Job Description

Senior Scientist, Quality Control (m/f/d)

We are offering an attractive position for a Senior Scientist, Quality Control (m/f/d) with a strong technical background and hands-on experience in biochemical analytical methods to join our Biologics Analytical Department located in Lucerne/Schachen, Switzerland.

You will be part of a multidisciplinary team and support the development of novel biopharmaceuticals. As an active member of our global bioanalytical development team, you will work with your counterparts at our US research sites to apply state-of-the-art technology to support biotechnology process development.

The integrated Biologics Analytical Department provides support to the Biotechnology Department by performing release and stability testing of biological drug substances and is supporting global outsourcing of analytics for biologics, followed by study and quality monitoring to guarantee adherence to regulatory requirements and internal guidelines. Furthermore, the department conducts raw-/starting material and in-process testing for biological drug substances. The position offers development potential; responsibilities can be adjusted to the candidate’s qualifications and ambitions.

Your main accountabilities include:

First time establishment of new ELISAs and transfer to CRO and commercialization laboratories.

Performing analytical method qualification and method bridging in the laboratory including strategy development and alignment with global company requirements.

Release and stability testing of biologics to determine relative biological potency.

Second Scientist Review of analytical release and stability data in electronic laboratory notebooks.

Writing technical protocols, reports, Standard Operating Procedures (SOPs), etc.

Representing the area as a subject matter expert in global development teams.

Supporting the local and global department strategies and initiatives.

Supporting ELISA lab investigations, change controls, deviations.

Qualifications:

Ph.D. in Biochemistry/Chemistry/Biological Sciences, Master’s degree with 3+ years of industry experience, or a Bachelor’s degree with 7+ years of experience. 

Hands-on experience with ELISAs for biological potency determination.

Work experience in a GMP laboratory.

Experience with analytical method qualification/validation and method transfer.

Experience in protein biochemistry and protein analytics/characterization.

Strong oral and written communication skills in English and German.

Strong team player, demonstrating mutual respect.

Experience in the field of residual host cell protein analysis, residual protein A analysis or critical reagent management is beneficial.

Do you find yourself in the description and are you interested in taking this opportunity? Please send us your complete application documents and become part of a modern company with attractive working conditions.

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

CMR, OEB

Job Posting End Date:

01/20/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R328801