Qualification & Validation Manager

Jobdescription

For one of our clients, a leading global

pharmaceutical company, we are currently looking for

a Qualification and Validation

Manager.

General

Information : Start

date :  05.01.2026

Duration :  until

30.09.2026

Workplace : Basel

• Workload :  100%

Remote / Home

Office :  possible, max 20%

Working

hours :  Standard

Department :  MSAT

(MMNGF)

Team :  10

people

About the

job :

The Qualification Manager is

responsible for the CSV and qualification program at

Basel DS Manufacturing, as well as activities to maintain qualified

status in collaboration with the engineering and operators at Basel

Drug Substance Manufacturing (for biochemical and chemical

manufacturing processes).

Your

Profile :

Master's degree in chemical

engineering, biotechnology, or a similar discipline and more than

two years of experience in a pharmaceutical GMP

environment.

Familiarity with the qualification

and validation of pharmaceutical production facilities and

laboratory equipment.

strong IT skills

and excellent German and English language

skills.

Tasks &

Responsibilities : Management and

coordination of CSV and qualification projects, approval of

qualification plans and reports in

eVal

Creation of qualification strategies, risk

analyses, qualification plans and

reports

Processing of changes, deviations,

CAPAs, and creation of technical assessments for

stakeholders

Development and implementation of

suggestions for improvements to the device qualification and system

validation concepts

Representation of

qualification and validation topics during authority inspections as

well as in local and global networks, task forces or project

teams

Collaboration with partners from site

engineering, IT, manufacturing companies and compliance

departments.

Work in an environment with a

strong team spirit, timely and effective communication, a sense of

urgency and a high motivation to achieve the company's

goals

Must

Haves :

Master's degree in chemical

engineering, biotechnology, a similar discipline or chemical

engineer

At least 2 years of solid experience

in the cGMP environment relevant to the

pharmaceutical

Experience in the operation,

qualification and validation of pharmaceutical production plants

and laboratory equipment

Very good written and

spoken German and English skills

MS Office,

Gsuite, Visio, eVal, Lucid Chart knowledge

Good

interaction with stakeholders

Team

spirit

Sense of

urgency

Nice to

haves : Veeva and eVal

experience

Sounds

interesting? Apply now – we’re looking forward to receiving your

applications!

Application Submission

Deadline :  27.11.2025