Analista de Controle de Qualidade Sr - Barueri, Brasil - Kerry

Kerry

Empresa verificada

Barueri, Brasil

há 3 semanas

Postado por:

Ana Silva

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Descrição

About Kerry:

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries.

Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world.

Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition.

A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.

About the role:

Quality Control Sr. Analyst - Pharma Division

Responsible for the overall direction and operation of quality assurance documentation systems, including the change management system, global quality management system, batch master records, and standard operating procedures/instruction circulation system.

job.

The role involves training staff, maintaining records of product and raw material quality and testing procedures, informing production of quality issues and compliance with Good Manufacturing Practices and Kerry Standard Operating Procedures.

Location
:
Barueri - SP

Key responsibilities:

Maintain Quality Assurance Management of the Control System.
Maintain the Global Quality Management System.
Update and maintain Batch Master Records and Packaging Records.
Maintain the Barueri System of Standard Operating Procedures, Work Instructions and Laboratory Methods.
Provide quality assurance assistance for quality control, product development, production, supply chain and regulatory as required.
Lead, maintain and support quality standards initiatives (i.e. ISO 9001 and FSSC 22000)
Comply with Quality Assurance documentation.
Performs other duties and responsibilities as required.
Responsible for all customer responses and lead pharmaceutical audits.
Responsible for Sheffcoat analyzes (QC) and follow productions if necessary.
Final approval and review of finished product labels created by regulation.
Final approval and review of product formulas entered by Regulatory.
Creation of repackaging, relabeling and packaging records for production.

Qualifications and skills:

Bachelor's Degree in Chemistry, Pharmacy, Biochemistry, Microbiology, or similar science.
Advanced English
Desirable Spanish
At least 5 years of experience in the pharmaceutical industry, in the areas of R&D, Quality, regulatory.
Experience in monitoring audits, investigating nonconformities, action plans with knowledge of Pharmaceutical requirements (excipients).
Indepth knowledge of RDC's relevant to the pharmaceutical and excipients segment