sen. lab associate physical chemistry quality control in Stein

posted
contact
Dimitri Michos, Basel Professionals Health Care & Life Sciences
job type
temporary
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job details

posted
location
stein, aargau
sector
life sciences
job type
temporary
reference number
13591
contact
dimitri michos, basel professionals health care & life sciences
phone
058 201 55 50

job description

Sen. Lab Associate Physical Chemistry Quality Control

For the Drug Product Services (DPS), the successful Contract Development and Manufacturing Organization (CDMO) branch of our client, located in Basel and Stein we are looking for you as Sen. Lab Associate in Physical Chemistry Quality Control

Key responsibilities:

o   Plan and carry-out analytical tests according to current good manufacturing practices (cGMP) standards on drug products in clinical development or commercial phase (specifically focused on HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visible particles, subvisible particles and related DP analytics)

o   Contribute to planning of analytical method validation as well as execute and evaluate validation experiments

o   Support cGMP regulated analytical method transfer

o   Ensure proper maintenance of equipment, safety and health protection following lab and safety instructions and all cGMP regulations

o   Install, qualify and maintain instruments according to best practices and regulations

o   Support establishment of DP analytical infrastructure and services for biologics, small molecule and peptide parenteral products for clinical and commercial products

Key requirements:

o   Completed vocational training as BTA, PTA, CTA or equivalent or a degree as B.Sc. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related subject

o   Extensive (> 2 years) working experience as a technical assistant in the pharmaceutical or chemical industry, preferably in analytics

o   Strong working knowledge in majority of relevant analytical techniques

o   Very good reporting, interpretation and documentation skills of scientific results

o   Good knowledge of written and spoken English

o   Experience working in a cGMP-regulated environment is advantageous

Proficiency in development of parenteral dosage forms and protein analytics is beneficial