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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/Engineer

Job Description

  • Location: New Brunswick, New Jersey
  • Type: Contract
  • Job #80663

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

Job ID #: 80663

Work Location:
New Brunswick, NJ – 50% on site

Summary:
The Scientist provides technical support related to one or more Technology Transfer (TT) projects as well as provide support to the Product Champion cluster.
This position is accountable for working together with the TT Lead to ensure various project aspects are supported from a technical perspective as well as a timeline perspective.
This position is responsible for supporting the Product Champion group through Data Verification (DV) activities, change control support, improvement projects, etc.

Education/Experience:

  • Required Bachelors degree in engineering/science-related field with 3 years of relevant experience. Time spent in advanced degree program may consider as equivalent experience.
  • Work in a matrix environment and effectively support the decentralized manufacturing function.
  • Effectively collaborate with other functions

Knowledge/Skills:

  • Knowledge in Biologics/sterile liquid drug products, aseptic processing
  • Experience in Biologics/Vaccine Aseptic Drug Product Manufacturing and/or Technology Transfer
  • Ability to serve as a technical expert for Drug Product manufacturing
  • Strong critical thinking, technical writing, and verbal communication

Desired:

  • Thorough knowledge of quality systems, Quality by Design, validation principles for product and engineering design and process control fundamentals

Responsibilities:

  • Support TT Lead for one or more projects
  • Actively participates in TT meetings, collaborating with cross-functional group.
  • Responsible for detailed reviews of project documents such as protocols, reports, risk assessments, and MBRs.
  • Provides assistance to sites to review/resolve quality events as needed.
  • Collaborate on TT project definition and support chartered projects as needed.
  • Identifies TT issues/risks and proposes ideas for issue resolution. Supports issue resolution as needed.
  • Support Product Champion Cluster
  • Support DV of various product TTs and lifecycle projects.
  • Support improvement projects for Product Champion group.
  • Identify opportunities for improvement and provide ideas to implement.
  • Collaborate with Product Champions and work together to learn about different products and implement various improvements.
  • Reporting Relationship Reports to Product Champion Cluster Lead

 

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