<h1 style="text-align: center;"><strong>QA Technician </strong></h1><p style="text-align: center;"><strong>**3rd Shift: 4pm to 4am**</strong></p><p><br></p><h2>Job Description</h2><p>The Quality Assurance Tech plays a crucial role in ensuring the highest standards of product quality and compliance. The majority of the time will be spent on the production floor, collaborating with the operations team to perform verifications, conduct general walkthroughs, and execute onsite reviews and mini audits. This role requires the ability to initiate solutions to problems, such as initiating deviations, and involves reviewing various documents, including executed batch records, cleaning records, and log books. Issuing batch records as needed is also part of the responsibilities. Approximately 80-85% of time will be spent on the production floor, with the remainder in the office. The role requires adherence to specific gowning requirements, from safety shoes to full gowning.</p><p><br></p><h2>Responsibilities</h2><ul><li>Collaborate with the operations team to perform verifications on the production floor.</li><li>Conduct general walkthroughs and onsite reviews to ensure compliance.</li><li>Execute mini audits to ensure processes are correctly followed.</li><li>Initiate solutions to problems, such as deviations.</li><li>Review and maintain various documents, including batch records and log books.</li><li>Issue batch records as needed.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance expertise.</li><li>FDA and GMP compliance knowledge.</li><li>Experience with batch record review and document control.</li><li>Audit skills.</li><li>Pharmaceutical industry knowledge.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in any science discipline preferred.</li><li>2+ years of experience in a regulated industry (GMP/FDA/ISO).</li><li>For Sr. roles, 5+ years of regulated industry experience.</li><li>For Lead roles, 7+ years of regulated industry experience with potential supervisory responsibilities.</li></ul><h2>Work Environment</h2><p>Training occurs on the first shift, Monday to Friday from 8am to 4:30pm, lasting 6-8 weeks depending on skills. Specific gowning requirements are in place, ranging from safety shoes to full gowning.</p>

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Quality Assurance Technician

<h1 style="font-weight: 700;">Job Title: Quality Assurance Technician</h1><br><h2>Job Description</h2><p>As a Quality Assurance Technician, you will be responsible for reviewing compliance documentation related to raw materials, in-process samples, and finished product analyses. You will monitor adherence to current Good Laboratory Practices (cGLP) by laboratory personnel during routine operations to ensure procedural compliance. Additionally, you will verify that laboratory chemicals, reagents, and standards are properly labeled in accordance with standard operating procedures (SOPs).</p><br><h2>Responsibilities</h2><ul><li>Review laboratory audit trails during data assessments to ensure alignment with SOPs.</li><li>Coordinate with Analytical Laboratory Teams to compile and provide necessary documentation to cross-functional teams.</li><li>Manage incoming documentation, including tracking, recording, storing, and archiving in an organized manner.</li><li>Identify system gaps during routine monitoring and notify supervisors of areas requiring improvement.</li><li>Understand laboratory equipment operation, qualification, and calibrations, including their software audit trail reviews.</li><li>Actively participate in the review of data related to laboratory investigations and incidents to ensure regulatory compliance.</li><li>Support departmental and cross-functional initiatives and complete assignments as directed by the manager or supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Strong documentation and technical writing skills, with the ability to apply relevant scientific principles and practices.</li><li>Ability to work under minimal supervision, independently, and in a team environment.</li><li>Proficiency in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.</li><li>Experience in analytical quality assurance with a focus on inhalation products (MDI) is a plus.</li><li>Effective interpersonal relationship skills and the ability to work in a team environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Possess a minimum bachelor&#39;s degree in Chemistry, Pharmaceutical Sciences, or related field from an accredited institution. A master&#39;s degree is preferred.</li><li>A minimum of 1-3 years of experience in analytical quality assurance.</li><li>Proficiently speak English as a first or second language and ability to read, write, and communicate effectively.</li><li>Self-starter with the initiative to seek additional training or direction as needed.</li><li>Knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP).</li><li>Willingness to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday.</li></ul><h2>Work Environment</h2><p>Work primarily during the first shift from 8:30 AM to 5:00 PM, Monday to Friday. You will be part of a supportive team of 15-20 people, collaborating with the manufacturing team. Reporting directly to the QA Manager, you will be required to stand or walk unassisted for 75% or more of an 8-hour period and may need to lift up to 10 kg unassisted. Appropriate personal protective equipment must be worn when required. You will spend considerable time sitting at a desk and working at a computer or other screens.</p><br>

<h1><strong>Job Title: Quality Assurance Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Assurance Technician is responsible for reviewing and confirming compliance documentation related to raw materials, in-process samples, and finished product analyses. The role involves monitoring adherence to current Good Laboratory Practices (cGLP) by laboratory personnel and verifying that laboratory chemicals, reagents, and standards are properly labeled according to standard operating procedures (SOPs). The technician will also review laboratory audit trails, coordinate with analytical laboratory teams, manage documentation, identify system gaps, and support cross-functional initiatives.</p><p><br></p><h2>Responsibilities</h2><ul><li>Review and confirm compliance documentation related to raw materials, in-process samples, and finished product analyses.</li><li>Monitor adherence to current Good Laboratory Practices (cGLP) by laboratory personnel during routine operations.</li><li>Verify proper labeling of laboratory chemicals, reagents, and standards in accordance with SOPs.</li><li>Review laboratory audit trails during data assessments to ensure alignment with SOPs.</li><li>Coordinate with Analytical Laboratory Teams to compile and provide necessary documentation to cross-functional teams.</li><li>Manage incoming documentation, including tracking, recording, storing, and archiving.</li><li>Identify system gaps during routine monitoring and notify supervisors of areas requiring improvement.</li><li>Understand laboratory equipment operation, qualification, and calibrations, including software audit trial reviews.</li><li>Actively participate in the review of data related to laboratory investigations and incidents to ensure regulatory compliance.</li><li>Support departmental and cross-functional initiatives and complete assignments as directed.</li></ul><h2>Essential Skills</h2><ul><li>Strong command of English language communication skills, both verbal and written.</li><li>Solid documentation and technical writing skills, with the ability to apply relevant scientific principles and practices.</li><li>Ability to work under minimal supervision, both independently and in a team environment.</li><li>Proficient computer skills and software applications such as Microsoft Office tools and Quality applications.</li><li>Experience in analytical quality assurance, preferably in pharmaceutical manufacturing.</li><li>Knowledge of analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, and analytical development.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related field from an accredited institution required; Master’s degree preferred.</li><li>1-3 years of experience in analytical quality assurance.</li><li>Experience with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP).</li><li>Self-motivated with excellent organizational skills and the ability to focus on details.</li><li>Experience with inhalation products (MDI) is a plus.</li><li>Ability to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday.</li></ul><h2>Work Environment</h2><p>The position operates on a first shift from 8:30 AM – 5:00 PM, Monday through Friday, within a team of 15-20 people collaborating with manufacturing. The role requires standing or walking unassisted for 75% or more of an 8-hour period, with occasional lifting of up to 10 kg. Appropriate personal protective equipment must be worn when required. Additionally, the technician will spend 75% or more of the time sitting at a desk or working at a computer.</p><p><br></p><p>Company is offering up to 6K for relocation </p>

<h1><strong>Job Title: Quality Technician</strong></h1><p>Join our team as a Quality Technician, where you will play a crucial role in ensuring our products meet established criteria. This role is very documentation heavy and will spend about 90% of the day in the office. We are seeking candidates with <strong>Batch Record Review and Lot Release</strong> experience. </p><p><br></p><h2>Essential Skills</h2><ul><li>Proficiency in quality assurance and documentation review.</li><li>Strong attention to detail.</li><li>Experience in a Good Manufacturing Practices (GMP) environment.</li><li>Experience participating in formal audits.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minimum 3 years’ experience in a manufacturing environment, with previous quality experience preferred.</li></ul><h2>Work Environment</h2><p>Work in a mid-sized manufacturing environment where most of the day is spent at a desk. The company is growing rapidly, offering great opportunities for advancement.</p>

Quality Assurance Technician (Documentation)

