<h1><strong>Job Title: Project Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>As a Project Engineer, you will manage technology or integration projects, successfully delivering solutions to meet project goals. You may work directly with external equipment vendors, customers, or partners, and must have a solid understanding of design approaches and industry technologies utilized in fulfillment and distribution center designs.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage technology or integration projects to ensure successful delivery of solutions.</li><li>Collaborate with external equipment vendors, customers, or partners.</li><li>Understand and apply design approaches and industry technologies in fulfillment and distribution center designs.</li><li>Coordinate project activities, including equipment installation and commissioning.</li><li>Oversee vendor management and project coordination.</li><li>Handle project budgets ranging from $0.5 million to $50 million.</li><li>Provide technical leadership for large-scale industrial engineering projects.</li><li>Design and implement integrated automation solutions, including complex material handling systems, high-speed packaging lines, and manufacturing lines.</li></ul><h2>Essential Skills</h2><ul><li>Vendor management</li><li>Conveyor belt systems</li><li>Project management</li><li>Equipment installation</li><li>CAD software proficiency</li><li>Engineering</li><li>Project coordination</li><li>Facilities management</li><li>Material-handling equipment expertise</li><li>Distribution center knowledge</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Engineering Operations, Business Administration, or a related field.</li><li>4+ years of experience as a project engineer, process engineer, project manager, manufacturing engineer, or related occupation.</li><li>Direct management of cumulative automation project budgets ranging from $0.5 million to $50 million.</li><li>Proven technical leadership for large-scale industrial engineering projects.</li><li>Experience with integrated automation solutions, such as complex material handling systems and high-speed packaging lines.</li><li>Proficiency in Microsoft Office products: Excel, Project, and Outlook.</li><li>Highly proficient CAD skills with the capability to independently develop an integrated automation layout.</li><li>Ability to travel up to 75% of the time to installation sites throughout North America.</li></ul><h2>Work Environment</h2><p>This role offers an excellent opportunity to travel to multiple states and build a substantial internal network. You will work with various internal vendors, developing project management skills and experience across multiple disciplines. The work involves frequent travel, with up to 90% of the time spent traveling to installation sites throughout the United States. Typically, travel involves flying out Monday morning, staying at the site all week, and returning home Friday afternoon. It is rare, but some may choose to stay over the weekend.Tra</p>

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Traveling - Project Manager

Traveling - Project Manager/Engineer

<p><strong>[Job Description]</strong></p><p><br></p><p>Globally recognized eCommerce company based in Seattle, WA is currently hiring for a Traveling Conveyor System Project Engineer. These Engineers are responsible for the completion of the project/program. Oversees all aspects of projects. Sets deadlines, assigns responsibilities, and monitors and summarizes progress of project/program. Prepares reports for upper management regarding status of the project/program.</p><p><br></p><p>The Project Engineer is mainly responsible for traveling to various warehouse facilities to support the project of retrofitting or replacing the old conveyor belt system. The Project Engineer will not be responsible for the hands-on work, but be the main point of contact as a project manager to work with various vendors in bring them into the warehouse facilities to conduct these replacements and installations.</p><p><br></p><p><br></p><p><strong>Pay - $65/hr. (Set final pay, no room for negotiation)</strong></p><p><strong>Contract Duration - 5 Months To Start</strong></p><p><strong>Location - NC, DC, MD, VA, NJ, or NYC local candidates</strong></p><p><strong>Travel Requirement - 80% - 100% (travel compensated)</strong></p><p><br></p><p><br></p><p><strong>[Responsibilities]</strong></p><p><br></p><ul><li>Will be responsible for generating leads for untapped territories using 3rd party and outside resources.</li><li>Engage in the agricultural package manufacturing machinery selling to manufacturing companies and offer solutions for machine add-ons.</li><li>Travel to untapped territories to establish in-person meetings and sell-over opportunities.</li></ul><p><strong>[Key Projects]</strong></p><p><br></p><ul><li>Will be travelling to various warehouses and retrofit/update old conveyor belts to new modern ones (focused on automation and MHE equipment).</li><li>Will utilize engineering knowledge to partner with other vendors who will come out to the facilities and perform duties (project management experience).</li></ul><p><br></p><p><strong>[Qualification Requirements]</strong></p><p><br></p><ul><li>3-5 years of experience within engineering industry.</li><li>3-5 years of project management experience.</li><li>Bachelors Degree (in Engineering preferred).</li><li>Comfortability travelling 80%-100% to work site locations.</li><li>Must have automation experience and conveyor belts/systems experience.</li><li>Experience / comfortability working with 3<sup>rd </sup>party vendors.</li></ul>

Traveling Conveyor System Project Engineer

<h1><strong>Job Title: Field Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Project/Field Engineer will be a part of the industrial group, traveling to various complex industrial projects across the country. Project durations will range from 3 weeks to 18 months on-site, with scheduled visits home.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform analysis of construction methods, including crane reaches, formwork design, erosion control, and grading modifications.</li><li>Produce miscellaneous sketches and drawings to show field conditions to the architect, clarify plan details for craft persons, and propose alternate details.</li><li>Verify quality and compliance of installation with specifications and drawings for all work.</li><li>Process and expedite answers to RFIs generated from the field, ensuring correct incorporation of answers.</li><li>Participate in and contribute to Operation Planning Process and weekly coordination meetings, superintendent meetings, daily crew huddles, and foreman meetings.</li><li>Schedule and conduct pre-installation meetings for any subcontractor with on-site labor. Prepare meeting agendas and ensure attendance by all parties.</li><li>Prepare and monitor written delivery schedule logs. Inspect shipments of all deliveries as directed by the Superintendent.</li><li>Expedite project closeout by tracking and verifying completion of punch list items.</li></ul><h2>Essential Skills</h2><ul><li>Four-year engineering degree related to construction preferred.</li><li>1-4 years of experience as a Project Engineer on industrial projects preferred.</li><li>Excellent communication and interpersonal skills.</li><li>Valid Driver&#39;s License.</li><li>Willingness to travel.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with construction, RFIs, change orders, project engineering, project coordination, commercial construction, estimation, project scheduling, blueprints, construction management, project management, field engineering, general contracting, ground-up projects, and building systems.</li></ul><h2>Work Environment</h2><p>The position will report to the Madison, WI office but requires heavy travel. Engineers will spend a few weeks on-site followed by a few weeks back home. The work involves managing various industrial projects, predominantly upgrades to existing manufacturing food and beverage facilities. The role includes working alongside a superintendent and project manager, managing subcontractors. The company supports some solar work locally, though most projects are expansions and remodels. Typical work weeks are 40-50 hours, with mileage reimbursement, housing or per diem offered depending on project specifics. The health plan varies by location, with Milwaukee Network Health coverage in Milwaukee.</p>

Traveling Project Engineer

<p style="text-align: center;"><strong style="font-size: 22px;">Traveling Quality Control Manager</strong></p><p><strong>Description:</strong></p><p>Are you passionate about ensuring the highest standards of quality in construction projects? Join our dynamic team as a Travelling Quality Control Manager, where you&#39;ll play a pivotal role in the comprehensive development, implementation, and management of Project Quality Control requirements. This position is crucial for the safe, high-quality, and timely delivery of our projects.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Quality Control Planning: Develop and oversee the approval process for the Project Quality Control Plan (QCP) and Inspection and Testing Plan (ITP).</li><li>Resource Coordination: Collaborate with the Project Manager to ensure adequate quality control personnel and necessary equipment, including testing tools and site laboratories, are available for project execution.</li><li>Client Collaboration: Coordinate with Client Quality Assurance personnel to execute and inspect the works.</li><li>Third Party Management: Manage Third Party Testing Agencies, including coordinating testing activities, utilizing on-site personnel, and reviewing related reports and commercial documents.</li><li>Safety Compliance: Ensure that site staff and subcontractors adhere to current safety legislation and company procedures, promoting Health, Safety, and Welfare as core values.</li><li>Training and Briefing: Brief site staff and subcontractors on QCP and ITP requirements and ensure compliance, including the preparation of testing reports.</li><li>Material and Process Review: Review all material and work process submissions before client approval. Conduct inspections of off-site subcontractor and supplier facilities if necessary to meet project requirements.</li><li>Documentation: Prepare and review quality control documentation, such as Client QC Daily Reports, Monthly QC Reports, and Logs.</li><li>Three Phase Control: Implement the Three Phase Stage of Control for work activities: Preparatory, Initial, and Follow-up.</li><li>Specification Compliance: Understand Specification and Contract requirements to ensure work is executed to the correct standards.</li><li>Decision Making: Make key decisions independently while keeping the Project Manager and Upper Management Team informed and aligned with company procedures and Delegation of Authority (DLA).</li><li>Task Delegation: Delegate tasks appropriately and promote independence, decision-making, and accountability within the project team.</li><li>Communication: Communicate key issues to the Project Manager and Upper Management Team.</li><li>Meetings: Attend daily and weekly internal briefings and progress meetings.</li></ul><p><strong>Skills:</strong></p><ul><li>Quality control</li><li>OSHA 30</li><li>Construction</li><li>USACE</li><li>QCM</li><li>CQM</li></ul><p><strong>Top Skills Details:</strong></p><ul><li>Quality control</li></ul><p><strong>Additional Skills &amp; Qualifications:</strong></p><ul><li>QCM certification is ideal, but can be obtained after hiring.</li></ul><p><strong>Experience Level:</strong></p><ul><li>Expert Level</li></ul>

