<h1 style="font-weight: 700;">Job Title: Project Manager/Estimator</h1><br><h2>Job Description</h2><p>We are seeking a skilled and experienced Project Manager/Estimator to join our team. This role involves developing accurate cost estimates for concrete and masonry projects while overseeing project planning and coordination from inception to completion. The ideal candidate will demonstrate strong leadership abilities and have a keen understanding of industry standards.</p><br><h2>Responsibilities</h2><ul><li>Prepare Estimates: Develop accurate and comprehensive cost estimates for concrete and masonry projects, including material, labor, equipment, and overhead.</li><li>Review Project Plans: Analyze blueprints, specifications, and other project documents to determine the scope of work and calculate material and labor needs.</li><li>Bid Submissions: Submit detailed and timely bids for projects while maintaining competitive pricing.</li><li>Vendor &amp; Supplier Relations: Establish relationships with suppliers and subcontractors to obtain competitive quotes for materials and labor.</li><li>Cost Analysis: Continuously evaluate project costs against estimates and adjust for any changes or unforeseen challenges.</li><li>Project Planning &amp; Coordination: Oversee the planning and scheduling of concrete and masonry projects from inception to completion, ensuring all phases meet deadlines and budget requirements.</li><li>Team Management: Supervise, direct, and coordinate project teams, including subcontractors, laborers, and field supervisors.</li><li>Client Communication: Act as the primary point of contact for clients, ensuring their needs are met and providing progress updates.</li><li>Quality Control: Ensure work meets company standards, building codes, and client specifications.</li><li>Budget &amp; Schedule Management: Track project expenses and timelines, ensuring projects remain within budget and deadlines are met.</li><li>Problem Solving: Address and resolve any issues or delays in a timely and efficient manner.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 3-5 years of experience in estimating and managing concrete and masonry projects.</li><li>Bachelor’s degree in Construction Management, Civil Engineering, or a related field preferred (or equivalent work experience).</li><li>Strong knowledge of concrete and masonry materials, techniques, and industry standards.</li><li>Proficiency in estimating software (e.g., PlanSwift, Precontractor, Procore).</li><li>Excellent communication, negotiation, and interpersonal skills.</li><li>Proven ability to manage multiple projects simultaneously.</li><li>Strong understanding of project budgets, scheduling, and cost control.</li><li>OSHA 30 Certification and knowledge of construction safety.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Construction Management, Civil Engineering, or a related field preferred (or equivalent work experience).</li><li>OSHA Certification or similar safety certifications preferred.</li></ul><h2>Work Environment</h2><p>This role involves a mix of office-based work and onsite visits, requiring daily in-office presence as well as time spent with clients on walkthroughs of project sites. The work environment is dynamic and offers immediate responsibility in a growing concrete contractor that specializes in concrete/masonry and excavation.</p><br>

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Project Manager/estimator

<h1 style="font-weight: 700;">Job Title: Project Materials Coordinator</h1><br><h2>Job Description</h2><p>The Project Materials Coordinator will be responsible for ensuring that materials for various projects are delivered to their designated locations promptly. This role involves close collaboration with project managers to facilitate efficient material flow.</p><br><h2>Responsibilities</h2><ul><li>Coordinate with project managers to ensure timely delivery of materials.</li><li>Work closely with development, manufacturing, and supply chain teams.</li><li>Manage inventory and track materials using SAP or MS Office Excel.</li><li>Collaborate with development engineers, supplier quality engineers, and production teams.</li></ul><h2>Essential Skills</h2><ul><li>Experience in inventory management.</li><li>Proficiency in project coordination.</li><li>Familiarity with SAP or MS Office Excel.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to work effectively with diverse teams.</li><li>Full-time availability for the initial three months, transitioning to part-time.</li></ul><h2>Work Environment</h2><p>The role requires daily in-office presence, collaborating with various teams to ensure timely delivery of materials. The environment involves working with development engineers, supplier quality engineers, production, and supply chain teams. Dress code is professional, suitable for an office setting.</p><br>

Project Materials Coordinator

<h1 style="font-weight: 700;">Job Title: Project Scheduler</h1><br><h2>Job Description</h2><p>This role involves collaboration with internal teams and customers to efficiently schedule engineering projects within the pulp/paper and food and beverage sectors.</p><br><h2>Responsibilities</h2><ul><li>Coordinate project scheduling with internal teams and customers.</li><li>Utilize Primavera P6 and MS Project to manage and control project timelines.</li><li>Implement cost control measures on engineering and construction projects.</li><li>Lead scheduling efforts for projects ranging from $500k to $5 million.</li><li>Analyze complex financial data sets and integrate them into MS Project.</li></ul><h2>Essential Skills</h2><ul><li>5+ years of experience with Primavera P6 and MS Project.</li><li>Proficiency in project controls and management.</li><li>Intermediate Microsoft Excel skills, including data analysis and pivot tables.</li><li>Understanding of Power BI.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with project coordination and cost control.</li><li>Ability to manage cloud-based project tools.</li></ul><h2>Work Environment</h2><p>This position offers a hybrid schedule with approximately 30% travel required.</p><br>

Project Scheduler

<h1 style="font-weight: 700;">Job Title: Project Superintendent – Federal Construction</h1><br><h2>Job Description</h2><p>We are seeking a highly experienced and dedicated Project Superintendent to lead the daily on-site construction operations for a large-scale federal renovation project valued at over $30 million. The ideal candidate will have a minimum of 10 years of verifiable experience supervising complex government construction projects of comparable or larger size and scope. This role requires deep expertise in federal construction processes, jobsite logistics, phasing coordination, quality and safety enforcement, and strong leadership skills to manage both subcontractors and internal crews in a high-stakes environment with mission-critical constraints.</p><br><h2>Responsibilities</h2><ul><li>Provide full-time on-site supervision for all phases of construction, ensuring work progresses according to the approved schedule, drawings, and specifications.</li><li>Coordinate closely with the Project Manager, SSHO, and QCM to maintain alignment with safety, quality, and performance standards.</li><li>Manage daily subcontractor activities, site access, and ensure all trades perform in compliance with USACE/NAVFAC contract requirements, EM 385-1-1, and OSHA standards.</li><li>Develop and lead daily site meetings and weekly coordination meetings with field personnel, subcontractors, and federal agency representatives.</li><li>Maintain accurate daily reports, field documentation, and photos; proactively identify and mitigate schedule impacts or field conflicts.</li><li>Monitor and enforce compliance with approved submittals, RFIs, changes, and quality control procedures.</li><li>Oversee site logistics planning, laydown, deliveries, and access around secure and occupied facilities.</li><li>Ensure proper execution of temporary protection, utility interruptions, shutdowns, and restoration work in collaboration with base personnel and stakeholders.</li><li>Participate in three-phase quality control inspections and enforce jobsite safety at all times.</li><li>Collaborate in project closeout, punch list management, and turnover documentation.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 10 years serving as a Superintendent on federal construction projects with individual contract values exceeding $30 million.</li><li>In-depth understanding of USACE and NAVFAC construction standards, including EM 385-1-1 safety requirements, quality control systems, and federal site safety protocols.</li><li>Proven track record managing complex renovations, phased construction, and operations within occupied federal or military facilities.</li><li>Strong leadership capabilities with demonstrated success in managing diverse teams of subcontractors and vendors.</li><li>Advanced skills in project scheduling using Primavera P6 or Microsoft Project.</li><li>High proficiency in interpreting blueprints, technical specifications, and contract documentation.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with hangar construction, secure military facilities, aviation infrastructure, or other high-complexity vertical construction projects.</li><li>OSHA 30-Hour Certification.</li><li>Current First Aid/CPR Certification.</li><li>Familiarity with RMS/QCS reporting systems and federal documentation protocols.</li><li>Eligibility for access to military installations.</li></ul><h2>Work Environment</h2><p>This is a full-time, on-site position requiring presence throughout the duration of the project. The schedule is 4x10s, from Monday to Thursday, 6:00 AM to 4:30 PM. Flexibility to work early mornings, extended hours, and occasional nights or weekends is needed to meet project milestones or accommodate federal facility access restrictions. Candidates must be physically capable of navigating and inspecting all areas of the construction site, including walking, climbing, and working in various environmental conditions. Dress code is professional as required by federal standards.</p><br>

Project Superintendent – Federal Construction

<p><strong>Description</strong></p><p>Seeking a Bilingual (Spanish) Project Assistant/Onboarding Coordinator to support the Davie, FL office. This individual will support administrative functions for the project management and talent acquisitions team.</p><p><br></p><p><strong>Responsibilites:</strong></p><ul><li>Assist project managers with administrative functions (schedule meetings, take notes, etc.)</li><li>Initiate <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> checks and drug screening according to FCRA regulations.</li><li>Coordinate new hire onboarding by ensuring all new hire paperwork is accurately completed on time.</li><li>Manage spreadsheets, ensuring data accuracy and accessibility.</li><li>Able to effectively handle sensitive and confidential information with discretion.</li><li>Excellent communication and interpersonal skills.</li><li>Manage the applicant tracking system ensuring accurate and up-to-date information for all candidates.</li><li>Maintain regular communication with managers, providing status updates</li><li>Knowledge within the industry’s best practices, emerging trends, and recruitment tools and technologies.</li><li>Knowledge and familiarity with employment laws and regulations.</li><li>Excellent organizational skills with demonstrated attention to detail and the ability to handle multiple priorities with strict deadlines.</li><li>Professional with strong work ethic but approachable with excellent judgement in working with candidates and diverse levels of staff.</li><li>Participate in a variety of special projects and ad hoc reporting.</li></ul><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>Bi-lingual (English/Spanish) a MUST</li><li>1+ year of experience in administration, HR, talent acquisition, or recruitment coordination.</li><li>iCIMS experience</li><li>Onboarding coordination experience</li><li>Experience working in a dynamic, high volume, customer-focused environment supporting multiple locations and disciplines.</li><li>Proficiency in Microsoft Office Suite.</li><li>Ability to operate office equipment.</li><li>Good written and verbal communication skills.</li><li>Proven experience with attention to detail a must.</li></ul>