<h1 style="font-weight: 700;">Job Title: Quality Compliance Manager</h1><br><h2>Job Description</h2><p>The Quality Compliance Manager will lead compliance efforts for AS9100, ISO9001, ITAR, and support CMMC certification processes. This role is crucial in ensuring that all quality and compliance processes meet customer and industry standards.</p><br><h2>Responsibilities</h2><ul><li>Lead compliance efforts for AS9100, ISO9001, ITAR, and support CMMC certification processes.</li><li>Ensure all quality and compliance processes meet customer and industry standards.</li><li>Review flow-down requirements from quote requests and purchase orders for compliance with standards and contracts.</li><li>Assess customer drawings for inspection feasibility and conformance to GD&amp;T standards.</li><li>Evaluate manufacturing and inspection methods.</li><li>Provide quality input into manufacturing processes, including inspection planning and identification of key characteristics.</li><li>Support root cause analysis and corrective actions in response to customer complaints or field failures.</li><li>Collaborate across departments to promote quality awareness and implement best practices.</li><li>Serve as the primary contact for auditors, regulatory bodies, and customers on quality and compliance issues.</li><li>Champion a data-driven culture of continuous improvement to enhance product and process quality.</li><li>Perform additional duties as needed to support broader business objectives.</li></ul><h2>Essential Skills</h2><ul><li>Experience in compliance management, audit, document management, and quality systems management.</li><li>Proficiency in AS9100 standards with practical experience.</li><li>Experience in quality assurance and continuous improvement initiatives.</li><li>Knowledge of ISO9001, ITAR, and CMMC processes.</li><li>At least 5 years of progressive experience in quality or compliance roles within a manufacturing setting.</li><li>Minimum 2 years in a supervisory or managerial capacity.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Engineering or related field; ASQ Certification preferred.</li><li>Experience with government contract review, blueprint reading, and quality inspection processes.</li><li>Familiarity with CMMC is preferred.</li><li>Additional certifications in Quality Management, Compliance, or Continuous Improvement are advantageous.</li></ul><h2>Work Environment</h2><p>The role is onsite with a dog-friendly facility, offering a collaborative environment with a small company and engineering team. Benefits include a substantial 401k match, ESOP eligibility after 1 year, annual bonuses, and 80% company-paid benefits. The company boasts a long average tenure among employees.</p><br>

Quality Compliance Manager

<h1><strong>Quality Control - Roof Observer</strong></h1><p><br></p><h2><strong>Job Description</strong></h2><p>The Roof Observer is responsible for maintaining a presence at the construction site to ensure compliance with contract documents, approved submittals, schedule, and safety procedures. This role involves completing daily quality and safety reports and other submittals throughout the week.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Maintain a presence at the construction site on a day-to-day basis.</li><li>Interact with roofing contractors and client representatives to coordinate site requirements per job specifications.</li><li>Take photographs of job-site progress and document daily activities.</li><li>Ensure the roofing contractor complies with Contract Documents.</li><li>Complete and submit daily quality and safety reports.</li><li>Inform the Project Manager of quality issues and safety violations by the contractor.</li><li>Ensure incomplete work is finished prior to the final inspection.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>Proficiency in Excel and Microsoft Office.</li><li>Coordination skills, particularly in Roofing Inspection.</li><li>Quality control and inspection capabilities.</li><li>2 years of experience with roofing, either residential or commercial, including demo, inspection, or shingling.</li><li>1 year of experience using an iPad.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Experience with insurance companies is a plus</li></ul>

Quality Control - Roof Observer

<h1 style="font-weight: 700;">Job Title: Quality Control Analyst</h1><br><h2>Job Description</h2><p>The Quality Control Analyst is responsible for performing critical testing on raw materials, environment, utilities, validation samples, and manufactured materials. The analyst ensures that samples are tested and reviewed according to quality requirements and that results are valid, accurate, and documented per applicable regulatory and corporate standards. Tasks may include method validation and transfers.</p><br><h2>Responsibilities</h2><ul><li>Perform testing and associated tasks without errors according to applicable SOPs and protocols.</li><li>Comply with policies and procedures to maintain compliance with legal regulations, health and safety, and regulatory requirements.</li><li>Develop and maintain SOPs.</li><li>Develop expertise in assigned assays and techniques.</li><li>Author lab investigations and invalid assay assessments.</li><li>May be required to perform shift work as needed to support operations.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in a Scientific discipline.</li><li>Quality control expertise.</li><li>Knowledge of GMP and QC testing.</li><li>Understanding of microbiology and critical testing on raw materials, environment, utilities, validation samples, and manufactured materials.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree in Biology or Microbiology is highly preferred.</li><li>Experience with environmental monitoring in a pharmaceutical manufacturing environment.</li><li>Experience in analytical testing labs, whether academic or industry-based.</li><li>Experience working in a cGMP Pharmaceutical Laboratory.</li><li>Knowledge of Laboratory Information Management Systems (LIMS).</li><li>Experience with Bioburden, Endotoxin, and Sterility testing.</li><li>Intermediate knowledge of GMPs, safety regulations, and data integrity.</li><li>Intermediate knowledge of analytical methods and related instrumentation.</li></ul><h2>Work Environment</h2><p>The role may require shift work to support operations. The work environment involves compliance with GMP and safety regulations, ensuring the integrity of data and results. The facility operates under strict health and safety protocols and utilizes advanced analytical methods and instrumentation.</p><br>

Quality Control Analyst

<h1><strong>Job Title: Quality Control Chemist</strong></h1><p><br></p><h2>Job Description</h2><p>This position performs routine testing using various chemistry techniques within the pharmaceutical industry. We seek an experienced professional who can make an immediate impact.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct routine testing or other analysis in a specific group or department setting.</li><li>Perform advanced or critical testing as required.</li><li>Operate specialized equipment or conduct specialized skill testing.</li><li>Apply working knowledge of raw materials testing and release.</li><li>Utilize instruments such as HPLC, GC, and ICP.</li><li>Lead investigation activities.</li><li>Ensure compliance with all data integrity and cGMP practices, procedures, and expectations.</li><li>Maintain compliance with all good documentation practices.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in HPLC, GC, ICP, and GC-MS.</li><li>Experience in quality control and wet chemistry.</li><li>Knowledge of pharmaceutical raw materials and data entry.</li><li>Analytical chemistry expertise.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>1-3 years of experience in the industry for Chemist I positions; co-op experience in a cGMP pharmaceutical manufacturing setting is acceptable.</li><li>3-5 years of industry experience for Chemist II positions.</li></ul><h2>Work Environment</h2><p>Work within a small, collaborative team of 15 people in quality, with cross-departmental collaboration. The position operates on the first shift, Monday through Friday, from 8:00 AM to 5:00 PM. The main site for product testing is in Fall River, with a focus on expanding the product line, particularly inhalants.</p>

Quality Control Chemist

<h1><strong>Job Title: Quality Control Chemist </strong></h1><h1><strong>Pay: $62k+ </strong></h1><h1><strong>Shift: 3pm-11pm</strong></h1><p><br></p><h2>Job Description</h2><p>The principal focus of this position is to test raw materials, intermediates, and finished products to determine if they meet specifications. The role involves method development, instrument optimization, troubleshooting, and statistical monitoring of method performance. You will use analytical results to guide the production and packaging of hydrochloric acid, and documentation of work is required to meet customer and regulatory requirements.</p><p><br></p><h2>Responsibilities</h2><ul><li>Determine if tankage is acceptable for packaging based on HCl analytical results for specific customer orders.</li><li>Enter production movements of hydrochloric acid in SAP.</li><li>Consistently work safely and responsibly, using designated personal protective equipment.</li><li>Perform laboratory testing of raw materials to confirm suitability for production.</li><li>Test intermediate product samples to ensure they are suitable for further processing.</li><li>Test finished products against quality control specifications to ensure they meet agreed Sales Specifications and maintain high quality.</li><li>Accurately report laboratory test results to generate completed Certificates of Analysis.</li><li>Prepare Certificates of Analysis with precision.</li><li>Record and maintain accurate and complete records of test results, calculations, and data following ISO 9001 procedures and Quality Assurance System.</li><li>Manage and store manufactured product and raw material retain samples in compliance with ISO 9001 procedures and Laboratory Quality Assurance.</li><li>Identify specification anomalies in manufactured products and raw materials and report to Supervisor for corrective actions.</li><li>Maintain high standards of laboratory cleanliness and tidiness according to good housekeeping guidelines.</li><li>Actively contribute to the daily function of the laboratory service by preparing shared consumables and ensuring instruments and equipment are clean for the next use.</li><li>Maintain stocks of laboratory reagents and consumables to prevent delays in quality control testing and product dispatch.</li><li>Develop methods of analysis as required by the lab manager, including gauge R&amp;R, instrument optimization, validation, and statistical long-term stability monitoring.</li><li>Primarily operate during second shift hours.</li></ul><h2>Essential Skills</h2><ul><li>Quality control expertise</li><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in chemistry</li><li>Experience with HPLC</li><li>Proficiency in laboratory techniques</li><li>Analytical chemistry skills</li><li>Wet chemistry techniques</li><li>Ability to work second shift with minimal supervision</li><li>Experience in various wet chemical techniques</li><li>Competence in statistical analysis</li><li>Elemental analysis using ICP, ICPMS, or XRF instruments</li><li>Three years of laboratory experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in chemistry</li><li>3+ years of laboratory experience</li><li>Problem-solving and analytical abilities</li><li>Strong communication and interpersonal skills</li><li>Prior experience using ICP for trace metals analysis</li><li>Preferred experience in wet chemistry, pH measurements, FTIR, X-Ray spectrometer, and auto titrations</li><li>Commitment to documenting testing via established forms, paperwork, and computer data entry</li><li>Willingness to follow established procedures and work within cGMP, FDA, and ISO 9001 environments</li><li>Ability to plan daily/weekly workload and function independently</li><li>Must pass a Department of Homeland Security <span style="color: rgb(8, 7, 7); background-color: none;">background</span> check, pre-placement physical, and pre-employment drug screen</li><li>Specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus</li></ul><h2>Work Environment</h2><p>This job operates in a professional laboratory environment. The role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. Some work requires exposure to loud noises or fumes in the plant facility. The physical demands include occasionally sitting, climbing, balancing, stooping, kneeling, crouching, or crawling. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.</p>

