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

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We are looking for a  Global MSAT Quality Systems (QMS) Specialist (m / f / d) – EW | Basel

Background

The Global MSAT Quality Systems (QMS) Specialist is a key global matrix role acting as the interface between Global MSAT / Engineering / Device, Packaging & Distribution MSAT (PTT) and the Quality Systems organization (PTQ). The position ensures that global quality processes are consistently applied, compliant, and efficiently executed across the Large Molecule Drug Product manufacturing network.

Within Pharma Technical Operations (PT), Pharma Technical Technology (PTT) is responsible for industrialization and technical product management, with a strong focus on robustness, operational efficiency, and sustainable manufacturing performance. The global Manufacturing Science and Technology (gMSAT) organization oversees commercial products, technology implementation, standardization initiatives, and proactive risk mitigation in close collaboration with cross-functional stakeholders worldwide.

This role requires solid GMP expertise, strong organizational capabilities, and a proactive mindset to manage complex global quality system activities.

Candidate Profile

The ideal candidate holds a scientific degree in Pharmaceutical Sciences or a related discipline and brings at least three years of professional experience in Quality Systems within a GMP-regulated environment. Experience supporting MSAT or Engineering organizations is highly valued. Proficiency in electronic document and learning management systems is essential. Fluent English communication skills are required; German language skills are considered an advantage.

General Information

Start Date : 01 February 2026

Contract Duration : 2 years (extension very likely)

Location : Basel / Kaiseraugst

Workload : 100%

Remote Work : Limited to 1–2 days per week

Travel : Approximately 10%

Criminal Record Extract : Required

Key Responsibilities

QMS Process Ownership : Manage the end-to-end lifecycle of changes to PTT-owned QMS documents, including change initiation, coordination of global action items, follow-up with responsible owners, and securing final approval prior to implementation

Document and System Support : Provide operational support for Veeva Vault QualityDocs, oversee QMS document lifecycles, and maintain standardized templates

Inspection and Audit Support : Coordinate, track, and ensure timely closure of PTT-related CAPAs resulting from health authority inspections and internal audits

Training Coordination : Assign and manage training activities via Cornerstone and act as the interface between Global MSAT and the PTQ Learning organization

Must-Have Qualifications

Bachelor’s, Master’s, or PhD degree, preferably in Pharmaceutical Sciences, Quality Management, or related fields

Minimum of 3–5 years of experience in Quality Systems and GMP operations

Proven hands-on experience with Quality Management Systems, including Change Control and CAPA management

Knowledge of MSAT (Manufacturing Science and Technology) or Engineering operations in a pharmaceutical environment

Strong user-level experience with electronic Document Management Systems and Learning Management Systems (e.g., Veeva Vault QualityDocs, Cornerstone)

Collaborative leadership skills with experience in matrix organizations, strong communication, negotiation, and decision-making abilities

Fluent English; German language skills are a plus

Nice-to-Have Qualifications

Experience in global or cross-site roles supporting international teams

Strong technical writing skills with the ability to translate complex technical topics into clear, compliant documentation

Dissatisfied, underchallenged, or curious about something new?

What are you waiting for? Apply now, unlock your potential, and strive for more satisfaction in your career. I am here to support you with my expertise and guide you through the entire application process. I look forward to meeting you and hearing your story!

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