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.

Bio Process Associate - 1st Shift

Job Description

• Location: Devens, Massachusetts
• Type: Contract
• Job #79562

Our client, a leading pharmaceutical company, is hiring a Bio Process Associate on a contract basis.

Job ID #: 79562

Work Location:
Devens, MA - on site

Summary:
The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease.

Education/Experience:

• High school diploma is required.
• Knowledge of science generally attained through completion of a certificate program or Associates Degree in Biotechnology or a related field is desired.
• Prior experience successfully participating on work teams where personal accountability, attention to detail, collaboration, and results were expected.
• Demonstrated proficiency in common computer tools and web based applications.
• Prior experience with Good Manufacturing Practices (GMP) regulations and/or prior work experience in a clean room or highly regulated environment desired.

Responsibilities:

• Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices and standard operating procedures.
• Revise and create process documents and assist with process related investigations.
• Train for proficiency in process automation and supporting business systems and in the operation of primary production equipment within the assigned functional area.
• Lead in maintaining material and components inventory level. Weigh and check raw materials.
• Support a safe work environment and contribute to area specific initiatives associated with work safety.
• Weighs and checks raw materials. Assembles, cleans and autoclaves process components. Assists in maintaining material and component inventory levels.
• Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions. Assists in revising and creating process documents, i.e. SOPs and Batch Records, and assists with process-related investigations.