<h1 style="text-align: center;"><strong><u>Quality Control Chemist</u></strong></h1><p style="text-align: center;"><br></p><p style="text-align: center;">INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM </p><p style="text-align: center;">OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823</p><p style="text-align: center;"><br></p><p><strong><u>Job Description</u></strong></p><p>The principal focus of this position is to test raw materials, intermediates, and finished products to determine if they meet specifications. As a chemist, the scope will include method development, instrument optimization, troubleshooting, and statistical monitoring of method performance. You will use analytical results to guide the production and packaging of hydrochloric acid. Documentation of work is required to meet customer and regulatory requirements.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Determine if tankage is acceptable for packaging based on HCl analytical results for specific customer orders daily.</li><li>Enter production movements of hydrochloric acid in SAP.</li><li>Work safely and responsibly at all times, including using designated personal protective equipment, safeguarding health and safety.</li><li>Conduct laboratory testing of raw materials to confirm suitability for production.</li><li>Perform laboratory testing of intermediate product samples to confirm suitability for further processing.</li><li>Test finished products against quality control specifications to ensure products released for shipment conform to agreed Sales Specifications and are of consistent, high quality.</li><li>Accurately report laboratory test results to generate completed Certificates of Analysis.</li><li>Prepare Certificates of Analysis accurately.</li><li>Record and maintain accurate and complete records of test results, calculations, and data in accordance with ISO 9001 procedures and Quality Assurance System.</li><li>Manage storage of manufactured product and raw material retain samples in accordance with ISO 9001 procedures and Laboratory Quality Assurance guidelines.</li><li>Identify specification anomalies in manufactured products and raw materials for corrective actions.</li><li>Maintain high levels of laboratory cleanliness and tidiness, in line with good housekeeping guidelines.</li><li>Actively contribute to the day-to-day function of the laboratory service, preparing shared consumables and ensuring instruments and equipment are clean and ready for use.</li><li>Maintain stocks of laboratory reagents and consumables to ensure no delays in quality control testing and dispatch of products.</li><li>Develop methods of analysis per lab manager requirements, including gauge R&amp;R, instrument optimization, validation, and statistical long-term stability monitoring of methods.</li><li>Primarily work during second shift operations.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>Quality control</li><li>Chemistry</li><li>HPLC</li><li>Laboratory techniques</li><li>Analytical chemistry</li><li>Wet chemistry</li><li>Willingness to work second shift with minimal supervision</li><li>Experience in a variety of wet chemical techniques</li><li>Statistical analysis</li><li>Elemental analysis using ICP, ICPMS, or XRF instrumentations</li><li>Three years of lab experience</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Bachelor’s degree in chemistry</li><li>Problem-solving, analytical ability, communication, and interpersonal skills</li><li>Prior experience using ICP for trace metals analysis preferred</li><li>Experience in wet chemistry, pH measurements, FTIR, X-Ray spectrometer, and Auto titrations preferred</li><li>Commitment to documenting testing via established forms, paperwork, and computer data entry</li><li>Willingness to follow established procedures and work within cGMP, FDA, and ISO 9001 environments</li><li>Ability to plan daily/weekly workload and function independently of supervision</li><li>Must pass Department of Homeland Security check, pre-placement physical, and pre-employment drug-screen</li><li>Specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus</li></ul><p><strong><u>Work Environment</u></strong></p><p>This job operates in a professional laboratory environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. Some of the work will require exposure to loud noises or fumes in the plant facility. The physical demands include occasionally sitting, climbing or balancing, and stooping, kneeling, crouching, or crawling. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.</p>

<h1><strong>Job Title: Quality Control Chemist</strong></h1><p><br></p><h2>Job Description</h2><p>The principal focus of this position is to test raw materials, intermediates, and finished products to determine if they meet specifications. As a chemist, the scope will include method development, instrument optimization, troubleshooting, and statistical monitoring of method performance. You will use analytical results to guide the production and packaging of hydrochloric acid. Documentation of work is required to meet customer and regulatory requirements.</p><p><br></p><h2>Responsibilities</h2><ul><li>Determine if tankage is acceptable for packaging based on HCl analytical results for specific customer orders daily.</li><li>Enter production movements of hydrochloric acid in SAP.</li><li>Work safely and responsibly at all times, including using designated personal protective equipment, safeguarding health and safety.</li><li>Conduct laboratory testing of raw materials to confirm suitability for production.</li><li>Perform laboratory testing of intermediate product samples to confirm suitability for further processing.</li><li>Test finished products against quality control specifications to ensure products released for shipment conform to agreed Sales Specifications and are of consistent, high quality.</li><li>Accurately report laboratory test results to generate completed Certificates of Analysis.</li><li>Prepare Certificates of Analysis accurately.</li><li>Record and maintain accurate and complete records of test results, calculations, and data in accordance with ISO 9001 procedures and Quality Assurance System.</li><li>Manage storage of manufactured product and raw material retain samples in accordance with ISO 9001 procedures and Laboratory Quality Assurance guidelines.</li><li>Identify specification anomalies in manufactured products and raw materials for corrective actions.</li><li>Maintain high levels of laboratory cleanliness and tidiness, in line with good housekeeping guidelines.</li><li>Actively contribute to the day-to-day function of the laboratory service, preparing shared consumables and ensuring instruments and equipment are clean and ready for use.</li><li>Maintain stocks of laboratory reagents and consumables to ensure no delays in quality control testing and dispatch of products.</li><li>Develop methods of analysis per lab manager requirements, including gauge R&amp;R, instrument optimization, validation, and statistical long-term stability monitoring of methods.</li><li>Primarily work during second shift operations.</li></ul><h2>Essential Skills</h2><ul><li>Quality control</li><li>Chemistry</li><li>HPLC</li><li>Laboratory techniques</li><li>Analytical chemistry</li><li>Wet chemistry</li><li>Willingness to work second shift with minimal supervision</li><li>Experience in a variety of wet chemical techniques</li><li>Statistical analysis</li><li>Elemental analysis using ICP, ICPMS, or XRF instrumentations</li><li>Three years of lab experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in chemistry</li><li>Problem-solving, analytical ability, communication, and interpersonal skills</li><li>Prior experience using ICP for trace metals analysis preferred</li><li>Experience in wet chemistry, pH measurements, FTIR, X-Ray spectrometer, and Auto titrations preferred</li><li>Commitment to documenting testing via established forms, paperwork, and computer data entry</li><li>Willingness to follow established procedures and work within cGMP, FDA, and ISO 9001 environments</li><li>Ability to plan daily/weekly workload and function independently of supervision</li><li>Must pass Department of Homeland Security check, pre-placement physical, and pre-employment drug-screen</li><li>Specific vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus</li></ul><h2>Work Environment</h2><p>This job operates in a professional laboratory environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. Some of the work will require exposure to loud noises or fumes in the plant facility. The physical demands include occasionally sitting, climbing or balancing, and stooping, kneeling, crouching, or crawling. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.</p>

<h1><strong>Job Title: Quality Control Chemist</strong></h1><p><br></p><h2>Job Description</h2><p>This position performs routine testing using various chemistry techniques within the pharmaceutical industry. We seek an experienced professional who can make an immediate impact.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct routine testing or other analysis in a specific group or department setting.</li><li>Perform advanced or critical testing as required.</li><li>Operate specialized equipment or conduct specialized skill testing.</li><li>Apply working knowledge of raw materials testing and release.</li><li>Utilize instruments such as HPLC, GC, and ICP.</li><li>Lead investigation activities.</li><li>Ensure compliance with all data integrity and cGMP practices, procedures, and expectations.</li><li>Maintain compliance with all good documentation practices.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in HPLC, GC, ICP, and GC-MS.</li><li>Experience in quality control and wet chemistry.</li><li>Knowledge of pharmaceutical raw materials and data entry.</li><li>Analytical chemistry expertise.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>1-3 years of experience in the industry for Chemist I positions; co-op experience in a cGMP pharmaceutical manufacturing setting is acceptable.</li><li>3-5 years of industry experience for Chemist II positions.</li></ul><h2>Work Environment</h2><p>Work within a small, collaborative team of 15 people in quality, with cross-departmental collaboration. The position operates on the first shift, Monday through Friday, from 8:00 AM to 5:00 PM. The main site for product testing is in Fall River, with a focus on expanding the product line, particularly inhalants.</p><p><br></p><p><strong>Relocation Bonus</strong></p><p>Up to 6K for relocation bonus offered </p>