Project/Onboarding Administrator

<h1><strong>Job Title: Project Manager </strong></h1><p><br></p><h2>Job Description</h2><p>Join a dynamic team responsible for overseeing start-up activities and finalization work toward the launch of grocery components in specific types of buildings. This role involves implementing grocery operations post-launch and managing retrofit projects for existing buildings. The position requires close collaboration with third-party vendors to ensure successful project completion.</p><p><br></p><h2>Responsibilities</h2><ul><li>Monitor the main vendor responsible for installing racking and coordinate with teams for taping, hanging signs, and other tasks to ensure a finished product before handing it over to operations.</li><li>Manage and track 100-200 tasks using an established playbook, ensuring other teams stay on track.</li><li>Utilize Fieldwire to monitor vendor tasks, assess completion through pictures, and ensure compliance with standards.</li><li>Communicate with vendors, troubleshoot delays, and ensure work meets quality standards and deliveries are timely.</li></ul><h2>Essential Skills</h2><ul><li>Proven experience in project management and construction management.</li><li>Proficiency in using Asana for project tracking and management.</li><li>Ability to communicate effectively with vendors and troubleshoot issues.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with grocery program implementation.</li><li>Willingness to travel 50-75%, primarily regionally.</li></ul><h2>Work Environment</h2><p>This is a fast-paced, high-standard environment with a focus on virtual teamwork and collaboration with vendors and operations. The role involves significant travel, especially during site launches, which can require onsite presence for up to a few weeks. The work is mainly heads-down with some vendor interaction and collaboration with operational leaders to maintain strong relationships.</p>

Project/Program Manager III

<p><strong>An architecture firm in Chicago is looking for a well-organized proposal/marketing coordinator with strong writing skills and a good graphic eye to join their international design practice!</strong></p><p><br></p><p><u>Responsibilities will include</u>:</p><ul><li>Working with the Chief Marketing Office, Partners, and Principals on qualification packages, proposals, award submissions, and other promotional pieces</li><li>Leading the organization of marketing materials and imagery in the Adobe Creative Suite</li></ul><p><u>Qualifications</u><strong>:</strong></p><ul><li>Bachelor&#39;s Degree</li><li>3+ years of experience in the AEC industry</li><li>Communication skills that are attuned to the architectural industry, as well as graphic sensibilities</li><li>Proficiency in InDesign, Photoshop, Affinity Publisher, Word, Excel, and OpenAsset</li><li>Skills in Video editing, website maintenance, and creative writing are preferred</li></ul>

Proposal Coordinator

<h1 style="font-weight: 700;">Job Title: Propulsion Test Engineer</h1><br><h2>Job Description</h2><p>We are seeking experienced Propulsion Test Engineers to join our team at Kennedy Space Center, FL. As a key player in our engineering team, you will be responsible for performing critical test engineering activities to support spacecraft propulsion systems.</p><br><h2>Responsibilities</h2><ul><li>Perform test engineering activities, including detailed operating procedure authoring and execution, to achieve test verification and vehicle production objectives.</li><li>Engage in hypergolic propellant servicing.</li><li>Develop and execute steps for component removal, replacement, and re-test on systems containing hypergolic propellants.</li><li>Conduct leak testing of spacecraft propulsion systems.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor of Science degree in engineering, engineering technology, chemistry, physics, mathematics, data science, or computer science.</li><li>5 years of propulsion-related fluids test engineering experience on spacecraft.</li><li>Experience loading hypergolic propellants or performing other test-related operations on hypergol-contaminated propellant systems.</li><li>Experience in leak checking spacecraft fluid systems.</li><li>Experience developing procedures for leak checks and functional testing of spacecraft hypergolic propellant systems.</li><li>Experience operating high-pressure pneumatic equipment to pressurize flight hardware.</li><li>Ability to lead technicians, QA team members, and other test engineers in executing tests.</li><li>Strong troubleshooting skills to document and resolve non-conformances on both ground support equipment and flight hardware.</li><li>Willingness to work overtime and off-shift operations, including 2nd and 3rd shifts.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Current non-Destructive Test (NDT) Leak Test certification.</li><li>Current SCAPE/SAR certification.</li></ul><h2>Work Environment</h2><p>The position is based at Kennedy Space Center, FL. The work environment involves handling advanced aerospace technologies and requires adherence to safety standards when working with hypergolic propellants. Engineers should be prepared to work in shifts and may need to work overtime to meet project deadlines.</p><br>

Propulsion Test Engineer

<h2>Job Title: Propulsion Test Engineer</h2><p><strong>Location:</strong> Kennedy Space Center, Florida  </p><p><br></p><p>Join a high-performing engineering team at Kennedy Space Center supporting spacecraft propulsion testing and verification. As a Propulsion Test Engineer, you will play a critical role in authoring, executing, and troubleshooting test procedures for hypergolic propulsion systems to ensure flight readiness and compliance with mission requirements</p><p><br></p><p>Key Responsibilities</p><ul><li>Author and execute detailed operating procedures for spacecraft propulsion systems</li><li>Handle and service hypergolic propellants in accordance with stringent safety protocols</li><li>Conduct removal, replacement, and re-test procedures for components in hypergolic systems</li><li>Perform leak testing and functional verification of spacecraft fluid systems</li><li>Operate high-pressure pneumatic systems to pressurize flight hardware</li><li>Lead multidisciplinary testing teams, including technicians, QA, and fellow engineers</li><li>Investigate, document, and resolve equipment and hardware non-conformances</li><li>Support mission-critical test operations across all shifts (including 2nd and 3rd) and overtime as needed</li></ul><p><br></p><p>Required Qualifications</p><ul><li>Bachelor’s degree in Engineering, Engineering Technology, Chemistry, Physics, Mathematics, Data Science, or Computer Science</li><li>Minimum 5 years experience in propulsion fluids test engineering on spacecraft</li><li>Experience handling hypergolic propellants and working on contaminated systems</li><li>Proficient in leak checking, functional testing, and procedure development for hypergolic systems</li><li>Skilled in pneumatic pressurization of flight systems</li><li>Demonstrated leadership in testing environments with cross-functional teams</li><li>Exceptional troubleshooting and documentation capabilities</li></ul><p><br></p><p><br></p>

<h1 style="font-weight: 700;">Job Title: Propulsion Test Engineer</h1><br><h2>Job Description</h2><p>We are seeking dedicated Propulsion Test Engineers to join our team at Kennedy Space Center, FL. This role involves performing test engineering activities on spacecraft propulsion systems to achieve test verification and vehicle production objectives.</p><br><h2>Responsibilities</h2><ul><li>Author and execute detailed operating procedures on spacecraft propulsion systems.</li><li>Conduct hypergolic propellant servicing.</li><li>Develop and execute steps for component removal, replacement, and re-test on systems containing hypergolic propellants.</li><li>Perform leak testing of spacecraft propulsion systems.</li><li>Lead technicians, QA team members, and other test engineers in executing testing.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor of Science degree from an accredited course of study in engineering, engineering technology, chemistry, physics, mathematics, data science, or computer science.</li><li>Experience in loading hypergolic propellants or performing test-related operations on hypergolic contaminated propellant systems.</li><li>Experience in leak checking spacecraft fluid systems.</li><li>Experience in developing procedures for leak checking and performing functional testing of spacecraft hypergolic propellant systems.</li><li>Experience operating high-pressure pneumatic equipment to pressurize flight hardware.</li><li>Strong troubleshooting capabilities to document and resolve non-conformances on ground support equipment and flight hardware.</li><li>5 years of propulsion-related fluids test engineering experience on spacecraft.</li><li>Willingness to work overtime and off-shift operations, including 2nd and 3rd shifts.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Current Non-Destructive Test (NDT) Leak Test certification.</li><li>Current SCAPE/SAR certification.</li></ul><h2>Work Environment</h2><p>The work environment at Kennedy Space Center involves working with advanced technologies and equipment. The role may require overtime and off-shift operations, including 2nd and 3rd shifts. The facility operates under stringent safety protocols and requires adherence to dress codes suitable for handling spacecraft propulsion systems.</p><br>

<h1 style="font-weight: 700;">Job Title: Protection and Control Engineer</h1><br><h2>Job Description</h2><p>We are seeking a skilled Protection and Control Engineer to join our dynamic substation team. The role involves developing and revising existing drawings for one-line and three-line diagrams, grounding, schematics, and wiring, as well as control and relaying panels. You will coordinate with CAD operators to produce high-quality CAD drawings, integrate protection and control drawings with the physical layout of substations, and design interfacing with SCADA systems and communications, including RTUs, HMIs, and IEDs. Additionally, you will be responsible for developing control and relay panel layouts, assembling specifications, creating project criteria, and developing design specifications, including the overall bill of materials.</p><br><h2>Responsibilities</h2><ul><li>Develop and revise existing drawings for one-line and three-line diagrams, grounding, schematics, and wiring.</li><li>Coordinate with CAD operators to develop organized and quality CAD drawings.</li><li>Integrate protection and control drawings with the physical layout and design of substations.</li><li>Design interfacing with SCADA systems and communications, including RTUs, HMIs, and IEDs.</li><li>Develop control and relay panel layouts and assemble specifications.</li><li>Create project criteria and develop design specifications, including the overall bill of materials.</li></ul><h2>Essential Skills</h2><ul><li>3-6 years of Protection &amp; Controls Design Engineering experience in projects up to 500kV.</li><li>Engineering Degree.</li><li>Experience with AutoCAD/MicroStation.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Substation design experience.</li><li>Experience in electrical engineering.</li><li>Ability to work remotely with 5+ years of relevant experience.</li></ul><h2>Work Environment</h2><p>This position offers a hybrid work environment, allowing the engineer to work from home 1-2 days per week. The role is part of a Substation Group consisting of around 22 people, including engineers, designers, and drafters. The team is divided into both Physical and P&amp;C groups. The engineer must work out of one of two offices located in Lansdale, PA or Orlando, FL. Our team is growing, providing excellent opportunities for career advancement, as well as bonuses and profit-sharing once direct.</p><br>

