Are you ready to contribute to a pioneering team revolutionizing medicine through mRNA technology? We are looking for a passionate, detail-oriented QC Raw Materials Associate to join our cutting-edge manufacturing hub in Norwood, MA. This is a high-impact, on-site role where your expertise in analytical testing and compliance will directly power a global mission to transform patient lives.
The Role As a key member of our Quality Control team, you will support GMP Manufacturing through hands-on quality control of raw materials, consumables, and product samples. You will thrive in a fast-paced, digital-first environment, utilizing advanced analytical tools and emerging technologies like Generative AI to ensure the highest standards of lab data integrity and operational excellence.
Key Responsibilities
- Analytical Testing: Perform critical testing using HPLC, Bioanalyzer, osmolality, pH, conductivity, and raw material spectroscopy.
- Sample Coordination: Manage the requesting, sampling, and shipping of raw materials while coordinating logistics across internal and external laboratories.
- Inspections & Compliance: Execute AQL visual inspections of drug products and dimensional verifications of materials in strict alignment with SOPs and GxP regulations.
- Data Management: Log samples and results into LabVantage (LIMS) and maintain meticulous records following Good Documentation Practices (GDP).
- Quality Support: Contribute to the QC Stability Program, write and revise technical reports/SOPs, and support quality systems like deviations, CAPAs, and change controls.
- Operational Excellence: Manage QC inspection labels, troubleshoot controlled temperature units, and practice aseptic techniques in cleanroom environments.
- Education: BS in a relevant scientific discipline.
- Experience: 3+ years in a GMP Quality Control laboratory setting.
- Technical Aptitude: Demonstrated ability to learn and apply complex GxP regulations and digital platforms.
- Mindset: A "behave like an owner" attitude with a commitment to innovation and continuous improvement.
Apply today to be part of a team that digitizes everywhere possible to maximize our impact on patients!
FOR MORE IMMEDIATE CONSIDERATION, email a current resume to iris.levy@randstadusa.com
salary: $38 - $38.19 per hour
shift: First
work hours: 6 AM - 4 PM
education: Bachelors
Responsibilities
As a QC Raw Materials Associate, you will support GMP Manufacturing through hands-on quality control of raw materials, consumables, and product samples. Key responsibilities include:
- Sample Management: Request, sample, release, and ship raw materials to support GMP operations while coordinating logistics across internal and external laboratories.
- Analytical Testing: Perform testing using HPLC, Bioanalyzer, osmolality, pH, conductivity, and spectroscopy.
- Inspections: Execute AQL visual inspections of drug products and dimensional verifications of raw materials and retain samples.
- Data Integrity: Log samples into LabVantage (LIMS), maintain compliant data records, and follow Good Documentation Practices.
- Quality Systems: Support the QC Stability Program, write/revise SOPs, and participate in deviations, CAPAs, and non-conformance investigations.
- Lab Operations: Manage QC inspection labels, troubleshoot controlled temperature units, and maintain lab supplies/housekeeping.
- Compliance: Practice aseptic techniques, gown for cleanrooms, and execute all tasks in strict alignment with GxP regulations and work instructions.
Skills
Qualifications
Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.
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.