<h1><strong>Job Title: Quality Control Chemistry Technician</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Control Chemistry Technician will work in a fast-paced laboratory environment, performing a variety of chemical tests including HPLC, GC, pH, FTIR, percent solids, viscosity, color, odor, appearance, some titrations, and other wet chemistry techniques. This role primarily involves GC testing, with the majority of time spent conducting product tests in the lab, blending samples, and documenting results. The technician will test liquid contents destined for aerosols and occasionally the aerosolized products themselves.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct product testing using HPLC, GC, pH, FTIR, and various wet chemistry techniques.</li><li>Document test results thoroughly in paperwork and notebooks.</li><li>Blend samples and perform some filling tasks in production.</li><li>File paperwork and enter data accurately.</li><li>Test liquid contents for aerosol products and occasionally test aerosolized products.</li></ul><h2>Essential Skills</h2><ul><li>High School Diploma.</li><li>1-2+ years of experience in GC or LC, open to various industries.</li><li>Experience with HPLC, GC, pH, FTIR, and wet chemistry techniques.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associates or Bachelor&#39;s degree in Chemistry, Biochemistry, or a related field is preferred.</li><li>GC experience is critical for this role.</li></ul><h2>Work Environment</h2><p>The work environment is a laboratory setting with 3rd shift hours from 10pm-6:30am, Monday to Friday, with occasional weekend work or overtime after the first month. Initially, the technician will work on 2nd shift from 2-10:30pm. Safety is paramount, with proper PPE such as safety glasses, gloves, lab coats, and ear plugs provided and required. Physical demands include standing 75% of the time, sitting 25%, and occasional lifting up to 25 lbs. The team operates on a three-shift system with one Quality Lab Technician per shift.</p>

Quality Control Chemistry Technician

<h1 style="text-align: center;"><strong>Hiring for a Quality Control Engineer in Stony Point!</strong></h1><p style="text-align: center;"><br></p><p><br></p><h2>Job Description</h2><p>The Quality Control Engineer operates as the quality partner with manufacturing engineering, focusing on incoming materials inspection processes, root cause analysis of production issues to enhance yield improvements, and revising documentation to support quality engineering.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct inspections of purchased parts and subassemblies using standard inspection tools such as calipers and hard gages.</li><li>Accurately document the results of quality control inspections and testing.</li><li>Maintain all controlled document files and test records.</li><li>Assist in creating and updating inspection templates and tools.</li><li>Evaluate problems and make initial recommendations within quality engineering and manufacturing engineering.</li><li>Demonstrate experience as a Change Agent by successfully implementing process improvements and SPC metrics in a technical manufacturing environment.</li></ul><h2>Essential Skills</h2><ul><li>Quality control</li><li>Inspection</li><li>Quality engineering</li><li>Quality assurance</li><li>Root cause analysis</li><li>Electronics manufacturing</li><li>Quality management system</li><li>Use of inspection equipment like calipers and gages</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree in engineering or physical sciences preferred: electrical, industrial, manufacturing, materials science, or mechanical engineering, or electrical technology</li><li>Minimum of five years of technical experience in Manufacturing and Quality Control</li><li>Practical competence in Six Sigma analytical tools and Lean Manufacturing methods</li><li>Experience working in an electronics manufacturing facility strongly preferred</li><li>Knowledge of MIL-Specs and MIL-STDs is a plus</li><li>Strong analytical ability and computer skills</li><li>Strong MS Office skills, specifically Word, Excel, PowerPoint, and Outlook</li></ul><h2>Work Environment</h2><p>This position is based in Stony Point, NY, and is fully onsite. </p>

Quality Control Engineer

<h1 style="font-weight: 700;">Job Title: Quality Control Engineer</h1><br><h2>Job Description</h2><p>The Quality Control Engineer operates as the quality partner with manufacturing engineering, focusing on incoming materials inspection processes, root cause analysis of production issues to enhance yield improvements, and revising documentation to support quality engineering.</p><br><h2>Responsibilities</h2><ul><li>Conduct inspections of purchased parts and subassemblies using standard inspection tools such as calipers and hard gages.</li><li>Accurately document the results of quality control inspections and testing.</li><li>Maintain all controlled document files and test records.</li><li>Assist in creating and updating inspection templates and tools.</li><li>Evaluate problems and make initial recommendations within quality engineering and manufacturing engineering.</li><li>Demonstrate experience as a Change Agent by successfully implementing process improvements and SPC metrics in a technical manufacturing environment.</li></ul><h2>Essential Skills</h2><ul><li>Quality control</li><li>Inspection</li><li>Quality engineering</li><li>Quality assurance</li><li>Root cause analysis</li><li>Electronics manufacturing</li><li>Quality management system</li><li>Use of inspection equipment like calipers and gages</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree in engineering or physical sciences preferred: electrical, industrial, manufacturing, materials science, or mechanical engineering, or electrical technology</li><li>Minimum of five years of technical experience in Manufacturing and Quality Control</li><li>Practical competence in Six Sigma analytical tools and Lean Manufacturing methods</li><li>Experience working in an electronics manufacturing facility strongly preferred</li><li>Knowledge of MIL-Specs and MIL-STDs is a plus</li><li>Strong analytical ability and computer skills</li><li>Strong MS Office skills, specifically Word, Excel, PowerPoint, and Outlook</li></ul><h2>Work Environment</h2><p>This position is based in Stony Point, NY, and is fully onsite. The role follows a business casual dress code with an 8 am start time.</p><br>

<h1 style="text-align: center;"><strong>Hiring for a Quality Control Engineer in Stony Point!</strong></h1><p style="text-align: center;">For immediate consideration, please send your resume and availability to abhurd@actalentservices.com!</p><p><br></p><h2>Job Description</h2><p>The Quality Control Engineer operates as the quality partner with manufacturing engineering, focusing on incoming materials inspection processes, root cause analysis of production issues to enhance yield improvements, and revising documentation to support quality engineering.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct inspections of purchased parts and subassemblies using standard inspection tools such as calipers and hard gages.</li><li>Accurately document the results of quality control inspections and testing.</li><li>Maintain all controlled document files and test records.</li><li>Assist in creating and updating inspection templates and tools.</li><li>Evaluate problems and make initial recommendations within quality engineering and manufacturing engineering.</li><li>Demonstrate experience as a Change Agent by successfully implementing process improvements and SPC metrics in a technical manufacturing environment.</li></ul><h2>Essential Skills</h2><ul><li>Quality control</li><li>Inspection</li><li>Quality engineering</li><li>Quality assurance</li><li>Root cause analysis</li><li>Electronics manufacturing</li><li>Quality management system</li><li>Use of inspection equipment like calipers and gages</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree in engineering or physical sciences preferred: electrical, industrial, manufacturing, materials science, or mechanical engineering, or electrical technology</li><li>Minimum of five years of technical experience in Manufacturing and Quality Control</li><li>Practical competence in Six Sigma analytical tools and Lean Manufacturing methods</li><li>Experience working in an electronics manufacturing facility strongly preferred</li><li>Knowledge of MIL-Specs and MIL-STDs is a plus</li><li>Strong analytical ability and computer skills</li><li>Strong MS Office skills, specifically Word, Excel, PowerPoint, and Outlook</li></ul><h2>Work Environment</h2><p>This position is based in Stony Point, NY, and is fully onsite. The role follows a business casual dress code with an 8 am start time.</p>

<h1><strong>Job Title: Quality Control Lab Assistant</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Control Lab Assistant plays a crucial role in supporting the testing and preparation of materials in a laboratory setting. This position involves aiding certified professionals in conducting various laboratory tests and handling samples through front-end automation, storage, and retrieval processes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist in the preparation of materials for testing.</li><li>Aid certified individuals in performing laboratory tests.</li><li>Receive and prepare samples using front-end automation.</li><li>Store and archive samples in refrigerated and frozen conditions.</li><li>Use computerized reports to retrieve and reconcile samples from archives.</li><li>Prepare buffer materials for testing.</li><li>Receive specimens and supplies, and process information from collection centers.</li><li>Handle and track donor samples from receipt to final testing.</li><li>Dispose of samples properly into biohazard containers post-testing.</li><li>Operate, maintain, and troubleshoot laboratory instrumentation.</li><li>Use computerized inventory management systems to track testing status of samples.</li><li>Assist in monitoring inventory levels for laboratory supplies.</li><li>Notify supervisor of inventory needs.</li></ul><h2>Essential Skills</h2><ul><li>High School Diploma or equivalent.</li><li>Basic computer skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Laboratory experience or in production line work is preferred.</li><li>Skills in data entry and inspection.</li></ul><h2>Work Environment</h2><p>The work environment is within a donor processing/manufacturing facility, providing a positive atmosphere with opportunities for growth and training in the medical field. Employees benefit from a competitive package including tuition reimbursement. The position offers a set shift with no &#39;on call&#39; or STAT labs, ensuring a standard daily operating rhythm. Two shift options are available: 6:30 AM to 3:00 PM or 10:00 AM to 6:30 PM, Monday to Friday. The first day orientation typically occurs from 10:00 AM to 12:00 PM. The facility operates in a warehouse setting.</p>

Quality Control Lab Assistant

<h1 style="text-align: center;"><strong><u>Quality Control Lab Technician</u></strong></h1><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>

