Process Engineer

Description

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.

Position Summary

The Process Engineer will organize, coordinate, or perform modifications, validations, and enhancements of processes, equipment, and tooling to new and existing products to ensure safety, maximum yields, quality, cost effectiveness and throughput of our processes. This role will primarily focus on the facilities high value processes surrounding pharmaceutical washing and sterilization.

Primary Duties And Responsibilities

Support the development and improvement of products and processes assuring the Plant’s competitive position. Support projects and initiatives stemming from Global Process Engineering team for High Value Products. Initiate, support, execute CAPA and other quality initiatives. Ensure compliance with cGMPs, FDA and other regulations as necessary. Guide, coordinate, or perform modifications, improvements, or validations of existing or new products, processes, tooling, equipment, and related research and development activity. Plan, schedule, or perform projects within the approved time schedules and budgets. Support/lead Operations Excellence lean and continuous improvement activities. Support new and experimental product development activities. Review procedures to ensure they reflect the most effective means and contain the most current and correct information. Maintain engineering records and documents as required. Lead the way in supporting the plant’s efforts in meeting corporate and plant goals. Review processes continually to ensure their quality. 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.

Required Qualifications

Education: Bachelor's in Engineering or Sciences Must have 2-3 years of experience in Biotechnology/Pharmaceutical manufacturing. Must have excellent written and verbal skills. Excellent interpersonal skills: good team player and individual contributor as well.

Preferred Qualifications

Lean Six Sigma Black Belt (or Green Belt with solid track of lean improvements). Working knowledge of SPC and Minitab software. Knowledge of cGMP for aseptic/ clean room manufacturing. Ability of authoring/revising SOIs, SOPs and validation documents.

Physical & Travel Requirements

Travel up to 10% Office environment

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 and/or a pre-employment drug screening.