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Entry-Level Qc Analyst
Job in
Woburn, Middlesex County, Massachusetts, 01813, USA
Listed on 2026-01-22
Listing for:
Greenkey Resources LLC
Full Time
position Listed on 2026-01-22
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Medical Science, Data Scientist
Job Description & How to Apply Below
Overview
- Embark on a rewarding career as an Entry-Level QC Analyst in a dynamic, innovation-driven environment.
- Contribute to cutting-edge research and quality control in gene therapy applications.
- Gain hands‑on experience with advanced laboratory techniques, including immunoassays and cell‑based bioassays.
- Collaborate with multidisciplinary teams to ensure compliance with GMP standards.
- Enhance your technical skills through method transfer and reagent qualification activities.
- Participate in drafting and reviewing technical documents and SOPs.
- Ideal for individuals passionate about advancing their expertise in quality control.
- Work in a supportive environment that fosters professional growth and development.
- Conduct immunoassays and cell‑based assays to support product testing and stability analysis.
- Assist in drafting and reviewing SOPs and technical documentation for laboratory operations.
- Support method transfer and qualification of reagents under expert supervision.
- Maintain laboratory instruments and ensure proper calibration and upkeep.
- Collaborate with internal and external teams to achieve project goals efficiently.
- Contribute to investigations and deviation reports to uphold quality standards.
- Ensure compliance with GMP regulations in all laboratory activities.
- Review and analyze QC data to ensure accuracy and reliability.
- Bachelor’s degree in Cell Biology, Molecular Biology, Biochemistry, or related field required.
- Experience with mammalian cell culture and ELISAs is preferred.
- Proficiency in basic laboratory techniques and data analysis methods essential.
- Strong organizational and communication skills are critical for success.
- Detail‑oriented with a commitment to maintaining high‑quality standards.
- Ability to work collaboratively within a team and independently as needed.
- Enthusiasm for learning and growing in a regulated laboratory environment.
- Dedication to upholding compliance with GMP and regulatory guidelines.
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