Quality Control Lab Technician

<h1><strong>Job Title: Quality Control Analyst </strong></h1><h1><strong>Shift: M-F 3:00pm-11:30pm </strong></h1><h1><strong>Pay: $22/hr</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Control Analyst, you will be responsible for testing raw materials and finished products in our Quality Control laboratory. This role requires precision and attention to detail to ensure compliance with established specifications and standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations, and final products.</li><li>Utilize and operate laboratory equipment and instruments according to laboratory procedures, including pH, conductivity, UV, KF, FTIR, and titrations.</li><li>Understand and follow Quality Control test methods or compendia methods (USP, EP, BP, JP, or ACS) and EXCIPACT standards.</li><li>Calculate and generate data for compliance to specifications and report results.</li><li>Perform technical review of lab data forms, such as water, environmental monitoring, and direct measure analysis.</li><li>Calibrate and maintain lab equipment.</li><li>Enter final results and raw data for tested materials or products in the Laboratory Information Management System (LIMS) as needed.</li><li>Perform investigative analysis to support investigations, complaints, or instrument troubleshooting.</li><li>Conduct Environmental Monitoring duties, which require gowning into cleanroom and collecting air and surface samples.</li><li>Review for discrepancies in data, manufacture COA, COC, and perform data verification in accordance with company procedures.</li><li>Apply appropriate disposition labels to materials (accepted, rejected, etc.).</li><li>Handle hazardous materials using all appropriate or mandatory safety PPE and safety equipment.</li><li>Complete documentation in a legible manner and review for accuracy.</li><li>Perform sampling and testing for USP Purified water and Water for Injection.</li><li>Author, review, or update lab procedures and Lab instruments Work Instructions.</li><li>Perform microbiological tests such as bioburden, endotoxin, Dnase, Rnase, Protease, and Phosphatase using proper aseptic techniques.</li><li>Prepare and properly dispose of microbial media.</li></ul><h2>Essential Skills</h2><ul><li>Quality control</li><li>GMP</li><li>Laboratory</li><li>Chemistry</li><li>Microbiology</li><li>Quality assurance</li><li>Biology</li><li>Environmental monitoring</li><li>Biochemistry</li><li>Wet chemistry</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in a science discipline with knowledge and experience in Chemistry, Biology, or Biochemistry.</li><li>3 years of laboratory experience in a related field.</li><li>Wet chemistry and microbial testing experience preferred (e.g., Acid/Base Titrations, water content, Bioburden, Endotoxin).</li></ul><h2>Work Environment</h2><p>Typically works in a lab and office environment with adequate lighting and ventilation and a normal range of temperature and noise level. At times, may be exposed to various chemicals, including flammables, corrosives, and oxidizers. Work assignments are diversified, with examples of past precedent used to resolve work problems, and new alternatives may be developed to resolve issues. A frequent volume of work and deadlines impose strain on a routine basis. Minimal physical effort is required, as work is mostly sedentary but does require walking, standing, bending, reaching, lifting, or carrying objects that typically weigh less than 10 lbs.</p>

Quality Control Laboratory Technician

<p><strong>Quality Control Manager – Hyperscale AI Data Center</strong></p><p>Location: Ellendale, ND</p><p>Industry: Commercial &amp; Mission-Critical Construction</p><p>Are you passionate about precision, performance, and building excellence? Do you thrive in environments where quality is non-negotiable and every detail matters? We’re looking for a Quality Control Manager to lead quality assurance and control efforts on a high-profile construction project in Ellendale, ND.</p><p>This is your opportunity to play a pivotal role in delivering complex, high-tech facilities—ensuring every system, surface, and structure meets the highest standards of performance and compliance.</p><h3>What You’ll Do</h3><ul><li>Lead the implementation of the QA/QC management system on-site.</li><li>Oversee inspections, testing, and documentation across all trades and vendors.</li><li>Manage exterior mockups and ensure proper installation of waterproofing, curtain walls, roofing, and transition details.</li><li>Coordinate with construction managers, subcontractors, and design teams to uphold quality standards.</li><li>Conduct pre-installation meetings, mockup reviews, and first-work inspections.</li><li>Ensure compliance with applicable codes, standards, and project specifications.</li><li>Guide forensic evaluations, site investigations, and performance testing.</li><li>Maintain comprehensive quality documentation for project closeout.</li></ul><h3>What You Bring</h3><ul><li>5+ years of experience in construction leadership roles such as Quality Control, Superintendent, or Project Manager.</li><li>Strong knowledge of building systems, including passive fire-rated assemblies, mechanical, and electrical systems.</li><li>Experience leading teams and mentoring others in quality-focused environments.</li><li>Proficiency with construction software such as Bluebeam, Microsoft Office, and Procore.</li><li>Excellent communication, problem-solving, and critical thinking skills.</li><li>Ability to remain calm and collaborative under pressure.</li></ul><h3>Preferred Qualifications</h3><ul><li>Bachelor’s degree in Construction Management, Engineering, or a related field.</li><li>Prior experience managing quality on data center or mission-critical projects.</li></ul><h3>Physical Requirements</h3><ul><li>Ability to work outdoors in varying weather conditions and on elevated structures such as ladders and scaffolds.</li><li>Regular physical activity, including standing, walking, climbing, kneeling, and lifting, as part of site inspections.</li></ul><p><br></p><p>This is more than a job—it’s a chance to shape the future of high-performance construction. If you’re ready to lead with integrity, precision, and purpose, we want to hear from you.</p>

Quality Control Manager - Data Center

<h1 style="font-weight: 700;">Job Title: QC Scientist I/II</h1><br><h2>Job Description</h2><p>The QC Scientist I/II will perform HPLC/UPLC testing on various samples, including In-Process DS release, DP release, DS stability, DP Stability, process validation, analytical method validation/transfer, method establishment/qualification, and non-routine samples. The role involves demonstrating proper laboratory safety and housekeeping practices through regular audits and inspections, ensuring all activities meet EHS requirements. Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods, including Reverse Phase, SEC, Titer concentration, and CEX.</p><br><h2>Responsibilities</h2><ul><li>Accurately record and report analysis results following lab procedures and quality systems.</li><li>Recognize and report out-of-specification/out-of-trend results to laboratory management and recommend solutions.</li><li>Maintain and troubleshoot analytical instrumentation and workspace as needed.</li><li>Perform method validation and/or qualification testing as required.</li><li>Author and/or review SOPs, test methods, forms, etc., in the document management system eDMS.</li><li>Ensure compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.</li><li>Work with internal and external customers to ensure clear and open communication when resolving and raising issues.</li><li>Collaborate with QC leads, PMs, and clients to maintain the health of client programs.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 1 year of HPLC/UPLC experience in quality/analytical/pharmaceutical industry or similar experience.</li><li>Proficiency in HPLC, GMP, chemistry, and EMPOWER.</li><li>Knowledge of GMP regulations in a cGMP manufacturing environment.</li><li>Working knowledge of scientific principles for a wide range of analytical techniques.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with a multitude of HPLC/UPLC assays, such as SEC, CEX, Glycans, Peptide Map, is a plus.</li><li>Prior use of EMPOWER is preferred.</li></ul><h2>Work Environment</h2><p>The work environment consists of bench work with standard hours from Monday to Friday, 8am-4:30pm. The position offers opportunities for growth and learning in a culture that empowers development, with the potential for conversion into a full-time role based on performance.</p><br>

Quality Control Scientist

<h1><strong>Job Title: Quality Control Expert Associate</strong></h1><p><br></p><h2>Job Description</h2><p>This position is based 100% onsite in Holly Springs, NC, following a standard weekday schedule. The Quality Control Expert Associate will play a critical role in the startup and operations of the ANC facility, focusing on quality records management, including deviations, CAPAs, and change controls. The ideal candidate will have at least one year of experience in a GMP-regulated lab or manufacturing setting, with proficiency in the Veeva Quality system being highly desirable. Strong communication and grammar skills, along with a proactive, detail-oriented approach, are essential for success in this fast-paced environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Work collaboratively with Quality and Quality Assurance teams to author and own change control records and deviations in the DQMS Veeva System.</li><li>Lead investigation teams and help collect and report metrics for the systems team.</li><li>Assist with the review of validation documents to support equipment and computerized system onboarding.</li><li>Author, revise, and review documents and reports, including SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, and technical reports.</li><li>Support the startup of a GMP QC laboratory.</li><li>Support routine activities over weekends and public holidays as required.</li></ul><h2>Essential Skills</h2><ul><li>At least one year of experience in a GMP-regulated lab or manufacturing setting.</li><li>Strong writing and grammar skills.</li><li>Proficiency in Deviation and Change Control writing.</li><li>Experience with the Veeva Quality system.</li><li>Ability to lead meetings and drive investigations independently.</li><li>Proactive and detail-oriented.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school/GED with 2 years of work experience, or Associates with 6 months of work experience, or Bachelors degree.</li><li>Leadership capabilities and practical aptitude.</li><li>Collaborative approach and proactive mindset.</li></ul><h2>Work Environment</h2><p>This role requires working collaboratively with Quality and Quality Assurance teams onsite. The position includes authoring and owning change control records and deviations, leading investigation teams, and supporting the startup of a GMP QC laboratory. Routine activities may be required over weekends and public holidays, emphasizing a fast-paced and dynamic work setting.</p>

