QA Documentation Specialist

MANPOWER AG – Your career, our focus!

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ManpowerGroup is the world's leading company for workforce solutions.

With our three brands – Manpower, Experis, and Talent Solutions – we support companies from various industries with their recruitment needs. For 75 years, we have been operating in over 75 countries and accompany our clients throughout Switzerland to successfully carry out their tasks and projects.

QA Documentation Specialist

Purpose of the Role Responsible for reviewing executed paper\-based batch records to ensure manufacturing activities were performed according to GMP procedures, internal SOPs, and regulatory requirements. The role requires strong attention to detail, independence, and a solid understanding of pharmaceutical manufacturing processes.

Key Responsibilities

Review executed paper\-based batch records within agreed timelines.

Verify compliance with GMP requirements, SOPs, and manufacturing procedures.

Track, monitor, and report batch review progress and critical release metrics.

Support on\-time batch release activities.

Identify observations/deviations and raise them with Operations in a timely manner.

Participate in discussions and meetings related to batch documentation findings.

Bachelor's or Master's degree in

Pharmaceutical Technology

Biotechnology

Chemistry

Pharmacy

Or another relevant scientific discipline

Equivalent industry experience may be considered.

Required Experience

Minimum 2 years of GMP experience in a pharmaceutical or biotech manufacturing environment.

Experience with quality procedures and SOP execution.

Batch Record Review experience is highly preferred.

Knowledge of pharmaceutical manufacturing documentation and compliance requirements.

Required Skills

Strong attention to detail.

Ability to work independently.

Excellent communication and stakeholder management skills.

Strong understanding of GMP regulations and documentation practices.

Language Requirements

Business\-fluent German (mandatory)

English preferred.

Working Model

100% On\-Site in Visp

No home office / remote work option.

Paper\-based documentation environment.

Ideal Candidate Profile

A GMP professional with pharmaceutical manufacturing experience who has hands\-on exposure to batch record review, is highly detail\-oriented, fluent in German, and capable of managing documentation review timelines to support compliant and timely batch release. jpide7b3615jm jit0834jm jiy26jm