Protection And Control Engineer

<p><strong>Description</strong></p><p>PURPOSE</p><p>The Manager - Publications works with minimal direction from a Director Level Team Member on the efficient and compliant development and execution of NNI publication plan(s) across assigned therapies and therapeutic areas.</p><p><br></p><p>This position tracks (database entry), updates, reports and communicates NNI publication projects and deliverables with minimal direction. The Manager, Publications leverages his/her technical experience and understanding of the organization and its processes to guide the successful completion of key publications.</p><p><br></p><p>RELATIONSHIPS</p><p>This position reports to a Director Level Team Member within Scientific Communications (SC), Medical Affairs.</p><p><br></p><p>The Manager-Publications is expected to develop and utilize a network of internal relationships with local and global publication stakeholders, including colleagues from Medical Affairs, Clinical Data Science &amp; Evidence, legal, regulatory affairs, global publication team, and commercial publications colleagues from market access and marketing.</p><p><br></p><p>The Manager - Publications is also expected to network effectively with external resources (e.g., authors) and work closely with external vendors, stakeholders, and agencies.</p><p><br></p><p><strong><u>GENERAL</u></strong>:</p><ul><li>Works with minimal direction; their manager conducts periodic reviews of progress and results.</li><li>Functions at a proficient level.</li><li>Participates in cross-functional project teams locally and/or globally.</li><li>May act as a project leader with own manager oversight.</li><li>Has the ability to identify and resolve problems related to publication projects, processes, or tasks, with management support as needed.</li><li>Exercises judgment within defined procedures and policies</li><li>Acts as a key contact point for publication activities for internal and external stakeholders for assigned therapeutic areas/therapies.</li><li>Provides guidance/conducts training of internal and external stakeholders on publication planning and processes.</li><li>Engages directly with external HCPs/KOLs that are potential authors.</li><li>Applies their experience to the quality assessment of documents.</li><li>Has knowledge of external publication and industry guidelines. Educates others as needed.</li><li>Remains current with respect to assigned therapeutic areas and competitor products.</li></ul><p><br></p><p><strong><u>PUBLICATIONS:</u></strong></p><ul><li>Drives the development and update of NNI publication strategies and publication plans for the assigned therapeutic area in alignment with global and NNI medical strategies and publication plans with minimal direction from a Director Level Team Member</li><li>Drives the execution and reporting of publication plan activities</li><li>Interacts with local and global publication groups, journals, editors, authors, and others as necessary to ensure the successful completion of publication projects.</li><li>Manages agency partners and other external stakeholders involved in developing and submitting publications to peer-reviewed scientific journals and scientific/medical conferences.</li><li>Works closely with agency partners and consultants (as a day-to-day contact) to manage project status, publication drafts, author comments, NNI reviews/approvals, and maintains Datavision publication records and reporting.</li><li>As needed, prepare and review manuscripts, meeting abstracts, scientific poster presentations, including digital solutions for publication support with support from a Director Level Team Member.</li><li>May be responsible for planning author meetings.</li><li>Participates as needed in PPG functions, prepares required PPG proposals, follows up on meetings, etc.</li><li>Contributes to publication communication, e.g., newsletters, announcements, etc.</li><li>Coordinates, prepares, manages, and tracks author engagements in HCP Rex and Datavision.</li><li>Advanced level of system use of publication systems, Datavision, Medical Toolbox, etc. Develop training and guide authors, internal and external stakeholders, and vendors in the correct use of publication systems. Develops/aids in developing guidance documents and process descriptions to improve processes related to publication planning and execution at NNI.</li><li>Manages, tracks, and reports publication budget and vendor deliverables for assigned therapeutic areas/therapies.</li></ul><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>An MS, MD, or PhD in a Life Science or a PharmD required.</li><li>CMPP preferred but not required</li><li>A minimum of 2 years of relevant experience in pharma or a medical communication agency required with a PhD, MD, or PharmD, and 4 years of relevant experience with an MS.</li><li>Demonstrated experience in the preparation of publications.</li><li>Basic disease and therapeutic area knowledge in diabetes, obesity, and rare diseases an added advantage</li><li>General understanding of regulatory requirements and drug development processes.</li><li>Demonstrated proficiency in the use and understanding of computer software (e.g., word processing, graphics, document management).</li><li>Excellent project management and organizational skills, including the ability to plan, prioritize, and execute on competing projects and timelines.</li><li>Ability to multitask and work both independently and within multi-disciplinary teams</li><li>Strong interpersonal and written communication skills for effective professional communications, with demonstrated ability to cultivate strong working relationships, both with internal and external stakeholders,</li></ul>

Publications Manager

<h1 style="font-weight: 700;">Job Title: QA Analyst I</h1><br><h2>Job Description</h2><p>The QA Analyst will play a pivotal role in maintaining food safety and quality assurance systems and controls within the plant. This includes ensuring compliance with SQF, HACCP, FSMA, HARPC, process controls, and regulatory compliance.</p><br><h2>Responsibilities</h2><ul><li>Collaborate with the Food Safety Manager to uphold food safety and quality assurance standards.</li><li>Participate in food safety and quality assurance systems such as SQF, HACCP, FSMA, and HARPC.</li><li>Ensure regulatory compliance through pH and water testing.</li><li>Utilize systems like TraceGains, SafeFood360, and SnapQC for QA testing.</li><li>Assist in reviewing labels to ensure accuracy and compliance.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in regulatory compliance and quality assurance procedures.</li><li>Experience with TraceGains and other food safety systems.</li><li>Strong written and communication skills.</li><li>Laboratory skills including pH and water testing.</li><li>Knowledge of SQF, FSMA, and food safety protocols.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in food science, nutrition, microbiology, biology, or related fields.</li><li>HACCP certification required.</li><li>PCQI certification preferred, with the opportunity to become certified while employed.</li><li>Minimum of 2 years of experience in the food industry, preferably in a bakery.</li><li>Familiarity with the Code of Federal Regulations (21 CFR Sections).</li><li>Experience with cloud-based food safety and quality management systems.</li></ul><h2>Work Environment</h2><p>The position is based in a food manufacturing plant that offers a sensory-rich environment, reminiscent of a delightful bakery. Employees will work amidst the aromas of freshly baked goods, contributing to an engaging and dynamic work setting.</p><br>

QA Analyst I

<h1><strong>Job Title: QA Analyst </strong></h1><p><br></p><h2>Job Description</h2><p>The QA Analyst will play a pivotal role in maintaining food safety and quality assurance systems and controls within the plant. This includes ensuring compliance with SQF, HACCP, FSMA, HARPC, process controls, and regulatory compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Collaborate with the Food Safety Manager to uphold food safety and quality assurance standards.</li><li>Participate in food safety and quality assurance systems such as SQF, HACCP, FSMA, and HARPC.</li><li>Ensure regulatory compliance through pH and water testing.</li><li>Utilize systems like TraceGains, SafeFood360, and SnapQC for QA testing.</li><li>Assist in reviewing labels to ensure accuracy and compliance.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in regulatory compliance and quality assurance procedures.</li><li>Experience with TraceGains and other food safety systems.</li><li>Strong written and communication skills.</li><li>Laboratory skills including pH and water testing.</li><li>Knowledge of SQF, FSMA, and food safety protocols.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in food science, nutrition, microbiology, biology, or related fields.</li><li>HACCP certification required.</li><li>PCQI certification preferred, with the opportunity to become certified while employed.</li><li>Minimum of 2 years of experience in the food industry, preferably in a bakery.</li><li>Familiarity with the Code of Federal Regulations (21 CFR Sections).</li><li>Experience with cloud-based food safety and quality management systems.</li></ul><h2>Work Environment</h2><p>The position is based in a food manufacturing plant that offers a sensory-rich environment, reminiscent of a delightful bakery. Employees will work amidst the aromas of freshly baked goods, contributing to an engaging and dynamic work setting.</p>

<h1 style="font-weight: 700;">Job Title: QA Associate</h1><br><h2>Job Description</h2><p>The QA Associate is responsible for the rigorous review, verification, and archival of batch records and associated documentation to ensure compliance with internal SOPs, cGMP, and FDA regulations. This role is primarily desk-based and involves close collaboration with production, warehouse, and quality teams to resolve discrepancies and maintain data integrity.</p><br><h2>Responsibilities</h2><ul><li>Perform comprehensive batch record reviews for completeness, accuracy, and compliance with GDP and SOPs.</li><li>Review supporting documentation including logbooks, protocols, packaging records, and inventory records.</li><li>Collaborate with production and management to resolve discrepancies or missing information in batch records.</li><li>Scan and archive completed records into the electronic database and physical storage system.</li><li>Input data into warehouse management systems (e.g., Dynamics 365) and quality systems (e.g., Reliance).</li><li>Ensure inventory values and documentation are accurately recorded and support initiatives within the QA team to build flexibility and coverage.</li><li>Participate in continuous improvement efforts and assist in training production staff on documentation best practices.</li><li>Cross-trained with other QA Associate functions including Document Control and Inventory Control.</li><li>Issue and control batch records, cleaning records, test sheets, and logbooks.</li><li>Maintain and control the company lot number system and ensure proper documentation flow.</li></ul><h2>Essential Skills</h2><ul><li>Strong interpersonal skills; able to work respectfully with cross-functional teams.</li><li>Self-motivated and organized with a high level of accountability.</li><li>Willingness to learn and adapt to evolving processes and systems.</li><li>Proficient in Microsoft Office and comfortable using ERP and quality systems (e.g., Dynamics 365, Reliance).</li><li>Excellent written and verbal communication skills.</li><li>Ability to work independently and collaboratively with minimal supervision.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma or GED required; Associate’s or Bachelor’s degree in a scientific or technical field preferred.</li><li>1+ year of experience in pharmaceutical QA or FDA-regulated environment preferred.</li><li>Strong attention to detail and ability to work in a fast-paced, documentation-heavy environment.</li></ul><h2>Work Environment</h2><p>This position is a Monday to Friday Day Shift role with a flexible start time between 7:00 - 8:30 AM, working 8-9 hours from there. The role includes 90% desk-based work in a shared office setting, with occasional lifting of up to 50 lbs. The manufacturing building is dusty due to the powdered products produced and is not a sterile environment. The team comprises 3 Inspectors, 1 Supervisor, 3 Batch Record Reviewers, 1 Document Control, and 1 Inventory Control.</p><br>

QA Associate - Batch Record Reviewer

<h1 style="text-align: center;"><strong>QA Auditor</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a motivated and detail-oriented QA Auditor to join our team. In this role, you will perform essential line audits of pharmaceutical filling and packaging operations and ensure compliance with SOPs. You will also conduct line clearances, in-process, and end-item inspections, and review specifications for acceptance of packaging components, raw materials, and finished products. Additionally, you will be responsible for generating, reviewing, and issuing batch production records, releasing materials for production, and organizing printed materials for production. The position requires a strong knowledge of contemporary cGMP practices and procedures, as well as excellent written and oral communication skills.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform in-house line audits of pharmaceutical filling and packaging operations.</li><li>Review manufacturing activities and documentation for compliance with SOPs.</li><li>Conduct line clearances, in-process, and end-item inspections.</li><li>Apply specifications for acceptance of incoming packaging components, raw materials, and finished products.</li><li>Generate, review, and issue batch production records.</li><li>Release materials and components for use in production.</li><li>Organize and issue printed materials to production.</li><li>Monitor and interpret charts and gauges.</li><li>Review, issue, and archive log books.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance and auditing skills.</li><li>Experience with internal audits, compliance, and inspections.</li><li>Proficiency in using micrometers, calipers, and light inspection units.</li><li>Knowledge of Good Documentation Practices.</li><li>Ability to review large executed production batch records thoroughly.</li><li>Strong attention to detail and ability to coordinate activities simultaneously.</li><li>Effective time management skills.</li><li>Excellent written and oral communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associates degree in Science or equivalent is required.</li><li>Bachelors degree in Science or equivalent is preferred.</li><li>1-4 years&#39; experience in Quality Assurance or Manufacturing, preferably in an FDA regulated environment.</li><li>Working knowledge of cGMPs is preferred.</li><li>Technical writing skills are a plus.</li></ul><h2>Work Environment</h2><p>The work environment includes clean rooms, manufacturing facilities, and labs. The typical first shift schedule consists of four 10-hour days, with standard work hours from 6:00 AM to 4:30 PM. Flexibility in availability for various days of the week and a five-day schedule may be required. Overtime rates apply for hours worked over 40 per week. Alternative work hours or schedules may be required at the discretion of management.</p>

