Quality Control Associate

Title: Quality Control Associate I 
Location: Norwood, MA
Pay:  $25-33/hr 
Contract: 6+ months 

Job Summary

The Quality Control Associate I will perform a routine support role for GMP testing and support various laboratory activities at client’s manufacturing facility and affiliated contract organizations. This position will focus on molecular and cell biology general lab support activities. The role involves supporting the QC operations for raw materials, drug substance, and drug product, including data management and documentation. This is an on-site position.

Job Responsibilities

• Perform routine bioassay and analytical testing, including Cell Based Potency, qPCR, sequencing, electrophoresis.
• Support raw material testing.
• Prepare reagents, maintain lab equipment, and perform housekeeping tasks.
• Order, receive, and inventory supplies and materials.
• Write, revise, and follow SOPs and protocols.
• Data management activities such as scanning and uploading records.
• Participate in audits and continuous improvement initiatives.
• Establish and maintain a safe laboratory working environment.
• Accountable for all mandatory training and assigned tasks.
• Additional duties may be assigned.

Education & Qualifications 

• BA/BS Degree
• STEM degree with 0-2 years of experience in a GMP QC laboratory setting, focusing on molecular biology and/or Bioassays
• Hands-on experience with mammalian cell culture, PCR, qPCR, sequencing, gel electrophoresis, and lab equipment.
• Ability to prepare reagents, pipette small volumes, work in a Biological Safety Cabinet
• Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS)
• Excellent troubleshooting skills and the ability to communicate scientific issues clearly
• Strong written and oral communication skills and organizational abilities
• Knowledge of GMP, aseptic techniques, and general laboratory instrumentation (e.g. pH meters, balances, pipettes
• Ability to work effectively in a fast-paced, cross-functional matrix environment
• Familiarity with relevant FDA, EU, ICH guidelines, and regulations.