Management of the quality control department with raw material, packaging material and release analysis
GMP-compliant and timely analytical testing of raw materials, intermediate and end products
Responsibility for stability management
Monitoring and coordination of release analysis with HPLC, GC, wet-chemical methods and titrations of
Supporting the development and validation of methods and accompanying their transfer into routine practice
Documentation, evaluation and assessment of analytical tests in the GMP environment (OOS, OOE, OOT and deviations)
Preparation of customer and authority audits
Advising customers on specific analytical issues
Your profile
Degree in chemistry or pharmacy (university/university of applied sciences) - ideally with a focus on analytics or an apprenticeship as a chemical laboratory technician with corresponding further training (HFP, HTL)
Many years of professional experience in release analysis or quality control in a regulated environment (GMP experience is a plus)
Management experience as laboratory manager / team leader an advantage
Broad know-how in analytical methods such as HPLC and wet-chemical methods
German and English fluently spoken and written
Your advantages
You will benefit from an environment in which personal responsibility is encouraged and you will receive constant further training
You will find a familiar team with a good working atmosphere and exciting opportunities for development
You will receive a salary in line with the market and above-average social benefits
Our customer
is an internationally active company that specializes in the development and production of active pharmaceutical ingredients. As a CDMO, the company supports its customers from the initial idea through synthesis route development and method development to routine production. The company is characterized by an informal working atmosphere, good social benefits and a broad range of responsibilities. Place of work: Liestal region