QA Auditor

<h1><strong>QA Auditor</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a motivated and detail-oriented QA Auditor to join our team. In this role, you will perform essential line audits of pharmaceutical filling and packaging operations and ensure compliance with SOPs. You will also conduct line clearances, in-process, and end-item inspections, and review specifications for acceptance of packaging components, raw materials, and finished products. Additionally, you will be responsible for generating, reviewing, and issuing batch production records, releasing materials for production, and organizing printed materials for production. The position requires a strong knowledge of contemporary cGMP practices and procedures, as well as excellent written and oral communication skills.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform in-house line audits of pharmaceutical filling and packaging operations.</li><li>Review manufacturing activities and documentation for compliance with SOPs.</li><li>Conduct line clearances, in-process, and end-item inspections.</li><li>Apply specifications for acceptance of incoming packaging components, raw materials, and finished products.</li><li>Generate, review, and issue batch production records.</li><li>Release materials and components for use in production.</li><li>Organize and issue printed materials to production.</li><li>Monitor and interpret charts and gauges.</li><li>Review, issue, and archive log books.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance and auditing skills.</li><li>Experience with internal audits, compliance, and inspections.</li><li>Proficiency in using micrometers, calipers, and light inspection units.</li><li>Knowledge of Good Documentation Practices.</li><li>Ability to review large executed production batch records thoroughly.</li><li>Strong attention to detail and ability to coordinate activities simultaneously.</li><li>Effective time management skills.</li><li>Excellent written and oral communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associates degree in Science or equivalent is required.</li><li>Bachelors degree in Science or equivalent is preferred.</li><li>1-4 years&#39; experience in Quality Assurance or Manufacturing, preferably in an FDA regulated environment.</li><li>Working knowledge of cGMPs is preferred.</li><li>Technical writing skills are a plus.</li></ul><h2>Work Environment</h2><p>The work environment includes clean rooms, manufacturing facilities, and labs. The typical first shift schedule consists of four 10-hour days, with standard work hours from 6:00 AM to 4:30 PM. Flexibility in availability for various days of the week and a five-day schedule may be required. Overtime rates apply for hours worked over 40 per week. Alternative work hours or schedules may be required at the discretion of management.</p>

<h1 style="text-align: center;"><strong>Internal Auditor</strong></h1><p><br></p><h2><strong>Job Description</strong></h2><p>This position requires outstanding decision-making and problem-solving skills. As an Internal Quality Auditor, you will ensure that the organization&#39;s processes, and the goods and services that result, comply with customer requirements, business requirements, and industry standards, including AS9100, ISO 9001, P&amp;W ASQR-01, and internal quality manuals.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Conduct routine shop audits to prepare for internal and third-party audits.</li><li>Support third-party audit preparation and execution.</li><li>Participate in internal and external quality/technical audits.</li><li>Assist in the development of audit plans and schedules.</li><li>Support external supplier/vendor audits in collaboration with the supplier performance team.</li><li>Develop audit reports with the audit team.</li><li>Obtain, analyze, and evaluate documentation, reports, data, and flowcharts for compliance.</li><li>Coordinate and communicate audit schedules and plans with process areas.</li><li>Collaborate with auditees and other auditors during audits.</li><li>Support lead auditor in supplier process/performance reviews.</li><li>Deliver training associated with audits and quality requirements compliance.</li><li>Generate quality forms and records associated with audits.</li><li>Take initiative to identify solutions to problems that are not always well-defined.</li><li>Other duties as assigned.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>Internal audit experience.</li><li>ETQ Reliance proficiency.</li><li>AS9100 audit certification.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>High School diploma or equivalent, with 2 years&#39; experience in a regulated industry such as Food, Drug, Medical, or Aviation.</li><li>Eligibility to obtain necessary export authorizations.</li><li>Proficiency in English, both written and spoken.</li><li>Proficient computer skills, including Microsoft Outlook, Word, Excel, and PowerPoint.</li><li>AS9100 Lead Auditor Certification from an accredited institution or completion of an AS9100 auditor course and passing of the exam within the first 12 months of employment.</li><li>Good attendance record.</li><li>Strong communication skills.</li><li>Ability to work overtime when required.</li></ul><h2><strong>Work Environment</strong></h2><p>This position is fully onsite and operates on a schedule of Monday to Friday, 7:00am - 3:30pm (1st Shift). You will report to the designated supervisor.</p>

<h1 style="font-weight: 700;">Job Title: QA Deviation Investigator</h1><br><h2>Job Description</h2><p>As a QA Deviation Investigator, you will play a crucial role in analyzing and investigating deviations or non-conformances within a regulated environment. Utilizing problem-solving tools like root cause analysis, you will collect and analyze relevant data to identify patterns and potential causes. Your findings will be documented comprehensively, and you will collaborate with various departments to implement corrective and preventive actions (CAPAs). You will also participate in client communications and provide timely written documentation of investigations.</p><br><h2>Responsibilities</h2><ul><li>Analyze and investigate deviations or non-conformances using problem-solving tools such as root cause analysis.</li><li>Collect and analyze relevant data to identify patterns, trends, or potential causes.</li><li>Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information.</li><li>Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs).</li><li>Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes.</li><li>Participate in client communications and responses, working closely with program team leads, quality, and management.</li></ul><h2>Essential Skills</h2><ul><li>Experience in CAPA, quality assurance, and root cause analysis.</li><li>Knowledge of deviations in pharmaceutical settings and GMP/FDA regulations.</li><li>Strong technical writing and communication skills.</li><li>Proficiency in quality processes and Six Sigma methodologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS/BA in biology, biochemistry, chemistry, or other science-related fields.</li><li>1+ years of experience with problem-solving tools like Root Cause Analysis and/or LEAN/Six Sigma.</li><li>1+ years of experience in technical writing and/or deviation writing.</li><li>3+ years of experience in a regulated environment, preferably in biologics/pharmaceuticals.</li><li>Ability to evaluate data and make recommendations based on trends and trend analysis.</li><li>Ability to work effectively in a fast-paced environment and prioritize tasks.</li><li>Ability to facilitate meetings for desired outcomes.</li></ul><h2>Work Environment</h2><p>The role requires working Monday through Friday, with core hours of 9am to 3pm, and flexibility in start and end times. You will collaborate with any department needed for deviations, not necessarily limited to upstream or downstream processes.</p><br>

QA Deviation Investigator

<h1 style="font-weight: 700;">Job Title: QA Inspector</h1><br><h2>Job Description</h2><p>The QA Inspector ensures that all products released for distribution comply with applicable specifications. This role involves managing materials in the warehouse to ensure they are appropriately identified as to status and stored correctly. The QA Inspector is responsible for verifying that only released materials are used in production and that all materials are appropriately sampled, tested, and meet specifications before their use in production.</p><br><h2>Responsibilities</h2><ul><li>Assure compliance with applicable SOPs.</li><li>Ensure manufacturing complies with Batch Record Instructions and requirements.</li><li>Receive and sample all raw materials and components for appropriate testing.</li><li>Quarantine and release finished products for shipping.</li><li>Ensure all items in the plant, including raw materials, components, packaging, labels, finished products, reject materials, and rework materials, are appropriately labeled and stored according to SOPs.</li><li>Administer the label program.</li><li>Inspect production lines.</li><li>Conduct appropriate sampling, storage, and status labeling of pallets of incoming materials until tested for compliance with specifications and released for use.</li><li>Conduct appropriate sampling and storage of finished products until tested and released for production.</li><li>Review batch records to ensure only released ingredients, components, and labeling are used in production.</li><li>Assist the Quality Manager in product investigations where deviations have occurred in manufacturing, or complaints or product failures have been reported.</li><li>Maintain label inventory, issue labels to production, return labels to inventory, and facilitate reconciliation of label inventory.</li><li>Inspect production lines, checking for PPE, labels, codes, weights, and compliance with product specifications.</li></ul><h2>Essential Skills</h2><ul><li>1+ years of quality inspection experience in a GMP environment required, 3+ years preferred.</li><li>HS Diploma required.</li><li>Proficient computer skills to work within the QMS/Database, including basic skills or experience in a similar system like SAP or equivalent ERP.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in quality assurance, quality inspection, and quality check processes.</li></ul><h2>Work Environment</h2><p>The QA Inspector will work primarily Monday through Friday from 8:00 AM to 4:30 PM, with moderate overtime of 4-6 hours weekly. There is a possibility of Saturday work, typically one Saturday a month. The team consists of three inspectors and a supervisor, interfacing with production and warehouse personnel. Sampling duties are typically performed one day a week, constituting 80% of the workday compared to 20% in the office. Other days will involve 70% office release work and 30% inspections and auditing in production/warehouse environments. The work environment can be dusty due to the powdered products or animal feed-based products. The role offers 6 paid holidays and 40 hours of PTO, with a plan for conversion at the end of the assignment as there is an open headcount already approved.</p><br>

QA Inspector (Pharmaceuticals)

