Sr. Quality Assurance Specialist

Siegfried • Pennsville, NJ

8d • $82,000 - $110,000 • Onsite

About The Position

The incumbent assures compliance to all regulatory requirements, current Good Manufacturing Practices, and company Policies, Standard Operating Procedures and Work Instructions. Siegfried is a trusted and respected partner to the pharmaceutical industry, upholding the highest standards in safety, quality and sustainability, while fostering a culture that empowers employees to thrive. It is a rapidly expanding global company where diverse perspectives and experiences come together in a collaborative environment, valuing both collective success and individual contributions, offering long-term opportunities to grow and make an impact.

Requirements

• A BA/BS degree in microbiology, biology, chemistry, or engineering and 3-5 years of experience in QA in a pharmaceutical manufacturing environment required, or an equivalent combination of education and experience.
• Excellent communication skills.
• Conscientious and detail oriented.
• Excellent computer skills (MS Office 365).
• Team player.
• Able to self-manage daily work and set priorities.
• Able to manage projects and prioritize appropriately.
• Able to adhere to deadlines.

Nice To Haves

• Thorough knowledge of cGMP in active pharmaceutical ingredient (API) manufacturing is preferable.

Responsibilities

• Reviews, approve and tracks executed production records.
• Reviews and approves production and QC investigations.
• Reviews lab sample results and manufacturing records related to qualification/validation activities.
• Conducts, write, and reviews quality related investigations as appropriate.
• Reviews and approves Master Production Records.
• Responsible for cGMP compliance of assigned manufacturing operations / areas.
• Completes QMS items as assigned.
• Is responsible for the conditional / final release of materials.
• Hosts customer and internal audits, as needed.
• Conduct internal and external audits, as needed.
• Participates in inspections by regulatory authorities.
• Writes and reviews Annual Product Reviews/Product Quality Reviews.
• Writes and reviews Product Validation / Qualification / Assessments documents.
• Writes and reviews Equipment Qualifications / Assessments documents.
• Writes and reviews Computerized Systems Validations / Assessments documents.
• Reviews, evaluates and approves minor equipment changes.
• Conducts GMP inspections.
• Conducts environmental monitoring.
• Reviews and approves CMC sections of DMFs as appropriate.
• Maintains QA databases for products / equipment as appropriate.
• Adheres to personal moral, ethical, legal, and behavioral conduct that is in compliance with the Siegfried Code of Conduct.
• Adheres to all applicable SHE and cGMP regulations e.g. ICH Q7, FDA, 21 CFR 210 and 211, etc.

Benefits

• Explore and provide reasonable accommodations to assist any qualified individual with a disability in performing the essential functions of his/her job.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior