Manufacturing Specialist / Sr. Manufacturing Specialist– Downstream Processing (DSP)/ Drug Product — Siegfried
- Location
- Schlieren
- Contract
- full-time
- Posted
- Yesterday
Role overview
Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents.
As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive.
Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment.
- Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents.
- As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive.
- Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemical Engineering, or a related scientific field with 3–6 years of relevant experience, ora Master's degree with 1–3 years of relevant experience.
- Equivalent combinations of education and experience may be considered.
Key requirements
- Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemical Engineering, or a related scientific field with 3–6 years of relevant experience, ora Master's degree with 1–3 years of relevant experience.
- Equivalent combinations of education and experience may be considered.
- Experience in biopharmaceutical, gene therapy, cell therapy, or viral vector manufacturing with a focus on DSP.
- Hands-on experience with chromatography, filtration, and TFF/UF-DF operations.
- Working knowledge of cGMP regulations, cleanroom operations, aseptic processing, and GMP documentation.
- Experience with manufacturing systems such as MES, LIMS, or SAP is preferred.
- Experience in Drug Product manufacturing (formulation, sterile filtration, aseptic fill-finish) is a plus.
- Experience writing and maintaining SOPs and work instructions.
- Strong troubleshooting, communication, and documentation skills.
- Willingness to support flexible working hours, including weekends.
- English speaking and writing, German is a plus. Technical Skills
- Viral vector purification processes (e.g., AAV, lentivirus, adenovirus).
Company and context
- Siegfried DINAMIQS is a Contract Development and Manufacturing Organization (CDMO) based in Schlieren-Zurich, Switzerland, specializing in the manufacturing of viral vector gene therapies.
- At DINAMIQS we offer a comprehensive range of services, including vector design optimization, cutting-edge process development and analytics, as well as manufacturing.
- With a R&D facility running and a newly constructed GMP facility, we are dedicated to supporting gene therapy projects with scalable and efficient solutions.
- DINAMIQS became part of Siegfried's global network in 2023 and is now looking to grow its dedicated team of experts by hiring a Manufacturing Specialist / Sr.
- Manufacturing Specialist.
- If you are highly motivated, self-driven, and passionate about driving operational excellence in a dynamic environment, you are the person we are looking for.
- Execute DSP operations including chromatography, filtration, TFF, and UF/DF in a cGMP environment.
- Perform manufacturing activities according to batch records, SOPs, and GMP requirements.
- Prepare, operate, and maintain manufacturing equipment.
- Perform manufacturing support activities, including cleaning, monitoring, buffer preparation, material handling, and inventory management.
Additional details
- Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.
- English speaking and writing, German is a plus.
- Knowledge of contamination control and aseptic manufacturing practices.
- High level of accountability, quality mindset, and attention to detail.
- A unique and amazing work experience, being part of one of the most dynamic, diverse and inclusive CDMOs in the industry. Competitive and attractive compensation
Notes and original content
- Position Summary:
- Your Profile:
- Technical Skills
- Soft Skills
- Your Benefits:
- A unique and amazing work experience, being part of one of the most dynamic, diverse and inclusive CDMOs in the industry.
- Competitive and attractive compensation
Questions about this listing
What salary does Siegfried offer for this role?
Siegfried lists CHF 101'500 - 154'000 gross per year for this position in Schlieren. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Siegfried offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Siegfried during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Zürich?
EU/EFTA residents living in the border zone of the country adjoining Canton Zürich can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Zürich's cantonal migration office or with HR during the application.
How do I apply for this position at Siegfried?
Use the "Apply now" button on this page — it links directly to Siegfried's original listing at siegfried.wd103.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