Quality Control Senior Associate

<h1><strong>Job Title: Quality Control Specialist</strong></h1><p><br></p><p>*Per diem available for non local candidates- first project is near Columbus, GA.*</p><p><br></p><h2>Job Description</h2><p>We are seeking a Quality Control Specialist for a barracks project at Fort Benning. The role involves being on-site with a Quality Control Manager (QCM), where you will oversee either the electrical or mechanical scope under the direction of the Project Manager and QCM.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist with the development and implementation of audit protocols.</li><li>Audit third-party vendors to ensure quality and compliance.</li><li>Create weekly reports to locate errors.</li><li>Ensure that requests from management or customers are handled in a timely manner.</li><li>Perform specified tests to verify that control measures are adequate for contract requirements.</li><li>Schedule, document the results of, and maintain a log of all required inspections.</li><li>Clearly document, correct, and re-inspect all non-conformances before covering up work.</li></ul><h2>Essential Skills</h2><ul><li>Degree in Construction Management, Mechanical Engineering, or Electrical Engineering.</li><li>2+ years of building construction experience.</li><li>OSHA 30-hour Construction Safety &amp; Health training.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Engineering, Architecture, or Construction Management with 2 years of experience in either Architectural, Mechanical, or Electrical disciplines; OR a High School diploma/GED plus 5 years of construction management experience.</li><li>Experience establishing and maintaining effective quality control systems in compliance with contract requirements.</li><li>Experience using Army RMS/CQC system, preferred.</li><li>Strong knowledge of project plans, specifications, shop drawings, samples, and testing.</li><li>Proficiency with computer software used in the construction industry.</li><li>Ability to create and administer new QC programs.</li><li>Time management skills.</li><li>Professional communication skills both verbally and in writing.</li><li>Credentials showing completion of the course &#39;Construction Quality Management for Contractors&#39; offered by USACE, or willingness to complete the course upon hire.</li></ul><h2>Work Environment</h2><p>The position offers a per diem for 5 days of full per diem at $178/day and 2 days of partial per diem for lodging for non local candidates. The role will involve working on-site, overseeing either electrical or mechanical scope under direction. The work environment is dynamic and requires adherence to safety protocols, with an emphasis on maintaining quality standards in construction management.</p>

Quality Control Specialist

<p>﻿<strong><u>Job Description:</u></strong></p><p>The Quality Control Specialist has broad responsibility for Quality Control auditing of finished goods and the manufacturing facility. This position will also be responsible for database maintenance, troubleshooting, and product disposition, including product hold/release authority, quality inspection, investigation, and reporting issues associated with Food Safety and Quality. The position requires employees to receive cross-training in other QC functions to provide backup support as needed. The role involves inspecting finished goods, representing Medical Foods, Dietary supplements, and other high-profile contract customer products.</p><p><br></p><p><strong><u>Responsibilities:</u></strong></p><ul><li>Enter data into company databases</li><li>Perform inspection of equipment, product, and/or production lines</li><li>Ensure conformance to GMP guidelines and company policies/procedures</li><li>Inspect/audit facilities, manufacturing equipment, and products as require</li><li>Identify non-conforming conditions and products relating to food safety and food quality</li><li>Place on hold products or materials that do not conform to specifications</li><li>Initiate investigations into the causes of material or product non-conformance, gathering pertinent information without prompt from Supervisor</li><li>Investigate customer complaints with guidance from Supervisor</li><li>Perform internal audits based on SQF guidelines</li></ul><p><strong><u>Qualifications:</u></strong></p><ul><li>1 year of quality control experience in food &amp; beverage</li><li>Ability to work independently</li><li>Good analytical skills</li><li>Experience following GMPs</li></ul><p><strong><u>About Actalent</u></strong></p><p>Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.</p><p><br></p><p><strong><u>Diversity, Equity &amp; Inclusion</u></strong></p><p>At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&amp;I Are Embedded Into Our Culture Through:</p><ul><li>Hiring diverse talent</li><li>Maintaining an inclusive environment through persistent self-reflection</li><li>Building a culture of care, engagement, and recognition with clear outcomes</li><li>Ensuring growth opportunities for our people</li></ul><h2><br></h2>

<p><strong>Description</strong></p>
					<p>• Supervise, train, and support QC staff in daily tasks and ensure adherence to procedures, including CMM and inspection tool maintenance, probe care, NCR follow-up, and 5S practices.
• Coordinate daily inspector assignments, delegate projects, monitor overtime usage in line with departmental goals, and track task completion.
• Create and maintain a visual queue system to clearly indicate inspection priorities for parts on QC shelves.
• Identify skill gaps within the team and propose individual development plans, with a focus on improving PIWEB software proficiency. Adjust team roles to enhance department efficiency.
• Mentor inspectors through training, goal setting, and performance reviews. Keep the department’s skill matrix current.
• Develop and implement standardized PIWEB reports for component families. Train CMM programmers to adapt and reuse these templates. Create CMM programs and corresponding PIWEB reports.
• Provide daily quality updates to Production and Engineering. Identify trends, support root cause analysis, and refine quality feedback and reporting. Create custom reports as needed.
• Draft, implement, and review SOPs and work instructions related to equipment maintenance, gauge calibration, and inspection processes. Work to align procedures across QC Baker and QC Fischer.
• Collaborate with QC, Manufacturing Engineering, and Design teams to manage the Drawing Change Request (DCR) process. Recommend improvements and track request statuses.
• Define and apply best metrology practices for inspection. Implement systems to verify data accuracy and enhance troubleshooting capabilities.
• Maintain the PIWEB database to ensure it is current, well-structured, and supports efficient analysis and investigations.
• Oversee software used in QC (e.g., Calypso, PIWEB), including repairs, license renewals, and upgrades. Serve as the liaison with software vendors.
• Schedule and manage calibration services for equipment and ensure accurate recordkeeping.
• Communicate critical equipment or personnel issues to the management team promptly.
• Identify and implement process improvements. Track inspection times by product and operation point to support cost analysis and prioritize optimization efforts.</p>
					<p><strong>Skills</strong></p>
					<p>calypso, cmm, cmm programming, gd&amp;t, asme, gage rr, cad software, Quality engineering, Quality control, Engineering</p>
					<p><strong>Top Skills Details</strong></p>
					<p>calypso,cmm,cmm programming,gd&amp;t,asme,gage rr,cad software,Quality engineering</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>- Must have Bachelors in Mechanical Engineering (or related) 
- Must have leadership experience
- Must be an expert in Zeiss Calypso</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

Quality Control Supervisor

<h3>&#128663; Quality Control Supervisor – Drive Excellence at a Leading Automotive Company</h3><p>Are you ready to lead quality operations at the heart of automotive performance? An exciting and forward-thinking automotive company is seeking a Quality Control Supervisor to take charge of inspection excellence, team development, and process innovation.</p><p>This is your chance to make a real impact—supporting high-precision manufacturing that powers everything from cutting-edge vehicles to motorsport-grade components.</p><h3>&#128295; What You’ll Do</h3><ul><li>Lead and mentor a skilled QC team, ensuring daily operations run smoothly and procedures are followed with precision.</li><li>Coordinate inspection schedules, assign projects, and manage overtime to meet department goals.</li><li>Implement a visual system to prioritize inspections and streamline workflow.</li><li>Identify skill gaps and champion team development—especially in PIWEB software and CMM programming.</li><li>Drive performance through coaching, goal setting, and annual reviews while maintaining an up-to-date skills matrix.</li><li>Develop and standardize PIWEB reports and CMM programs for complex components.</li><li>Collaborate with Production and Engineering to report quality issues, analyze trends, and support root cause investigations.</li><li>Create and refine SOPs and work instructions for inspection, calibration, and maintenance processes.</li><li>Partner with cross-functional teams to improve the Drawing Change Request (DCR) process and support OnePlan integration.</li><li>Define best practices in metrology and ensure data integrity through robust inspection systems.</li><li>Maintain and optimize the PIWEB database for fast, insightful analysis.</li><li>Oversee QC software tools (Calypso, PIWEB), including upgrades, licensing, and vendor coordination.</li><li>Manage calibration services and ensure accurate documentation.</li><li>Communicate critical issues to leadership and drive continuous improvement initiatives.</li></ul><h3>&#129504; What You Bring</h3><ul><li>Bachelor’s degree in Mechanical Engineering or a related field (or equivalent experience).</li><li>Proven leadership experience in a manufacturing or quality environment.</li><li>Expert-level proficiency in Zeiss Calypso software and CMM programming.</li><li>Strong knowledge of GD&amp;T (ASME Y14.5, ISO), Gage R&amp;R, and calibration techniques.</li><li>Skilled in CAD/CAM and inspection software tools.</li><li>Proficient in PIWEB database management and Microsoft Office Suite (Excel, Word, Access, Project, PowerPoint).</li><li>Ability to assess manufacturability and define effective inspection strategies.</li></ul>

