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About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee’s voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.

Sample Management

Job Description

  • Location: Devens, MA
  • Type: Contract
  • Job #70791

Our client, a leading pharmaceutical company, is hiring a Sample Management on a contract basis.

Work Location

Devens, MA


The QC Sample Management Technician is responsible for the movement and control of QC samples and materials, including in-process, finished drug product, characterization, retain, and stability samples processed through the QC laboratories. This includes, but is not limited to, sample collection and distribution, inventory control, chain of custody, sample tracking, and sample delivery.


Associates degree in Chemistry, Microbiology or related science; or a high school diploma/GED with 2+ years of relevant work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute.



• Experience with cold chain sample storage and transfer in a GMP regulated environment is desirable.

• Knowledge of basic electronic systems (email, MS Office, etc.).

• Experience with LIMS and ELN computer applications preferred.

• Able to perform light to moderate lifting and carrying objects up to 20 lbs.

• Knowledge of regulatory standards as they apply to GMP laboratories is preferred.

• Attention to detail and demonstrated organizational skills.

• Ability to adapt and adjust to changing priorities and to manage assignments with challenging/conflicting deadlines.

• Ability to work in a high-paced team environment and meet deadlines.

• Ability to communicate effectively with peers and department management.



• Handle test samples throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples.

• Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with regulatory requirements and written procedures.

• Maintain inventory and distribution of QC samples and materials to functional groups as scheduled or requested.

• Record performance metrics for the sample management group.

• Support identification and implementation of process efficiencies.

• Communicate effectively with management regarding task completion, roadblocks, and needs.



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