Position:  Quality Control Manager
Location:  Cantanhede, Portugal
Job Id:  1296
# of Openings:  1

 
Quality Control Manager
Cantanhede (Portugal)

Tilray is a global leader in medical cannabis research and production dedicated to providing safe, consistent and reliable therapy to patients. We are the only GMP certified medical cannabis producer currently supplying products to thousands of patients, physicians, pharmacies, hospitals, governments and researchers in Australia, Canada, the European Union and the Americas.  Our team of PhD scientists, botanists and master horticulturists are leaders in cannabis research and related agricultural sciences. We strive to improve scientific understanding of the potential applications of medical cannabis and have invested in developing continuing medical education programs for health care practitioners around the globe.
 
 
Looking to develop your career at the forefront of a rapidly expanding industry?
Ready to apply your talents to make a positive difference in the lives of patients across the country?
 
 
Reporting to the Sr. Quality Manager, working closely with the Tilray quality management team The Quality Control Manager will be responsible for performing different analytical quality control analysis to ensure the highest quality of Tilray products.
 
Role and Responsibilities
  • Perform required analysis (analytical chemistry, endurance, and others) for quality control of samples (raw material, intermediate and finished products)
  • Be involved in the acquisition, setting up, and qualification of QC Lab equipment,
  • Assist in development and maintenance of validated methods for quality control
  • Perform calibration and coordinate all the maintenance programs of the equipment
  • Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site Standard Operating Procedures
  • Document test results, maintaining batch records and coordinating for batch approval and release
  • Ensure the proper disposal of all hazardous, chemical waste
  • Monitor use and inventories of laboratory chemicals and supplies, maintaining appropriate laboratory supply levels
  • Supervise laboratory technicians in the quality control laboratory
  • Identify areas of opportunity for improvement of analytical methods
  • Develop, author, implement and revise all Quality Control SOPs
  • Keep up to date with technical advances in analytical and pharmaceutical sciences
  • Stay abreast of current trends in regulatory requirements in the field of Quality Control
  • Review analytical methods, validation protocols, reports, and method transfer protocols
  • Review release and stability specifications and propose and revise specifications as necessary
  • Review and approve all analytical data to support product testing, stability and release
Qualifications and Education Requirements
  • Degree in Pharmacist, Chemistry, Biochemistry or Biotechnology with 3 years of experience in quality control analysis
  • A minimum of 1 years’ experience with analytical instrumentation (HPLC, GC-MS, and other analytical instrumentation)
  • Experience with method validation, GMP compliance and working creating SOP’s
  • Must have the proven ability to organize and prioritize work for efficient operations
  • Substantial attention to detail is required
  • Proven ability to effectively use Microsoft Office Applications

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