Quality Compliance Team Leader

No Relocation Assistance Offered
# 162830 - Sanford, Maine, United States

Who We Are
Colgate-Palmolive Company is a caring, innovative growth company that is reimagining a healthier future for all people, their pets and our planet. Focused on Oral Care, Personal Care, Home Care and Pet Nutrition, we sell our products in more than 200 countries and territories under brands such as Colgate, Palmolive, elmex, hello, meridol, Sorriso, Tom’s of Maine, EltaMD, Filorga, Irish Spring, PCA SKIN, Protex, Sanex, Softsoap, Speed Stick, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill’s Pet Nutrition.

We are recognized for our leadership and innovation in promoting sustainability and community wellbeing, including our achievements in decreasing plastic waste and promoting recyclability, saving water, conserving natural resources and improving children’s oral health.

If you want to work for a company that lives by their values, then give your career a reason to smile and join our global team!
 

The Quality Compliance Supervisor directs conformance to the GMP/Quality standards and establishes a culture to enable the site to deliver consistent, safe, and effective products.   Positive Release of Finished Goods is at the core of this position’s daily responsibility.  A key role is to maintain a comprehensive site documentation system, author and maintain the site Validation Master Plan, and ensure site-wide compliance to 21 CFR Parts 11, 210, 211, and 820.

Responsibilities Include:

• The Compliance Supervisor coaches and mentors site personnel in regards to Compliance issues.  

• Lead/participate in consumer/customer satisfaction improvement initiatives. 

• Support the development, implementation, and monitoring of the manufacturing site Quality Plan to ensure compliance with both GMP’s and CP Global Quality Standards.

• Responsible for daily documentation authorizing product release and the execution of release procedure.

• Interpret and communicate regulatory policies and requirements to CP personnel (local resident expert and leader for compliance and related GMP concerns).

• Supervision and management of plant Documentation system (This includes all documents vital to an FDA inspection- SOP’s, Management of Change, Notices of Deviation, Batch Records, Non conformances, and Validations)

• Supervise Consumer Complaint trends and history.  Ensures that all returned samples and adverse event complaints are fully investigated and documented.

• Manage the Site Annual Product Review and provide vital compliance documentation and corrective action strategies for continuous improvement.

• Ensure that the designs, specifications, implementation, and maintenance of a cGMP system follows current regulations and CP standards.

• Supervision and management of site’s Management of Change (MOC) program.

• Supervision and management of FDA Drug Listings and international drug registrations.

• Contribute to the local Automation, Digitization and Analytics (ADA) strategy; in specific with the paperless initiatives.

• Ensures the development of people, teams, and organizational capabilities by empowering team members through training, information sharing, mentor, feedback, and delegation.

Required Qualifications: