Process Engineer

Largo, FL

Posted: 11/22/2019 Job Number: JN -112019-11244

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.

Title: Process Engineer I-III (various levels)
Location: Largo/Clearwater Area, Florida
Industry: Pharmaceutical and Chemical Manufacturing
Shifts Available: Monday-Friday, 8am-5pm (expect over-time, up to 10 hour days)

Salary: $50,000-$75,000 depending on experience
Employment Type: Direct hire

Environment: This client innovates, formulates and creates consumer brands. They serve companies in pharmaceutical, cosmetic, personal care and chemical applications. Using state-of-the-art equipment, their team of experts work to ensure high quality. Highly differentiated products are brought to market with exceptional customer service. Isn t this the type of company you want to work for?

Primary Purpose:
  • Provide engineering services for pilot batches, validation, commercial product support, and capital projects.
Responsibilities:
  • Provide technical support for manufacturing. Conduct technical investigations, write reports and provide assistance in the close-out of deviations.
  • Lead technology transfers by conducting laboratory and/or pilot plant experiments, and providing technical risk assessments for new manufacturing processes. Interpret and communicate results to the technology transfer team.
  • Designs and implements manufacturing processes, equipment (from pilot to fully operational) for complex products.
  • Utilize lean or six sigma tools to generate process improvements for inline products.
  • Keep current on regulatory and quality requirements for manufacturing.
  • Write and/or approve SOPs, as needed, to support GMP manufacturing.
  • Develop process validation protocols and mentor engineers as to validation requirements.
  • Write/execute protocols (IQ/OQ/PQ) for equipment as required
  • Develops user specifications/ requirements for equipment purchase and/ or requirements for process validation
  • Makes decisions with designated assignments that influence the goals of the project and department
  • At the discretion of VP or Director of Engineering, approve master batch records and/or protocols in areas where the engineer is deemed a subject matter expert
  • Interacts regularly with senior technical peers and colleagues and executive management
  • Demonstrates leadership skills and the ability to influence
  • Has proficiency in more than one functional area (process, project, etc.)
  • Other functions as required to support existing operations and customer focused projects.
Qualification:
  • Bachelor s degree in Chemical Engineering required
  • Background in or working knowledge of chemical manufacturing or pharmaceutical industry
  • Background in or working knowledge of Pharmaceutical industry and cGMP s preferable
  • Minimum 3 years experience in Chemical or pharmaceutical Manufacturing
  • Project skills appropriate for leadership of tech transfer projects
  • Data analysis with a good understanding of statistical process control
  • PAT (process analytical technology) experience is preferred
  • Technical skills appropriate for execution of technical transfers of topical products
  • Demonstrates strong technical and/or regulatory expertise and ability to adapt to changing circumstances
  • Excellent communication skills, able to adapt a fast paced environment and deadline driven
  • Ability to wear Personal Protective Equipment including a respirator, gloves, and eye protection
  • Must be able to work extended hours on evenings and weekends as required.
  • Must be able to wear personal protection equipment which includes gloves and respirator, when required. Must be able to lift up to 20 pounds on a regular basis.
EOE/ADA
Search words; validation, process, Engineer, Process Engineer, chemical, technical transfer, tech transfer, manufacturing, IQ/OQ/PQ
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