Traveling Quality Control Manager

<h1 style="font-weight: 700;">Job Title: Traveling Superintendent</h1><br><h2>Job Description</h2><p>This position will be supporting a 2-year multi-family project in Philadelphia, PA. Interested candidates will need to travel to Columbus, OH to work and train with the company before <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">beginning</span></span> on the project in Philadelphia in the fall.</p><br><h2>Responsibilities</h2><ul><li>Professionally represent the company and effectively support company strategic initiatives.</li><li>Demonstrate strong knowledge of commercial construction and exceptional jobsite management skills; deliver on key projects and commitments via professional knowledge and leadership abilities.</li><li>Develop and maintain positive long-term relationships with subcontractors and business partners.</li><li>Possess detailed process and application knowledge relating to building codes, budget management, construction practices, project scheduling, etc.</li><li>Ensure on-time delivery while maintaining team focus on safety, quality, and budget.</li><li>Fully understand and effectively utilize drawings, specifications, subcontract agreements, and purchase orders.</li><li>Assist the Project Manager with material delivery schedules and effectively manage the change management process.</li><li>Assume primary responsibility for leading, implementing, and enforcing jobsite safety requirements and the company&#39;s Quality Assurance Program.</li><li>Lead and/or assist with job set-up, communications, safety compliance, record-keeping, quality control, and closeout as needed.</li></ul><h2>Essential Skills</h2><ul><li>Strong knowledge of commercial construction</li><li>Exceptional jobsite management skills</li><li>Ability to develop and maintain long-term relationships with subcontractors and business partners</li><li>Detailed process and application knowledge relating to building codes, budget management, construction practices, and project scheduling</li><li>Proficiency in utilizing drawings, specifications, subcontract agreements, and purchase orders</li><li>Experience in leading and enforcing jobsite safety requirements and quality assurance programs</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Construction Management (or related field) desired but not required</li><li>4+ years of commercial construction experience as a Superintendent</li><li>Experience in multi-family construction is desired but not required</li></ul><h2>Work Environment</h2><p>100% on a job site, working out of a construction trailer. The company offers opportunities to work on exciting multi-family related projects, with potential to move around and experience new types of projects. Recognized as a top workplace and a leading commercial contractor.</p><br>

Traveling Superintendent

<h2>Job Description</h2><p>This position will be supporting a 2-year multi-family project in Philadelphia, PA. Interested candidates will need to travel to Columbus, OH to work and train with the company prior to starting on the project in Philadelphia in the fall.</p><p><br></p><h2>Responsibilities</h2><ul><li>Professionally represent the company and effectively support company strategic initiatives.</li><li>Demonstrate strong knowledge of commercial construction and exceptional jobsite management skills; deliver on key projects and commitments via professional knowledge and leadership abilities.</li><li>Develop and maintain positive long-term relationships with subcontractors and business partners.</li><li>Possess detailed process and application knowledge relating to building codes, budget management, construction practices, project scheduling, etc.</li><li>Ensure on-time delivery while maintaining team focus on safety, quality, and budget.</li><li>Fully understand and effectively utilize drawings, specifications, subcontract agreements, and purchase orders.</li><li>Assist the Project Manager with material delivery schedules and effectively manage the change management process.</li><li>Assume primary responsibility for leading, implementing, and enforcing jobsite safety requirements and the company&#39;s Quality Assurance Program.</li><li>Lead and/or assist with job set-up, communications, safety compliance, record-keeping, quality control, and closeout as needed.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Construction Management (or related field) desired but not required</li><li>4+ years of commercial construction experience as a Superintendent</li><li>Experience in ground up multi-family construction is preferred. Will consider high rise, Sr. Living, Hotel project experience</li></ul><h2>Recruiter: Eisen Hardy - &#39;ehardy@actalentservices.com&#39;</h2>

Traveling Superintendent - Multifamily

<h1><strong>Hiring a Licensed Practical Nurse in CT! </strong></h1><h2>Job Description</h2><p>We are seeking a dedicated and compassionate Licensed Practical Nurse to join our team. The ideal candidate will be responsible for triaging calls, prepping rooms, and scheduling follow-up appointments, ensuring a smooth and efficient patient care experience.</p><p><br></p><h2>Responsibilities</h2><ul><li>Triaging patient calls</li><li>Prepping rooms for patient visits</li><li>Scheduling follow-up appointments</li><li>Maintaining accurate medical documentation</li><li>Updating and managing medical records</li></ul><h2>Essential Skills</h2><ul><li>Triage</li><li>Medical documentation</li><li>Medical record management</li><li>Good personality</li><li>Strong work ethic</li><li>Proficiency in Epic</li><li>Healthcare experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Active LPN license in CT</li></ul><h2>Work Environment</h2><p>The position operates in a healthcare setting with a Monday to Friday schedule from 8am to 5pm, occasionally requiring work until 5:15pm. The environment is supportive and patient-focused, providing entry-level opportunities with training for individuals with the right attitude and work ethic.</p>

Triage Licensed Practical Nurse

<p style="text-align: center;"><em>﻿INTERESTED </em>CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR</p><p style="text-align: center;">TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW!</p><p style="text-align: center;"><br></p><p><u>Urgently hiring a Entry Level Sample Technician who will be working with lubricant samples. An ideal candidate will have a high school diploma or an Associates of Science degree with at least 6 months of shipping and/ or sample preparation experience.</u></p><p><br></p><h2>Job Description</h2><p>The Sample Technician is responsible for the intake, logging, preparation, and processing of samples, as well as maintaining the laboratory shipping area. This role ensures accurate sample management and efficient laboratory operations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Scan reports and log samples by typing in and matching product codes in the sample management systems.</li><li>Unbox samples, place them onto trays, and deliver them to the laboratory.</li><li>Measure and weigh samples.</li><li>Mix and batch samples.</li><li>Operate basic laboratory equipment to initiate tests.</li><li>Perform basic wet chemistry tasks.</li><li>Fill test tubes, place them on a hot tray, and de-gas samples</li><li>Maintain laboratory shipping area</li></ul><h2>Essential Skills</h2><ul><li>High school diploma or equivalent.</li><li>Experience with sample preparation or shipping is preferred.</li><li>Must be able to lift up to 50 pounds</li><li>BACHELOR DEGREE IS OVERQUALIFIED</li></ul><h2><strong>SHIFT: M-F 8AM-5PM</strong></h2>

URGENTLY HIRING: Sample Processor

URGENTLY HIRING: Sample Technician

<h1><strong>Job Title: Research Associate III - Scientific</strong></h1><p><br></p><h2>Job Description</h2><p>This role is onsite at our Round Lake facility and involves providing analytical and technical support for nitrosamines and impurities analysis. You will collaborate with subject matter experts and lead laboratory experiments.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct routine and non-routine nitrosamines and impurities evaluations using LC/MS/MS and associated wet chemistry and sample preparation techniques.</li><li>Perform chemical analyses, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE), to support nitrosamines studies.</li><li>Perform experiments for nitrosamines and EL analysis within specified timelines.</li><li>Operate, maintain, and troubleshoot MS instrumentation.</li><li>Participate in investigations related to atypical or out-of-specification/out-of-trend results.</li><li>Independently plan and execute method development activities utilizing LC/MS/MS.</li><li>Generate scientifically sound experimental data following protocols and SOPs.</li><li>Independently author and contribute to experimental protocols, summaries, and technical reports.</li><li>Document and review laboratory work using an electronic laboratory notebook, adhering to good documentation practices (GDP) and general good laboratory practices (GLP).</li><li>Follow Quality Manual, SOPs, and Environmental Health Safety Sustainability (EHSS) guidelines to ensure compliance and continuous improvement.</li><li>Provide support to maintain a compliant, safe, and clean working environment/laboratory.</li><li>Evaluate analytical results, identify trends, exceptions, and interpret results relative to product requirements and project goals.</li><li>Interpret analytical data and present it in a form suitable for a diverse audience.</li><li>Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences, sharing project status and seeking input.</li></ul><h2>Essential Skills</h2><ul><li>Extensive hands-on experience with mass spectrometry analysis, specifically MS/MS via HPLC or UHPLC with APCI or ESI ionization.</li><li>Experience with MassHunter is preferred.</li><li>Strong knowledge and experience in analytical chemistry and relevant laboratory skills.</li><li>Proficiency in wet chemical techniques and instrumental analysis.</li><li>Analytical problem-solving mindset with high learning agility.</li><li>Innovative experimental attitude with strong presentation skills.</li><li>Excellent written and verbal communication skills in English.</li><li>Ability to provide and accept critical feedback constructively.</li><li>Collaborative attitude with team members and cross-functional teams.</li><li>Objective assessment, organization, and clear communication of information.</li><li>Ability to plan and complete assigned work to meet project deliverables in a timely manner.</li><li>Proficiency in Microsoft Office applications: Excel, Word, Outlook.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>PhD with 0-3 years of experience, a master&#39;s with 3-5 years of experience, or a bachelor&#39;s with 5-7 years of experience in a chemistry-related field.</li><li>Experience in analytical or organic chemistry is preferred.</li></ul><h2>Work Environment</h2><p>This position is based onsite at our Round Lake facility, requiring daily in-person laboratory work. The environment is equipped with advanced LC/MS/MS instrumentation and requires adherence to strict safety and quality guidelines. The dress code is professional laboratory attire.</p>

USA - Research Associate Scientific III

<h1 style="font-weight: 700;">Job Title: UX Designer</h1><br><h2>Job Description</h2><p>We are seeking a skilled UX Designer to develop and refine user-centered experiences across digital touchpoints, including in-vehicle systems, mobile apps, and web. The UX Designer will work independently on design initiatives, leveraging research insights and industry best practices to create intuitive and user-friendly designs. This role involves collaboration with cross-functional teams to ensure alignment between business goals and user needs.</p><br><h2>Responsibilities</h2><ul><li>Support UX design efforts on mid-sized projects, ensuring consistency and usability across platforms.</li><li>Design and iterate on wireframes, prototypes, and interaction flows to communicate design intent.</li><li>Partner with UX researchers to analyze user data and translate findings into actionable design improvements.</li><li>Conduct experience audits, competitive/comparative analysis and confirm design proposals are meeting market expectations.</li><li>Develop and refine information architecture and user flows.</li><li>Participate in and occasionally lead design critiques and stakeholder reviews.</li><li>Advocate for best practices in usability, accessibility, and interaction design.</li><li>Work closely with product teams and developers to understand product goals, requirements, and constraints, ensuring design implementation meets standards.</li><li>Support UX strategy development and contribute to design system evolution.</li></ul><h2>Essential Skills</h2><ul><li>4+ years of UX design experience.</li><li>Proficiency in Figma.</li><li>Bachelor&#39;s degree in Design, HCI, or a related field OR equivalent experience.</li><li>Experience working within an Agile development process.</li><li>Strong ability to balance user needs with business objectives.</li><li>Excellent presentation and stakeholder communication skills.</li><li>Understanding of accessibility and usability principles.</li></ul><h2>Work Environment</h2><p>The position offers a small team environment, combining a mix of American team members and ADC. The role provides a long-term consultant-to-hire opportunity.</p><br>

