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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.

Clinical Manufacturing Associate

Job Description

  • Location: Warren, New Jersey
  • Type: Contract
  • Job #79113

Our client, a leading pharmaceutical company, is hiring a Clinical Manufacturing Associate on a contract basis.

Job ID #: 79113

Work Location:
Warren, NJ – On site


  • Bachelors degree in an applicable science or engineering field and 2 years relevant experience.
  • Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.
  • Experience within cGMP/FDA regulated industry.
  • Basic mathematical skills.
  • Technical writing capability.
  • Proficient in MS Office applications.
  • Background to include an understanding and application within industry of biology, chemistry, medical or clinical practices.


  • Production of blood component lots through cell culture, harvest, and cryopreservation.
  • Aseptic technique
  • Become fully trained and qualified in all aspects of assigned processes.
  • Develop a high level of technical knowledge of project(s).
  • Weigh and measure in-process materials to ensure proper quantities are added/removed.
  • Adhere to the production schedule ensuring on-time, internal production logistics.
  • Record production data and information in a clear, concise format according to proper GDPs.
  • Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
  • Assist tech transfers in and out of the clinical facility.
  • Motivated, team conscious individuals are needed to fulfill job requirements.
  • No direct reports will be assigned to this job role.
  • Perform other tasks as assigned.
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