Global MSAT Quality Systems Specialist

Global MSAT Quality Systems (QMS) Specialist (m/f/d) | Basel

We are looking for a motivated and reliable (m/f/d) Global MSAT Quality Systems (QMS) Specialist for our client Roche in Basel.

The Perfect Candidate possesses a degree in Pharmaceutical Science and over three years of experience in Quality Systems and GMP operations. Essential knowledge includes MSAT, proficiency with electronic Document Management Systems, and fluent English communication skills.

Latest Possible

Start Date:

Depending on the candidate, we could consider

Planned Duration of Employment: 2 years

Home Office: Home office limited to 1-2 days a week max

• QMS Process Management:
  Oversee the full lifecycle of changes for PTT owned QMS documents, from change initiation and action item assignment to responsible owners across the global network, driving completion and secure the final "approval to execute" before documentation is made effective
• Document & System Support:
  Provide operational support for Veeva Vault Quality Docs, manage the lifecycle of QMS documents and maintain standardized templates.
• Inspection & Audit Support:
  Coordinate and track PTT owned CAPAs from Health Authority inspections and audits, ensuring the timely closure of all commitments.
• Training Coordination:
  Manage training assignments via Cornerstone and act as the liaison between Global MSAT and the PTQ Learning Team.

• BS/MS/PhD degree (Preferably in Pharmaceutical Science or Quality System related fields)
• Min. 3-5 years of experience in Quality Systems and GMP operations
• Demonstrated experience with Quality Management Systems (QMS), specifically CAPA management and Change Control
• Knowledge of MSAT (Manufacturing Science and Technology) or Engineering operations in a pharma setting
• Proficiency with electronic Document Management Systems (e.g., Veeva Vault Quality Docs) and Learning Management Systems
• Leadership: collaborative, matrix team leadership experience and decision‑making skills. Network mindset as well as strong communication and negotiation skills enabling you to establish trustful and successful relationships.
• English fluent, German is a plus

• Experience in a global role or supporting global teams.
• Proven technical writing skills with an ability to translate complex technical information into clear, compliant documentation.

Are you interested and would you like to seize this opportunity? Then we should definitely get to know each other! Simply click on "Apply now" and we look forward to receiving your complete application documents

Seniority level:
Associate

Employment type:

Contract

Job function:
Other

Industries:
Pharmaceutical Manufacturing and Biotechnology Research