Senior QC Coordinator in Analytical Development Team Lead
4 weeks ago
We are seeking an experienced Senior QC Coordinator to lead our Analytical Development team. This is an exciting opportunity for a highly skilled professional to join our dynamic organization and contribute to the success of our clients.
The ideal candidate will have a strong scientific background, excellent project management skills, and experience working in a cGMP QC laboratory environment. They will be responsible for coordinating method transfer activities, generating transfer plans, and leading meetings with customers and internal stakeholders.
Key Responsibilities:
- Lead analytical development projects from inception to completion
- Coordinate method transfer activities with customers and contract laboratories
- Develop and maintain quality documentation, including transfer plans and summary reports
- Collaborate with cross-functional teams to ensure smooth project execution
- Ensure compliance with regulatory requirements and industry standards
Requirements:
- Masters degree in Pharmaceutical Sciences, Biochemistry, Protein Chemistry, or related field
- At least 3 years of experience in a cGMP QC laboratory environment
- Strong project management skills, with experience leading cross-functional teams
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
What We Offer:
- Competitive salary: $90,000 - $110,000 per annum
- Benefits package, including health insurance, retirement plan, and paid time off
- Opportunities for career growth and professional development
- A dynamic and supportive work environment
About Fujifilm Diosynth Biotechnologies:
Fujifilm Diosynth Biotechnologies is a world-leading Contract Development and Manufacturing Organization (CDMO) serving the pharmaceutical industry. We are committed to advancing tomorrow's medicines and improving patient outcomes.
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