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QA Associate II/III
Astrix Inc
- California, Maryland, United States
- California, Maryland, United States
À propos
Job Title Scientific & Technical Recruiter @ Astrix | Driving Innovation by Connecting Top Talent with Leading Life Science Companies
Position: QA Associate II/III
Job Type Contract until January 2026 (possibility of extension)
Summary: We are seeking a QA Associate to support quality operations within our manufacturing facility. This role ensures compliance with cGMP requirements, supports batch release activities, and provides QA oversight for day-to-day production operations.
Our client is a global player in the biotech field, primarily focusing on creating building blocks for advanced research and development, often supporting other companies in highly technical industries.
Key Responsibilities
Review and approve GMP documents, including SOPs, specifications, and batch records.
Perform batch record reviews and support product release activities.
Support deviation, CAPA, investigation, and change control processes.
Provide on-the-floor QA oversight (line clearance, material verification, compliance checks).
Assist with internal and external audits and regulatory inspections.
Support validation and qualification activities (equipment, processes, cleaning).
Maintain QA logs, training records, and document control systems.
Qualifications
Bachelor’s degree in a scientific or related field.
1–3+ years of experience in a GMP-regulated environment (Pharma or Biotech preferred).
Working knowledge of cGMP and regulatory guidelines.
Strong attention to detail and excellent communication skills.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
Seniority level Mid-Senior level
Employment type Contract
Job function Quality Assurance
Benefits
Medical insurance
401(k)
Vision insurance
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Compétences linguistiques
- English
Avis aux utilisateurs
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