Buffers & Media Technician I- 12-hour Rotating Shifts

at  Thermo Fisher Scientific

St. Louis, MO 63134, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate30 Dec, 2024USD 21 Hourly06 Oct, 2024N/AManufacturing,Jewelry,Operations,Cgmp PracticesNoNo
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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