Quality Control Analyst

For a leader in the pharmaceutical industry with an excellent work,life balance.

Responsibiliites:
Performs analytical testing according to raw material and product release specifications (HPLC,
GC, UV/VIS, IR, dissolution, pH, conductivity, TOC, titration, weighing, wet chemistry
experiments etc.).
Performs review of analytical data.
Performs basic laboratory work (buffer preparation, waste disposal management, washing of lab
dishes, cleaning of the labs etc.)
Supports management supply of consumables.
Supports maintenance/calibration of equipment and keeps relationship with suppliers.
Supports stability studies (set up, sampling, testing, coordination)
Writes specific standard operations procedures (e.g. operation and maintenance of equipment)
Participates in method transfer and method validation activities
Supports selection, purchase and commissioning of new equipment.
Handling of deviations and change controls
Can be assigned special tasks and project work

Profile:
Federal Certificate of Capacity as Laboratory Technician or similar education
2 – 3 years of work experience in a GMP environment
Solid knowledge in HPLC and GC techniques and CDS
Knowledge of dissolution, UV/VIS and IR techniques.
Knowledge of analytical method transfer and analytical method validation.
Experience of doing analytical testing according to Ph. Eur. and USP prescriptions.
Good writing skills.
Excellent team spirit.
Good knowledge in English and French.
Knowledge of most common office software.