Supervisor, Buffers & Media
at Thermo Fisher Scientific
St. Louis, MO 63134, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 04 Dec, 2024 | Not Specified | 04 Sep, 2024 | 2 year(s) or above | Disabilities,Pharmaceutical Industry,Cgmp Practices,Analytical Skills,Communication Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
REQUIREMENTS:
- Equivalent experience accepted; Bachelor’s degree in science or engineering preferred
- 2+ years of supervisory experience in the pharmaceutical industry preferred
- 3+ years of proven experience in a related field or industry required
- Knowledge of cGMP practices and deviation investigations preferred
- Strong mechanical and analytical skills
- Proficiency in MS Office and strong math skills
- Meticulous with strong prioritization and communication skills
- Able to work independently and as part of a team
- Strong problem-solving and decision-making abilities
Thermo Fisher Scientific is an equal opportunity employer and provides reasonable accommodations for applicants with disabilities. We value diversity and inclusion in our workforce, and we are committed to creating a supportive and inclusive environment for all employees.
Apply today to be part of our exceptional team! Visit http://jobs.thermofisher.co
Responsibilities:
- Maintain a safe and clean work environment, ensuring compliance with established policies and procedures
- Follow manufacturing batch records and work instructions with a focus on achieving flawless execution.
- Complete department functions such as equipment maintenance, documentation, and data management
- Act as an On-The-Job Trainer for various job functions
- Document all activities to meet cGMP requirements and actively provide feedback
- Evaluate processes critically and identify areas for improvement
- Perform equipment testing, troubleshooting, and routine maintenance
- Schedule and assign personnel, prioritize tasks, and supervise progress
- Complete production plan, ensuring timely consumption of materials and quality documentation
- Identify deviations, aid in investigations, and provide input on major deviations
- Participate in cross-functional teams and act as a Subject Matter Expert
REQUIREMENT SUMMARY
Min:2.0Max:3.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Science or engineering preferred
Proficient
1
St. Louis, MO 63134, USA