UX Designer

<h1 style="font-weight: 700;">Job Title: Medical Assistant</h1><br><h2>Job Description</h2><p>Assist in the delivery of primary health care and patient care management in a fast-paced clinic environment. This role involves performing nursing and administrative duties, preparing patients for examinations and treatments, and ensuring all necessary instruments and supplies are ready and sterilized. You will also be responsible for taking patient vital signs, reviewing medications and allergies, entering information into the EMR system, and assisting physicians or PAs with medical procedures.</p><br><h2>Responsibilities</h2><ul><li>Assist in the delivery of primary health care and patient care management.</li><li>Perform nursing and administrative duties.</li><li>Prepare patients for examination and treatment.</li><li>Take patient vital signs, review medications and allergies, and enter all health questionnaire information into the EMR system (WebChart).</li><li>Prepare exam and treatment rooms with necessary instruments and supplies.</li><li>Help room patients.</li><li>Prepare and maintain supplies and equipment for treatments, including sterilization.</li><li>Assist physicians or PAs in preparing for medical procedures.</li><li>Verify all patients by DOB and full name.</li><li>Perform procedures and accompanying paperwork.</li><li>Promote office discharge process by scheduling requested testing, outside physician appointments, writing or entering required lab orders and prescriptions, and providing all information to patients with instructions or faxing orders/prescriptions to the appropriate facility or pharmacy.</li><li>Triage telephone calls for referral to physician or nurse practitioner.</li><li>Restock examination rooms weekly.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in taking patient vital signs.</li><li>Experience with patient care and insurance billing.</li><li>Certified Medical Assistant (CMA) credentials.</li><li>Ability to perform blood collection and phlebotomy.</li><li>Proficiency in using EMR systems (WebChart).</li><li>Excellent patient care/customer service skills.</li><li>Ability to work calmly and effectively in a busy or stressful situation.</li><li>Adherence to all policies for safety, attendance, punctuality, and personal appearance.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Completion of MA schooling.</li><li>MA certification in good standing (CMA, CCMA, RMA, AAMA, NHA, etc.).</li><li>Experience in rheumatology or internal medicine.</li><li>Experience in pediatrics.</li></ul><h2>Work Environment</h2><p>The hours for this role are from 8:00 AM to 5:30 PM, with the possibility of starting as early as 7:00 AM depending on patient lab needs. No weekend work is required. The primary location is in Greenwood, but occasional travel to Noblesville for coverage may be needed. A six-week training program is provided to ensure you are well-prepared for your responsibilities.</p><br>

Urgent Hiring For Medical Assistant At Greenwood, IN

<h1 style="text-align: center;"><br></h1><p style="text-align: center;"><br></p><h1 style="text-align: center;"><strong>Our client, a leading healthcare organization, is seeking a talented Certified Medical Assistant to join their team across Westchester!</strong></h1><p><br></p><h2>Job Description</h2><p>Monitor patient arrival and assist with patient flow, ensuring that patients and visitors are greeted promptly and courteously. Escort patients to exam rooms, monitor patient wait times, assist patients in preparing for exams, and advise physicians when patients are ready. Assist during examinations if required or requested. Obtain and record patients&#39; chief complaints, data, and histories, including vital signs, venipuncture, allergies, specimen collection, temperature, blood pressure, pulse, and respiration, documenting results within the scope of practice. Perform, prep, and assist with clinical and technical services as assigned. Prepare medical records, take heights, weights, and vital signs, and record them. Ensure lab and other reports are on records before each patient&#39;s appointment. Provide interpretation services and clerical support necessary for the efficient and effective functioning of the office. Maintain examination rooms and medical areas in a clean and orderly fashion. Stock examination rooms with supplies and check supplies from vendors against packing slips as assigned. Update pertinent patient information, including medical insurance coverage and eligibility, in the appropriate EMR system. Retrieve and file medical reports/lab results. Maintain knowledge of HIPPA rules to ensure patients&#39; health information is confidential.</p><p><br></p><h2>Responsibilities</h2><ul><li>Monitor patient arrival and assist with patient flow.</li><li>Greet patients and visitors promptly and courteously.</li><li>Escort patients to exam rooms and monitor wait times.</li><li>Assist patients in preparing for exams and advise physicians when patients are ready.</li><li>Assist during examinations if required or requested.</li><li>Obtain and record patients&#39; chief complaints, data, and histories.</li><li>Record vital signs, venipuncture, allergies, specimen collection, temperature, blood pressure, pulse, and respiration.</li><li>Document results in patients&#39; charts within the scope of practice.</li><li>Perform, prep, and assist with clinical and technical services as assigned.</li><li>Prepare medical records and take heights, weights, and vital signs.</li><li>Ensure lab and other reports are on records before each patient&#39;s appointment.</li><li>Provide interpretation services and clerical support.</li><li>Maintain examination rooms and medical areas in a clean and orderly fashion.</li><li>Stock examination rooms with supplies and check supplies from vendors against packing slips.</li><li>Update patient information, including medical insurance coverage and eligibility, in the EMR system.</li><li>Retrieve and file medical reports/lab results.</li><li>Maintain knowledge of HIPPA rules to ensure patient confidentiality.</li></ul><h2>Essential Skills</h2><ul><li>2+ years of MA experience</li><li>Certified Medical Assistant (CMA) or Registered Medical Assistant (RMA)</li><li>Basic Life Support (BLS) certification</li><li>Experience with vitals and EMR systems</li><li>Knowledge of cardiology and internal medicine</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with Epic EMR system</li><li>Strong patient care skills</li><li>Willingness to float to different offices if necessary</li></ul><h2>Work Environment</h2><p>This position is in a busy outpatient office environment with a schedule of Monday to Friday, 08:30 am – 05:00 pm. The office handles 50-100 patients a day. There are openings in three different offices: Scarsdale, Hawthorne, and Yonkers. The Scarsdale office, which is the busiest, has two openings and requires strong candidates. The Hawthorne office is located at 40 Saw Mill River Road, Hawthorne, NY (Cardiology office). The Scarsdale office is at 688 &amp; 696 White Plains Road, Scarsdale, NY (Cardiology &amp; Internal Medicine). The Yonkers office is at 1086 N Broadway STE 240, Yonkers, NY (Cardiology office).</p>

Urgent Hiring For Medical Assistant Paying Upto $22/hr

Urgent Hiring For Medical Assistant, Paying Upto $22/hr

<h1><strong>Job Title: Medical Assistant</strong></h1><p><br></p><h2>Job Description</h2><p>The role of a Clinical Medical Assistant is to provide care and education to patients, following established standards and practices. This position involves updating patient charts in EMR systems and documenting changes. The assistant coordinates with other members of the care team to ensure seamless care delivery, maximal coordination of efforts, and active patient participation in planning and care. Additionally, the assistant is responsible for restocking rooms.</p><p><br></p><h2>Responsibilities</h2><ul><li>Provide patient care and education following established standards and practices.</li><li>Update patient charts in electronic medical records (EMR) systems and document changes.</li><li>Coordinate with other members of the care team for seamless care delivery and maximal coordination of efforts.</li><li>Ensure active patient participation in planning and care.</li><li>Restock examination and treatment rooms.</li></ul><h2>Essential Skills</h2><ul><li>Medical assisting</li><li>Customer service</li><li>Knowledge of medical terminology</li><li>Experience with electronic medical records (EMR) systems, such as NextGen and Epic</li><li>Patient access and interaction skills</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent</li><li>At least one year of clinical experience in a medical office, clinic, or hospital setting, or graduation from an accredited medical assistant program</li><li>Demonstrated history of stable employment and/or favorable references</li></ul><h2>Work Environment</h2><p>The position operates Monday through Friday from 8:30 AM to 5:30 PM. </p><p>The dress code requires wearing scrubs. </p><p><br></p><p><strong>Company Benefits</strong></p><p><br></p><p>• Medical, dental &amp; vision</p><p>• Critical Illness, Accident, and Hospital</p><p>• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available</p><p>• Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)</p><p>• Short and long-term disability</p><p>• Health Spending Account (HSA)</p><p>• Transportation benefits</p><p>• Employee Assistance Program</p><p>• Time Off/Leave (PTO, Vacation or Sick Leave)</p>

Urgent Hiring For Medical Support Assistant, Paying Upto $22/hr

<h1 style="font-weight: 700;">Job Title: Engineering Project Manager</h1><br><h2>Job Description</h2><p>This position involves managing energy utility projects to ensure they adhere to budget, schedule, and scope. The role requires performing project management functions by creating and maintaining project budgets, schedules, and delivery expectations while evaluating and managing scope, risk, and profitability. Ensuring project safety and internal compliance through clear communication with customers, key stakeholders, and internal team members is paramount.</p><br><h2>Responsibilities</h2><ul><li>Partner with engineering and design production leadership teams to plan, execute, and review client-funded projects.</li><li>Communicate all relevant activities and action plans to key internal stakeholders while accepting feedback and direction from Program and Delivery Managers.</li><li>Develop and document project management plans that include project scope verification, schedules, timelines, milestones, budget estimates, cash flows, work breakdown structures, and resource requirements.</li><li>Lead process development and reporting advancements within the Operations team and drive continuous improvement for project management best practices.</li><li>Mentor and train project coordinators by directing coordination activities, providing constructive feedback, and observing performance.</li><li>Ensure compliance with best practices and guidelines. Provide input and feedback for project onboarding, funding, financial analysis, and status reporting for each project.</li><li>Develop timetables and priorities for the execution of all design and related field activities for assigned projects.</li><li>Coordinate various client and third-party contractor activities where necessary.</li><li>Ensure resource requirements are documented and accurately assigned to facilitate maximum efficient utilization and meaningful capacity planning.</li><li>Prepare regular financial and resource forecasts at the project and program level as required.</li><li>Evaluate executed contracts to ensure delivery and finance teams are informed and compliant with legal, ethical, and contractual requirements.</li><li>Ensure complete and timely project closeout including lessons-learned reviews to facilitate continuous improvement.</li><li>Travel to various Delivery Centers and customer site locations when necessary and appropriate.</li><li>Accept and deliver on various related tasks and duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Project tracking</li><li>Analysis</li><li>Status report</li><li>Project documentation</li><li>Multi-tasking</li><li>Project management</li><li>Project budgets</li><li>Scopes</li><li>Construction management</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s Degree in Engineering preferred</li><li>Four to twelve years of Project Manager/Engineering experience</li><li>Consulting experience preferred from services companies</li><li>Engineering <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span></span></span> preferred before entering Project Management</li></ul><h2>Work Environment</h2><p>The work environment is a quiet engineering office setting where teamwork is highly encouraged and happens frequently. The dress code is business casual.</p><br>

