Sign upLog in

Quality Control Senior Associate

Atrium

Boston, MA

Apply
JOB DETAILS
SALARY
$30–$33 Per Hour
SKILLS
Analysis Skills, Artificial Intelligence (AI), Asepsis, Assays, Biotech and Pharmaceutical, Cell Biology, Cross-Functional, Current Good Manufacturing Practice (cGMP), Detail Oriented, Equipment Maintenance/Repair, GMP (Good Manufacturing Practices), Gene Therapy, Genetics, Interviewing Skills, Laboratory, Laboratory Equipment, Laboratory Operations, Laboratory Techniques, Maintain Compliance, Manufacturing, Operational Support, Production Support, Quality Control, Quality Metrics, Quality Monitoring, Real-time PCR (qPCR), Record Keeping, Regulatory Compliance, Short Messaging Service (SMS), Team Player, Test Lab, Testing
LOCATION
Boston, MA
POSTED
1 day ago
Client Overview:
Our client, a growing biotech organization in Boston, is seeking a Quality Control Senior Associate to support critical Cell Therapy quality operations within a fast-paced GMP environment. This is an excellent opportunity for candidates with biologics testing experience, aseptic technique expertise, and exposure to Cell & Gene Therapy (CGT).

Salary/Hourly Rate:
$30/hr - $33/hr

Position Overview:
The Quality Control Senior Associate will perform in-process, release, and stability testing while supporting laboratory operations and maintaining compliance with cGMP standards. The ideal Quality Control Senior Associate will have hands-on QC laboratory experience and thrive in a collaborative manufacturing environment. The schedule is from Sunday to Wednesday, 7:30 am to 6:00 pm. This is a 12-month contract with a strong possibility of extension.

Responsibilities of the Quality Control Senior Associate:
  • Perform Quality Control testing on Cell Therapy in-process, release, and stability samples within a GMP-regulated laboratory environment.
  • Execute laboratory assays including flow cytometry, qPCR (MycoTOOL), ELISA, cell counts, sterility testing (BACT), gram stain, and endotoxin (LAL) testing.
  • Analyze, document, and review test results while ensuring accuracy and compliance with laboratory procedures.
  • Support QC data tracking and trending activities to assist with product quality monitoring.
  • Maintain detailed laboratory records and complete technical review of raw data in accordance with cGMP and cGDP standards.
  • Assist with routine laboratory upkeep, equipment maintenance, and general operational support.
  • Collaborate cross-functionally with Quality and Manufacturing teams to support Cell Therapy production timelines.
  • Adhere to aseptic techniques and strict quality standards in all laboratory activities.
Required Experience/Skills for the Quality Control Senior Associate:
  • 1+ years of laboratory experience within QC, biologics, or pharmaceutical environments.
  • Experience with aseptic techniques is required.
  • Strong attention to detail and ability to work independently and within a team.
Preferred Experience/Skills for the Quality Control Senior Associate:
  • Exposure to Cell & Gene Therapy (CGT) environments is highly preferred.
  • An understanding of biological or cell-based assays is preferred.
Education Requirements:
  • Bachelor's degree in a scientific discipline is required.
Benefits:
  • Client-provided benefits available, upon eligibility.
About Atrium:What you do matters. Guided by our Applicant-Centric™ approach, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated. Join us and become part of an inclusive team committed to your growth and success.
By applying to this job, you agree to receive calls, AI-generated calls, text messages, and/or emails from Atrium and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to opt out on any message you receive. For more details, please review our Terms of Use and Privacy Policy .

As a woman-owned firm, we value diversity. We are an equal opportunity and affirmative action employer and will consider all applications without regard to race, sex (including gender, pregnancy, sexual orientation and gender identity), age, color, religion or creed, national origin or ancestry, veteran status, disability (physical or mental), genetic information, citizenship or any other characteristic protected by law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Candidates who apply for roles through the Atrium website will be added to our candidate pool and may be considered for additional roles of a similar title. Please contact us to request an accommodation.
EOE/M/F/D/V/SO

Position ID: 397164

About the Company

A

Atrium

Resume Resources

Free Resume TemplatesFree Resume Builder