QC Bioassay Associate
- Premium Pay: Earn a competitive $41.00/hour, plus a 10% shift differential for your evening availability.
- Schedule for Balance: Work a consistent Monday-Friday (12:00 PM – 8:00 PM) shift.
- Career Growth: Start with a 6-month contract that has potential for extension or conversion based on your performance and business needs.
- High-Impact Work: Gain hands-on experience with commercially approved products and clinical-stage breakthroughs while working in a state-of-the-art cGMP facility.
- Education: A Bachelor’s degree (BS) in Biochemistry or a relevant scientific discipline.
- Experience: 2–3 years of professional experience in a laboratory setting.
- Regulatory Knowledge: A solid understanding (or a rapid ability to learn) GxP regulations and Good Documentation Practices.
- The Mindset: You are bold, curious, and collaborative. You thrive in fast-paced environments and have a "relentless" drive to solve complex technical puzzles.
- Location: Fully on-site in Norwood, MA (Not eligible for remote work).
- Shift: Monday-Friday, 2nd Shift (12:00 PM – 8:00 PM).
- Target Start Date: March 16, 2026.
shift: Second
work hours: 12 PM - 8 PM
education: Bachelors Responsibilities Here’s What You’ll Do As a Quality Control Specialist , you will drive operational excellence in the Bioassay lab through technical leadership and rigorous cGMP compliance.
- Lead & Execute: Support routine testing for Raw Materials, Drug Substances, and Drug Products for clinical and commercial use.
- Technical SME: Troubleshoot complex equipment and assay performance issues; lead method transfers (Bioassays, qPCR, sequencing) in collaboration with development teams.
- Quality Ownership: Conduct technical assessments for deviations and investigations; write/revise SOPs, protocols, and reports to ensure "Right First Time" results.
- Mentorship & Leadership: Perform On-the-Job Training (OJT) for staff, manage scheduling/resource allocation, and represent the team in management's absence.
- Operational Integrity: Oversee equipment validation, maintain CTU alarm response, and ensure strict adherence to GxP, Data Integrity, and Good Documentation Practices.
- Continuous Improvement: Lead lab optimization projects and support audit readiness to maintain a high-standard, inclusive, and innovative work culture.
- Bioassay (5 years of experience is required)
- Quality Control (5 years of experience is required)
- GMP (1 year of experience is required)
- cGMP (5 years of experience is required)
- Raw Materials (1 year of experience is required)
- Biochemistry (1 year of experience is required)
- GxP (4 years of experience is required)
- Years of experience: 5 years
- Experience level: Experienced
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected]. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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