QC Associate I, Raw Materials - NorwoodApply Now
Location: Norwood, Massachusetts
Employment Type: Contract
Job Description
Title: QC Associate I – Raw Materials
Location: Norwood, MA
Work Arrangement: 100% Onsite
Employment Type: Contract
Duration: 6+ months
About the Role
We are seeking a QC Associate I to support routine GMP Quality Control testing and laboratory operations for raw materials, drug substance, and drug product.
This role will focus on molecular biology and bioassay support, laboratory documentation, reagent preparation, data management, and general QC laboratory activities within a regulated manufacturing environment.
Key Responsibilities
Key Skills
Quality Control | GMP | Raw Materials | Molecular Biology | Bioassays | Cell-Based Potency | PCR | qPCR | Sequencing | Gel Electrophoresis | Mammalian Cell Culture | LIMS | SAP | eQMS
Compensation
In accordance with applicable pay transparency requirements, the anticipated hourly rate for this role is $30.00–$35.00/hr, based on experience and qualifications.
Location: Norwood, MA
Work Arrangement: 100% Onsite
Employment Type: Contract
Duration: 6+ months
About the Role
We are seeking a QC Associate I to support routine GMP Quality Control testing and laboratory operations for raw materials, drug substance, and drug product.
This role will focus on molecular biology and bioassay support, laboratory documentation, reagent preparation, data management, and general QC laboratory activities within a regulated manufacturing environment.
Key Responsibilities
- Perform routine bioassay and analytical testing, including cell-based potency, qPCR, sequencing, and electrophoresis
- Support raw material testing activities
- Prepare reagents and support routine laboratory equipment maintenance and housekeeping
- Order, receive, and maintain inventory of laboratory supplies and materials
- Follow, write, and revise SOPs and laboratory protocols
- Support QC data management activities, including scanning and uploading records
- Participate in audits, continuous improvement initiatives, and general laboratory compliance activities
- Bachelor's degree in a STEM discipline
- 0–2 years of experience in a GMP QC laboratory environment
- Experience or academic exposure to molecular biology and/or bioassay techniques
- Hands-on experience with mammalian cell culture, PCR, qPCR, sequencing, or gel electrophoresis
- Ability to prepare reagents, pipette small volumes, and work in a Biological Safety Cabinet
- Strong written and verbal communication skills
- Strong organizational and troubleshooting skills
- Ability to work effectively in a fast-paced, cross-functional laboratory environment
- Knowledge of GMP and aseptic techniques
- Experience with general laboratory instrumentation such as pH meters, balances, and pipettes
- Experience with LIMS, SAP, eQMS, or similar electronic laboratory systems
- Proficiency with Microsoft Office applications
- Familiarity with FDA, EU, and ICH guidelines and regulations
- Prior experience supporting raw material, drug substance, or drug product testing
Key Skills
Quality Control | GMP | Raw Materials | Molecular Biology | Bioassays | Cell-Based Potency | PCR | qPCR | Sequencing | Gel Electrophoresis | Mammalian Cell Culture | LIMS | SAP | eQMS
Compensation
In accordance with applicable pay transparency requirements, the anticipated hourly rate for this role is $30.00–$35.00/hr, based on experience and qualifications.