Scientist IMP In-Process Controls

Jobdescription

For one of our clients, a global pioneer in

pharmaceuticals, we are currently looking for a Scientist IMP

In-Process

Controls.

General

Information : Start

date : ASAP

Latest start date : 01.03.2026

Planned duration : 30.09.2026 with

the possibility of extension

Contract :

temporary contract via Randstad

Workplace : Basel

Workload : 80-100%

Home Office : not

possible

Team : 8

People

Department : Analytical Research &

Development (MMDCA)

Working Hours : Standard

About

the job : The department

is responsible for the process analytics during the manufacturing

of chemically synthesized Active Pharmaceutical Ingredients (APIs).

This includes reaction controls and the analysis of isolated

intermediates, strictly adhering to cGMP, safety, and regulatory

requirements. We are seeking motivated individuals to actively

contribute to a variety of engaging tasks within our Manufacturing

Analytics Team.

The

Perfect Candidate : The

ideal candidate is a hands-on analytical expert with a Master’s

degree and at least three years of experience mastering

physical-chemical techniques like chromatography within a cGMP

environment. They bridge the gap between development and production

by seamlessly implementing new methods while ensuring rigorous data

integrity, documentation accuracy, and proactive management of

deviations. Fluency in both German and English is essential for

this role, as the candidate must navigate a dynamic matrix

organization to mentor colleagues and drive cross-functional

process

optimizations.

Tasks

Responsibilities : Provide

essential guidance to laboratory colleagues on the planning,

execution, and conclusion of analytical tests for in-process and

intermediate analytics

Ensure strict compliance

with cGMP (current Good Manufacturing Practice), safety standards,

and regulatory requirements across all analytical

activities

Thoroughly review analytical methods

and specifications originating from the analytical development

department

Implement and establish new

analytical methods from development into the

production-accompanying control

process

Generate and meticulously check

analytical documentation, maintaining a high focus on quality, data

integrity, and meeting defined deadlines

Take

initiative and ownership in the timely processing and documentation

of deviations and non-conformances

Actively

participate in crucial quality assessments and investigations to

uphold product integrity

Contribute to process

optimization by assisting in the development and implementation of

lean, efficient working

processes

Must

Haves : You

hold a Master's degree or university degree in Natural Sciences, or

have completed a Chemical Laboratory Technician apprenticeship with

extensive, relevant professional experience. Please note candidates

with a PhD degree are considered

overqualified.

Min. 3 year proven, hands-on

experience with a variety of analytical techniques relevant to

chemical manufacturing processes.

Confident

with physical chemical analytical techniques

(Chromatography)

Strong commitment to quality

and a high level of awareness regarding data integrity and

documentation accuracy.

Sound knowledge of GMP

principles (Good Manufacturing Practice) and regulatory

requirements in the pharmaceutical industry

To

perform effectively in this role, advanced German (C1) &

English language skills are required

Able to

demonstrate excellent organizational skills and the ability to

effectively manage and prioritize multiple tasks in a dynamic

environment

Proactive team player with a strong

sense of responsibility and a high willingness to learn and

adapt

You are capable of thriving in an agile

matrix organization and successfully contributing to shared,

cross-functional

objectives.

Sounds

interesting? Apply Now! We look forward to receiving your

application.