▷ [Apply Now] Supervisor Biotech Production
12 hours ago
Within this role you will be responsible for supervising the implementation of commercial manufacturing production schedules and supervising the manufacturing team in relation to process execution for manufacturing processes.
This is a shift position.
As a Supervisor Biotech Production, a typical day might include, but is not limited to, the following:
1. Supervising commercial scale manufacturing of recombinant proteins according to approved protocols, regulation, and schedule.
2. Supervising a team responsible for the manufacture of bulk drug substance in a cGMP regulatory environment.
3. Ensuring that the highest safety and housekeeping standards are maintained.
4. Supervising all aspects of respective areas of operations.
5. Reviewing and editing batch records in accordance with cGMP standards.
6. Ensuring availability of production batch records for upcoming lots.
7. Scheduling duties and batch tasks based on master production schedule.
8. Ensuring equipment readiness and coordinating regular equipment maintenance and calibrations; troubleshoots equipment.
9. Performing cGMP audits of production area.
10. Performing people management duties including time sheet submissions, scheduling of vacations, personnel development, disciplinary actions, hiring, terminations, and performance evaluations.
11. Scheduling individual and ongoing training.
12. Interfacing with other departments, such as Facilities, Process Development, Process Analytical Sciences, Regulatory, Quality Assurance and Quality Control.
13. Ensuring that safety standards are maintained at all times.
This role might be for you if you:
1. Demonstrate previous supervisory and/or leadership experience is required.
2. Possess logical troubleshooting and problem-solving skills.
3. Have excellent analytical, written and oral communication skills.
4. Demonstrate an ability to work within a successful team.
To be considered for this opportunity you should have a BS/BA in Life Sciences or related field with 5+ years of relevant cGMP manufacturing experience. Will substitute relevant experience in lieu of educational requirement.
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