Utilities Engineering Project Manager

<p>We are seeking a <strong>Utilities Inspector</strong> to join our team for a significant rail tunnel project in the New York / New Jersey area. In this role, you will play a critical role in ensuring the successful relocation, installation, and protection of essential utility infrastructure during the construction process. This role involves inspecting, monitoring, and documenting utility-related construction activities, ensuring compliance with project specifications, safety standards, and local regulations.</p><p><br></p><p><strong>Key Responsibilities:</strong></p><ul><li>Inspect utility work, including the relocation, installation, and protection of water, sewer, gas, electric, and telecommunications infrastructure.</li><li>Ensure utility construction activities comply with approved plans, specifications, contracts, and applicable codes.</li><li>Monitor construction progress to ensure adherence to project schedules.</li><li>Identify and document deficiencies, and recommend corrective actions as needed.</li><li>Serve as a point of contact between contractors, utility companies, and project management.</li><li>Coordinate with utility owners and agencies to minimize disruptions and resolve conflicts in a timely manner.</li><li>Provide updates on utility work progress and issues to the project team.</li><li>Maintain accurate daily inspection logs, photos, and reports detailing work performed, issues encountered, and resolutions.</li><li>Assist in reviewing contractor submittals, RFIs, and change order requests related to utility work.</li></ul><p><strong>Required Qualifications:</strong></p><ul><li>Bachelor’s degree in Civil Engineering, Construction Management, or similar related work experience.</li><li>Minimum of 10 years of experience in utility inspection, utility construction, or related infrastructure projects.</li></ul><p><strong>Key Skills and Abilities:</strong></p><ul><li>Strong understanding of utility systems (water, sewer, gas, electric, telecommunications).</li><li>Familiarity with excavation, trenching, and underground utility installation standards and best practices.</li><li>Knowledge of utility relocation processes and coordination with utility owners.</li><li>Familiarity with local, state, and federal regulations related to utility construction (e.g., OSHA, NJDEP, and local codes).</li><li>Excellent attention to detail and ability to identify and document non-conformance issues.</li><li>Strong interpersonal and communication skills for effective coordination with contractors, utility companies, and project stakeholders.</li></ul><p><strong>Preferred Qualifications:</strong></p><ul><li>Certification as a Construction Inspector (e.g., NICET or ICC certification).</li><li>Experience working in rail, tunnel, or other heavy civil infrastructure environments.</li><li>Familiarity with New Jersey utility providers and permitting processes.</li><li>Experience managing union electrical contractors or any prior experience dealing with utility companies (like PSE&amp;G or Con Edison) would be a bonus.</li></ul><p><br></p>

Utilities Inspector

<h1><strong>Job Title: Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Utility Inspector to oversee the replacement of lead service lines with copper ones. This role involves inspecting water mains and various structures such as roads, dams, and bridges to ensure structural soundness, safety, and compliance with regulations. You will document inspection results, monitor progress, and contribute to construction and project status reports. You will also oversee and coordinate construction-related services and conduct on-site investigations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect water mains and other structures to ensure structural soundness, safety, and compliance with codes and regulations.</li><li>Document inspection results, including structural conditions and deficiencies between design and execution.</li><li>Monitor progress and contribute to construction reports and project status updates.</li><li>Oversee and coordinate construction-related services on projects.</li><li>Conduct on-site investigations and review relevant data including maps, reports, tests, and drawings.</li><li>Ensure compliance with guidelines and regulations, including permits and safety requirements.</li><li>Deliver technical files and documentation as required.</li></ul><h2>Essential Skills</h2><ul><li>OSHA 10 certification</li><li>Strong communication skills, with the ability to interact with clients daily.</li><li>Bilingual in Spanish.</li><li>1+ years of construction experience.</li><li>Bachelor&#39;s degree in Civil Engineering.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma.</li><li>Ability to pass a federal <span style="color: rgb(8, 7, 7); background-color: none;">background</span> check.</li><li>Technical proficiency and design application knowledge.</li><li>Understanding of the construction process for large commercial, municipal, or federal projects.</li><li>Strong organizational skills.</li><li>Excellent attention to detail.</li><li>Comfortable using computers, tablets, and phones.</li><li>Strong writing and oral communication skills.</li><li>Good interpersonal skills for relationship cultivation.</li></ul><h2>Work Environment</h2><p>The role involves canvassing and surveying areas in North/Central NJ, particularly between Edison NJ and Newark. You will use a mobile app on a tablet to conduct inspections and take photos. The position requires a personal vehicle, with mileage reimbursement available, and offers opportunities for overtime pay. Benefits include an employee discount program, 401k, and medical/dental/vision insurance.</p>

Utility Inspector

<h1><strong>Job Title: Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Utility Inspector to oversee the replacement of lead service lines with copper ones. This role involves inspecting water mains and various structures such as roads, dams, and bridges to ensure structural soundness, safety, and compliance with regulations. You will document inspection results, monitor progress, and contribute to construction and project status reports. You will also oversee and coordinate construction-related services and conduct on-site investigations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect water mains and other structures to ensure structural soundness, safety, and compliance with codes and regulations.</li><li>Document inspection results, including structural conditions and deficiencies between design and execution.</li><li>Monitor progress and contribute to construction reports and project status updates.</li><li>Oversee and coordinate construction-related services on projects.</li><li>Conduct on-site investigations and review relevant data including maps, reports, tests, and drawings.</li><li>Ensure compliance with guidelines and regulations, including permits and safety requirements.</li><li>Deliver technical files and documentation as required.</li></ul><h2>Essential Skills</h2><ul><li>OSHA 10 certification</li><li>Strong communication skills, with the ability to interact with clients daily.</li><li>Bilingual in Spanish.</li><li>1+ years of construction experience.</li><li>Bachelor&#39;s degree in Civil Engineering.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma.</li><li>Ability to pass a federal <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span> check.</li><li>Technical proficiency and design application knowledge.</li><li>Understanding of the construction process for large commercial, municipal, or federal projects.</li><li>Strong organizational skills.</li><li>Excellent attention to detail.</li><li>Comfortable using computers, tablets, and phones.</li><li>Strong writing and oral communication skills.</li><li>Good interpersonal skills for relationship cultivation.</li></ul><h2>Work Environment</h2><p>The role involves canvassing and surveying areas in North/Central NJ, particularly between Edison NJ and Newark. You will use a mobile app on a tablet to conduct inspections and take photos. The position requires a personal vehicle, with mileage reimbursement available, and offers opportunities for overtime pay. Benefits include an employee discount program, 401k, and medical/dental/vision insurance.</p>

<h1><strong>Job Title: Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Utility Inspector to join our team in replacing lead service lines with copper ones. The role involves inspecting water mains and other structures to ensure structural soundness, safety, and compliance with codes and regulations. This is a fantastic opportunity to contribute to significant infrastructure projects and work with prestigious clients in the environmental and construction industry.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect water mains and other structures such as roads, dams, and bridges.</li><li>Document inspection results, including deterioration, structural condition, and compliance with design and regulations.</li><li>Monitor progress and contribute to construction and project status reports.</li><li>Oversee and coordinate construction-related services on projects.</li><li>Conduct on-site investigations and review relevant data such as maps, reports, tests, and drawings.</li><li>Comply with guidelines and regulations including permits and safety requirements.</li><li>Deliver technical files and other required documentation.</li></ul><h2>Essential Skills</h2><ul><li>OSHA 10 certification</li><li>Strong communication skills for daily interactions with clients and property owners</li><li>1+ years of construction experience</li><li>Experience in excavation, site development, and construction inspection</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma</li><li>5 years of relevant construction experience</li><li>Ability to pass a federal BG Check</li><li>Technical proficiency and design application knowledge</li><li>Understanding of the construction process for large commercial, municipal, or federal projects</li><li>Strong organizational skills</li><li>Attention to detail</li><li>Proficiency with computers, tablets, and phones</li><li>Strong writing and oral communication skills</li><li>Good interpersonal skills</li></ul><h2>Work Environment</h2><p>The role involves canvassing and surveying various project sites, including areas between Edison, NJ and Newark, NJ. Inspectors will use a mobile app on a tablet for guidance and documentation, including taking photos of inspected pipes. Work hours are 8:30 AM to 5:30 PM with opportunities for overtime pay. The position requires a vehicle, and mileage will be reimbursed. Benefits include an employee discount program, 401k, medical, dental, and vision insurance.</p>

<h1><strong>Job Title: Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Utility Inspector to oversee the replacement of lead service lines with copper ones. This role involves inspecting water mains and various structures such as roads, dams, and bridges to ensure structural soundness, safety, and compliance with regulations. You will document inspection results, monitor progress, and contribute to construction and project status reports. You will also oversee and coordinate construction-related services and conduct on-site investigations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect water mains and other structures to ensure structural soundness, safety, and compliance with codes and regulations.</li><li>Document inspection results, including structural conditions and deficiencies between design and execution.</li><li>Monitor progress and contribute to construction reports and project status updates.</li><li>Oversee and coordinate construction-related services on projects.</li><li>Conduct on-site investigations and review relevant data including maps, reports, tests, and drawings.</li><li>Ensure compliance with guidelines and regulations, including permits and safety requirements.</li><li>Deliver technical files and documentation as required.</li></ul><h2>Essential Skills</h2><ul><li>OSHA 10 certification</li><li>Strong communication skills, with the ability to interact with clients daily.</li><li>Bilingual in Spanish.</li><li>1+ years of construction experience.</li><li>Bachelor&#39;s degree in Civil Engineering.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma.</li><li>5 years of relevant construction experience.</li><li>Ability to pass a federal <span style="color: rgb(8, 7, 7); background-color: none;">background</span> check.</li><li>Technical proficiency and design application knowledge.</li><li>Understanding of the construction process for large commercial, municipal, or federal projects.</li><li>Strong organizational skills.</li><li>Excellent attention to detail.</li><li>Comfortable using computers, tablets, and phones.</li><li>Strong writing and oral communication skills.</li><li>Good interpersonal skills for relationship cultivation.</li></ul><h2>Work Environment</h2><p>The role involves canvassing and surveying areas in North/Central NJ, particularly between Edison NJ and Newark. You will use a mobile app on a tablet to conduct inspections and take photos. The position requires a personal vehicle, with mileage reimbursement available, and offers opportunities for overtime pay. Standard working hours are from 8:30 am to 5:30 pm. Benefits include an employee discount program, 401k, and medical/dental/vision insurance.</p>

