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West Pharmaceutical Services is seeking a mid-level Process Engineer in Kinston, NC to lead improvements in rubber mixing and extrusion for pharmaceutical packaging. The role emphasizes on-site work, adherence to GMPs, and process validation activities, with a focus on reducing variability and enhancing throughput.
You will drive CAPA, support project transfers between plants, and ensure documentation and regulatory compliance while collaborating with a global Process Engineering team.
Crosslinked Jobs/Elastomers/rubber/Process Engineer One of 8,182 open polymer and materials roles on Crosslinked, each read for materials, degree, visa and salary. See roles like this WP H-1B history This employer has filed H-1B petitions with the U.S. Department of Labor in the past. That is a record of prior filings, not a statement about this role. Whether any given position is eligible for sponsorship is decided by the employer, case by case. Confirm before you apply. From Jan to Dec 2025 it filed 5 H-1B labor applications for scientist and engineer roles.
Process Engineer West Pharmaceutical Services Kinston, NC, today
BS-level Process Engineering roles on Crosslinked list a median of $117k (755 that show pay). This posting does not list pay.
Improve, validate and support rubber mixing and extrusion processes and equipment at a pharmaceutical packaging plant.
Own process validation and transfer for rubber compounding and extrusion in a regulated pharma packaging environment
Heavily GMP, CAPA and change-control documentation rather than open-ended materials R&D
Bench and desk Generalist Methodical pace BS acceptable
Adjacent materials role: Process focus on 'mixing and extrusion of rubber'; evaluates 'rheological data'; supports formulation/product process validations
This is an onsite position requiring the team member to be onsite for all scheduled workdays. This position offers relocation assistance. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
In this role, you will organize, coordinate, or perform modifications, validations, and enhacements of processes and equipment to ensure safety, maximum yields, quality, cost effectiveness and throughput of our processes. This role will primarily focus on the processes surrounding mixing and extrusion of rubber. Essential Duties and Responsibilities Lead assigned process improvement projects. Plan, schedule, or perform projects within the approved time schedules and budgets. Guide, coordinate, or perform modifications, improvements or validations of existing or new formulations/products, processes and equipment. Ensure that all projects and activities are in compliance with local, regional and best practice requirements on HSE and meet other applicable authority requirements. All internal change control procedures include, e.g. adequate risk assessment / FMEA are to be followed strictly. Support product transfer projects between plants from a process standpoint as assigned. Support & Manage process or technology transfer projects between plants from a process standpoint as assigned. Support new and experimental development activities. Support projects and initiatives stemming from the Global Process Engineering team. Support/lead Operations Excellence lean and continuous improvement activities. Review procedures to ensure they reflect the most effective means and contain the most current and correct information. Maintain Process engineering records and documents as required. Gather and evaluate in-process control date (CPP graphs, rheological data, etc.) in order to support process improvements and ensure the process Quality. Initiate, support, execute CAPA and other quality initiatives. Ensure compliance with cGMPs, FDA and other regulations as necessary. Prepare reports as may be required on a routine basis or on demand within establish deadlines. Safeguard confidential information. Maintain effective team member relations. Performs other duties as assigned based on business needs. Conforms with and abides by all regulations, policies, work procedures, instruction and all safety rules. Other duties as assigned.
excellent written and vebal skills. Excellent interpersonal skills: good team player and individual contributor.
5%: Up to 13 business days per year
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
The ability to be able to lift and carry various items up to 40 pounds. The employee is occasionally exposed to wet and/or humid conditions, industrial odros, smells and dust or powders. The employee occasionally works near moving mechanical parts and or equipment. The employee occasionally works in clean room environments requiring special gowning and training to operate in these environments. The noise level in the office work environment is usually quiet. The noise level in the manufacturing work environment is moderate to loud. Hearing protection is required as posted in the manufacturing work environment.
While performing the duties of this job, the employee is regularly required to, sit, stand, walk, talk, hear, see and use hands and fingers to operate office equipment (ie phones, computers, copies, etc.). Sitting and/or standing for extended periods may occur as well as getting to and from offices and building sites.
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.
If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.
Does West Pharmaceutical Services sponsor H-1B visas?
West Pharmaceutical Services has filed H-1B petitions with the US Department of Labor in past years, but this specific posting does not explicitly mention sponsorship for the Process Engineer role. Confirm with the employer before applying if visa support is required.
Where is the Process Engineer role at West Pharmaceutical Services based?
This role is based in Kinston, NC.
What degree is required for the Process Engineer role at West Pharmaceutical Services?
This role asks for a bachelor's degree.
How many years of experience does this Process Engineer role require?
The posting calls for at least 3 years of relevant experience.
What polymers or materials does this Process Engineer role work with?
rubber.
What techniques or methods are required for this Process Engineer role?
rheology.