Biopharmaceutical Technician - Days/Nights
at Thermo Fisher Scientific
St. Louis, MO 63134, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Jul, 2024 | USD 21 Hourly | 28 Apr, 2024 | 1 year(s) or above | English,Chemistry,Instructions,Biology,Jewelry,Manufacturing,Cgmp Practices,Biochemistry | 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:
EDUCATION
- High School Diploma/GED required. Associates in a relevant scientific field preferred. Bachelor’s degree in Biology, Biochemistry or Chemistry seen as a plus.
EXPERIENCE
- 1-3 years of relevant lab experience in a related field or industry preferred
- Experience in manufacturing and/or GMP environment preferred
KNOWLEDGE, SKILLS, ABILITIES
Knowledge
- Understanding ‘why’ and not just the ‘how’ of processes and practices
- Knowledge of cGMP practices, aseptic techniques, or chemical concepts seen as a plus
Skills
- Mechanical Skills/ Analytical Skills/Method Automation
- MS Office
- Strong math skills
- Strong prioritization skills
- Detail oriented
- Results driven
Abilities
- Able to read, write, and communicate in English
- Able to understand and carry out instructions
- Reliable
- Strong communication (written and verbal)
- Effectively multi-task
- Able to work in an environment of change
- Able to work independently and as part of a team
- Able to recognize problems developing, not just occurring
- Be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These items are prohibited: makeup, jewelry, nail polish, cologne / perfume, scented lotions or hair care products, etc.)
Responsibilities:
- Execution of manufacturing batch records, work instructions and/or SOPs, with focus on proactive ‘right the first time’ executions. Assist with batch record reconciliation.
- Assist in all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies.
- Documentation of all activities to meet cGMP requirements. Complete document reviews and revisions. Daily record review, tasks, and databases. Actively provide feedback.
- Critical evaluation of processes, including foresight and thinking ahead.
- Complete preventative maintenance and work notifications tasks on time. Perform equipment testing and routine trouble-shooting.
- Ensure tasks are performed with a method of prioritization - interpret production schedules and complete tasks accordingly.
- Participate in shift exchanges, 1-1’s, meetings, attend meetings as needed to facilitate area needs based on changes, etc. (lean activities).
REQUIREMENT SUMMARY
Min:1.0Max:3.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Proficient
1
St. Louis, MO 63134, USA