Quality Control Chemist-Entry Level

Collabera; Frederick (MD); On-site; USD 50,000 - 65,000; Full time

Job summary

A leading company in the biotechnology sector is seeking a Quality Control Chemist to conduct analytical testing and ensure compliance with GMP standards. The role involves routine testing of materials and supporting lab maintenance. Ideal candidates will have a relevant degree and experience in the biotech or pharma industry. Strong analytical skills and familiarity with regulatory compliance are essential for success in this entry-level position.

Qualifications

• Bachelor’s Degree or equivalent experience in QC/biotech.
• Experience in biotech/pharma industry preferred.

Responsibilities

• Execute analytical testing per established methods.
• Support laboratory maintenance and equipment calibration.
• Review and trend test data.

Skills

Analytical Techniques

Technical Writing

Data Analysis

Education

Bachelor’s Degree

Associate Degree

High School Diploma

Tools

Flow Cytometry

ELISA

PCR

Bioassays

MS Office

Job description

We are seeking a Quality Control Chemist to perform routine and complex analytical testing of raw materials, intermediates, and final products using techniques such as cell-based bioassays, Flow Cytometry, ELISA, and qPCR. This role supports GMP compliance, lab maintenance, data review, investigations, and documentation updates.

Key Responsibilities:

1. Execute analytical testing per established methods.
2. Support laboratory maintenance and equipment calibration.
3. Review and trend test data; assist with Certificate of Analysis (CoA) generation.
4. Participate in OOS investigations and deviation root cause analysis.
5. Author/revise SOPs and validation documents.
6. Present updates in team meetings and ensure GMP compliance.

Basic Qualifications:

• Bachelor’s Degree; OR
• Associate Degree with 2+ years of QC/biotech experience; OR
• High School Diploma with 3+ years of QC/biotech experience.

Preferred Qualifications:

• Proficiency in analytical techniques (Flow Cytometry, ELISA, PCR, bioassays).
• Familiarity with GMP, SOPs, and regulatory compliance (21 CFR Part 11/210/211).
• Experience in biotech/pharma industry.
• Strong technical writing and data analysis skills.
• Competency with MS Office applications.

Additional Details:

• Seniority level: Entry level
• Employment type: Contract
• Job function: Engineering and Science
• Industries: Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing