Fill Finish Project Engineer -Clinical Drug Product Manufacturing

Fill Finish Project Engineer -Clinical Drug Product Manufacturing

Fill Finish Project Engineer -Clinical Drug Product Manufacturing

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We are seeking an enthusiastic and detail-oriented Fill Finish Project Engineer to support the planning and execution of clinical drug product manufacturing projects, with a focus on aseptic fill finish and device assembly operations.

Fill Finish Project Engineer

Employment type: Permanent

In this role, you will collaborate closely with senior engineers, project managers, and cross-functional teams to help ensure the successful and compliant execution of clinical manufacturing.

Key Responsibilities:

• Representation of Fill Finish Pilot Plant interfacing with the Drug Product Development group, the Drug Delivery Systems group, the supply management team ensuring timely clinical supplies.
• Ensure that manufacturing relevant information and technical capabilities are in place for the operations team to flawlessly produce the DP/DA according to GxP, EHS and business requirements
• Ensure timely plant readiness and support the operations team in the execution of the experimental/clinical activities
• Ensure timely delivery of clinical material from to Pack&Label sites (internal and/or external)
• Manage the overall relationship with internal/external stakeholders and act as the single point of contact between the organization and pilot plant facility
• Provide pilot plant input & requirements as required
• Source raw materials and components when required
• Ensure that manufacturing processes are consistent with agreed platforms and are scalable and transferable to commercial operations
• Ensure and/or support planning, execution and documentation (protocols, reports, memo)
• Support investigations, CAPAs, change controls according to assigned responsibilities, and performs critical raw data review for key documents
• Forecasts and monitor actual spending vs budget
• Maintain compliance with all company policies and procedures

Qualifications:

• Bachelor’s degree in Pharmaceutical Sciences, Chemical Engineering, Biochemical Engineering, or related discipline.
• At least 3+ years of experience in biologics drug product development, fill finish, or device assembly (1+ year for PhD candidates)
• Strong understanding of aseptic processing, fill finish operations, or combination product assembly is an advantage.
• Prior experience in technology transfer, pilot plant operations, or clinical supply chain is highly desirable. Working knowledge of GMP/GxP compliance, CAPA management, and regulatory documentation.
• Strong organizational and communication skills with the ability to work in cross-functional teams.
• Proactive mindset with a willingness to learn and take on increasing responsibilities.
• Fluent in English; German is a plus.

Why Join Us?

Adryan is an internationally operating services group, providing a full range of services for the life sciences industry, and working with top clients in the sector to make a meaningful impact on the way that they operate.

• You will be part of a dynamic and growing organisation, working on impactful hiring projects.
• Benefits include a laptop, phone, and personal training budget.
• Hybrid- flexible working hours and conditions.
• General 2nd class abonnement for Swiss public transportation.
• Employer-covered accident and illness insurance contributions
• Access to our employee benefits program
• Annual training budget and internal knowledge-sharing platform
• Supportive and collaborative work environment
• Monthly team dinners
• Annual international team event (Switzerland & the Netherlands)

To apply, please submit your resume in word and a brief cover letter outlining your experience with fill finish operations and tech transfer or clinical supply coordination.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Engineering and Project Management

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