<h1><strong>Job Title: Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Utility Inspector to oversee the replacement of lead service lines with copper ones. This role involves inspecting water mains and various structures such as roads, dams, and bridges to ensure structural soundness, safety, and compliance with regulations. You will document inspection results, monitor progress, and contribute to construction and project status reports. You will also oversee and coordinate construction-related services and conduct on-site investigations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect water mains and other structures to ensure structural soundness, safety, and compliance with codes and regulations.</li><li>Document inspection results, including structural conditions and deficiencies between design and execution.</li><li>Monitor progress and contribute to construction reports and project status updates.</li><li>Oversee and coordinate construction-related services on projects.</li><li>Conduct on-site investigations and review relevant data including maps, reports, tests, and drawings.</li><li>Ensure compliance with guidelines and regulations, including permits and safety requirements.</li><li>Deliver technical files and documentation as required.</li></ul><h2>Essential Skills</h2><ul><li>OSHA 10 certification</li><li>Strong communication skills, with the ability to interact with clients daily.</li><li>Bilingual in Spanish.</li><li>1+ years of construction experience.</li><li>Bachelor&#39;s degree in Civil Engineering.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma.</li><li>Ability to pass a federal <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> check.</li><li>Technical proficiency and design application knowledge.</li><li>Understanding of the construction process for large commercial, municipal, or federal projects.</li><li>Strong organizational skills.</li><li>Excellent attention to detail.</li><li>Comfortable using computers, tablets, and phones.</li><li>Strong writing and oral communication skills.</li><li>Good interpersonal skills for relationship cultivation.</li></ul><h2>Work Environment</h2><p>The role involves canvassing and surveying areas in North/Central NJ, particularly between Edison NJ and Newark. You will use a mobile app on a tablet to conduct inspections and take photos. The position requires a personal vehicle, with mileage reimbursement available, and offers opportunities for overtime pay. Benefits include an employee discount program, 401k, and medical/dental/vision insurance.</p>

<h1><strong>Job Title: Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Utility Inspector to oversee the replacement of lead service lines with copper ones. This role involves inspecting water mains and various structures such as roads, dams, and bridges to ensure structural soundness, safety, and compliance with regulations. You will document inspection results, monitor progress, and contribute to construction and project status reports. You will also oversee and coordinate construction-related services and conduct on-site investigations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect water mains and other structures to ensure structural soundness, safety, and compliance with codes and regulations.</li><li>Document inspection results, including structural conditions and deficiencies between design and execution.</li><li>Monitor progress and contribute to construction reports and project status updates.</li><li>Oversee and coordinate construction-related services on projects.</li><li>Conduct on-site investigations and review relevant data including maps, reports, tests, and drawings.</li><li>Ensure compliance with guidelines and regulations, including permits and safety requirements.</li><li>Deliver technical files and documentation as required.</li></ul><h2>Essential Skills</h2><ul><li>OSHA 10 certification</li><li>Strong communication skills, with the ability to interact with clients daily.</li><li>Bilingual in Spanish.</li><li>1+ years of construction experience.</li><li>Bachelor&#39;s degree in Civil Engineering.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma.</li><li>Ability to pass a federal <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span></span> check.</li><li>Technical proficiency and design application knowledge.</li><li>Understanding of the construction process for large commercial, municipal, or federal projects.</li><li>Strong organizational skills.</li><li>Excellent attention to detail.</li><li>Comfortable using computers, tablets, and phones.</li><li>Strong writing and oral communication skills.</li><li>Good interpersonal skills for relationship cultivation.</li></ul><h2>Work Environment</h2><p>The role involves canvassing and surveying areas in North/Central NJ, particularly between Edison NJ and Newark. You will use a mobile app on a tablet to conduct inspections and take photos. The position requires a personal vehicle, with mileage reimbursement available, and offers opportunities for overtime pay. Benefits include an employee discount program, 401k, and medical/dental/vision insurance.</p>

<h1><strong>Job Title: Civil/Utility Inspector</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced Utility Inspector to oversee the relocation, installation, and protection of water, sewer, gas, electric, and telecommunications infrastructure. The Inspector will ensure compliance with plans, specifications, contracts, and codes while monitoring construction progress and adherence to schedules. This role requires identifying deficiencies, recommending corrective actions, and acting as a liaison between contractors, utility companies, and project management. The position also involves coordinating with utility owners/agencies to minimize disruptions and resolve conflicts, updating the project team on utility work progress and issues, maintaining daily inspection logs, photos, and reports, and reviewing contractor submittals, RFIs, and change order requests.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect relocation, installation, and protection of water, sewer, gas, electric, and telecommunications infrastructure.</li><li>Ensure compliance with plans, specifications, contracts, and codes.</li><li>Monitor construction progress and adherence to schedules.</li><li>Identify deficiencies and recommend corrective actions.</li><li>Act as a liaison between contractors, utility companies, and project management.</li><li>Coordinate with utility owners/agencies to minimize disruptions and resolve conflicts.</li><li>Update the project team on utility work progress and issues.</li><li>Maintain daily inspection logs, photos, and reports.</li><li>Review contractor submittals, RFIs, and change order requests.</li></ul><h2>Essential Skills</h2><ul><li>Inspection experience in civil infrastructure projects.</li><li>Knowledge of excavation, trenching, and underground systems installation.</li><li>Understanding of Utilities such as water, sewer, gas, and electric systems.</li><li>Bachelor&#39;s Degree in Civil Engineering, Construction Management, or a similar field.</li><li>Minimum 10 years of experience in rail, tunnel, roadway, or other heavy civil infrastructure projects.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>NICET or ICC certification.</li><li>Experience working with PSEG or ConEd.</li></ul><h2>Work Environment</h2><p>This role involves working on a multi-billion dollar infrastructure project, requiring five days on site. The successful candidate will join a team of inspectors, Resident Engineers, Construction Managers, Field Engineers, and more. The position involves monitoring, inspecting, and documenting utility-related construction activities.</p>

<h1><strong>Currently Hiring - Utilities Inspector for exciting project with TOP Engineering company!!</strong></h1><p><br></p><h2>Job Description</h2><p>The Inspector will be responsible for overseeing the relocation, installation, and protection of water, sewer, gas, electric, and telecommunications infrastructure. The role ensures compliance with plans, specifications, contracts, and codes, while monitoring construction progress and adherence to schedules.</p><p><br></p><h2>Responsibilities</h2><ul><li>Inspect the relocation, installation, and protection of water, sewer, gas, electric, and telecommunications infrastructure.</li><li>Ensure compliance with plans, specifications, contracts, and codes.</li><li>Monitor construction progress and adherence to schedules.</li><li>Identify deficiencies and recommend corrective actions.</li><li>Act as a liaison between contractors, utility companies, and project management.</li><li>Coordinate with utility owners/agencies to minimize disruptions and resolve conflicts.</li><li>Update the project team on utility work progress and issues.</li><li>Maintain daily inspection logs, photos, and reports.</li><li>Review contractor submittals, RFIs, and change order requests.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Civil Engineering, Construction Management, or similar.</li><li>Minimum 10 years of experience in rail, tunnel, roadway, or other heavy civil infrastructure projects.</li><li>Strong understanding of water, sewer, gas, and electric systems.</li><li>Experience with excavation, trenching, and underground systems installation.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>NICET certification or ICC certification.</li><li>Experience working with PSEG or CONED.</li></ul><h2>Work Environment</h2><p>This position is part of a multi-billion dollar infrastructure project, requiring work 5 days on-site. You will collaborate with a team of inspectors, Resident Engineers, Construction Managers, and Field Engineers, focusing on monitoring, inspecting, and documenting utility-related construction activities. The role offers opportunities for growth within the company, 20 days of PTO, 9 holidays, and a competitive retirement savings plan with employer match. Additional benefits include exclusive discounts and special offers for theme parks, shows, sporting events, and more.</p>

<h1><strong>Job Title: Laser Scanning Technician</strong></h1><p><br></p><h2>Job Description</h2><p>Work with project managers, clients, and other project stakeholders to plan scan operations. Travel to client sites throughout the USA and beyond to perform scanning and photogrammetry services (up to 50% travel). Utilize Trimble laser scanner to capture existing site data on primarily industrial sites. Process scan data utilizing Trimble Realworks to ensure accuracy and produce files for integration into project models and viewing platforms. Support drone scanning and photogrammetry services. Coordinate scan-to-BIM modeling based on cloud data. Maintain scanning equipment. Support BIM team with model coordination and initiatives. Quickly learn new tools and disseminate knowledge to others.</p><p><br></p><h2>Responsibilities</h2><ul><li>Plan scan operations with project managers, clients, and stakeholders.</li><li>Travel nationwide and beyond to perform scanning and photogrammetry services.</li><li>Utilize Trimble laser scanner to capture existing site data on industrial sites.</li><li>Process scan data using Trimble Realworks for accuracy and integration.</li><li>Support drone scanning and photogrammetry services.</li><li>Coordinate scan-to-BIM modeling based on cloud data.</li><li>Maintain scanning equipment.</li><li>Assist the BIM team with model coordination and initiatives.</li><li>Learn new tools quickly and share knowledge with the team.</li></ul><h2>Essential Skills</h2><ul><li>Experience with Trimble.</li><li>Experience with Revit, AutoCAD, or Navisworks.</li><li>Associate&#39;s degree in architecture or related field.</li></ul><h2><br></h2>

