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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.

Assistant Process Engineer

Job Description

  • Location: East Syracuse, NY
  • Type: Contract
  • Job #72940

Our client, a leading pharmaceutical company, is hiring an Assistant Process Engineer on a contract basis.

Work Location

East Syracuse, NY

Summary

BACHELORS is a MUST. CHEMICAL, ENGINEERING OR LIFE SCIENCES.

Chemical Engineering, Bioengineering, Biology, Chemistry..

 

The Manufacturing Support Assistant Process Engineer will support Manufacturing Operations (Upstream/Downstream processing, cryogenics facility, facilities, and materials management) on a daily basis, as well contribute to strategic projects

 

Duties/Responsibilities:

1. Compile process data, perform statistical analysis and identify opportunities for improvement of process performance.

2. Support Quality Investigations to determine root cause, assess product impact and recommend CAPA.

3. Support OpEx projects and identify opportunities for productivity, compliance and safety excellence. Originate, review and evaluate change controls.

4. Support technical transfer of new molecules, facility fit and implementation of product/process into the manufacturing facility.

5. Support protocols and final technical reports for requested initiatives/ studies.

6. Follow cGMP requirements.

7. Responsible for entry and management of data which consists of alphanumeric or symbolic data into a software based hierarchy or electronic forms

 

QUALIFICATIONS

• The candidate must have demonstrated verbal, written, and communication skills and a successful proven history of working with technical teams.

• Technical writing ability a must.

 

Education/Experience/ Licenses/Certifications:

• BS or MS with 1-3 years experience or relevant internships required. Degree in Engineering field (e.g. Chemical, Biological) or relevant biotechnology coursework preferred.

 

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