<h1 style="font-weight: 700;">Job Title: QA QMS Associate</h1><br><h2>Job Description</h2><p>The QA QMS Associate is responsible for ensuring compliance with both internal and external quality standards, playing a pivotal role in maintaining and enhancing the Quality Management System (QMS) in accordance with Good Manufacturing Practice (GMP) and regulatory requirements.</p><br><h2>Responsibilities</h2><ul><li>Assist in the development, implementation, and maintenance of the QMS in line with GMP and regulatory requirements.</li><li>Maintain and ensure proper documentation of all quality systems and records.</li><li>Oversee document control processes, ensuring SOPs, work instructions, and other quality documents are up to date and correctly implemented.</li><li>Assist in the collection, analysis, and reporting of quality data, including quality metrics, CAPA reports, and audit findings.</li><li>Support investigations of deviations, non-conformances, and customer complaints, ensuring appropriate follow-up and resolution.</li><li>Provide training and guidance to employees on QMS-related processes and regulatory requirements.</li><li>Ensure compliance with all regulatory requirements.</li><li>Support risk assessments and help mitigate potential quality risks to product safety and compliance.</li><li>Familiarity with pharmaceutical operations, preferably MDI, to ensure required compliance.</li><li>Familiarity with TrackWise applications for handling Deviation and CAPA.</li><li>Prepare and review investigations related to deviation, OOS, market complaints, and microbiological failure.</li><li>Prepare and review trends related to various QMS elements like Deviations, CAPA, Change Request, and Environmental monitoring.</li><li>Preparation and review of the Annual Product Quality Review.</li><li>Fulfill the requirements of regulatory submission while closely working with regulatory teams.</li><li>Prepare and review risk assessments (FMECA) for various facilities, equipment, processes, and particular events.</li><li>Prepare and review elemental impurities risk assessment and nitrosamine-related risk assessment.</li><li>Prepare audit reports, document findings, and provide actionable recommendations for improvement.</li></ul><h2>Essential Skills</h2><ul><li>Quality auditing</li><li>Quality assurance</li><li>Quality management system</li><li>GMP</li><li>Batch record review</li><li>Deviation investigations</li><li>Out of Specifications (OOS)</li><li>Out of Trends (OOT)</li><li>CAPA</li><li>Change control</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Advanced vocational training or education in pharmaceutical manufacturing, industrial management, or related field from an accredited institution.</li><li>Bachelor&#39;s degree in a scientific discipline such as biology, chemistry, pharmacy, or related field is preferred.</li><li>Minimum of 3 years of experience in MDI or combination products is preferred.</li><li>Proficient in Microsoft Office tools, SAP, and other business applications.</li><li>Ability to influence decision-making and facilitate completion of work towards achieving business goals.</li><li>Effective interpersonal relationship skills and ability to work in a team environment.</li><li>Proficiency in English, including usage, spelling, grammar, and punctuation.</li><li>Current Good Manufacturing Practices (cGMP) knowledge.</li><li>Self-starter demonstrating initiative with seeking additional training or direction.</li><li>Strong organization and leadership skills, both written and verbal.</li><li>Detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.</li></ul><h2>Work Environment</h2><p>You will be working with a small team of 15 people in the quality department, with significant cross-collaboration with different departments. This role operates on a first shift from 8:00 am to 5:00 pm, Monday to Friday.</p><br>

QA QMS Associate

<h1><strong>Job Title: QA Regulatory Affairs Specialist</strong></h1><p><br></p><h2>Job Description</h2><p>This position requires reviewing label content to ensure accuracy, consistency, and compliance. The role involves using labeling software to prepare and submit SPL, collaborating with customers for private labeling, and communicating labeling requirements and timelines to internal stakeholders.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate label approvals and manage version controls and updated labeling.</li><li>Support change control processes related to labeling updates.</li><li>Coordinate labeling projects to ensure regulatory compliance.</li><li>Facilitate project completion through effective and detailed project management.</li><li>Provide guidance to team members on labeling regulations and process requirements.</li><li>Initiate, review, and implement label creation/updates with extreme attention to detail.</li><li>Identify and recommend process improvements to enhance business practices.</li><li>Provide regular updates regarding labeling projects to cross-functional departments.</li><li>Foster collaborative, efficient, and effective working relationships with internal teams.</li><li>Prepare and submit Annual Reports.</li><li>Mentor team members and act as a recognized resource to local team.</li><li>Perform other duties as assigned based on business requirements.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance expertise.</li><li>Knowledge of FDA regulations.</li><li>Understanding of SOPs.</li><li>Ability to partner with members across departments like Regulatory and Quality to ensure compliance.</li><li>Proficient knowledge of GMP and Quality Management Systems.</li><li>Computer literacy in Windows applications and MS Office (Word, Excel, Outlook).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>A minimum of a BS in a scientific discipline.</li><li>1-3 years of experience in pharmaceutical manufacturing.</li><li>1-2 years of quality experience with pharmaceutical FDA submissions.</li></ul><h2>Work Environment</h2><p>This role operates within a GMP environment on the QA team, offering room for growth. The position requires collaboration with teams based both in the US and India.</p>

QA Regulatory Affairs Specialist

<h1><strong>Job Title: QA Sanitation Lead</strong></h1><p><br></p><h2>Job Description</h2><p>This role involves ensuring the highest standards of quality and safety in a food manufacturing environment. The QA Sanitation Lead will be responsible for overseeing the sanitation processes and procedures, focusing on HACCP, GMP, and raw materials management. Additionally, the role includes maintaining documentation, implementing SOPs, and ensuring the effective operation of metal detectors and quality review on production lines.</p><p><br></p><h2>Responsibilities</h2><ul><li>Implement and oversee HACCP and GMP protocols.</li><li>Manage raw materials and ensure proper documentation.</li><li>Develop and enforce SOPs for sanitation and quality control.</li><li>Operate and maintain metal detectors.</li><li>Conduct quality reviews on production lines.</li><li>Apply the 7 steps of cleaning process.</li><li>Calculate concentration levels of chemical cleaners.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in microbiology and HACCP.</li><li>Experience in inspection and sampling.</li><li>Strong cleaning and swabbing skills.</li><li>Ability to follow SOPs, HACCP, and GMP guidelines.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or greater.</li><li>Experience in food manufacturing is preferred.</li><li>Excellent communication skills across departments.</li></ul><h2>Work Environment</h2><p>The role is set in a production environment where you will be required to walk different lines and collect samples for testing. The position involves working third shift from Monday to Friday, starting between 7/8pm and ending at 3:30/4:30am, or a seniorrole from Sunday to Thursday from 8pm to 4:30am. The workplace offers competitive benefits, including a 401K plan. Employees are encouraged to build their resumes in a top-tier food manufacturing setting.</p>

QA Sanitation Lead

<h1 style="font-weight: 700;">Job Title: QA Specialist</h1><br><h2>Job Description</h2><p>This position requires reviewing label content to ensure accuracy, consistency, and compliance. The role involves using labeling software to prepare and submit SPL, collaborating with customers for private labeling, and communicating labeling requirements and timelines to internal stakeholders.</p><br><h2>Responsibilities</h2><ul><li>Coordinate label approvals and manage version controls and updated labeling.</li><li>Support change control processes related to labeling updates.</li><li>Coordinate labeling projects to ensure regulatory compliance.</li><li>Facilitate project completion through effective and detailed project management.</li><li>Provide guidance to team members on labeling regulations and process requirements.</li><li>Initiate, review, and implement label creation/updates with extreme attention to detail.</li><li>Identify and recommend process improvements to enhance business practices.</li><li>Provide regular updates regarding labeling projects to cross-functional departments.</li><li>Foster collaborative, efficient, and effective working relationships with internal teams.</li><li>Prepare and submit Annual Reports.</li><li>Mentor team members and act as a recognized resource to local team.</li><li>Perform other duties as assigned based on business requirements.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance expertise.</li><li>Knowledge of FDA regulations.</li><li>Understanding of SOPs.</li><li>Ability to partner with members across departments like Regulatory and Quality to ensure compliance.</li><li>Proficient knowledge of GMP and Quality Management Systems.</li><li>Computer literacy in Windows applications and MS Office (Word, Excel, Outlook).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>A minimum of a BS in a scientific discipline.</li><li>1-3 years of experience in pharmaceutical manufacturing.</li><li>1-2 years of quality experience with pharmaceutical FDA submissions.</li></ul><h2>Work Environment</h2><p>This role operates within a GMP environment on the QA team, offering room for growth. The position requires collaboration with teams based both in the US and India.</p><br>

QA Specialist

<h1 style="font-weight: 700;">Job Title: QA Specialist</h1><br><h2>Job Description</h2><p>We are seeking a proactive and detail-oriented Quality Assurance (QA) Associate to support clinical and commercial manufacturing operations. This role will focus on reviewing and managing documentation for registration and clinical batches, ensuring compliance with regulatory requirements, and supporting R&amp;D and feasibility projects. The ideal candidate will be comfortable working independently on smaller projects, collaborating cross-functionally, and maintaining high standards of quality and accountability.</p><br><h2>Responsibilities</h2><ul><li>Review and understand batch records, manufacturing protocols, and registration/clinical batch documentation.</li><li>Ensure documentation aligns with FDA and other regulatory agency requirements.</li><li>Manage deviations, change controls, and CAPAs as they arise.</li><li>Evaluate method validation and equipment qualification protocols and reports.</li><li>Ensure SOPs are followed and documentation is complete and accurate.</li><li>Provide feedback on validation documents and ensure alignment with regulatory expectations.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance experience with a focus on batch record review and GMP compliance.</li><li>2-4 years of experience in a QA role, specifically in document review of Batch Records, Equipment Records, Validation Records, etc.</li><li>Collaboration and initiative to seek help or additional work.</li><li>Attention to detail and accountability.</li><li>Ability to prioritize tasks and review protocols effectively.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>AS/BS Degree Preferred, HS Diploma Required.</li><li>2+ years in a Quality/GMP Environment with at least 2 years directly in a QA role.</li><li>Pharmaceutical industry experience strongly preferred.</li><li>Experience reviewing batch records in a commercial setting and understanding supporting documents such as Deviations and Change Controls.</li><li>Well-rounded experience in reviewing documentation for GMP compliance.</li></ul><h2>Work Environment</h2><p>The QA Specialist will work on the R&amp;D side of the building, which offers a quieter environment than the operations side. The role involves walking through scale-up production environments or entering the operations building for final clinical batch compliance. The position provides an individual office space, with primarily onsite work and occasional flexibility for minimal remote work if necessary. The work schedule is Monday to Friday, from 7:30 AM to 4:00 PM, or a similar variation. Collaboration with internal teams is essential, and the position occasionally supports CDMO-related tasks. The role promises exposure to diverse QA experiences and a supportive R&amp;D team, with potential for role extension into 2026.</p><br>

QA Specialist (Pharmaceutical Batch Records)

