Job description

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

Responsibilities of the Validation Engineer include:

• Understand Process Validation
• Write Technical reports from lab findings
• Knowledge of Asceptic Sterile pharmaceutical process
• Execute process performance qualifications, trial batches, scale-up batches, and validation batch protocols to support process development
• Knowledge of (IQ/OQ/PQ), and Summary Reports

Qualifications of the Validation Engineer include:

• Bachelor's degree or higher in Chemical Engineering or Science
• 1+ years of process validation in the pharmaceutical industry
• Aseptic and sterile pharmaceutical process knowledge is preferred.

Compensation for the Validation Engineer includes:

• $40-$50/hour 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: $40.00 - $50.00 per hour

Benefits:

• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 8 hour shift

Work setting:

• Manufacturing facility

Work Location: One location

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