As a Process Development Strategist, you will play a crucial role in driving harmonization and leading drug product process development within our global team. We are committed to delivering game-changing therapies from clinical phase I into the market to serve every patient, every day.
The Position
Our core business is to develop safe, innovative and effective drugs using cutting-edge technologies for manufacturing processes (Drug Substance and Drug Product), clinical supply, formulation, device, packaging, and analytical development.
As an integrated partner within the drug development ecosystem, we are dedicated to effectively developing innovative and patient-centered parenteral drug products including Formulation and Process Development and Drug Delivery Systems.
The Principal Process Engineer and Strategy Realization Lead ensures robust clinical and commercial process designs for effective process validation and successful commercialization. The incumbent is responsible for the development of drug product processes for the holistic parenteral DP process development portfolio, running from Biologics, synthetic molecules, peptides to Gene & Cell Therapy.
This includes overseeing the development of filling, lyophilization, and freeze/thawing processes, applying Quality by Design principles where appropriate, and executing process characterization and validation programs. The role will provide process design and validation support for drug product transfers across the network and offer engineering support for equipment and processes.
Furthermore, you will collaborate within the Global Drug Product Process Engineering group to drive strategy harmonization and oversee seamless harmonized strategy deployment and right-first-time clinical and launch technology transfers and major market approvals. Harmonizing work across technical development functions and other Pharma Technical Operations network partners is crucial for success.
A key component of the role involves providing strategic guidance across the DP process engineering network, ensuring the team's work supports the broader PTD Parenterals Development organization, including clinical and commercialization development phases, Drug Delivery, and Device Departments.
The Opportunity
As an experienced Principal Process Engineer and Strategy Realization Lead with expertise in process development and launch experience in parenteralia, you will play a crucial role in driving strategy harmonization and leading drug product process development within our global team.
* Develop, optimize, and validate robust processes for clinical and commercial parenteral drug products.
* Lead process design, validation studies, and technical transfers for seamless commercialization.
* Collaborate cross-functionally and across the parenteralia pipeline portfolio to ensure strategic alignment and successful project execution.
* Foster innovation and continuous improvement in drug product and equipment processes.
* Ensure compliance with GMP and regulatory standards.
Who You Are
Our ideal candidate will meet the following criteria:
* While a Ph.D. in a related scientific or engineering field is preferred, all candidates possessing equivalent experience are encouraged to apply.
* 10+ years of biopharmaceutical industry experience and proven ability to lead cross-functional teams.
* Experience with implementing advanced Process Analytical Technologies and/or drug device combination product processes is a plus.
* Expertise in parenteral process development and regulatory submissions.
* Strong leadership and project management capabilities.
* Excellent communication, strategic thinking, and problem-solving skills.
We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Roche is an Equal Opportunity Employer.