P&G is the largest consumer packaged goods company in the world. We have operations in over 75 countries, with 65 trusted brands that improve lives for 5 billion consumers worldwide.  This brings many advantages, including the opportunity for our employees to enjoy a diverse and rewarding lifelong career filled with new and exciting challenges.

Are you looking for a position that offers a rewarding lifelong career filled with new and exciting challenges? P&G is looking for a Quality Assurance Senior Manager to be a key interface for the functional organizations operating within the innovation center for our Global Health Care organization.  In this role a successful candidate will 1) assure site product quality work processes are delivered with excellence, 2) partner with R&D to grow Quality Assurance (QA) capability and continue the journey to build a quality culture, 3) support innovation/simplification/standardization of work processes and systems throughout the site, and finally 4) deliver continual improvement of the quality systems by identifying and resolving opportunities in existing systems. 

This role offers an opportunity to be part of P&G's largest innovation center. You will get to play a critical role in the Quality program for the site operations.  You will collaborate with site operational leaders to ensure systems and controls are suitable to produce product of appropriate “QUALITY our consumers, customers and regulators trust everywhere, every time”. You will be the Quality Leader for the pilot scale production facility as well as on site materials management.  Key responsibilities will be leading laboratory and operations-based Investigations, owning the site Validation master plans, defining effective CAPAs, and managing the site self-inspection program.  You will also have system ownership responsibilities for other site-based Quality systems. 

You know this is the right role if you have:

• A strong foundation and experience in Quality systems and regulated businesses for OTC Drug, cosmetic, medical device, or dietary supplement regulations- ISO and/or FDA (or other BOH)

• Knowledge and application of base QA systems including validations, deviations, CAPAs, investigations, self-inspection.  Experience in Computer System Validation activities is preferred.

• Understand and can apply validation principles for equipment, processes/procedures, and computer systems

• Proven track record of risk assessment and management, including risk identification tools and communication processes

Qualifications

You’re a good fit if:

• You have at minimum a Bachelor’s degree in Engineering, Physical Sciences (Chemistry, Microbiology, etc.)

• You have experience with manufacturing operations

• You have demonstrated leadership and communication skills at an individual and team level

• You have critical thinking skills

• You have excellent written and verbal communication as well as attention to detail