<p><strong>Description</strong></p><p>- Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc.</p><p>- Conduct functional tests and verify conformance to detailed specifications and tolerances</p><p>- Interpret engineering drawings, specifications, and work instructions</p><p>- Record and maintain accurate inspection data, including lot history and traceability records</p><p>- Support lot release, material review, and root cause analysis for nonconforming parts</p><p>- Participate in audits and provide complete, well-organized inspection documentation</p><p>- Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations</p><p>- Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements</p><p>- Nonconformance, CAPA, and Material Review Board Support</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>- Minimum 3–5 years of quality technical experience in the medical device industry required.</p><p>- Proven experience inspecting critical or high-precision components and/or devices.</p><p>- Familiarity with ISO 13485, and Good Documentation Practices (GDP).</p><p>- Proficiency with inspection equipment and interpreting engineering drawings and GD&amp;T.</p><p>- Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems.</p><p>- Excellent attention to detail, organization, and communication skills.</p><p><br></p><p><strong>Preferred Qualifications:</strong></p><p>- CQI or CQT certification</p><p>- Experience with cleanroom manufacturing in a medical device setting.</p><p>- Working knowledge of SPC and data analysis tools such as Minitab.</p><p>- Familiarity with Failure Investigation techniques.</p><p><br></p><p><br></p><p><br></p>

Quality Control Technician

<h2>Responsibilities</h2><ul><li>Own the mold quality process from design through production.</li><li>Perform dimensional and visual inspections to ensure molds meet specifications.</li><li>Troubleshoot mold-related issues and coordinate maintenance or repairs.</li><li>Maintain mold identification, tracking, and preventive maintenance programs.</li><li>Conduct mold audits and manage technical documentation and internal databases.</li><li>Participate in internal and external audits and continuous improvement initiatives.</li><li>Operate in both office and production environments, including exposure to heat, noise, and heavy equipment.</li></ul><h2>Essential Skills</h2><ul><li>Proficient in reading and understanding CAD drawings and technical blueprints.</li><li>Skilled in using calipers, tape measures, and precision tools for dimensional checks.</li><li>Experienced in conducting inspections, audits, and standardized tests.</li><li>Knowledgeable in mold tracking, preventive maintenance, and repair coordination.</li><li>Actively contributes to continuous improvement initiatives.</li><li>Comfortable working in industrial environments with adherence to safety protocols.</li><li>Strong grasp of basic math, including percentages, averages, and algebra.</li><li>Maintains detailed records of inspections, test results, and mold performance.</li></ul>

<h1><strong>Job Title: Construction Quality Control Technician</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a detail-oriented and proactive Quality Technician to support our construction projects by ensuring compliance with quality standards and regulatory requirements. This role is critical in maintaining the integrity of our work through audits, inspections, documentation, and reporting.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct regular audits and inspections on construction sites to ensure adherence to project specifications, codes, and safety standards.</li><li>Perform specification checks on materials and workmanship to verify compliance with engineering drawings and client requirements.</li><li>Maintain accurate and timely documentation of inspection results, non-conformance reports, and corrective actions.</li><li>Prepare and submit quality reports to project managers and stakeholders.</li><li>Collaborate with project teams to resolve quality issues and implement continuous improvement initiatives.</li><li>Support internal and external audits, including client and regulatory inspections.</li><li>Ensure all quality control procedures are followed throughout the project lifecycle.</li></ul><h2>Essential Skills</h2><ul><li>Construction management</li><li>Quality assurance</li><li>Construction</li><li>Audit</li><li>Inspection</li><li>General contractor</li><li>Project coordination</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent required; associate degree or technical certification in construction, engineering, or quality management preferred.</li><li>2+ years of experience in a quality control or quality assurance role, preferably within a construction or EPCM environment.</li><li>Strong understanding of construction processes, materials, and quality standards.</li><li>Familiarity with ISO standards and QA/QC documentation practices.</li><li>Excellent attention to detail, organizational, and communication skills.</li><li>Proficiency in Microsoft Office and quality management software.</li><li>Experience with root cause analysis and corrective/preventive action (CAPA) processes.</li><li>Knowledge of industry-specific regulations and standards (e.g., ASTM, OSHA).</li><li>Ability to read and interpret technical drawings and specifications.</li></ul><h2>Work Environment</h2><p>On-site at large pharma project in Sanford.</p>

<h1 style="text-align: center;"><strong>Quality Control Technician</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Control Technician, you will play a crucial role in ensuring the production of high-quality oil products. Your responsibilities will include checking and verifying production records, spot checking labels, and creating labels for oil products. You will monitor the flow of products and take samples from production to perform PV and OSI testing in the lab. Additionally, you will conduct pH and density testing and oversee the production floor to perform quality checks.</p><p><br></p><h2>Responsibilities</h2><ul><li>Check and verify production records</li><li>Spot check labels for accuracy</li><li>Create labels for oil products</li><li>Monitor the flow of product through the production process</li><li>Take samples from production and conduct PV and OSI testing in the laboratory</li><li>Conduct pH and density testing</li><li>Oversee the production floor and perform routine quality checks</li><li>Engage in frequent moving, standing, lifting, and other active movements</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Preferred experience in food and beverage or quality lab environments</li><li>Associates degree in biotech or biology is preferred but not required</li><li>Commitment to wearing proper personal protective equipment (PPE)</li></ul><h2>Work Environment</h2><p>This position offers a balanced work environment, with 60% of time spent in office working with labels, 30% on the production floor overseeing products, and 10% in the lab. The role is situated in a food-grade environment where accuracy is paramount to prevent recalls. The facility is climate-controlled, manufacturing vegetable oil and dried goods, and candidates should be comfortable getting dirty. The schedule is 6AM to 2:30PM, Monday through Friday. PPE, including safety glasses, lab coat, respirator, and gloves, is provided. Dress code requires no jewelry, jeans without holes, steel-toe boots, and t-shirts or sweatshirts without holes. The company values promoting from within and offers opportunities for advancement to candidates who demonstrate strong work ethics, quality of work, and attendance.</p>

<h1 style="font-weight: 700;">Job Title: Quality Control Technician</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Control Technician to perform analysis of various materials using standardized procedures and support production by conducting quality inspections. This role is vital in ensuring the highest standards of quality and safety within our facility.</p><br><h2>Responsibilities</h2><ul><li>Perform analysis of incoming, in-process, and finished materials using standardized analytical procedures, including tests such as pH, Turbidity, Brix, Salt, Alcohol, Total Nitrogen, and Microbiological Sampling and testing.</li><li>Conduct standardized quality sampling and checks during production, reporting variances and non-conformities to management.</li><li>Support production and perform quality inspections before, during, and between product runs.</li><li>Monitor plant sanitation and personal hygiene according to Good Manufacturing Practices (GMP) for food processing facilities and current company GMP policies, reporting repeat offenders to management.</li><li>Prepare samples for shipment and send for outside testing, updating results and alerting management to any discrepancies or issues.</li><li>Place product on hold and release product from hold according to company policy.</li><li>Receive new ingredients, contact suppliers for documentation, and maintain ingredient information files.</li><li>Organize and update all laboratory quality control documentation, including SOPs, forms, charts, tables, and analysis data, ensuring data entry is up-to-date.</li><li>Maintain lab equipment, including calibration, performance verification, and troubleshooting equipment and systems as needed.</li><li>Manage laboratory supply stock for general analysis, including solutions and general office supplies.</li><li>Support the QC Manager in all customer service issues.</li><li>Assist the QC team with any projects as designated.</li><li>Pursue excellence and continuously develop technical and personal skills.</li></ul><h2>Essential Skills</h2><ul><li>Basic laboratory skills through experience or a degree.</li><li>Proficiency in pipetting.</li><li>Micro plating techniques.</li><li>pH testing.</li><li>Ability to read a graduated cylinder.</li><li>Experience with Microsoft Office.</li><li>Effective and professional communication skills.</li><li>Quality control and HACCP understanding.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Strong organizational skills.</li><li>Effective time management.</li><li>Basic science skills.</li></ul><h2>Work Environment</h2><p>The typical schedule will be from 5 am to 1:30 pm. Work primarily takes place in a smaller lab, but there will be times when going out onto the production lines to gather samples is necessary. The team values work-life balance, and there is room for growth within the company, as demonstrated by the manager and assistant manager who both started as QC technicians themselves.</p><br>

<h1><strong>Job Title: Quality Control Technician</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Control Technician, you will play a crucial role in ensuring the production of high-quality oil products. Your responsibilities will include checking and verifying production records, spot checking labels, and creating labels for oil products. You will monitor the flow of products and take samples from production to perform PV and OSI testing in the lab. Additionally, you will conduct pH and density testing and oversee the production floor to perform quality checks.</p><p><br></p><h2>Responsibilities</h2><ul><li>Check and verify production records</li><li>Spot check labels for accuracy</li><li>Create labels for oil products</li><li>Monitor the flow of product through the production process</li><li>Take samples from production and conduct PV and OSI testing in the laboratory</li><li>Conduct pH and density testing</li><li>Oversee the production floor and perform routine quality checks</li><li>Engage in frequent moving, standing, lifting, and other active movements</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Preferred experience in food and beverage or quality lab environments</li><li>Associates degree in biotech or biology is preferred but not required</li><li>Commitment to wearing proper personal protective equipment (PPE)</li></ul><h2>Work Environment</h2><p>This position offers a balanced work environment, with 60% of time spent in office working with labels, 30% on the production floor overseeing products, and 10% in the lab. The role is situated in a food-grade environment where accuracy is paramount to prevent recalls. The facility is climate-controlled, manufacturing vegetable oil and dried goods, and candidates should be comfortable getting dirty. The schedule is 6AM to 2:30PM, Monday through Friday. PPE, including safety glasses, lab coat, respirator, and gloves, is provided. Dress code requires no jewelry, jeans without holes, steel-toe boots, and t-shirts or sweatshirts without holes. The company values promoting from within and offers opportunities for advancement to candidates who demonstrate strong work ethics, quality of work, and attendance.</p>

