Sr QC Technician - Sample Management

at  Thermo Fisher Scientific

St. Louis, MO 63134, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate30 Oct, 2024Not Specified31 Jul, 2024N/AGloves,Cgmp Practices,Software,Management SystemNoNo
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Description:

KNOWLEDGE, SKILLS, ABILITIES

Knowledge

  • Working knowledge of GMP regulations in a GMP environment
  • Knowledge of cGMP practices and aseptic techniques

Skills

  • Accurate Pipetting Skills
  • MS Office – must be good with computers and a variety of software,
  • MS Excel experience is a plus
  • Detail oriented
  • Results driven
  • Safety Attitude
  • Electronic document system
  • Trackwise or equivalent deviation system
  • Electronic Sample Management System (LIMS)

PHYSICAL REQUIREMENTS / WORK ENVIRONMENT:

A flexible work schedule is required.
Ability to lift up to 25 lbs independently, with occasional heavier objects of up to 50lbs with assistance.
Routine push/pull/lift activities involving sample carts, sample freezer trays, and other objects.
Must be able to wear gloves and other PPE to handle samples.
Must be able to stand for extended periods of time. This role is actively moving between desk and laboratory work.

DISCLAIMER:

This job description presents the general content and requirements for the performance of this job. The description is not to be construed as an extensive statement of work, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.
Nothing contained herein should be construed to describe an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully abide by all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
Thermo Fisher Scientific is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We strive to build an inclusionary work environment and prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Responsibilities:

  • Pickup and transport samples from the manufacturing areas to quality control testing/storage areas. Report sample issues to the appropriate management as required per procedures.
  • Receive samples into the analytical and microbiology laboratories. Receive samples for storage into the QC Sample Management storage units.
  • Manage receipt of incoming sample shipments and outgoing sample shipments.
  • Work in a biological safety cabinet with some level of gowning to sub-aliquoting bulk samples to smaller aliquots. Login samples to the LIMS system, properly label aliquots and receive to final storage as required per the label.
  • Clearly and accurately communicates status of samples (picked up, for testing, for send-out) to cross-functional area teams
  • Support the team by helping manage the team’s inventory supplies stock.
  • Maintain up to date training records.
  • Effectively train department employees in the execution of Sample Management tasks
  • Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintains the necessary compliance status required by company and facility standards.
  • May author Sample Management documents in the site electronic document management system
  • May investigate and complete investigation of minor sample management deviations
  • Assist with additional laboratory support duties as necessary to meet departmental goals.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

St. Louis, MO 63134, USA