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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.

Scientist

Job Description

  • Location: Harvard, Massachusetts
  • Type: Contract
  • Job #83287

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

Job ID: 83287

Work Location:  
Devens, MA – 50% on site

Summary:
The Scientist in Manufacturing Sciences & Technology will support the Materials and Cryogenics Science group in the life cycle management of raw materials, consumables and single-use systems utilized for biopharmaceuticals commercial manufacturing operations. The successful candidate will collaborate closely with Manufacturing, Manufacturing Technology, Quality Assurance, Quality Control, Supply Chain, and Global Procurement groups on cross-functional teams.

Education/Experience:

  • BS/MS with 2 years of industry experience post-graduation or PhD in Material Science Engineering, Chemistry or equivalent scientific background.
  • Awareness of cGMP compliance and regulatory agency requirements.
  • Demonstrated problem solving ability (familiarity with root cause analysis techniques and CAPAs a plus)
  • Strong organizational, oral communication and technical writing skills
  • Effective team player and strong individual contributor
  • Familiarity with analytical techniques (FTIR, SEM-EDS, etc.)
  • Knowledge of data trending and tracking, including use of statistical analysis software a plus

Knowledge/Skills:

  • Demonstrated Technical Writing Ability
  • Worked in Cross matrix Teams
  • Project Management – fast paced environment and can manage multiple projects at once
  • Independent Contributor – personable and can work with multiple stakeholders
  • Change Controls – GMP environments preferred
  • Investigation Experience
  • Bio Pharma experience preferred

Responsibilities:

  • Qualify alternative raw material suppliers
  • Work with procurement to identify new suppliers
  • Recommend and/or lead necessary testing to qualify material for use in GMP manufacturing
  • Author technical equivalency assessments, specification comparisons and material characterization reports
  • Support risk assessments
  • Author change controls
  • Support material and consumable manufacturing investigations
  • Evaluate and manage material associated supplier changes notifications to maintain GMP compliance.
  • Support material specification development

Pay: $73-$75/hr
 

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