Lonza Biotechnology & Biology Job – Candidates Apply Online
Lonza Cell and Gene Therapy Facility is the largest in the world and our facility is growing. We are looking for professionals to grow with us and we have this exciting opportunity in Viral Vector Therapy. The Manufacturing Supervisor will be responsible for leading and directing daily work activities in the batch viral suites to ensure schedule attainment is met.
Job Title: Viral Vector Manufacturing Supervisor
Eligibility Criteria
- Must be available to work Nights, Weekends and Holidays
- Bachelor’s Degree in Biotechnology, Biology, Chemistry, or equivalent with Associates degree
- High School Diploma or Equivalent may be considered with relevant experience
- Advanced Level knowledge of various commonly used biological processing techniques including cell culture, ultra-filtration and column chromatography.
- Extensive experience in writing technical documents and protocols.
- Advanced Level knowledge of cGMP facilities and cGMP requirements.
- Senior Level experience in biomanufacturing; GMP setting preferred, and/or 12-24 months experience as an Associate Level IV/Supervisor in bio-pharm industry.
Key responsibilities:
- Adherence to safety and cGMP regulations of the team.
- Execution of USP/DSP activities in the clean room.
- Planning of daily activities in the clean room and provide first line of problem solving in case of any event.
- Ensure critical supplies are in stock and available for production.
- Responsible and accountable of the Kanban system.
- Trainer, coach and mentor to the Core levels in the technical aspects of the department.
Coaching, mentoring and performance review of the team. - Escalation to management and interaction with other stakeholders in case of any event (Deviation Investigation Team, QA, MSAT, FE, etc.)
Contributor or leader on MFG and OE projects to optimize and streamline processes. - Responsible to interact with customer while performing operations in the clean room.
- Completes and reviews batch records and production documents.
- Reviews and approves Batch Records, Change Controls, Deviations and other documentation required for production operations.
Lonza Biotechnology & Biology