VDC/Bim Technician

<h1><strong>Job Title: Validation Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Validation Engineer is responsible for ensuring the accuracy, reliability, and compliance of inspection methods used in the manufacturing of medical devices. This role focuses on validating automated inspection programs in accordance with FDA, ISO, and ICH guidelines. The ideal candidate will have experience with automated inspection systems, including those integrated into Coordinate Measuring Machines (CMMs) and other measuring systems. Strong technical writing skills are essential for developing validation protocols, test scripts, and reports.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and execute validation protocols (IQ, OQ, PQ) for inspection methods, ensuring compliance with FDA, ISO, and ICH guidelines.</li><li>Validate inspection programs for automated optical inspection systems, including CMMs and other measuring systems.</li><li>Conduct risk assessments and define validation acceptance criteria based on statistical analysis and industry best practices.</li><li>Collaborate with Quality, Engineering, and Manufacturing teams to ensure inspection methods meet product and regulatory requirements.</li><li>Analyze and document validation results, authoring comprehensive reports and justifications for validation conclusions.</li><li>Maintain validation documentation to support audits and regulatory submissions.</li><li>Investigate validation-related nonconformances and recommend corrective actions as needed.</li><li>Stay up to date with industry regulations and best practices for validation of automated inspection systems.</li></ul><h2>Essential Skills</h2><ul><li>Engineering Degree</li><li>5+ years of validation experience</li><li>Experience with IQ/OQ/PQ</li><li>Test Method Validation</li><li>Technical Writing</li><li>Familiarity with FDA, ISO, and ICH guidelines</li><li>Proficiency in Minitab</li><li>Quality Inspection experience</li></ul><h2>Apply to learn more!</h2>

Validation (TMV) Engineer

<p>Job Title: Quality Engineer/Validation Engineer</p><p>Location: Irvine, CA</p><p>Job Family Group: Quality Assurance</p><p>Job Family: Quality Engineering</p><h3>Job Summary</h3><p>We are seeking a highly skilled and experienced Quality Engineer/Validation Engineer to join our team. In this role, you will be responsible for ensuring that our products and processes meet the highest standards of quality and regulatory compliance. You will play a critical role in validating equipment, processes, and systems, with a specific focus on utilizing ValGenesis for electronic validation management.</p><h3>Key Responsibilities</h3><ul><li>Validation Management: Utilize ValGenesis for managing and executing validation protocols, ensuring compliance with regulatory standards.</li><li>Quality Assurance Integration: Collaborate with product development and manufacturing teams to integrate quality standards into all processes.</li><li>Document Review and Approval: Review and approve validation-related documents and plans to ensure conformance with quality system requirements.</li><li>Risk Assessments: Conduct risk assessments and failure mode effects analysis (FMEA) for new and existing products.</li><li>Quality Control Methods: Develop and implement quality control methods, procedures, and performance metrics for product design and manufacturing.</li><li>Problem Solving: Lead problem-solving and improvement activities to address quality issues and reduce product and process nonconformities.</li><li>Process Audits: Conduct audits of design and manufacturing processes to ensure compliance with quality system requirements and identify opportunities for improvement.</li><li>Data Analysis: Compile and analyze statistical data to identify and prioritize areas for quality improvement.</li><li>Reporting: Prepare and present reports on product and process quality to management and customers.</li><li>Training and Mentoring: Train and mentor staff on quality system requirements, quality tools, and best practices.</li></ul><h3>Qualifications</h3><ul><li>Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field.</li><li>Experience: 1-3 years of experience in quality assurance or validation engineering.</li><li>Skills:<ul><li>Proficiency in using ValGenesis for electronic validation management.</li><li>Strong knowledge of validation principles and practices.</li><li>Thorough understanding of quality assurance methodologies.</li><li>Familiarity with product design and manufacturing processes.</li><li>Proficiency in quality tools and statistical analysis.</li><li>Excellent analytical and problem-solving skills.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work collaboratively in a team environment.</li></ul></li></ul><h3>Preferred Qualifications</h3><ul><li>Experience with ISO 13485:2016 and 21 CFR Part 820 standards.</li><li>Knowledge of risk management and FMEA.</li><li>Experience in conducting process audits and quality control.</li></ul><h3>Work Environment</h3><ul><li>Moderate to loud production environment.</li><li>Working around equipment and machinery.</li><li>Ability to work flexible hours, including evenings and weekends if necessary.</li></ul><p><br></p>

Validation Engineer

<p><strong>Job Description:</strong></p><p>We are seeking a highly skilled Validation Engineer with a strong focus on manufacturing and equipment validation to join our team dedicated to continuous improvement in the development of implantable medical devices. The ideal candidate will possess expertise in equipment validation processes such as Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), and have experience working with specialized equipment like lasers and epoxy machines. This position is a contract role.</p><p><br></p><p><strong>Responsibilities:</strong></p><ul><li>Support continuous improvement activities within the business</li><li>Qualify and validate equipment, processes, and protocols for manufacturing development of class 3 medical devices</li><li>Ensure compliance with relevant industry standards and regulations</li><li>Collaborate with cross-functional teams to drive process improvements and sustainment efforts</li></ul><p><strong>Qualifications:</strong></p><ul><li>Bachelor’s degree in Mechanical Engineering or related field</li><li>2-10 years of experience in mechanical design and development</li><li>Strong technical writing skills</li><li>Experience with CAD software (SolidWorks, CREO)</li><li>Familiarity with manufacturing processes and assembly</li><li>Excellent teamwork, communication, and project management skills</li><li>Experience with design for manufacturability and reliability principles</li><li>Experience with design verification and validation, including the use of statistical analysis</li></ul><p><em>Preferred Qualifications:</em></p><ul><li>Knowledge of design control processes (ISO 13485:2016, FDA regulations)</li><li>Experience with mechanical design and development within the medical device industry</li></ul><p><strong>Work Environment:</strong></p><p>Medical device manufacturing environment based in Longmont, CO. The facility includes a variety of clean room setups across multiple buildings within the business park. We offer PTO and 11 paid holidays.</p>

<h1><strong>Job Title: Validation Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Validation Engineer will be responsible for creating process flows, control plans, and PPAPs. They will work directly with internal and external customers to develop PPAP documentation for products, including prototype builds. This role is documentation-heavy, with approximately 75% of the time spent at a desk and 25% on the floor reviewing assemblies and monitoring builds.</p><p><br></p><h2>Responsibilities</h2><ul><li>Generate PPAP documentation for new programs, transfers, or engineering changes as required, including submittal of customer PPAPs.</li><li>Develop and write Validation Documents: Risk Assessment, Validation Plan (OQ, PQ), User Requirements, Functional Requirements, and Validation Report.</li><li>Monitor and control validation samples in manufacturing.</li><li>Develop Process Flow Charts, PFMEAs, and Control Plans.</li><li>Identify key process and quality characteristics and monitoring methods.</li><li>Plan and perform MSA&#39;s and process capability studies.</li><li>Develop and perform Design of Experiments (DOEs).</li><li>Monitor and measure process changes and analyze the effects.</li><li>Identify and assist in the resolution of non-conformances.</li><li>Identify and implement continuous improvements.</li></ul><h2>Essential Skills</h2><ul><li>2+ years&#39; experience working as a Quality Engineer or Validation Engineer within Manufacturing.</li><li>ISO 9001 or ISO 13485 experience.</li><li>Experience creating process flows, control plans, and PPAPs.</li><li>Gage R&amp;R experience.</li><li>Experience with circuit boards or electronics.</li><li>Process capability and capability measurements (CPK) experience.</li></ul><h2>&quot;Nice to have&quot; Skills &amp; Qualifications</h2><ul><li>Experience working with circuit boards or electronics is preferred.</li><li>Process capability and capability measurement (CPK) experience is a plus.</li><li>Minitab experience is a nice-to-have.</li></ul><h2>Work Environment</h2><p>The Validation Engineer will report to the Quality Manager and work within a team of four, including Validation Engineers, a documentation specialist, and a trainer. The company has a strong team environment with many veteran employees, providing ample opportunities for learning and growth. The company is rapidly growing and currently employs 175 people. They manufacture Printed Circuit Board Assemblies (PCBAs) for the global electronics market, meeting stringent regulatory demands of medical device, military, and defense industries. Most manufacturing processes are assembly-based, including coating, housing, and soldering assemblies, with a mix of manual and automated processes. The standard workweek is 40 hours, with minimal overtime as needed. The company offers industry-specific training and development programs, including Safari University. Employees receive 10 days of PTO, 6 standard holidays, and access to Udemy after 6 months of employment.</p>

<p><strong>Description</strong></p><p>We are seeking a highly skilled and experienced Quality Engineer/Validation Engineer to join our team. In this role, you will be responsible for ensuring that our products and processes meet the highest standards of quality and regulatory compliance. You will play a critical role in validating equipment, processes, and systems, with a specific focus on utilizing ValGenesis for electronic validation management.</p><p><br></p><p><strong>Key Responsibilities</strong></p><ul><li>Validation Management: Utilize ValGenesis for managing and executing validation protocols, ensuring compliance with regulatory standards.</li><li>Quality Assurance Integration: Collaborate with product development and manufacturing teams to integrate quality standards into all processes.</li><li>Document Review and Approval: Review and approve validation-related documents and plans to ensure conformance with quality system requirements.</li><li>Risk Assessments: Conduct risk assessments and failure mode effects analysis (FMEA) for new and existing products.</li><li>Quality Control Methods: Develop and implement quality control methods, procedures, and performance metrics for product design and manufacturing.</li><li>Problem Solving: Lead problem-solving and improvement activities to address quality issues and reduce product and process nonconformities.</li><li>Process Audits: Conduct audits of design and manufacturing processes to ensure compliance with quality system requirements and identify opportunities for improvement.</li><li>Data Analysis: Compile and analyze statistical data to identify and prioritize areas for quality improvement.</li><li>Reporting: Prepare and present reports on product and process quality to management and customers.</li><li>Training and Mentoring: Train and mentor staff on quality system requirements, quality tools, and best practices.</li></ul><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p><br></p><ul><li>Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field.</li><li>Experience: 1-3 years of experience in quality assurance or validation engineering.</li></ul><p><strong>Skills:</strong></p><ul><li>Proficiency in using ValGenesis for electronic validation management.</li><li>Strong knowledge of validation principles and practices.</li><li>Thorough understanding of quality assurance methodologies.</li><li>Familiarity with product design and manufacturing processes.</li><li>Proficiency in quality tools and statistical analysis.</li><li>Excellent analytical and problem-solving skills.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work collaboratively in a team environment.</li><li>Preferred Qualifications</li><li>Experience with ISO 13485:2016 and 21 CFR Part 820 standards.</li><li>Knowledge of risk management and FMEA.</li><li>Experience in conducting process audits and quality control.</li></ul><p><strong>Experience Level</strong></p><p>Intermediate Level</p>

