Job Title: Quality Assurance Technician Job Description 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. Responsibilities + Review and confirm compliance documentation related to raw materials, in-process samples, and finished product analyses. + Monitor adherence to current Good Laboratory Practices (cGLP) by laboratory personnel during routine operations. + Verify proper labeling of laboratory chemicals, reagents, and standards in accordance with SOPs. + Review laboratory audit trails during data assessments to ensure alignment with SOPs. + Coordinate with Analytical Laboratory Teams to compile and provide necessary documentation to cross-functional teams. + Manage incoming documentation, including tracking, recording, storing, and archiving. + Identify system gaps during routine monitoring and notify supervisors of areas requiring improvement. + Understand laboratory equipment operation, qualification, and calibrations, including software audit trial reviews. + Actively participate in the review of data related to laboratory investigations and incidents to ensure regulatory compliance. + Support departmental and cross-functional initiatives and complete assignments as directed. Essential Skills + Strong command of English language communication skills, both verbal and written. + Solid documentation and technical writing skills, with the ability to apply relevant scientific principles and practices. + Ability to work under minimal supervision, both independently and in a team environment. + Proficient computer skills and software applications such as Microsoft Office tools and Quality applications. + Experience in analytical quality assurance, preferably in pharmaceutical manufacturing. + Knowledge of analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, and analytical development. Additional Skills & Qualifications + Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related field from an accredited institution required; Master’s degree preferred. + 1-3 years of experience in analytical quality assurance. + Experience with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP). + Self-motivated with excellent organizational skills and the ability to focus on details. + Experience with inhalation products (MDI) is a plus. + Ability to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday. Work Environment 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. Company is offering up to 6K for relocation Pay and Benefits The pay range for this position is $62000.00 - $75000.00/yr. Health, Vision, Dental, 401K Workplace Type This is a fully onsite position in Fall River,MA. Application Deadline This position is anticipated to close on Aug 11, 2025. About Actalent 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. 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. 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.