Process Engineer Job Vacancy at West Pharmaceutical Services | Life Science Graduates Apply Now
West is offering a Process Engineer Job vacancy specializing in Sterilization in Kinston, North Carolina. This life science job opportunity allows candidates to lead process improvements, implement innovative sterilization techniques, and contribute to the production of life-saving injectable medicines. Ideal for those with experience in steam or gamma sterilization, this position combines engineering expertise, cGMP knowledge, and continuous learning within a collaborative and inclusive environment.
- Job Position: Associate Process Engineer, Sterilization
- Location: Kinston, North Carolina, US
- Job ID / Requisition Number: 68159
About the Company:
West has been a pioneer in healthcare innovation for over a century, delivering life-saving injectable medicines worldwide. Founded during World War II by Herman O. West, the company continues to make a difference in patient lives through cutting-edge technologies, sustainable practices, and community engagement. West offers an inclusive workplace that provides opportunities for lifelong learning, growth, and career advancement, making it an ideal life science job opportunity.
Qualifications:
- Bachelor’s or Master’s degree in Biology, Microbiology, or related scientific field.
- 1–3+ years of experience in steam/gamma sterilization or similar manufacturing roles.
- Knowledge of LEAN, Six Sigma, and cGMP principles.
- Excellent organizational, project management, and communication skills.
- An analytical and solution-oriented mindset, ideal for candidates seeking a life science job opportunity.
Job Description:
This Process Engineer Job vacancy in Sterilization is vital for implementing process improvements, life cycle management, and validation in steam and gamma irradiation processes. The engineer will support capital investments, technology transfers, and complex assignments while ensuring compliance with cGMP and safety standards. This role provides the chance to work on cutting-edge technologies, drive innovation, and collaborate with global teams.
Key Responsibilities:
- Lead and coordinate continuous process improvement projects in the sterilization process.
- Provide engineering support for daily production activities.
- Perform validations of sterilization and support equipment for initial and recurring implementation.
- Track and analyze process data to maintain optimal performance.
- Support product, process, or technology transfers between plants.
- Collaborate with engineering, QA, and global process teams to implement best practices.
- Ensure compliance with local, regional, and global regulations and internal change control procedures.
- Prepare routine and ad-hoc reports.
- Apply Six Sigma tools to reduce process variation and improve product quality.
Preferred Knowledge, Skills, and Abilities:
- OSHA/EPA/safety regulations knowledge.
- Familiarity with ISO9000, FDA, SAP, and MS Office applications.
- Experience with Lean manufacturing principles.
- Ability to write reports, SOPs, and process documents.
- Six Sigma Green Belt Certification preferred.
Travel Requirements: Up to 5% (13 business days per year)
Physical Requirements:
- Medium exertion: lifting up to 50 lbs occasionally, 20 lbs frequently.
- Ability to sit, stand, walk, and operate office and manufacturing equipment.
- Work in cleanroom environments with required gowning and training.
Additional Requirements:
- Ability to follow safety and quality policies at all times.
- Exposure to moderate-to-loud noise in manufacturing areas; hearing protection required.
