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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.

Senior Associate Scientist

Job Description

  • Location: Dublin, D
  • Type: Contract
  • Job #74034

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

Work Location

East Syracuse, NJ/Hybrid

Summary

 

This position is responsible for providing technical support to commercial operations. The position will be responsible for monitoring daily activities at our external manufacturing organization, interfacing with technical, quality and manufacturing representatives at site. This position will support all MS&T related activities at the CMO site and forms part of the MS&T external manufacturing team.

• Responsible for supporting commercial manufacturing performance at the external manufacturing sire. Represents MS&T external manufacturing team to provide person in plant technical support to the commercial manufacturing process including deviation resolution, change management, delivery of yield targets and optimization.

• Maintains strong working relationships with external partner(s).

• Interface with internal client functions such as MS&T, Quality, supplier Change Manager and Supply Chain.

• Develop and maintain strong technical familiarity with process and process equipment, process optimization evolution and technical problem solving.

• Tracks progress of routine manufacturing and tech transfer projects against schedule, provides routine updates and proactively identifies operational risks and remediation.

• Ensures timely escalation of potential technical, compliance or safety issues to the SRM/MS&T team and partners with internal MS&T resources to remediate.

• Ensures effective communication between technical and quality representatives at the contract manufacturing sire, including other PIP team members.

• Lead/support technology transfer activities as applicable.

• Implement and maintain high standard of quality and regulatory compliance to meet and exceed regulatory agency and quality requirements.

 

Required Experience and Education:

• Science or engineering degree in biotechnology, biochemical or related discipline.

• Experience in drug substance manufacturing essential to the role.

• A strong practical knowledge of the technologies related to mammalian cell culture, therapeutic protein purification and process engineering.

• Demonstrated ability to work independently and prioritize activities

• A proven ability to work on complex problems in which analysis of situations/data requires an in-depth evaluation of multiple factors is essential

• Experience in technology transfer of processes for commercial manufacture and associated regulatory requirements

• Ability to work in a multi-disciplinary team, partner with various functions to provide strong leadership to drive risk-based decisions

• Demonstrated ability in technical writing, computer-based knowledge and communication skills

 

Top 5 Measurable skills and experiences a candidate must have to be successful in this role:

 

• +5 years of experience with a strong practical knowledge of the technologies related to mammalian cell culture, therapeutic protein purification and process engineering.

• Demonstrated ability to work independently and prioritize activities

• A proven ability to work on complex problems in which analysis of situations/data requires an in-depth evaluation of multiple factors is essential

• Ability to work in a multi-disciplinary team, partner with various functions to provide strong leadership to drive risk-based decisions

• Demonstrated ability in technical writing, computer-based knowledge and communication skills

 

 

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