QC Lead
4 weeks ago
Job Summary
We are seeking a highly skilled QC Lead to join our team at GSK. The successful candidate will be responsible for scheduling and coordinating laboratory activities, ensuring compliance with GMP regulations and quality systems.
Key Responsibilities
- Scheduling and Coordination: Schedule and coordinate laboratory activities, including routine GMP testing and throughput.
- Quality Assurance: Demonstrate awareness of scientific principles and method validation for assays performed.
- Review and Communication: Review GMP assay data and communicate findings to manufacturing teams.
- Decision Making: Prioritize and decide appropriate course of action with minimal supervision.
- Leadership: Lead laboratory investigations and coordinate preventative maintenance activities with external vendors.
- Procedure Development: Perform revision of standard operating procedures and act as Process Owner for applicable methods.
- Training and Development: Train and teach team members on applicable procedures and serve as subject matter expert on various methods and topics.
- Communication and Teamwork: Effectively communicate across departments and lead others through high-pressure situations.
- Support and Compliance: Support non-routine tests, studies, or projects and ensure compliance with current GMP regulations and quality systems.
Requirements
- Education: Bachelor's Degree in a scientific discipline.
- Experience: 2+ years of GMP/pharmaceutical/lab experience.
- Skills: Computer skills and knowledge, basic proficiency with Microsoft Office programs, demonstrated ability to work successfully both independently and in a team environment, good verbal and written communication skills, and good time management skills.
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