Scientist Quality Control (a), 100%

Scientist Quality Control (a), 100% #

Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com.

To drive our continuous organic growth, we are constantly looking for highly qualified specialists. To strengthen our release laboratory in the QC Late Phase department, we are looking for a dedicated Scientist Quality Control (w/m/d).

Your tasks:

• Assessment and review of GMP-compliant analyses with a focus on (U)HPLC-UV/VIS and LC-MS within the framework of routine, release, and stability testing.
• Technical processing of OOS, OOT, deviation, and CAPA processes as well as scientific evaluation of analytical results.
• Maintenance and updating of Analytical Instructions and other GMP-relevant documents.
• Participation in the continuous optimization of an efficient QC routine operation with a focus on short turnaround times, high quality, and future-proof standardized processes.
• Technical guidance of laboratory technicians regarding analytical questions.
• Responsibility for analytical questions as well as close cooperation with scientists and laboratory specialists to ensure efficient and GMP-compliant analytics.

Your profile:

• Completed studies (BSc or MSc) in Analytical Chemistry, Pharmacy, or a comparable scientific field.
• Several years of GMP experience in pharmaceutical analytics with a Bachelor's degree; with a Master's degree, initial professional experience is a strong advantage.
• Sound knowledge in instrumental analytics, especially (U)HPLC-UV/VIS; LC-MS knowledge is an advantage.
• Experience in the analytics of peptides is an advantage.
• Experience in processing Quality Events (OOS, OOT, Deviations, CAPAs) is desirable.
• Knowledge of GMP-relevant IT systems such as LIMS, CDS, and SAP.
• Analytical mindset, high quality orientation, and enjoyment of technical responsibility.
• Team-oriented, communicative personality with a structured and independent way of working.
• Good German and English skills.

Our offer:

• A dynamic and rapidly growing work environment with internal development opportunities
• Employee promotion through numerous internal and external training offers
• 60% coverage of pension fund contributions by Bachem AG as well as the possibility for supra-mandatory provision with our optional savings plan
• Access to the benefits platform Swibeco with discounts at external partners
• Fresh, healthy, and diverse food in our staff restaurant
• Diverse free sports activities on the Bachem Campus

Would you like to drive innovations forward together with us?

Have we piqued your interest? Then we look forward to receiving your complete application documents via our application portal.

Learn more about the Bachem Group and be inspired by our inspiring working environment at our location in Bubendorf!

At Bachem, you-ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation-regardless of age, gender, background, religion, or sexual orientation.

Please note: unsolicited resumes from recruitment agencies will not be considered.

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