Senior Associate Specialist QC Services

vor 2 Monaten


Bern, Schweiz Randstad - Medium prio Vollzeit
Jobdescription

For more than 130 years, diversity, equity & inclusion have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.

That is why we in Switzerland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

For our QC department in Bern, we are looking for an open-minded, goal driven, motivated Sr Associate Specialist QC Services.

Tasks

  • Coordinates equipment/system qualification and validation activities within the QC department (e.g. clarification with vendors and the QC testing labs, writing technical documents) including collaboration with interdepartmental stakeholders
  • Decommissions qualified/validated equipment and systems through Change Control procedures
  • Executes or supports equipment lifecycle activities such as periodic reviews, calibration and maintenance tasks
  • Coordinates & manages the timely and effective completion of equipment related investigations, change controls and CAPA's related to equipment activities
  • Supports (improvement) projects regarding equipment and automated systems within the QC labs department
  • Helps to build a strong team to expand, strengthen and maintain the current knowledge base and expertise within QC to reflect changing business needs

Functie-eisen

Profile

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  • University degree in natural sciences, applied sciences or equivalent working professional experience
  • Good understanding of analytical technologies, GMP experience is a plus.
  • Know-how of commissioning, qualification and computer system validation requirements in a laboratory environment is a plus
  • Must be well organized, a self-starter, results oriented individual with the ability to multitask in a fast paced team environment with attention to detail and good documentation practice
  • Strong strategic and conceptual skills, analytical thinking and problem-solving ability
  • Strong project management skills
  • Proactive attitude, Team player, team builder
  • Good verbal and written skills in English and German


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