Process Engineer
Job Description
Process Engineer
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.
Title: Process Engineer
Location: Portsmouth, NH
Industry: Pharmaceutical
Hours: M-F: 8AM-5PM
Salary:$45.86 hourly paid weekly (Benefits Available)
Employment Type: Long term contract (potential for extension or direct offer)
Duties may include any of the following:
Manufacturing Support
Develop technical knowledge on manufacturing equipment and processes
Support resolution of major equipment breakdowns and quality issues in the suites
Provide SME support to Manufacturing and other departments for the
design and operation of process equipment.
Conduct troubleshooting and technical analyses on manufacturing equipment and processes including PI data analyses, CIP/SIP circuit review, MOC analyses, flow path analyses, etc.
Projects
Planning and execution of plant projects involving equipment changes and process improvements.
Execute commissioning protocols (installation, operation, CIP/SIP, wet
testing) with support and guidance from supervisor
Documentation
Review/revise Engineering and Manufacturing related SOP s, work instructions, and maintenance assessments/procedures as a result of CAPA, equipment/process changes, error prevention activities, etc.
Complete engineering review/approval of batch records
Initiate EDCRs for updates to Engineering documents including engineering drawings
Author commissioning protocols (installation, operation, CIP/SIP, wet testing).
Requirements:
Years of Experience: 3-7 years
Industry Experience: Biotech or Fluid Processing/Manufacturing
Education: B.S Chemical or Mechanical Engineering
EOE/ADA
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