Join our exciting growing Biotech client - they are hiring a QA Engineering Specialist/Senior level to join their team!
Position Title: Quality Assurance Engineering Specialist
Department: Quality Assurance
Location: Onsite Manufacturing Site, Philadelphia, PA
Shift: 3-11:30pm EST
Reports To: Quality Assurance Manager
Job Summary:
As a Quality Assurance Engineering Specialist in the pharmaceutical industry, you will play a critical role in ensuring the quality and compliance of our products throughout the development and manufacturing processes. You will collaborate with cross-functional teams to implement quality assurance strategies, conduct risk assessments, and ensure adherence to industry regulations and standards.
Key Responsibilities:
- Quality Oversight: Monitor and evaluate manufacturing processes, ensuring compliance with Good Manufacturing Practices (GMP), FDA regulations, and other applicable guidelines.
- Documentation Review: Review and approve quality documentation, including batch records, standard operating procedures (SOPs), and validation protocols.
- Risk Management: Conduct risk assessments and implement quality control measures to mitigate potential issues in product quality.
Qualifications:
Education: Bachelor’s degree in Pharmacy, Chemistry, Engineering, or a related field. Advanced degrees or certifications (e.g., CQE, CQA) are a plus.
Experience: Minimum 2-3 years of experience in quality assurance or quality control within the pharmaceutical or biotech industry.
Ready to take your career to the next level? Reach out directly to learn more ~