Pharmaceutical Development Laboratory Project Manager (Formulation expert) - Mendrisio site (Ticino) — Sintetica SA
- Location
- Mendrisio
- Contract
- other
- Posted
- —
Role overview
Pharmaceutical Development Laboratory Project Manager (Formulation expert)
Mendrisio site (Ticino) — Sintetica SA, Mendrisio (TI).
We do so in close cooperation with clinical experts, who shape our understanding of their unmet needs and drive our efforts to address them.
- Pharmaceutical Development Laboratory Project Manager (Formulation expert)
- Mendrisio site (Ticino) — Sintetica SA, Mendrisio (TI).
- Key responsibilities
- Coordinate and execute the activities related to the assigned formulation development projects:
- and skills
- Master’s degree or PhD in a scientific discipline (Chemistry, Industrial Chemistry, Pharmaceutical Chemistry).
Main responsibilities
- Key responsibilities
- Coordinate and execute the activities related to the assigned formulation development projects:
- Define qualitative and quantitative composition of formulations to ensure stability, compatibility, and bioavailability.
- Develop and optimize sterile injectable formulations (large and small volume parenteral, ophthalmic gels, suspensions, emulsions, lyophilized products) applying QbD principles and Design of Experiments (DoE) studies.
- Design and execute formulation trials, dissolution studies (including pilot-scale dissolutor testing), and data-driven optimization strategies.
- Evaluate extractables and leachable risk in collaboration with analytical team.
- Evaluate nitrosamines risk in collaboration with analytical team.
- Support aseptic processing or terminal sterilization strategy selection.
- Support scale-up activities and technology transfer to manufacturing.
- Collaborate cross-functionally with Manufacturing, Quality Assurance, Quality Control and Regulatory Affairs.
Key requirements
- and skills
- Master’s degree or PhD in a scientific discipline (Chemistry, Industrial Chemistry, Pharmaceutical Chemistry).
- At least 10 years of post-degree work experience, including at least 5 years in Pharma R&D context.
- Familiarity with both small and macro-molecules API.
- Demonstrated expertise in injectable and/or ophthalmic formulation development.
- Proven hands-on expertise in aseptic processing, sterilization strategies, and lyophilization cycle development.
- Practical experience applying QbD principles and/or DoE in drug product development.
- Strong experience with late-stage development, scale-up and commercial product support.
- Familiarity with ICH/EU/US/Swiss laboratory guidelines related to the technical subjects.
- Excellent command of written and spoken English.
- Preference will be given to candidates based in Switzerland.
- We offer Fulltime permanent employment in a young working environment and positive culture.
What the company offers
- Mendrisio site (Ticino) Founded in 1921 and headquartered in Mendrisio (Switzerland), Sintetica's mission is to continuously strive to improve therapies by enhancing its products' formulations and usability for the benefit of clinicians and patients.
Additional details
- Qualifications and skills
Questions about this listing
What salary does Sintetica SA offer for this role?
Sintetica SA lists CHF 68'000 - 103'000 gross per year for this position in Mendrisio. 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 Sintetica SA 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 Sintetica SA during the application process, since these details can vary by role even within the same contract category.
Do I need the G permit to apply for this role in Ticino as an Italian cross-border worker?
Yes, if you are resident in Italy within the 20 km border zone. The Swiss employer files the G-permit application at the Ticino cantonal migration office after the contract is signed — first issuance takes 2-6 weeks, then automatic yearly renewal for as long as the employment continues. Weekly return to your Italian home is required to keep the status.
How do I apply for this position at Sintetica SA?
Use the "Apply now" button on this page — it links directly to Sintetica SA's original listing at app.ncoreplat.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