<h1 style="font-weight: 700;">Job Title: Quality Assurance Technician</h1><br><h2>Job Description</h2><p>The Quality Assurance Technician is responsible for ensuring that all products manufactured in the plant meet customer expectations in terms of quality, cost, and service. This role provides effective support for all plant functions to achieve this goal and proactively complies with all local, state, federal regulations, and corporate/plant policies, rules, and procedures.</p><br><h2>Responsibilities</h2><ul><li>Perform all activities associated with testing the physical and performance attributes of test products.</li><li>Maintain current knowledge of accepted methods, specifications, standards, and tolerances.</li><li>Place product that does not meet requirements on hold as needed.</li><li>Evaluate all products, including test results and related information, to make informed decisions on passing, holding, rejecting, dispositioning, or reworking products and take appropriate action.</li><li>Communicate to the appropriate personnel when product samples do not meet requirements.</li><li>Record all data and information related to quality accurately and thoroughly.</li><li>Enter product testing/results into a computer system and ensure complete upkeep and maintenance of these records.</li><li>Maintain day-to-day working conditions in the lab, including cleanliness, orderliness, safety, routine maintenance, sanitation, and organization of controls, samples, records, and files.</li><li>Adhere to food safety, quality, and regulatory policies and procedures; execute duties as outlined in standard operating procedures; and report any related concerns to the Production or Quality Supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Line inspection</li><li>Quality assurance</li><li>Quality inspection</li><li>Biology</li><li>Lab experience</li><li>Quality control</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree in the Sciences OR 2 years of Quality Experience from FDA regulated industries.</li></ul><h2>Work Environment</h2><p>The role operates on a 12-hour 2-2-3 schedule, with openings from 6 a.m. to 6 p.m. and from 6 p.m. to 6 a.m. Training will be conducted directly on the shift.</p><br>

QA Tech

<h1><strong>Job Title: Quality Assurance Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Assurance Technician is responsible for ensuring that all products manufactured in the plant meet customer expectations in terms of quality, cost, and service. This role provides effective support for all plant functions to achieve this goal and proactively complies with all local, state, federal regulations, and corporate/plant policies, rules, and procedures.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform all activities associated with testing the physical and performance attributes of test products.</li><li>Maintain current knowledge of accepted methods, specifications, standards, and tolerances.</li><li>Place product that does not meet requirements on hold as needed.</li><li>Evaluate all products, including test results and related information, to make informed decisions on passing, holding, rejecting, dispositioning, or reworking products and take appropriate action.</li><li>Communicate to the appropriate personnel when product samples do not meet requirements.</li><li>Record all data and information related to quality accurately and thoroughly.</li><li>Enter product testing/results into a computer system and ensure complete upkeep and maintenance of these records.</li><li>Maintain day-to-day working conditions in the lab, including cleanliness, orderliness, safety, routine maintenance, sanitation, and organization of controls, samples, records, and files.</li><li>Adhere to food safety, quality, and regulatory policies and procedures; execute duties as outlined in standard operating procedures; and report any related concerns to the Production or Quality Supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Line inspection</li><li>Quality assurance</li><li>Quality inspection</li><li>Biology</li><li>Lab experience</li><li>Quality control</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree in the Sciences OR 2 years of Quality Experience from FDA regulated industries.</li></ul><h2>Work Environment</h2><p>The role operates on a 12-hour 2-2-3 schedule, with openings on both Day and Night Shift. Training will be conducted directly on the shift.</p>

<h1 style="font-weight: 700;">Job Title: QA Technician</h1><br><h2>Job Description</h2><p>The QA Technician will be responsible for testing raw ingredients, in-process, and finished products at the facility. The role involves working with general lab instrumentation and conducting wet chemistry analyses. You will perform tests for pH, solids, fats, and moisture, and be responsible for wastewater analysis and general wet chemistry. Additionally, you may engage in microbiological sample testing.</p><br><h2>Responsibilities</h2><ul><li>Conduct testing of raw ingredients, in-process, and finished products.</li><li>Utilize general lab instrumentation for analysis.</li><li>Perform wet chemistry tests including pH, solids, fats, and moisture analysis.</li><li>Conduct wastewater analysis.</li><li>Engage in microbiological sample testing as required.</li></ul><h2>Essential Skills</h2><ul><li>0-2 years of experience in a Food Manufacturing laboratory setting.</li><li>1 or more years of laboratory experience.</li><li>Quality assurance and quality control knowledge.</li><li>Inspection skills.</li><li>Biology and chemistry expertise.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associates Degree in Sciences preferred.</li></ul><h2>Work Environment</h2><p>The facility is dedicated to extracting whey protein for animal feed and includes a microbiology and chemistry lab. The technician may be required to work every other weekend.</p><br>

QA Technician

<h1><strong>Job Title: Quality Analyst</strong></h1><p><br></p><h2>Job Description</h2><p>You will play a crucial role in ensuring compliance and quality in our food manufacturing processes, working in a company that is expanding its operations due to increasing customer demands.</p><p><br></p><h2>Responsibilities</h2><ul><li>Review and approve records to ensure compliance.</li><li>Identify deviations and initiate corrective actions, including root cause analyses.</li><li>Manage the disposition of raw materials and products as Hold/Release/Quarantine using electronic WMS systems.</li><li>Conduct basic food safety, cGMP, and quality-related training for new hires.</li><li>Assist in developing SOPs related to manufacturing processes and production personnel compliance training.</li><li>Provide support during audits by regulatory and third parties.</li><li>Conduct and coordinate environmental testing as part of the Environmental Monitoring Program.</li><li>Collect raw materials for testing and sample finished products to identify sensory attributes.</li><li>Evaluate sensory characteristics for product approval and shelf life studies.</li><li>Collaborate with production personnel to correct processes if products are out of compliance.</li><li>Convey test results to appropriate personnel and follow up if needed.</li><li>Complete audits based on the production schedule.</li><li>Conduct and coordinate facility environmental testing.</li><li>Promote and follow GMPs for the facility.</li></ul><h2>Essential Skills</h2><ul><li>Quality control and assurance knowledge.</li><li>Understanding of GMP, HACCP, SQF, GFSI, and PCQI standards.</li><li>Food safety expertise.</li><li>Experience in food manufacturing and batch record review.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>2+ years of experience in Food or GMP Manufacturing Quality.</li><li>A degree in the sciences is preferred.</li><li>Training or experience in SQF, HACCP, GFSI, or PCQI is a plus.</li></ul>

QA Technician-3rd Shift

<h2 style="text-align: center;"><strong>**Immediate Opening: Quality Control Assurance Laboratory Technician**</strong></h2><p style="text-align: center;"><strong>Interested in this role? </strong>Reach out directly to apply <strong>TODAY </strong>to <strong>Grace Williams </strong>at <strong>grawilliams@actalentservices .com</strong></p><h2><br></h2><p style="text-align: center;"><br></p><p><br></p><p><br></p><p><strong>Position Summary</strong></p><p>Are you passionate about food safety, precision, and laboratory excellence? Join our team as a <strong>Quality Control Assurance Laboratory</strong></p><p><strong>Technician</strong> and play a vital role in upholding the highest standards of product quality and regulatory compliance. We are looking for a detail-oriented and dedicated professional to support our facility through comprehensive testing of finished products, packaging, and raw materials. In this hands-on role, you’ll dive into testing finished products, packaging, and raw materials—making sure everything is up to spec before it reaches our customers. You’ll be a key player in a fast-paced, collaborative environment where your work directly impacts the safety and satisfaction of consumers. This is an exciting opportunity to support finished product, packaging, and raw material testing within a dynamic production environment.</p><p><br></p><p>If you&#39;re detail-driven, science-savvy, and ready to make a difference in a dynamic production setting, we’d love to meet you!</p><p><br></p><p><strong>Key Responsibilities</strong></p><ul><li>Conduct laboratory testing to ensure products meet established specifications</li><li>Accurately enter and consolidate lab data, and report findings to operational teams</li><li>Support internal audits and maintain laboratory equipment</li><li>Participate in cross-training within chemistry labs to enhance team flexibility</li><li>Test finished goods, raw materials (milk, oil, corn syrup), and packaging for compliance.</li><li>Conduct cream release, component, and identity (ID) testing on incoming materials.</li><li>Execute quality control tests on raw, in-process, and finished products.</li><li>Perform mathematical calculations related to quality assurance.</li><li>Calibrate Charm SL equipment and prepare FT2 cleaning and zero solutions.</li><li>Maintain a clean, organized, and safe laboratory environment in compliance with safety and contamination policies.</li><li>Monitor and record temperatures of refrigerators and incubators daily.</li><li>Manage sample receipt, handling, and testing for finished products, raw materials, and packaging.</li><li>Record, review, and verify data using Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).</li><li>Execute laboratory procedures and the Internal Control Plan (ICP) with accuracy.</li><li>Enter test results and perform all required transactions in SAP and related data systems.</li><li>Consolidate, trend, and report laboratory data to operations; escalate out-of-spec results promptly.</li><li>Manage inventory and ordering of lab consumables.</li><li>Revise protocols and process flows as needed.</li><li>Conduct routine quality and food safety audits.</li><li>Support continuous improvement initiatives.</li><li>Obtain and maintain Appendix N certification; complete annual split samples.</li></ul><p><strong>Qualifications</strong></p><ul><li>Bachelor’s degree in a life science field (e.g., Biology, Chemistry, Food Science).</li><li>Understanding of GMP, HACCP, SQF, and food safety regulations.</li><li>Familiarity with wet chemistry, titration, and chemical testing.</li><li>Ability and understanding to follow quality assurance checks/inspections/lab tests</li></ul><p><br></p><p><strong>Work Environment</strong></p><ul><li>Time split between lab and production floor to conduct sampling and testing.</li><li>Tasks include sensory evaluation, instrument calibration, and bulk material testing (milk, sugar, oil).</li></ul><p><br></p><p><strong><u>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</u></strong></p><p><em><u>*Interview availability this week*</u></em></p><ul><li>I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to <strong>Grace Williams</strong>.</li><li><strong>HOW TO APPLY DIRECTLY: </strong>Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to <strong>grawilliams@actalentservices. com </strong>or call me directly at <strong>(317-567 -6610)</strong></li></ul><h2><br></h2>

