Candidates login or register below

Like Us

Candidate Login / Register
Sorry, but this job has expired. Please try another search or browse our jobs.

Scientific Associate Analytical Development and Quality Control

Job Field:
Regulatory and Drug Safety Jobs
Discipline:
QA Jobs
Country:
Switzerland
Region:
Switzerland All
Contract Type:
Temp / Locum / Contract
Currency:
EUR
Salary:
60 to 90 per hour
Posted:
19-Aug-19
Recruiter:
Key People
Job Ref:
mc24497

Our leading pharmaceutical company client is looking for a

Our client is looking for one Scientific Associate Analytical Development and Quality Control, working on site at their offices in Basel.

The individual will be responsible for performing lab activities related to CMC projects in terms of the development of analytical methodology and characterization of sterile drug products.

Role Responsibilities:
*Organization and execution of lab work for Idorsia's parenteral drug products
*Implementation of new analytical techniques required for parenteral drug products
*Development, optimization and implementation of analytical methods, e.g., for purity-, stability-, content and potentially genotoxic impurity determinations
*Conduct of release and stability tests under cGMP and non-GMP
*Planning and execution of method transfers and validations including respective documentation
*Review, interpretation and documentation of analytical data including results from method development, release, retest, validation, stability and transfer
*Assurance of adequate maintenance and operation of analytical equipment according to GMP

Qualifications:
*Apprenticeship, college-, or university-degree or equivalent education in the field of chemistry, biochemistry, biology, pharmacy, or chemical engineering. A minimum of 4 years of work experience in the analysis and method development for parenteral drug products.
*Skilled in the application of cGLP/cGMP.
*Extensive analytical development background and hands-on lab experience of analytics for sterile drug products.
*Experience in late phase development activities, e.g. analysis of drug product supplies for pivotal clinical trials, registration stability studies and process validation
*Detail-oriented. Ability to critically evaluate analytical data from a broad range of scientific disciplines.
*Prior experience with complex parenteral products and medical devices.
*Expertise in the development and validation of analytical methods used for the characterization and control of parenteral products.
*Excellent interpersonal/ organizational skills and the ability to multi-task.
*Strong oral/ written communication skills, proficiency in English. German/French is a plus.
*Computer literacy (e.g. Waters Empower, ELN).


Key People is a specialist international recruitment consultancy with over 25 years' experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment.

Please contact Mark Cussens, Clinical Research Recruiter on
Tel: +44 1727 817623 or email: mcussens@keypeople.co.uk
Tel: +41 4350 86620 or email: mark.cussens@keypeopleswitzerland.ch

Key People is a recruitment company with a reputation for providing good value that's been built up over 20 years.
-We achieve results faster
-Our candidates really are a cut above
-We add greater value
We think it's because we're a private company driven by clients, not by shareholders.

For our candidates, we have developed relationships with thousands of clients nationwide and across Europe, who choose to recruit through Key People, so you'll have a wide choice of opportunities to further your career.

Closing Date:
17/09/2019

Return to search.

This website uses cookies. Read our cookie policy for more information. By continuing to browse this site you are agreeing to our use of cookies.

Latest Job Listings