Step into a pivotal role supporting cutting-edge GMP manufacturing as a Quality Control Associate. This position offers high-impact, hands-on experience managing the lifecycle of raw materials and consumables within a fast-paced, inclusive environment that values operational excellence. You will work with advanced analytical tools and gain unique exposure to emerging technologies, including Generative AI systems designed to enhance lab data integrity and quality documentation.
Based at a state-of-the-art facility in Norwood that features modern laboratory spaces and collaborative hubs designed for high-throughput biopharmaceutical production, you will be part of a team dedicated to maintaining the highest standards of compliance. This is an ideal role for a detail-oriented professional looking to sharpen their technical skills in a continuously evolving setting while contributing to life-changing product development.
location: Norwood, Massachusetts
job type: Contract
salary: $25.00 - 34.84 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Raw Material Lifecycle Management: Perform sampling, inspection, and release of raw materials and consumables to ensure seamless support of GMP operations.
- Analytical Testing: Execute a variety of assays including HPLC, pH, conductivity, osmolality, and spectroscopy (TruScan) to verify material quality.
- Logistics & Coordination: Manage sample shipments to internal and external laboratories, ensuring proper documentation and domestic/international compliance.
- Data Integrity: Log samples and results into LabVantage (LIMS) while maintaining strict adherence to Good Documentation Practices (GDP).
- Quality Systems Support: Contribute to the authoring and revision of SOPs and technical reports while supporting deviations, CAPAs, and non-conformance investigations.
- Facility Oversight: Perform AQL visual inspections of drug products and manage controlled temperature units and lab housekeeping.
qualifications:
Required Skills
- Bachelor of Science (BS) in a scientific discipline.
- 3-4 years of experience working in a GMP Quality Control laboratory environment.
- Strong understanding of GxP regulations and compliance standards.
- Proficiency in aseptic techniques and cleanroom gowning protocols.
- Experience with LabVantage or similar LIMS platforms.
- Proven ability to execute tasks in strict alignment with SOPs and work instructions.
- Experience with analytical methods like HPLC, Bioanalyzer, or Spectroscopy.
- Experience writing or revising technical documents and SOPs.
- Exposure to Quality System processes (Deviations, CAPAs, Change Controls).
- Aptitude for learning new technologies, including AI-driven documentation tools
skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System
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 HRsupport@randstadusa.com.
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.