QA/QC Lab Tech - HIRING NOW

<h1><strong>Job Title: QA/QC Program Engineer V</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced M&amp;E QA/QC Support Engineer to join our team. The successful candidate will be responsible for developing and monitoring quality program metrics, analyzing trends, and working with applicable parties to correct any issues. This role will also involve assisting with the development of on-site partner construction QA and QC teams, as well as providing training to personnel regarding awareness and quality procedures. The ideal candidate is self-driven, possesses the ability to have difficult conversations on any misalignments that may arise, and is focused on leading and coaching a team.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and monitor quality program metrics to evaluate project performance.</li><li>Analyze metrics to understand the root cause of any disconcerting trends and work with applicable parties to correct those items.</li><li>Assist with the development of on-site partner construction QA and QC teams.</li><li>Assist with the development of QA/QC processes and standards to enable efficiency and effectiveness and support cross-functional communications.</li><li>Interface between design construction and facility operations, as well as general contractors.</li><li>Provide training to personnel regarding awareness and quality procedures and specific responsibilities in the QA/QC process.</li><li>Coordinate quality issues between design construction and facility operations teams.</li><li>Audit QA/QC activities of staff and subcontractors as necessary to assess conformance with QA/QC procedures.</li><li>Examine all submittals, particularly mechanical engineering and plumbing MEP submittals for quality assurance, and provide comments to ensure compliance.</li><li>Perform quality engineering reviews of design documentation for compliance with stated requirements, including vendor quality manuals and company quality records.</li><li>Develop, review, and approve levels 1 to 5 related to product and process quality, such as construction quality procedures (CQPs), checklists, technical deliverables, and test procedures and plans.</li><li>Recommend and verify effective implementation of corrective and preventive actions for project non-conformances and quality issues in coordination with project and quality management, design engineering, construction, and other functional disciplines.</li><li>Review commissioning agent level 4 and 5 commissioning scripts and provide feedback.</li><li>Assist construction manager in reviewing turnover documentation packages for completeness and accuracy.</li><li>Assist construction manager in reviewing level 3, 4, and 5 energization, start-up, and commissioning schedules and help ensure compliance.</li><li>Help drive closure to open issues in BIM360 and escalate outstanding open items not getting closed out promptly.</li><li>Attend factory witness tests (FWTs) as required for owner furnished contractor installed (OFCI) and contractor furnished contractor installed (CFCI) equipment and systems.</li><li>Provide an onsite visual inspection and/or observation for construction quality control of OFCI and CFCI equipment and systems, documenting site acceptance inspection in BIM360.</li><li>Assist in confirming that level 2 and level 3 testing documentation is properly completed and retained.</li><li>Provide assistance in reviewing installed labeling, signage, and tagging.</li><li>Assist in developing project-specific QA/QC dashboards, equipment tracking matrices, and semi-annual QA/QC deep dive presentations.</li><li>Attend required construction meetings such as weekly project and monthly global QA/QC meetings, MEP/owner architect contractor (OAC) weekly meetings, and daily start-up and commissioning meetings.</li></ul><h2>Essential Skills</h2><ul><li>5+ years of experience in quality control and quality assurance (QA/QC) programs for data centers or mission critical construction projects.</li><li>Strong mechanical and electrical QA knowledge.</li><li>Experience with Design-Build and Design-Bid-Build construction programs.</li><li>Experience in civil/structural building envelope, mechanical, electrical, and IC disciplines.</li><li>Experience leading QA/QC and Cx programs.</li><li>Experience in contractor, consultant, and vendor management.</li><li>Experience in mission critical power and cooling infrastructure or other critical systems.</li><li>Ability to apply experience to current data center challenges.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree, preferably in mechanical or electrical areas of study.</li><li>QA or PE certifications are highly valued.</li><li>People-focused with strong interpersonal skills.</li><li>Ability to work well with cross-functional partners.</li><li>QA/QC commissioning skills.</li><li>Vendor Management skills.</li></ul>

QA/QC Program Engineer V

<h1 style="font-weight: 700;">Job Title: QA/QC Program Engineer V</h1><br><h2>Job Description</h2><p>We are seeking an experienced M&amp;E QA/QC Support Engineer to join our team. The successful candidate will be responsible for developing and monitoring quality program metrics, analyzing trends, and working with applicable parties to correct any issues. This role will also involve assisting with the development of on-site partner construction QA and QC teams, as well as providing training to personnel regarding awareness and quality procedures. The ideal candidate is self-driven, possesses the ability to have difficult conversations on any misalignments that may arise, and is focused on leading and coaching a team.</p><br><h2>Responsibilities</h2><ul><li>Develop and monitor quality program metrics to evaluate project performance.</li><li>Analyze metrics to understand the root cause of any disconcerting trends and work with applicable parties to correct those items.</li><li>Assist with the development of on-site partner construction QA and QC teams.</li><li>Assist with the development of QA/QC processes and standards to enable efficiency and effectiveness and support cross-functional communications.</li><li>Interface between design construction and facility operations, as well as general contractors.</li><li>Provide training to personnel regarding awareness and quality procedures and specific responsibilities in the QA/QC process.</li><li>Coordinate quality issues between design construction and facility operations teams.</li><li>Audit QA/QC activities of staff and subcontractors as necessary to assess conformance with QA/QC procedures.</li><li>Examine all submittals, particularly mechanical engineering and plumbing MEP submittals for quality assurance, and provide comments to ensure compliance.</li><li>Perform quality engineering reviews of design documentation for compliance with stated requirements, including vendor quality manuals and company quality records.</li><li>Develop, review, and approve levels 1 to 5 related to product and process quality, such as construction quality procedures (CQPs), checklists, technical deliverables, and test procedures and plans.</li><li>Recommend and verify effective implementation of corrective and preventive actions for project non-conformances and quality issues in coordination with project and quality management, design engineering, construction, and other functional disciplines.</li><li>Review commissioning agent level 4 and 5 commissioning scripts and provide feedback.</li><li>Assist construction manager in reviewing turnover documentation packages for completeness and accuracy.</li><li>Assist construction manager in reviewing level 3, 4, and 5 energization, start-up, and commissioning schedules and help ensure compliance.</li><li>Help drive closure to open issues in BIM360 and escalate outstanding open items not getting closed out promptly.</li><li>Attend factory witness tests (FWTs) as required for owner furnished contractor installed (OFCI) and contractor furnished contractor installed (CFCI) equipment and systems.</li><li>Provide an onsite visual inspection and/or observation for construction quality control of OFCI and CFCI equipment and systems, documenting site acceptance inspection in BIM360.</li><li>Assist in confirming that level 2 and level 3 testing documentation is properly completed and retained.</li><li>Provide assistance in reviewing installed labeling, signage, and tagging.</li><li>Assist in developing project-specific QA/QC dashboards, equipment tracking matrices, and semi-annual QA/QC deep dive presentations.</li><li>Attend required construction meetings such as weekly project and monthly global QA/QC meetings, MEP/owner architect contractor (OAC) weekly meetings, and daily start-up and commissioning meetings.</li></ul><h2>Essential Skills</h2><ul><li>5+ years of experience in quality control and quality assurance (QA/QC) programs for data centers or mission critical construction projects.</li><li>Strong mechanical and electrical QA knowledge.</li><li>Experience with Design-Build and Design-Bid-Build construction programs.</li><li>Experience in civil/structural building envelope, mechanical, electrical, and IC disciplines.</li><li>Experience leading QA/QC and Cx programs.</li><li>Experience in contractor, consultant, and vendor management.</li><li>Experience in mission critical power and cooling infrastructure or other critical systems.</li><li>Ability to apply experience to current data center challenges.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree, preferably in mechanical or electrical areas of study.</li><li>QA or PE certifications are highly valued.</li><li>People-focused with strong interpersonal skills.</li><li>Ability to work well with cross-functional partners.</li><li>QA/QC commissioning skills.</li><li>Vendor Management skills.</li></ul><h2>Work Environment</h2><p>The work environment involves 100% onsite engagement with various stakeholders including third-party vendors, design teams, and construction teams. The role requires managing the entire work scope, providing guidance on QA scope, risk management reporting, and attending construction meetings. The position supports a collaborative environment aimed at achieving high standards of quality and efficiency.</p><br>

<h1 style="font-weight: 700;">Job Title: QC Associate II</h1><br><h2>Job Description</h2><p>We are seeking a motivated QC Associate II to join our team, where you will play a crucial role in testing and validating assays, implementing change controls, and conducting stability and raw material testing. You will also be responsible for thorough documentation and quality management systems.</p><br><h2>Responsibilities</h2><ul><li>Conduct testing using ELISA assays, PCR, SDS-Page, Gel Electrophoresis, and Microbiological assays.</li><li>Validate assays to ensure accuracy and reliability.</li><li>Manage change controls and contribute to stability and raw material testing.</li><li>Maintain detailed documentation and adhere to Quality Management Systems (QMS).</li><li>Revise Standard Operating Procedures (SOPs) as needed.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in ELISA assays, validation, and documentation.</li><li>Experience with Quality Control processes.</li><li>Familiarity with PCR, Gel Electrophoresis, and Microbiological assays.</li><li>Ability to document test data accurately.</li><li>Understanding of Good Manufacturing Practices (GMP).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in a science-related field.</li><li>Experience in a late-stage clinical trial environment or commercial setting is helpful.</li></ul><h2>Work Environment</h2><p>This role requires working in both office and lab settings, offering a dynamic environment for growth and development as we prepare for phase 3 of clinical trials. Exciting opportunities await as we embark on the next round of manufacturing and testing.</p><br>

QC Associate II

<h1><strong>Job Title: Quality Control Chemist</strong></h1><p><br></p><h2>Job Description</h2><p>This position involves supporting the Quality Control team by ensuring the effective operation of analytical instrumentation and methodologies. Recent chemistry grads with an emphasis on analytical chemistry are encouraged to apply!</p><p><br></p><h2>Responsibilities</h2><ul><li>Support the Quality Control team in various tasks and processes.</li><li>Operate and maintain analytical instruments such as HPLC and GCMS.</li><li>Ensure the accuracy and reliability of testing results.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Chemistry.</li><li>Experience with analytical instrumentation, specifically HPLC and GCMS.</li><li>Strong quality control abilities.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Typing skills.</li><li>Proficiency in mathematics.</li></ul><h2>Work Environment</h2><p>The role is based in a lab setting, requiring a focus on precision and attention to detail.</p>

