About this role
The team is seeking a Deputy Manager of Analytical Quality Assurance to join their team. This role is crucial for maintaining high-quality standards and ensuring compliance with regulatory requirements.
Key Responsibilities:
- Review the Validation Master Plan, Site Master File, Drug Master File, and Annual Product Quality Review.
- Evaluate Plant Layout and other documents related to Quality Assurance.
- Review quality systems related documents, including SOPs, vendor lists, audit plans, and audit schedules.
- Approve Certificates of Analysis (COA) for raw materials, in-process materials, intermediates, packing materials, and finished products.
- Ensure adherence to quality standards and regulatory guidelines.
- Collaborate with cross-functional teams to enhance quality assurance processes.
Required Skills & Qualifications:
- Bachelor's or Master's degree in a relevant field.
- Extensive experience in Analytical Quality Assurance, with 10-12 years in a similar role.
- Strong knowledge of quality assurance principles and regulatory requirements.
- Proficiency in reviewing and approving quality-related documentation.
- Excellent analytical and problem-solving skills.
- Strong communication and interpersonal skills.
What we offer:
The team provides a dynamic work environment, opportunities for professional growth, and the chance to be part of a dedicated team committed to quality excellence.
Applications are read by our talent team, usually within two working days.
If you look like a fit we will call you, and you will hear from us either way.