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Sample Management

Sunrise Systems
Devens, MA Full Time
POSTED ON 1/16/2025
AVAILABLE BEFORE 4/16/2025

Job Title : Quality Sample Management

Job ID : -

Location : Devens, MA,

Duration : Month’s Contract on W

Onsite role, Devens site

Work Schedule : Second Shift PM - PM. Monday through Friday.

Flex required as Holidays are required and weekend coverage as needed by Manufacturing Schedule.

  • Performs routine processing and data review of raw materials, in-process, batch release, and / or stability samples of Bulk Drug Substance in a cGMP compliant environment.
  • Performs routine inventory and sample management of routine samples, critical reagents and non-routine samples. Main responsibilities include Chain of Custody.
  • Executes routine procedures owned by the Sample Management functional area. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).
  • Knowledge of science generally attained through studies resulting in a AS or certificate program in the physical or life sciences, supply chain, a related discipline, or the equivalent in related experience.
  • Knowledge of basic laboratory techniques such as working in a BSC, pipetting, aseptic technique; basic laboratory safety practices preferred.
  • Familiarity with controlled temperature storage, sample inventory, and sample shipment and receipt.
  • Attention to detail and demonstrated organizational skills.
  • Demonstrated manual dexterity.
  • Will work in teams and have continual interaction with members of his / her team as well as other sub-teams within Quality Control Organization, in order to exchange information regarding sample management as it relates to meeting department goals and objectives
  • Daily contact with her / his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions.
  • Occasional contact with other line management staff relating to specific project responsibilities may be expected.
  • Occasional contact with Manufacturing and Stability organizations for escalation where appropriate
  • Occasional contact with other sites / vendors for tactical logistical purposes
  • Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials.
  • Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure.
  • Knowledge of basic electronic systems (email, MS Office, etc.)
  • Attention to detail is key.

Education :

HS Diploma required OR enrolled in a scientific program

Additional Job Requirements :

Position Handles Hazardous Materials

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