<p><strong>Description</strong></p><p>We are seeking a highly skilled and experienced Quality Engineer/Validation Engineer to join our team. In this role, you will be responsible for ensuring that our products and processes meet the highest standards of quality and regulatory compliance. You will play a critical role in validating equipment, processes, and systems, with a specific focus on utilizing ValGenesis for electronic validation management.</p><p><br></p><p>Key Responsibilities</p><p>Validation Management: Utilize ValGenesis for managing and executing validation protocols, ensuring compliance with regulatory standards.</p><p>Quality Assurance Integration: Collaborate with product development and manufacturing teams to integrate quality standards into all processes.</p><p>Document Review and Approval: Review and approve validation-related documents and plans to ensure conformance with quality system requirements.</p><p>Risk Assessments: Conduct risk assessments and failure mode effects analysis (FMEA) for new and existing products.</p><p>Quality Control Methods: Develop and implement quality control methods, procedures, and performance metrics for product design and manufacturing.</p><p>Problem Solving: Lead problem-solving and improvement activities to address quality issues and reduce product and process nonconformities.</p><p>Process Audits: Conduct audits of design and manufacturing processes to ensure compliance with quality system requirements and identify opportunities for improvement.</p><p>Data Analysis: Compile and analyze statistical data to identify and prioritize areas for quality improvement.</p><p>Reporting: Prepare and present reports on product and process quality to management and customers.</p><p>Training and Mentoring: Train and mentor staff on quality system requirements, quality tools, and best practices.</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Qualifications</p><p>Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field.</p><p>Experience: 1-3 years of experience in quality assurance or validation engineering.</p><p>Skills:</p><p>Proficiency in using ValGenesis for electronic validation management.</p><p>Strong knowledge of validation principles and practices.</p><p>Thorough understanding of quality assurance methodologies.</p><p>Familiarity with product design and manufacturing processes.</p><p>Proficiency in quality tools and statistical analysis.</p><p>Excellent analytical and problem-solving skills.</p><p>Strong communication and interpersonal skills.</p><p>Ability to work collaboratively in a team environment.</p><p>Preferred Qualifications</p><p>Experience with ISO 13485:2016 and 21 CFR Part 820 standards.</p><p>Knowledge of risk management and FMEA.</p><p>Experience in conducting process audits and quality control.</p><p><br></p>

<p><strong>Description</strong></p>
					<p>We are seeking a highly skilled and experienced Quality Engineer/Validation Engineer to join our team. In this role, you will be responsible for ensuring that our products and processes meet the highest standards of quality and regulatory compliance. You will play a critical role in validating equipment, processes, and systems, with a specific focus on utilizing ValGenesis for electronic validation management.

Key Responsibilities
Validation Management: Utilize ValGenesis for managing and executing validation protocols, ensuring compliance with regulatory standards.
Quality Assurance Integration: Collaborate with product development and manufacturing teams to integrate quality standards into all processes.
Document Review and Approval: Review and approve validation-related documents and plans to ensure conformance with quality system requirements.
Risk Assessments: Conduct risk assessments and failure mode effects analysis (FMEA) for new and existing products.
Quality Control Methods: Develop and implement quality control methods, procedures, and performance metrics for product design and manufacturing.
Problem Solving: Lead problem-solving and improvement activities to address quality issues and reduce product and process nonconformities.
Process Audits: Conduct audits of design and manufacturing processes to ensure compliance with quality system requirements and identify opportunities for improvement.
Data Analysis: Compile and analyze statistical data to identify and prioritize areas for quality improvement.
Reporting: Prepare and present reports on product and process quality to management and customers.
Training and Mentoring: Train and mentor staff on quality system requirements, quality tools, and best practices.</p>
					<p><strong>Skills</strong></p>
					<p>Validation, quality engineering, ValGenesis, Validation protocols, Process validation, Medical device</p>
					<p><strong>Top Skills Details</strong></p>
					<p>Validation,quality engineering,ValGenesis</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>Qualifications
Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field.
Experience: 1-3 years of experience in quality assurance or validation engineering.
Skills:
Proficiency in using ValGenesis for electronic validation management.
Strong knowledge of validation principles and practices.
Thorough understanding of quality assurance methodologies.
Familiarity with product design and manufacturing processes.
Proficiency in quality tools and statistical analysis.
Excellent analytical and problem-solving skills.
Strong communication and interpersonal skills.
Ability to work collaboratively in a team environment.
Preferred Qualifications
Experience with ISO 13485:2016 and 21 CFR Part 820 standards.
Knowledge of risk management and FMEA.
Experience in conducting process audits and quality control.</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

<h1><strong><u>Immediate Validation Engineering Opportunity! </u></strong></h1><p><strong><u>** For Immediate consideration please apply to this posting and email your resume to habels@actalentservices.com** </u></strong></p><p><br></p><h2>Job Description</h2><p>As a Validation Engineer, you will prepare installation and test validation procedures/protocols to ensure products are manufactured in accordance with appropriate regulatory agency validation requirements, internal company standards, and current industry practices. You will compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements. Additionally, you will investigate and troubleshoot problems to determine solutions, maintain validation documentation and files, and set up the ValGenesis Validation Program.</p><p><br></p><h2>Responsibilities</h2><ul><li>Prepare installation and test validation procedures/protocols</li><li>Ensure products are manufactured in accordance with regulatory agency validation requirements, internal company standards, and current industry practices</li><li>Compile and analyze validation data</li><li>Prepare reports and make recommendations for changes and/or improvements</li><li>Investigate and troubleshoot problems to determine solutions</li><li>Maintain validation documentation and files</li><li>Set up ValGenesis Validation Program</li></ul><h2>Essential Skills</h2><ul><li>Experience with ValGenesis</li><li>Bachelor of Science in Engineering or a related subject</li><li>3-5 years of experience in a quality or technical discipline</li><li>Ability to work independently with minimal supervision</li><li>Attention to detail and ability to make evaluative judgments based on the analysis of factual information</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in validation protocols, process validation, and equipment validation</li><li>Experience in the medical device industry</li><li>Role typically requires a university degree or extensive practical knowledge gained through experience</li></ul><h2>Work Environment</h2><p>This position is based onsite in Irvine, CA. The role offers 2 weeks of PTO and 10 paid holidays.</p>

<p><strong>Description</strong></p><p>We are seeking a highly skilled and experienced Quality Engineer/Validation Engineer to join our team. In this role, you will be responsible for ensuring that our products and processes meet the highest standards of quality and regulatory compliance. You will play a critical role in validating equipment, processes, and systems, with a specific focus on utilizing ValGenesis for electronic validation management.</p><p><br></p><p>Key Responsibilities</p><p>Validation Management: Utilize ValGenesis for managing and executing validation protocols, ensuring compliance with regulatory standards.</p><p>Quality Assurance Integration: Collaborate with product development and manufacturing teams to integrate quality standards into all processes.</p><p>Document Review and Approval: Review and approve validation-related documents and plans to ensure conformance with quality system requirements.</p><p>Risk Assessments: Conduct risk assessments and failure mode effects analysis (FMEA) for new and existing products.</p><p>Quality Control Methods: Develop and implement quality control methods, procedures, and performance metrics for product design and manufacturing.</p><p>Problem Solving: Lead problem-solving and improvement activities to address quality issues and reduce product and process nonconformities.</p><p>Process Audits: Conduct audits of design and manufacturing processes to ensure compliance with quality system requirements and identify opportunities for improvement.</p><p>Data Analysis: Compile and analyze statistical data to identify and prioritize areas for quality improvement.</p><p>Reporting: Prepare and present reports on product and process quality to management and customers.</p><p>Training and Mentoring: Train and mentor staff on quality system requirements, quality tools, and best practices.</p><p><strong>Skills</strong></p><p>Validation, quality engineering, ValGenesis, Validation protocols, Process validation, Medical device</p><p><strong>Top Skills Details</strong></p><p>Validation,quality engineering,ValGenesis</p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Qualifications</p><p>Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field.</p><p>Experience: 1-3 years of experience in quality assurance or validation engineering.</p><p>Skills:</p><p>Proficiency in using ValGenesis for electronic validation management.</p><p>Strong knowledge of validation principles and practices.</p><p>Thorough understanding of quality assurance methodologies.</p><p>Familiarity with product design and manufacturing processes.</p><p>Proficiency in quality tools and statistical analysis.</p><p>Excellent analytical and problem-solving skills.</p><p>Strong communication and interpersonal skills.</p><p>Ability to work collaboratively in a team environment.</p><p>Preferred Qualifications</p><p>Experience with ISO 13485:2016 and 21 CFR Part 820 standards.</p><p>Knowledge of risk management and FMEA.</p><p>Experience in conducting process audits and quality control.</p><p><br></p>

<h1 style="font-weight: 700;">Job Title: Validation Engineer</h1><br><h2>Job Description</h2><p>As a Validation Engineer, you will prepare installation and test validation procedures/protocols to ensure products are manufactured in accordance with appropriate regulatory agency validation requirements, internal company standards, and current industry practices. You will compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements. Additionally, you will investigate and troubleshoot problems to determine solutions, maintain validation documentation and files, and set up the ValGenesis Validation Program.</p><br><h2>Responsibilities</h2><ul><li>Prepare installation and test validation procedures/protocols</li><li>Ensure products are manufactured in accordance with regulatory agency validation requirements, internal company standards, and current industry practices</li><li>Compile and analyze validation data</li><li>Prepare reports and make recommendations for changes and/or improvements</li><li>Investigate and troubleshoot problems to determine solutions</li><li>Maintain validation documentation and files</li><li>Set up ValGenesis Validation Program</li></ul><h2>Essential Skills</h2><ul><li>Experience with ValGenesis</li><li>Bachelor of Science in Engineering or a related subject</li><li>3-5 years of experience in a quality or technical discipline</li><li>Ability to work independently with minimal supervision</li><li>Attention to detail and ability to make evaluative judgments based on the analysis of factual information</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in validation protocols, process validation, and equipment validation</li><li>Experience in the medical device industry</li><li>Role typically requires a university degree or extensive practical knowledge gained through experience</li></ul><h2>Work Environment</h2><p>This position is based onsite in Irvine, CA. The role offers 2 weeks of PTO and 10 paid holidays.</p><br>

