Job description

Technical Source is currently in search of a Process Engineer for our large pharmaceutical manufacturing client located in the Rocky Mount, NC area. The qualified candidate will have experience developing, executing, and documenting sterile drug processes in a GMP environment.

Responsibilities of the Process Engineer include:

• Author and execute process performance qualifications, and process simulation media fill protocols.
• Execute trial batches, scale up batches, and validation batch protocols to support process development
• Development of Verification/Qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports.

Qualifications of the Process Engineer include:

• Bachelors degree or higher in Engineering and/or Science
• 6 months. – 3 years’ of process validation and process development experience in working in the pharmaceutical industry
• Aseptic and sterile pharmaceutical process knowledge is preferred.

Compensation for the Process Engineer includes:

• $75,000-$110,000 based on experience and fit
• Full benefits, medical, dental and vision
• No Corp to Corp or Visa sponsorships currently

Key Words:

process engineer, specialist, chemistry, chemical engineer, sterile facility, manufacturing equipment, validation, qualification, technology transfer, testing, clean room, process engineer, pharmaceutical, commissioning, qualification, quality, biotech, sterile, full time, direct hire, contract, contract to hire, medical benefits, 401K, long term, stability,

Job Type: Full-time

Pay: $70,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift

Experience:

• Pharmaceutical: 1 year (Required)

Work Location: One location

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