Pharmaceutical Manufacturing Quality Specialist
4 weeks ago
Key Responsibilities:
- Ensure compliance with Good Manufacturing Practices (GMP) regulations.
- Conduct quality assurance activities, including batch record reviews and releases.
- Participate in audits and implement corrective actions.
- Develop and maintain Standard Operating Procedures (SOPs) and ensure compliance.
Requirements:
- Bachelor's degree in a relevant field or equivalent experience.
- Minimum 2 years of experience in pharmaceutical quality assurance or a related field.
- Experience with GMP regulations and quality systems.
About Actalent:
- Actalent is a global leader in engineering and sciences services and talent solutions.
- We help visionary companies advance their engineering and science initiatives through access to specialized experts.
- Our network of consultants and clients spans the U.S., Canada, Asia, and Europe.
Diversity, Equity & Inclusion:
- We prioritize diversity and inclusion in our hiring practices and company culture.
- We maintain an inclusive environment through self-reflection and continuous improvement.
- We foster a culture of care, engagement, and recognition with clear outcomes.
- We ensure growth opportunities for our people.
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