GMP QA Specialist - Materials & QC (Contract-to-Hire)

Astrix; New Jersey; On-site; USD 41,328 - 55,104; Full time

Job summary

A reputable staffing firm in New Jersey is seeking a Quality Assurance Specialist for a contract-to-hire position. The successful candidate will review and approve documentation, ensure compliance with GMP regulations, and collaborate with various departments. Candidates should have a Bachelor's degree in a scientific discipline and 2–5 years of experience in Quality Assurance within the biotechnology or pharmaceutical industry. Proficiency in Microsoft Office is preferred.

Qualifications

• 2–5 years of experience in Quality Assurance within the biotechnology, biopharmaceutical, or pharmaceutical industry.
• Strong knowledge of GMP regulations (21 CFR Part 210/211) and quality system principles.
• Experience reviewing QC data, raw material documentation, and stability reports.

Responsibilities

• Review and approve raw material documentation for accuracy and compliance.
• Perform raw material release activities in accordance with established SOPs and GMP requirements.
• Collaborate cross-functionally with Quality Control, Supply Chain, and Manufacturing.

Skills

Attention to detail

Strong organizational skills

Teamwork

Communication skills

Education

Bachelor’s degree in a scientific discipline

Tools

Microsoft Office

Quality management systems (QMS)

LIMS

Job description

A reputable staffing firm in New Jersey is seeking a Quality Assurance Specialist for a contract-to-hire position. The successful candidate will review and approve documentation, ensure compliance with GMP regulations, and collaborate with various departments. Candidates should have a Bachelor's degree in a scientific discipline and 2–5 years of experience in Quality Assurance within the biotechnology or pharmaceutical industry. Proficiency in Microsoft Office is preferred.