Senior/ Principal Scientist - Peptide parenteral formulation development at Roche
Basel, bs, Switzerland -
Full Time


Start Date

Immediate

Expiry Date

26 Sep, 25

Salary

0.0

Posted On

27 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Product Manufacturing, Management Skills, Chemistry, Solid State Characterization, Communication Skills, Peptides, Writing, Analytical Techniques

Industry

Pharmaceuticals

Description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
At Roche, we have an exciting opportunity for an expert in peptide parenteral formulation. You will be working on multiple innovative projects with cutting edge technologies that will have a meaningful impact on millions of lives.
As a Principal Scientist in Pharmaceutical Development, you are part of the Department “Pharmaceutical Development” in Pharma Technical Development (PTD) in Basel, Switzerland. The department Pharmaceutical Development is responsible for the development of parenteral drug products (Synthetic molecules and Biologics) from Phase 1 through Launch. Activities encompass formulation and manufacturing process development for parenteral drug products for all clinical stages and the market , the transfer of product and process to commercial manufacturing sites,as well as line extension development.

Responsibilities
  • Drive the pharmaceutical development of cutting-edge peptide parenteral formulations, from clinical development all the way to market launch, including line extensions.
  • Development of robust manufacturing processes for both liquid and lyophilized peptide and small molecule formulations, overseeing scale-up, process characterization & validation, and seamless transfer to our global commercial manufacturing sites.
  • Act as Pharmaceutical Project Leader representing Pharmaceutical Development, in global CMC (Chemistry, Manufacturing, and Controls) teams, cross-functional initiatives, and international committees within Roche. You will play a pivotal role in shaping global regulatory submissions for all phases (Phase 1-3) and market approvals (MAA/NDA), making a direct impact on bringing life-changing medicines to patients
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