<h3><strong>Job Title: QC Microbiologist – Environmental Monitoring</strong></h3><p><strong>Shift: Monday to Friday, 7:00 AM – 3:30 PM</strong></p><p>Location: On-site, Worcester, MA</p><p>Schedule Flexibility: Occasional weekend and holiday work required (pre-scheduled)</p><p>Experience Level: 3–5 years</p><p>Education: Bachelor’s degree in Biology or a related life science required</p><p>Note: Candidates with Master’s degrees or research-focused backgrounds will not be considered.</p><p><br></p><h3>Job Summary:</h3><p>We are seeking a detail-oriented and motivated QC Microbiologist to join our Environmental Monitoring (EM) team within a GMP-regulated environment. The ideal candidate will have hands-on experience in microbiological testing, aseptic techniques, and cleanroom practices. This role supports routine EM activities, fill operations, and various lab functions to ensure product and material quality.</p><h3>Key Responsibilities:</h3><ul><li>Perform routine Environmental Monitoring (EM) in GMP cleanroom environments, including during fill operations.</li><li>Execute laboratory test methods as written to support product and material release.</li><li>Maintain accurate and compliant laboratory records in accordance with GMP standards.</li><li>Assist with investigations by gathering and analyzing data.</li><li>Draft or revise procedures under supervision.</li><li>Manage time effectively to complete assigned tasks independently.</li><li>Trend and analyze EM data to support reporting.</li><li>Support lab operations, including gowning and working in biosafety cabinets.</li><li>Collaborate with cross-functional teams and maintain strong communication.</li></ul><h3>Required Skills &amp; Qualifications:</h3><ul><li>3–5 years of QC Microbiology experience, including hands-on EM and lab testing.</li><li>Proficiency in aseptic techniques and working in biosafety hoods.</li><li>Strong attention to detail and organizational skills.</li><li>Ability to prioritize tasks in a dynamic, fast-paced environment.</li><li>Comfortable standing for extended periods and moving between buildings.</li><li>Willingness to work weekends and holidays as needed.</li><li>Strong interpersonal and communication skills.</li><li>Familiarity with LIMS for data entry is preferred.</li></ul><h3>Preferred Qualifications (Nice to Have):</h3><ul><li>Knowledge of USP, EP, JP, ICH guidelines, and cGMP regulations.</li><li>Experience with cleanroom gowning and documentation practices.</li><li>Prior experience in a GMP or cleanroom environment.</li></ul><p><strong><em>If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. </em></strong></p>

Quality Control Technician II

<h1 style="text-align: center;"><strong>Quality Director</strong></h1><h2>Job Description</h2><p>The Director of Quality is a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span> leader responsible for overseeing all quality and regulatory functions within a cGMP-compliant manufacturing environment. This role ensures that products meet internal and external standards while fostering a culture of continuous improvement and compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead Quality Assurance, Quality Control, Regulatory Affairs, and Training teams.</li><li>Develop and execute quality and compliance strategies aligned with business goals.</li><li>Oversee Quality Management Systems (QMS) and ensure compliance with FDA, cGMP, and industry standards.</li><li>Manage audits, inspections, and regulatory submissions.</li><li>Supervise laboratory operations, including testing, validation, and equipment maintenance.</li><li>Promote a strong quality culture through training and cross-functional collaboration.</li></ul><h2>Essential Skills</h2><ul><li>Extensive experience in quality assurance and regulatory affairs within a cGMP-compliant environment.</li><li>Proven leadership in managing teams and developing quality strategies.</li><li>Strong understanding of Quality Management Systems (QMS) and compliance with FDA and industry standards.</li></ul><h2>Work Environment</h2><p>The work environment is a cGMP-compliant manufacturing setting. The role involves collaborating with cross-functional teams and promoting a culture of quality and continuous improvement.</p>

Quality Director

<h1 style="text-align: center;"><strong>Quality Director</strong></h1><h2>Job Description</h2><p>The Director of Quality is a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span> leader responsible for overseeing all quality and regulatory functions within a cGMP-compliant manufacturing environment. This role ensures that products meet internal and external standards while fostering a culture of continuous improvement and compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead Quality Assurance, Quality Control, Regulatory Affairs, and Training teams.</li><li>Develop and execute quality and compliance strategies aligned with business goals.</li><li>Oversee Quality Management Systems (QMS) and ensure compliance with FDA, cGMP, and industry standards.</li><li>Manage audits, inspections, and regulatory submissions.</li><li>Supervise laboratory operations, including testing, validation, and equipment maintenance.</li><li>Promote a strong quality culture through training and cross-functional collaboration.</li></ul><h2>Essential Skills</h2><ul><li>Extensive experience in quality assurance and regulatory affairs within a cGMP-compliant environment.</li><li>Proven leadership in managing teams and developing quality strategies.</li><li>Strong understanding of Quality Management Systems (QMS) and compliance with FDA and industry standards.</li></ul><h2>Work Environment</h2><p>The work environment is a cGMP-compliant manufacturing setting. The role involves collaborating with cross-functional teams and promoting a culture of quality and continuous improvement.</p>

<h1 style="text-align: center;"><strong>Quality Director</strong></h1><h2>Job Description</h2><p>The Director of Quality is a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span> leader responsible for overseeing all quality and regulatory functions within a cGMP-compliant manufacturing environment. This role ensures that products meet internal and external standards while fostering a culture of continuous improvement and compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead Quality Assurance, Quality Control, Regulatory Affairs, and Training teams.</li><li>Develop and execute quality and compliance strategies aligned with business goals.</li><li>Oversee Quality Management Systems (QMS) and ensure compliance with FDA, cGMP, and industry standards.</li><li>Manage audits, inspections, and regulatory submissions.</li><li>Supervise laboratory operations, including testing, validation, and equipment maintenance.</li><li>Promote a strong quality culture through training and cross-functional collaboration.</li></ul><h2>Essential Skills</h2><ul><li>Extensive experience in quality assurance and regulatory affairs within a cGMP-compliant environment.</li><li>Proven leadership in managing teams and developing quality strategies.</li><li>Strong understanding of Quality Management Systems (QMS) and compliance with FDA and industry standards.</li></ul><h2>Work Environment</h2><p>The work environment is a cGMP-compliant manufacturing setting. The role involves collaborating with cross-functional teams and promoting a culture of quality and continuous improvement.</p>

<h1 style="text-align: center;"><strong>Quality Director</strong></h1><h2>Job Description</h2><p>The Director of Quality is a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span> leader responsible for overseeing all quality and regulatory functions within a cGMP-compliant manufacturing environment. This role ensures that products meet internal and external standards while fostering a culture of continuous improvement and compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead Quality Assurance, Quality Control, Regulatory Affairs, and Training teams.</li><li>Develop and execute quality and compliance strategies aligned with business goals.</li><li>Oversee Quality Management Systems (QMS) and ensure compliance with FDA, cGMP, and industry standards.</li><li>Manage audits, inspections, and regulatory submissions.</li><li>Supervise laboratory operations, including testing, validation, and equipment maintenance.</li><li>Promote a strong quality culture through training and cross-functional collaboration.</li></ul><h2>Essential Skills</h2><ul><li>Extensive experience in quality assurance and regulatory affairs within a cGMP-compliant environment.</li><li>Proven leadership in managing teams and developing quality strategies.</li><li>Strong understanding of Quality Management Systems (QMS) and compliance with FDA and industry standards.</li></ul><h2>Work Environment</h2><p>The work environment is a cGMP-compliant manufacturing setting. The role involves collaborating with cross-functional teams and promoting a culture of quality and continuous improvement.</p>

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Talent Acquisition

Access skilled talent ready to excel via our AI-driven platform, virtual events, and recruitment services.

CareerCircle TalentConnect

Transform your workforce and hiring practices with essential training and continuing education.

InclusiveU

Broaden your talent pool with dedicated support for individuals with disabilities.

Getting Hired Powered by CareerCircle

Mission aligned solutions supporting Non-Profit Organizations, Educational Institutions, Local Workforce Development Boards, and Learning Providers.

Upskilling & Job Advocacy

Upskilling solutions designed to empower members with in-demand skills training and ongoing support for successful certificate completion.

CareerReady

Job advocacy solutions to connect job seekers to inclusive employers through dedicated recruiting support.

CareerAdvocacy

Learn how we connect all communities with careers and build skilled talent pipelines.

About CareerCircle

Discover answers to common questions and gain insights into our goals and services.

Reach out to us for inquiries, support, or to learn more about our mission and services.

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Access our virtual career fairs, job seeker workshops, and employer focused webinars.

Events

Discover valuable resources to enhance your hiring strategy and drive organizational success.

Employer Resources

Get the latest news and updates on our mission, partnerships, and community impact.

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