Biopharmaceutical Technician - Days/Nights

at  Thermo Fisher Scientific

St. Louis, MO 63134, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate20 Jul, 2024USD 21 Hourly29 Apr, 20241 year(s) or aboveEnglish,Jewelry,Chemistry,Cgmp Practices,Instructions,Biochemistry,Biology,ManufacturingNoNo
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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