Supplier Quality Engineer

Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate which all help contribute to a Healthier World.

At West, we are by the side of patients. The work we do impacts patients lives each and every day our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges. We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $2.14B in 2020. We serve by the side of our community. Giving back is in our DNAour team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West Without Borders team member-led giving program.

Job Summary :

Provide support for the validation program for the plant or assigned functional area regarding equipment, processes or procedures used. Ensure compliance to regulatory and ISO Management standards.

Essential Duties and Responsibilities :

• Responsible for compliance to Wests validation program
• Ensure that the validation requirements are documented to provide direction for meeting the validation needs of the customers, associated regulatory bodies and West functional groups
• Provide guidance to system / process stakeholders as to content and format of Validation life cycle documentation
• Candidate shall demonstrate hands-on experience planning, establishing and executing software validation activities
• Support Engineering and Operations groups during the process development and Validation phases of customer products life cycles
• Provide required training to support qualification activities
• Assume the QA responsibilities for reviewing and approval of validation life cycle documentation (PDD, IOQ / PQ protocols, protocol addendums, summary reports, etc.)
• Provide guidance during protocol incidents process, including reporting, investigations and approval of resolutions
• Keep current with all Industry standard practices and FDA requirements for validation, change control and complaint handling
• Monitor Change Control system and provide guidance for proper execution and timely closure of Change Controls and Action items
• Understanding and facilitation of Risk documentation to ensure compliance with ISO 14971 and ISO 31000
• Ensure compliance with Quality, Business Continuity, Safety and Environmental standards and applicable regulations
• Experience with risk management and task prioritization a must for this role
• Other duties as assigned

Basic Qualifications :

Preferred Knowledge, Skills and Abilities :

Travel Requirements :

Physical & Mental Requirements :

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@. 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.

About the company

West Pharmaceutical Services, Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products.

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