Buffers & Media Technician I- 12-hour Rotating Shifts
at Thermo Fisher Scientific
St. Louis, MO 63134, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Dec, 2024 | USD 21 Hourly | 06 Oct, 2024 | N/A | Manufacturing,Jewelry,Operations,Cgmp Practices | 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 or equivalent required.
EXPERIENCE:
- Required: No previous work experience required
- Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field
- Preferred: Experience in a cGMP environment
KNOWLEDGE
- Knowledge of cGMP practices, aseptic techniques, or chemical concepts preferred
SKILLS
- Strong math skills
- Detail oriented
- Focused on achieving outcomes
- MS Office
ABILITIES
- Able to read, write, and communicate in English
- Able to understand and carry out instructions
- Reliable
- Effectively multi-task
- Adaptable to a multifaceted work environment
- Possesses the ability to work both autonomously and collaboratively in a team environment.
PHYSICAL REQUIREMENTS / WORK ENVIRONMENT
- 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.)
- Able to adhere to clean room gowning requirements, including wearing Tyvek, Nitrile, and/or Latex gloves
- Ability to lift minimum of 25 lbs independently
- Ability to stand for 80% of shift
Responsibilities:
- Preparing for and execution of manufacturing batch records, work instructions, and/or SOPs, with focus on safety and “right the first time” executions with minimal oversight.
- Weigh, Transfer, and Mix chemicals
- Documentation of all activities to meet cGMP requirements. Maintain cGMP compliance in assigned work and follow all safety procedures, to include the use of Person Protective Equipment.
- Complete preventative maintenance and work notification tasks on time. Equipment testing and routine troubleshooting of process and analytical equipment.
- Draft, review, and revise documents as needed.
- Run in-process analytical testing as required per the batch record..
- Maintain Raw Materials inventory through use of systems such as Kanban.
- Maintain up to date training records
- Participate in other required activities (perform safety inspections, participate in improvement projects, etc.)
- 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:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Proficient
1
St. Louis, MO 63134, USA