Manager, R&d Quality, Gmp - Markham, Canada - Estée Lauder
Description
About The Estée Lauder Companies Inc.The Estée Lauder Companies Inc.
is one of the world's leading manufacturers, marketers, and sellers of quality skin care, makeup, fragrance, and hair care products.
The company's products are sold in approximately 150 countries and territories under brand names including:Estée Lauder, Aramis, Clinique, Lab Series, Origins, M-A-C, La Mer, Bobbi Brown, Aveda, Jo Malone London, Bumble and bumble, Darphin Paris, TOM FORD BEAUTY, Smashbox, AERIN Beauty, Le Labo, Editions de Parfums Frédéric Malle, GLAMGLOW, KILIAN PARIS, Too Faced, Dr.
Jart+, and the DECIEM family of brands, including The Ordinary and NIOD.Job Function
Implement, maintain and continuously improve the R&D GMP Quality Management System including creation/revision/review of SOPs, administration of change management, timely completion of deviations and investigations, implementation of corrective and preventive measures, compilation of quality metrics etc.
Exhibit professionalism and foster teamwork to create an environment of support that leads to productivity of R&D personnel and ensures GMP compliance.
Responsbilities
Provide expertise and leadership on the activities and quality systems necessary to ensure that R&D is operating in full compliance with sound scientific practice, current Good Manufacturing Practices, as applicable, and standard operating procedures.
Review and approve/reject data and documentation for GMP activities including, but not limited to, SOPs, batch documentation, IQ/OQ/PQ documents, protocols and reports, specifications, test reports etc.
Must have strong problem solving and decision making skills.Represent R&D QA on project teams and quality initiatives. Provide input into development strategies to support innovation, achieve business objectives and maintain GMP compliance. Reviews and approves dossiers to launch new products and line extensions.
Perform internal and external quality audits and facilitate corrective actions. Represent R&D QA in internal audits and/or regulatory inspections. Ensures responses to audit observations/inspection findings (internal and external) are completed in a satisfactory and timely manner.
Qualifications:
BS or BA in Chemistry or related degree.
Must have knowledge of cosmetic and OTC drug product regulations.
Requires excellent communication skills to direct R&D personnel and discuss quality related issues with management.
Must possess strong organizational and planning skills.
Expertise from R&D, manufacturing or process development experience is required.
Experience in a GMP regulated environment preferred.
Job:
Research & Development
Primary Location:
Americas-CA-ON-Markham
Job Type:
Standard
Schedule:
Full-time
Shift: 1st (Day) Shift
Job Number:
We are an equal opportunity employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply. Accommodations for job applicants with disabilities are available on request.
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