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Quality System Specialist open position

TRB Chemedica, an international Swiss pharmaceutical company, active in over 60 countries, is a major player since 40 years in the production and distribution of innovative therapies of ophthalmologic, rheumatologic and neurologic disease’s treatment. Human-sized company, TRB Chemedica fosters a corporate culture where autonomy, trust and innovation are a real force for professional growth.

Geneva’s head office pilots the whole marketing, commercials and logistics activities. The scientific sector is also taking care of the integrality of the development and the launching of our new products. This site meets the highest requirements and support, among other things, the product’s marketing that are GMP and ISO 13485 certified.

Your mission:

Reporting directly to the Quality Assurance Manager, you ensure that our company meets established standards of quality in all relevant areas of activities (manufacturing, development, post marketing) covering medical devices, medicinal products for human and veterinary use at the international and Swiss levels.  

Your responsibilities:

  • Be a reference for QA advices and recommendations;
  • Manage the TRB Int. Quality System;
  • Identify critical gaps in the quality systems and propose actions (CAPA);
  • Initiate procedures and revise SOPs;
  • Update the Learning Matrix;
  • Train collaborators on major SOPs;
  • Review and monitor the Quality Complaints;
  • Organize Quality section of the Management Review;
  • Responsible of the environment and product transport monitoring;
  • Coordinate and support regulatory inspections;
  • Collaborate with the QA and RA counterparts within the Company;
  • Support dedicated RA activities as needed (e.g. serialization);
  • QA attitude with a business/regulatory mindset;
  • Back-up for the Quality Assurance activities (Batch Release, Quality Agreement, Non-conformity, Change controls, Audits).

Your profile:

  • Life Science degree;
  • Ideally at least 2 years of experience as a QA specialist in a pharmaceutical company;
  • Medical device and drug experience essential – including a good experience in good distribution practices;
  • Fluent in French and English (German a plus);
  • Good written and oral communication, technical writing;
  • Strong attention to details and organizational skills required;
  • Ability to work independently with minimal supervision;
  • Ability to solve and optimize process problems;
  • Excellent interpersonal and collaborative skills.

Our proposal:

You will be welcome by a qualified, dynamic and caring team, which have for best interest to encourage self-development, autonomy and initiative spirit. We invite you to send us your complete application form (CV, covering letter, copies of work certificates and diplomas). All incomplete application will not be considered.  

Apply now

 

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