QC Chemist

<h1 style="font-weight: 700;">Job Title: QC Compendial Scientist II</h1><br><h2>Job Description</h2><p>In this role, you will utilize a range of analytical tools for large molecule analysis, including Compendial Testing (pH, UV, Osmolality), and other minor equipment. Your work will support GMP manufacturing through commercial product testing and Stability testing, among other client-requested endeavors. This position requires experience in a cGMP environment.</p><br><h2>Responsibilities</h2><ul><li>Perform Compendial Testing (pH, UV, Osmolality) using Spectrometer, Plate Readers, SoloVPE, qPCR, and color metric-based assays like Picogreen and Bradford on In-Process, DS release, and stability samples, ensuring timely project delivery.</li><li>Review laboratory data packets as assigned.</li><li>Perform and author laboratory investigations as assigned.</li><li>Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods such as Reverse Phase, SEC, CEX, etc.</li><li>Compile data for documentation of test procedures and prepare reports while collaborating with team members and other departments like quality assurance and data reviewers.</li><li>Contribute to the development of new concepts, techniques, and standards.</li><li>Recognize and report invalid/lab incident/out-of-specification/out-of-trend results to laboratory management and recommend solutions.</li><li>Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines.</li><li>Participate in laboratory activities, including performing safety inspections and ordering supplies.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Compendial Testing (pH, UV, Osmolality)</li><li>Experience with Spectrometer and Plate Readers</li><li>Qualitative pipetting skills</li><li>Knowledge of SoloVPE or A280 techniques</li><li>Bachelor’s degree in chemical pharmaceutical, biology, chemistry, biotechnology or related field</li><li>2+ years of experience in a GMP regulated environment, preferably in pharmaceuticals</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with qPCR and color metric-based assays like Picogreen and Bradford</li><li>Familiarity with wet chemistry and bioassay techniques</li><li>Flexibility, good organization and planning skills</li><li>Attention to details, positive and collaborative demeanor</li></ul><h2>Work Environment</h2><p>The role operates Monday to Friday from 8am to 4:30pm with a flexible start time. Training on all assays will occur during the first 3-6 months. The team currently consists of 3 members and is expected to grow to 6 members soon.</p><br>

QC Compendial Scientist II

<h1><strong>Job Title: QC Data Reviewer</strong></h1><p><br></p><h2>Job Description</h2><p>As a QC Data Reviewer, you will be responsible for overseeing a team of 14 chemists and lab technicians who test finished products, raw materials, and ANDA products within the laboratory. You will ensure data reviews are completed and aid in audits and investigations concerning deviations occurring during daily testing of pharmaceutical products. You will also assist with testing samples, including oral rinses and antiseptics, using titrations, pH, specific gravity, and HPLC as needed.</p><p><br></p><h2>Responsibilities</h2><ul><li>Supervise chemists and lab technicians testing finished products, raw materials, in-process samples, and components.</li><li>Perform data reviews and support audits and investigations on testing deviations for pharma products.</li><li>Assist in testing new ANDA pro</li><li>ducts, primarily Oral Dose products.</li><li>Conduct testing using HPLC, GC, TOC, FT-IR, UV-Vis, and pH meters.</li><li>Inspect supplies and ingredients used in pharmaceutical production.</li><li>Review SOPs and lab protocols for accuracy.</li><li>Participate in instrument validation when required.</li><li>Ensure adherence to GMP and FDA guidelines.</li></ul><h2>Essential Skills</h2><ul><li>3-5+ years of experience in HPLC/GC and Pharma/cGMP settings.</li><li>Bachelor’s degree with a major in chemistry.</li><li>Knowledge of GMP and GDP.</li><li>Experience in data review and documentation.</li><li>Proficiency in Microsoft Office.</li><li>Familiarity with OpenLab and LIMS software.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Preferred 4 years of pharmaceutical industry experience with hands-on GC, HPLC, FTIR, and wet chemistry.</li><li>Good handwriting for laboratory notebook documentation.</li><li>Knowledge of Agilent OpenLab software is an advantage.</li></ul><h2>Work Environment</h2><p>The position is based in a QC Lab at a pharmaceutical company specializing in oral rinse and antiseptic solutions, among other pharma products. Work primarily involves testing new ANDA products within the Oral Dose division. The company is rapidly growing and has recently expanded with a new lab site. The work schedule is during the 1st shift, from 8 AM to 4 PM or 9 AM to 5 PM.</p>

QC Data Reviewer

<h2 style="text-align: center;"><strong>**IMMEDIATE OPENING: QC Lab Analyst**</strong></h2><p style="text-align: center;"><em><u>*Interview availability this week*</u></em></p><p><br></p><p style="text-align: center;"><strong>Interested in this role? </strong>Reach out directly to apply <strong>TODAY </strong>to <strong>Grace Williams </strong>at <strong>grawilliams@actalentservices .com</strong> (HIRING NOW)</p><h2><br></h2><h2><strong>Position Summary</strong></h2><p>We are seeking a dedicated and detail-oriented Quality Control (QC) Lab Analyst to join our team at a leading ingredient manufacturing company specializing in corn starch products. The QC Lab Technician will play a crucial role in ensuring the quality and safety of our products through rigorous testing, analysis, quality control, and documentation.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Conduct raw materials testing to ensure compliance with quality standards.</li><li>The day-to-day testing is unique to the industry so most of the instrumentation will be new to most candidates.</li><li>Perform a variety of analytical tests independently and accurately, following established test procedures.</li><li>Utilize industry-specific instrumentation such as viscosity meters, moisture analyzers, Near-Infrared (NIR) spectroscopy, PH, Moisture Balance, Protein Analysis, Viscosity, Inductively Coupled Plasma (ICP) spectrometry, and other relevant equipment.</li><li>Maintain complete, accurate, and legible test records in accordance with company policies and record-keeping procedures.</li><li>Adhere to all safety and quality guidelines, including Good Laboratory Practices (GLP) and lab safety requirements.</li><li>Assist in the development and validation of new testing methods and procedures.</li><li>Collaborate with other departments to address quality issues and implement corrective actions.</li><li>Participate in routine equipment maintenance and calibration to ensure accurate test results.</li><li>Support continuous improvement initiatives within the QC department.</li></ul><h2><strong>Qualifications</strong></h2><ul><li>Bachelor&#39;s degree in Chemistry, Biology, or a related field required.</li><li>Strong attention to detail and ability to follow precise procedures.</li><li>Excellent organizational and record-keeping skills.</li><li>Ability to work independently and as part of a team.</li><li>Familiarity with GMP, GLP, and lab safety protocols.</li><li>Previous experience in a laboratory setting, particularly in the food or ingredient manufacturing industry, is a plus.</li></ul><h2>Work Environment</h2><p>This is a fast-paced food manufacturing environment where the candidate will be exclusively working in the laboratory. </p><p><br></p><h2><strong><u>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</u></strong></h2><p><em><u>*Interview availability this week*</u></em></p><ul><li>I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to <strong>Grace Williams</strong>.</li><li><strong>HOW TO APPLY DIRECTLY: </strong>Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to <strong>grawilliams@actalentservices. com </strong>or call me directly at <strong>(317-567 -6610)</strong></li></ul><h2><br></h2>

QC Lab Analyst - IMMEDIATE OPENING

<h1 style="text-align: center;"><strong><u> Quality Control Lab Technician</u></strong></h1><p style="text-align: center;">INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW!</p><p style="text-align: center;"><br></p><p>2nd Shift Quality Control Lab Technician</p><p>Location: Sharonville, OH</p><p>Schedule: Monday–Friday, 2:30 PM – 10:30 PM (occasional Saturdays based on production needs)</p><h3>About the Role</h3><p>We’re looking for a detail-orientedQuality Control Lab Technicianto join our 2nd shift team. This role is ideal for someone with adegree in Chemistryor ascience-related degree with strong chemistry courseworkwho can confidently speak to their chemistry knowledge. You’ll play a key role in ensuring our products meet the highest quality standards through hands-on lab testing and analysis.</p><h3>Key Responsibilities</h3><ul><li>Perform routine testing on production batches and finished products following SOPs and FDA/GMP guidelines.</li><li>Conduct chemical analyses using techniques such asHPLC, GC, TOC, andwet chemistry.</li><li>Record and evaluate test results, identify trends, and communicate necessary batch adjustments.</li><li>Assist with raw material inspection and environmental monitoring.</li><li>Maintain lab cleanliness, equipment, and inventory.</li><li>Support compliance with current Good Manufacturing Practices (cGMP).</li><li>Collaborate with other shifts to ensure smooth communication and continuity.</li></ul><h3>What We’re Looking For</h3><ul><li>Bachelor’s degree in Chemistryor ascience-related field with significant chemistry coursework.</li><li>Strong understanding of chemical principles and lab techniques.</li><li>Comfortable discussing chemistry concepts and applying them in a lab setting.</li><li>Experience with lab instrumentation (HPLC, GC, pH meters, etc.) is a plus.</li><li>Detail-oriented, organized, and able to work independently on the 2nd shift.</li></ul><h3>Why Join Us?</h3><ul><li>Family-owned and operatedcompany with a close-knit team environment.</li><li>Moreone-on-one trainingand development opportunities than larger organizations.</li><li>A workplace that valuescommunication, consistency, and meaningful work.</li><li>Job securityin a growing and stable industry.</li></ul><p style="text-align: center;"><br></p>

QC Lab Technician

<h1><strong>QC Lab Technician</strong></h1><h2>Job Description</h2><p>We are seeking QC Lab Technicians to support a food ingredient production facility specializing in powdered mixes for dairy products. </p><p><br></p><h2>Responsibilities</h2><ul><li>Test raw material samples from production and perform release of raw materials with appropriate documentation.</li><li>Prepare 50-60 sample batches per shift, which involves weighing ingredients and cooking them at appropriate temperatures.</li><li>Conduct basic lab testing including viscosity, moisture, water activity, and sensory testing such as taste, smell, and appearance.</li><li>Perform microbiology sample preparation duties as needed.</li><li>Handle basic duties including dishwashing, cleaning, sample preparation, and organization in the lab.</li><li>Participate in production room inspections and release, as well as final product release with documentation in the CPU system and QA Logbook.</li><li>Work on feet the majority of the day with occasional desk work for data entry and product release.</li></ul><h2>Essential Skills</h2><ul><li>Knowledge of moisture, raw materials, and quality control processes.</li><li>Ability to conduct sensory tests and basic lab testing.</li><li>Interest in working in a food production facility.</li></ul>

<h1 style="text-align: center;"><strong>QC Lab Technician</strong></h1><h2>Job Description</h2><p>We are seeking QC Lab Technicians to support a food ingredient production facility specializing in powdered mixes for dairy products. </p><p><br></p><h2>Responsibilities</h2><ul><li>Test raw material samples from production and perform release of raw materials with appropriate documentation.</li><li>Prepare 50-60 sample batches per shift, which involves weighing ingredients and cooking them at appropriate temperatures.</li><li>Conduct basic lab testing including viscosity, moisture, water activity, and sensory testing such as taste, smell, and appearance.</li><li>Perform microbiology sample preparation duties as needed.</li><li>Handle basic duties including dishwashing, cleaning, sample preparation, and organization in the lab.</li><li>Participate in production room inspections and release, as well as final product release with documentation in the CPU system and QA Logbook.</li><li>Work on feet the majority of the day with occasional desk work for data entry and product release.</li></ul><h2>Essential Skills</h2><ul><li>Knowledge of moisture, raw materials, and quality control processes.</li><li>Ability to conduct sensory tests and basic lab testing.</li><li>Interest in working in a food production facility.</li></ul>

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