​QA Associate QMS

Location Basel
Job type: Contract
Contact name: Jolie Trahar

Contact email: jolie.trahar@rbwconsulting.com
Contact phone: 01293364082
Job ref: JMTQAQMS
Published: 13 days ago
Expiry date: 25 Apr 2024 23:59

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QA Associate QMS

 

Are you ready to be part of cutting-edge pharmaceutical endeavors? Do you thrive in a dynamic environment where your expertise drives excellence? If so, we have an incredible opportunity for you!

Role Overview: As a QA Associate QMS, you'll be at the heart of ensuring GMP (Good Manufacturing Practice) standards are met with precision and efficiency. From reviewing batch records to supporting vital projects, your role will be pivotal in maintaining compliance and driving quality initiatives forward.

Key Responsibilities:

  • Reviewing manufacturing and analytical batch records, ensuring adherence to GMP standards.

  • Providing support for paper archiving.

  • Collaborating closely with internal teams to ensure timely release of GMP relevant documents and batches.

  • Upholding compliance with cGMP guidelines, regulatory requirements, and internal SOPs.

Why Join Us?

  • Location: Fully site-based in Basel, Switzerland, immerse yourself in a hub of innovation and pharmaceutical excellence.

  • Contract Duration: Embark on an 18-month journey, starting ASAP and running until 12th November 2025.

  • Team Collaboration: Work alongside experts in your field, contributing to departmental projects and objectives.

  • Professional Growth: Expand your skill set with tailored training and development opportunities.

  • Impact: Support the business in drug development, production, and life cycle management, making a tangible difference in global healthcare.

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Requirements:

  • Education: Apprenticeship (plus 5 years' QA experience) or Bachelor (plus 3 years' QA experience).

 

  • Language Skills: Applicants must be fluent in German and English, with strong oral and written communication abilities.

 

 

  • Experience: Proficiency in scientific, technical, and regulatory aspects related to GMP. Basic knowledge of drug development is essential.

 

  • Skills: Exceptional organizational skills, coupled with a keen eye for detail and a proactive approach to problem-solving.

 

Application Deadline: Don't miss your chance to join our team! Apply by 12noon CET on Wednesday, 24th April 2024.