Quality Control Supervisor Cantanhede

Quality Control Supervisor
Cantanhede
Cantanhede, Coimbra, Portugal

Tilray Brands is a leading global
- lifestyle and consumer packaged goods company with operations in Canada, the United States, Europe, Australia, and Latin America. The company aims to improve people's lives by inspiring and empowering the community to live their best life through products that meet their needs of mind, body, and soul, fostering a sense of wellbeing. Tilray’s mission is to be a trusted partner for patients and consumers by providing
- quality, differentiated brands and innovative products. As a pioneer in cannabis research, cultivation, and distribution, Tilray supports over 20 brands across more than 20 countries, offering a range of cannabis products,
- based foods, and alcoholic beverages.

Are you looking to develop your career at the forefront of a rapidly expanding industry? Are you ready to apply your talents to make a positive difference in the lives of patients worldwide?

The Quality Control Supervisor is responsible for performing analytical chemistry quality control testing to ensure the highest quality, potency, and purity of Tilray products. This role involves managing and supervising a team of Quality Control Technicians and analysts. The incumbent must maintain
- ready Quality Control operations at all times, in compliance with EU GMP standards.

Role and Responsibilities

• Develop specifications for new SKUs
• Manage analytical transfer and method validation for new SKUs
• Qualify new equipment and maintain qualification status of existing equipment
• Oversee analytical laboratory operations, including direct supervision of QC laboratory technicians
• Review and approve all analytical data to support product testing and release
• Document test results and maintain batch records
• Perform lab investigations, OOS/OOT investigations, and stability data monitoring in conjunction with QA
• Perform routine calibration and maintenance on laboratory instruments
• Assist in developing and maintaining validated quality control methods
• Ensure compliance with internal standards and external regulatory requirements
• Maintain
  - quality laboratory documentation in accordance with applicable regulatory guidance and SOPs
• Identify opportunities for analytical methods improvement
• Develop, author, implement, and revise all Quality Control SOPs
• Stay updated with advances in analytical sciences and relevant pharmacopeia
• Develop and review analytical methods, validation protocols, reports, and transfer protocols
• Serve as the single point of contact for pharmacopeial updates and global changes initiation
• Perform other relevant duties as assigned

Qualifications and Requirements

• B. Sc. in Chemistry, Biochemistry, or Biotechnology; M. Sc. preferred
• Minimum of 5 years supervisory experience
• At least 3 years’ experience with HPLC, GC-MS, and other analytical instrumentation
• Experience with method validation, GLP compliance, and SOP creation
• Excellent organizational skills with proven ability to prioritize tasks efficiently
• Experience with health authority inspections (e. g. , EMA, Infarmed)
• Experience with CMC documentation and submission is a plus
• Strong attention to detail