<p>Job Title: Quality Assurance Analyst I</p> <p>Are you passionate about quality and precision in pharmaceutical manufacturing? Join our team as a Quality Assurance Technician and play a critical role in ensuring our products meet the highest standards of safety, efficacy, and compliance.</p> <p>What You'll Do:</p> <ul> <li>Perform in-process quality checks (weight, thickness, hardness, disintegration, friability) as outlined in batch records. </li><li>Conduct pre-manufacturing inspections of cleanrooms and equipment using detailed SOPs. </li><li>Execute AQL sampling and inspections to ensure product integrity. </li><li>Inspect in-process and finished product samples for the QC Lab, ensuring accurate documentation and timely reporting. </li><li>Maintain standard weight records and verify balances daily. </li><li>Isolate and document rejected materials during batch processing. </li><li>Monitor environmental conditions that impact product and facility quality. </li><li>Review engineering logs (temperature/humidity, calibration, PM, pest control, contractor activity). </li><li>Audit batch records for completeness and accuracy before advancing to the next stage. </li><li>Verify equipment and control systems functionality during production runs. </li><li>Support investigations and reporting related to customer complaints. </li><li>Identify and escalate non-conformances or discrepancies to management. </li><li>Contribute to special projects and additional duties as assigned. </li></ul> <p>What You Bring:</p> <ul> <li>Vocational training or a degree in pharmaceutical manufacturing, industrial management, or a related field (preferred). </li><li>2-3 years of QA experience in a GMP-regulated pharmaceutical environment. </li><li>Experience with metered-dose inhalers (MDIs) or parenteral products is a strong plus. </li><li>Proficiency in Microsoft Office, SAP, and other business applications. </li><li>Strong organizational, communication, and leadership skills. </li><li>Ability to work independently and as part of a team. </li><li>Solid understanding of cGMP and regulatory compliance. </li><li>Detail-oriented with the ability to multitask and meet tight deadlines. </li></ul> <p>If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $65000.00 - $73000.00/yr.</p> <p>Health, Vision, Dental, 401K</p> <p>Workplace Type</p> <p>This is a fully onsite position in Fall River,MA.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Jun 27, 2025.</p> <p>About Actalent</p> <p>Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.</p> <p>The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.</p> <p>If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>