<h1><strong>Validation Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>The Validation Engineer ensures the accuracy, reliability, and compliance of inspection methods used in the manufacturing of medical devices. This role involves validating automated inspection programs according to FDA, ISO, and ICH guidelines. Experience with automated optical inspection systems, including those integrated into Coordinate Measuring Machines (CMMs), is essential. Strong technical writing skills are required for developing validation protocols, test scripts, and reports.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and execute validation protocols (IQ, OQ, PQ) for inspection methods, ensuring compliance with FDA, ISO, and ICH guidelines.</li><li>Validate inspection programs for automated optical inspection systems, including CMMs.</li><li>Conduct risk assessments and define validation acceptance criteria based on statistical analysis and industry best practices.</li><li>Collaborate with Quality, Engineering, and Manufacturing teams to ensure inspection methods meet product and regulatory requirements.</li><li>Analyze and document validation results, authoring comprehensive reports and justifications for validation conclusions.</li><li>Maintain validation documentation to support audits and regulatory submissions.</li><li>Investigate validation-related nonconformances and recommend corrective actions as needed.</li><li>Stay up to date with industry regulations and best practices for validation of automated inspection systems.</li></ul><h2>Essential Skills</h2><ul><li>Engineering Degree</li><li>3+ Years Equipment Validation Experience</li><li>IQ/OQ/PQ</li><li>Vision system, CMM and/or other inspection equipment validation</li><li>Test Method Validation</li><li>Technical Writing</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with Minitab</li><li>Knowledge of Quality Inspection standards</li></ul><h2>Work Environment</h2><p>This role requires onsite work. The company operates in two locations in Kendal, with one location in a high-rise building housing the Quality team, and the other in a two-story building with the doctor&#39;s surgery center on the first floor and the design team on the second floor. The company is a rapidly growing medical device manufacturer with around 100 employees, and their device assists individuals who are severely injured.</p>

<p>**If you are interested, please send the following to bmuratalla @astoncarter.com**</p><ul><li>updated resume</li><li>3-4 bullet points explaining how your experience relates</li><li>3 professional references</li></ul><p><br></p><p><strong>Key Responsibilities</strong></p><p>Validation Management: Utilize ValGenesis for managing and executing validation protocols, ensuring compliance with regulatory standards.</p><p>Quality Assurance Integration: Collaborate with product development and manufacturing teams to integrate quality standards into all processes.</p><p>Document Review and Approval: Review and approve validation-related documents and plans to ensure conformance with quality system requirements.</p><p>Risk Assessments: Conduct risk assessments and failure mode effects analysis (FMEA) for new and existing products.</p><p>Quality Control Methods: Develop and implement quality control methods, procedures, and performance metrics for product design and manufacturing.</p><p>Problem Solving: Lead problem-solving and improvement activities to address quality issues and reduce product and process nonconformities.</p><p>Process Audits: Conduct audits of design and manufacturing processes to ensure compliance with quality system requirements and identify opportunities for improvement.</p><p>Data Analysis: Compile and analyze statistical data to identify and prioritize areas for quality improvement.</p><p>Reporting: Prepare and present reports on product and process quality to management and customers.</p><p>Training and Mentoring: Train and mentor staff on quality system requirements, quality tools, and best practices.</p><p><br></p><p><strong>Skills</strong></p><p>Validation, quality engineering, ValGenesis, Validation protocols, Process validation, Medical device</p><p><br></p><p><strong>Top Skills Details</strong></p><p>Validation,quality engineering,ValGenesis</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Qualifications</p><p>Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field.</p><p>Experience: 1-3 years of experience in quality assurance or validation engineering.</p><p><br></p><p><strong>Skills</strong>:</p><p>Proficiency in using ValGenesis for electronic validation management.</p><p>Strong knowledge of validation principles and practices.</p><p>Thorough understanding of quality assurance methodologies.</p><p>Familiarity with product design and manufacturing processes.</p><p>Proficiency in quality tools and statistical analysis.</p><p>Excellent analytical and problem-solving skills.</p><p>Strong communication and interpersonal skills.</p><p>Ability to work collaboratively in a team environment.</p><p>Preferred Qualifications</p><p>Experience with ISO 13485:2016 and 21 CFR Part 820 standards.</p><p>Knowledge of risk management and FMEA.</p><p>Experience in conducting process audits and quality control.</p><p><br></p><p><strong>Experience Level</strong></p><p>Intermediate Level</p>

<p><br></p><p style="text-align: center;"><strong style="font-size: 14px;">Validation Engineer Manager</strong></p><p><br></p><p><strong>Validation &amp; Qualification:</strong></p><ul><li>Develop and execute Facility, Utility, and Equipment Qualifications.</li><li>Develop and execute Performance Qualifications and Process Validations.</li><li>Develop, execute, and maintain a robust Cleaning Validation program.</li><li>Develop, execute, and maintain a robust Computer System Validation program.</li></ul><p><br></p><p><strong>General:</strong></p><ul><li>Develop, update, maintain SOPs and provide training as appropriate.</li><li>Aid Process Engineering, Quality Assurance, Production, and other SMEs in the development and execution of pFMEAs.</li><li>Aid other departments in process trials, validation runs, and pilot batches to establish reliable manufacturing processes for new formulations.</li></ul><p><br></p><p><strong>Project Management:</strong></p><ul><li>Lead and manage multiple validation projects simultaneously, ensuring on-time completion.</li><li>Prepare and present technical reports, project updates, and validation metrics to <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span></span></span> management.</li></ul><p><br></p><p><strong>Compliance &amp; Quality:</strong></p><ul><li>Ensure qualification and validation processes comply with regulatory requirements (e.g., FDA, OTC monographs) and internal quality standards.</li><li>Support quality assurance initiatives by conducting risk assessments, participating in audits, and implementing corrective actions as necessary.</li></ul><p><br></p><p><strong>Equipment &amp; Facility Support:</strong></p><p>Provide technical support for the selection, installation, and qualification of manufacturing equipment and for the development process related documentation (i.e. batch records).</p><p><br></p><p><strong>Skills</strong></p><p>Equipment validation, Pharmaceutical, process validation, Quality engineering, regulatory, risk assessment, equipment qualification, performance qualification, validation, gmp, cgmp, fda, system validation</p><p><br></p><p><strong>Top Skills Details</strong></p><p>Equipment validation, Pharmaceutical, process validation</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>Required Education and Experience</li><li>Bachelor’s degree in chemistry or other physical science or a related field.</li><li>Minimum of 10+ years of experience in pharmaceutical and/or personal care validation, with at least 5 years in Rx or OTC manufacturing.</li><li>Demonstrated expertise in the development, execution, and maintenance of validation systems.</li><li>Strong knowledge of cGMP, FDA regulations, and OTC compliance standards.</li></ul><p><br></p><p><strong>Preferred Education and Experience</strong></p><p>Master’s Degree preferred.</p><p>Lean Six Sigma certification (Green Belt or higher) is a plus.</p><p><br></p><ul><li>Working knowledge or <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span></span></span></span></span></span></span></span> in the pharmaceutical care industry.</li><li>Working knowledge of industry best practices for risk assessment</li><li>Working knowledge of Facility, Utility and Equipment Qualification requirements</li><li>Working knowledge of Process Performance Qualification and Process Validation requirements.</li><li>Working knowledge of Computer System Validation Requirements.</li><li>Working knowledge of Cleaning Validation Requirements.</li><li>Strong technical and/or regulatory expertise.</li><li>Detailed record keeping and communication of results to others.</li><li>Project skills appropriate for leadership of validation projects.</li><li>Excellent written, verbal, and interpersonal communication skills.</li><li>High level of initiative, innovation, critical thinking, and problem-solving skills</li><li>Ability to work cross-functionally &amp; at all levels within the organization including <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span></span></span> leadership.</li><li>Ability to prioritize multiple responsibilities and manage deadlines accordingly.</li><li>Communicate effectively and professionally both internally and externally.</li><li>Exceptional attention to detail and high level of accuracy &amp; organization.</li><li>Ability to work as part of a team and excel independently in fast-paced environment.</li><li>Ability to adapt quickly to changing circumstances.</li><li>Demonstrated leadership skills.</li><li>Proficient with Microsoft Office</li></ul><p><strong>Experience Level</strong></p><p>Expert Level</p>

Validation Manager

<h1><strong>Validation Specialist</strong></h1><p><br></p><h2>Job Description</h2><p>As a Validation Specialist, you will perform revalidation on equipment and processes according to approved timelines. You will support validation activities related to changes in existing and new systems, including formulation, sterilization, cleaning, filling, and inspection processes. Your role will involve authoring and reviewing documents to ensure compliance with local, corporate, and regulatory regulations, and collaborating on IQ, OQ, and PQ protocols.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform and review revalidation activities.</li><li>Work and communicate effectively across departments to schedule and perform revalidations.</li><li>Author and review documents in accordance with local, corporate, and regulatory regulations.</li><li>Collaborate and review IQ, OQ, and PQ protocols for systems and processes.</li><li>Support and/or lead the closure of investigations using root cause analysis techniques.</li><li>Participate in continuous improvement initiatives using cLEAN tools.</li><li>Ensure executed protocol data is accurate and meets documented acceptance criteria.</li><li>Manage Change Requests related to revalidation and other validation activities.</li><li>Author and review validation procedures, specifications, and quality documents.</li><li>Present and support validation concepts during audits and inspections.</li><li>Follow all safety and environmental requirements.</li></ul><h2>Essential Skills</h2><ul><li>Experience in revalidation, validation, and GMP processes.</li><li>Hands-on experience with production equipment including CIP Skids, autoclaves, depyrogenation tunnels, and washers.</li><li>Strong data analysis, report generation, and document archival skills.</li><li>Bachelor&#39;s degree in Engineering, Computer Science, or a relevant scientific discipline.</li><li>Minimum of two years of experience in validation processes within the pharmaceutical or medical device industry.</li><li>Familiarity with technical documents related to validation efforts.</li><li>Experience in quality concepts and technical compliance review of validation documents.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with autoclaves, depyrogenation tunnels, filling lines, or washers.</li><li>Experience in cGMP documentation practices and regulations.</li><li>Basic computer skills including Microsoft Word and Excel.</li><li>Knowledge of statistical methods.</li><li>Strong oral and written communication skills.</li><li>Experience with validation test equipment like temperature mapping and data loggers.</li><li>Experience in project team collaboration.</li><li>Root cause analysis techniques experience.</li></ul><h2>Work Environment</h2><p>The role involves supporting revalidation efforts for annual production equipment cycles, with a mix of hands-on work and reporting/data analysis. The position supports a large pharmaceutical manufacturing site with significant growth potential. The work environment encourages collaboration and provides opportunities for project work in a legacy manufacturing site.</p>

Validation Specialist

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