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:

• 1. 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.
• 2. 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
• 3. 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).
  Specific Deliverables
• 1. Investigate and Implement Process/Equipment/Automation Design Changes as a result of 5205/5208 FRAS
  a. Changes driven through WorkFront
  b. Own or Influence Changes driven through change controls
  2. 5220 Tech Transfer OOF 08Apr25
  a. Delivery and Design
  i. Recipe Development Design and Execution Feb 25 ~20 days
  ii. Automation Configuration Specification Review & Approval
  iii. Chrom Skid Flow Path Analysis Generation & Approval
  iv. eBR Parameter Review & Approval
  v. Batch Record Review & Approval
  3. 5209 Scale Lump Sum Closure
  4. Incorporate Flow processing and cleaning flow paths into equipment functional specifications
  5. Automate CS Drain Hand Valve for SMCC and XFER-73500 SIP Circuits
  a. Change Control Ownership
  b. Project Ownership & Execution

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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