Executive Director & Head of Device Engineering
- Employer
- Coherus BioSciences
- Location
- Redwood City, CA
- Start date
- Aug 22, 2024
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- Discipline
- Engineering, Biomedical Engineer, Science/R&D, Biotechnology
- Required Education
- Masters Degree/MBA
- Position Type
- Full time
Employer: Coherus Biosciences, Inc. Ref #90828
Position: Executive Director & Head of Device Engineering
Duties:
Lead the Device Engineering Team in the development and commercialization of drug-device combination products for parenteral administration from discovery to transition to manufacturing. Lead characterization and development of device design and manufacturing processes, including managing the entire product lifecycle for a wide variety of drug delivery devices to support all therapeutic modalities in the pipeline. Work with device development team members, vendors, partners, consultants and external CMOs to ensure device development activities including development, verification, validation, risk management, and process validation are created and executed per device regulations and applicable standards for US distribution. Author, review, and approve device and combination product design control documents to support device development deliverables, including design inputs and outputs, design transfers, protocols, reports, risk management, and design validation. Lead and provide technical oversight over device manufacturing and combination product Contract Manufacturing Organizations (CMOs) to ensure successful clinical and commercial Good Manufacturing Practices (GMP) production of device constituents and drug-device combination products. Serve as the company device expert during regulatory agency interactions, partner audits, and inspections. Manage project budgets and device constituent purchasing controls and manage all contractor services spending.
Education: Master’s degree or foreign equivalent in Biomedical Engineering, Biotechnology, or related field
Experience: 8 years of experience as Director, Vice President, Program Manager, Consultant, or related occupation.
Special Requirements: Must have at least 5 years of prior work experience in each of the following:
- Drug device combination product leadership role managing key partner relationships including overseeing technical design & development activities, product & process characterization, product testing, and equipment & process validation activities.
- Application of 21 CFR 820 in medical device development engineering activities including design verification, validation, risk management and process validation for development of drug delivery device combination products, through development & commercial supply lifecycle.
- Leading the development and commercialization of combination biologic drug products in compliance with FDA and Ex-US health authority regulatory requirements, working with drug & process development teams to incorporate device design requirements driven by formulation and/or drug specifications.
- Leading a team of device engineers for the development of device and combination product programs in compliance with 21 CFR 820, 21 CFR Part 4, ISO 13485, cGMP, ISO 14971, ISO 10993, ISO 62366 and ISO 11608 requirements (ISO standards are internationally agreed upon by experts, promulgated by ISO – the International Organization for Standardization).
- Submitting and gaining approvals of regulatory submissions for drug delivery devices/combination products (e.g., Pre-filled syringes, Safety devices, Autoinjectors, On-body injectors for acute, chronic and/or emergency use applications).
- Establishing business and quality processes to manage supply, product technical complaints, investigations and post market surveillance activities for drug delivery device/combination products, as well as management of budget for ongoing device programs.
*TRAVEL: Position requires significant national and international travel (at least 25% of work time), fully reimbursed by employer.
*TELECOMMUTING: Position does allow telecommuting
Salary: $246,116 to $293,800 per year
Worksite: 333 Twin Dolphin Drive, Suite 600, Redwood City, CA 94065
Applicant Instructions: Include job code 90828 in reply. EOE.
Beginning July 19, 2021, Coherus BioSciences requires all new hires to be fully vaccinated against COVID-19 as of their start date. This requirement is a condition of employment at Coherus BioSciences, and it applies regardless of whether the position is located at a Coherus BioSciences facility or is fully remote. If you are unable to receive the vaccine due to a disability or serious medical condition, or because it is prohibited as a result of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.
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