Product Lifecycle Engineering Principal Scientist Medical Device & Combination Products

Job Description

Job Description

In June 2019 Vertex announced the establishment of new research sites in Boston and Providence where research development and clinical manufacturing for cell biologic and genetic therapies will be primarily based. Cell and genetic therapies represent two rapidly emerging therapeutic modalities with the potential to treatand even cureseveral diseases Vertex is focused on. At Vertex our teams bring together the best talent to ensure we bring these cutting-edge transformative therapies to patients as quickly as possible.

As the Product Lifecycle Engineering Principal Scientist you will focus on the sustaining activity with drug delivery devices and combination products. You will ensure design and development processes and risk documentation associated with drug delivery systems are maintained throughout commercialization post-market lifecycle. The successful candidate will work closely with Process Development Quality Assurance Regulatory Affairs Analytical and Manufacturing functions as position will be on-site in Boston MA.

Key Responsibilities

• Collaborate with highly cross-functional teams to Lead sustaining engineering activities for commercialized medical devices and drug delivery combination products.

• Maintain and update design history documentation engineering records and lifecycle deliverables in accordance with internal procedures and regulatory expectations.

• Ensure risk management documentation is current and aligned with post-market product changes investigations and ongoing commercialization needs.

• Support engineering assessments related to design changes component updates supplier changes and product improvements.

• Partner with Quality Assurance Regulatory Affairs Process Development Analytical Labeling and Manufacturing to assess product impact and implement lifecycle changes effectively.

• Evaluate technical issues arising during commercialization and post-market support and drive timely resolution.

• Provide engineering input to change control deviation investigations CAPA and nonconformance activities as applicable.

• Support continued compliance with applicable design control risk management and medical device / combination product requirements.

• Contribute to product robustness reliability and manufacturability through data-driven engineering decisions.

• Participate in cross-functional reviews to ensure product lifecycle activities are appropriately documented and executed.

• Identify opportunities for continuous improvement in sustaining engineering processes documentation practices and cross-functional workflows.

• Serve as a technical resource for lifecycle management activities associated with commercial drug delivery systems.

• Support Regulatory activities including authoring regulatory submission documentation.

Experience

• Must have experience with product development of combination products specifically drug delivery systems.

• Must have experience with design controls and risk management as it pertains to FDA EU MDR and associated harmonized standards (ISO 13485 ISOCFR.820 and 21CFR Part 4) and a thorough understanding of GxP principles and practices.

• Must have experience leading technical teams and projects in highly matrixed environments.

Required Qualifications

• Bachelors degree in Mechanical Engineering Biomedical Engineering Chemical Engineering Materials Engineering or related scientific/engineering discipline.

• Minimum of 10 years of experience working within a regulated medical device drug delivery and combination product environment.

• Strong knowledge of design controls and risk management for regulated products.

• Demonstrated experience in sustaining engineering product lifecycle management or post-market design assurance in collaboration with cross-functional product support from Quality Regulatory and Manufacturing teams.

• Working knowledge of process engineering and manufacturing methods analytical methods labeling and packaging and systems engineering.

• Strong technical writing problem-solving and communication skills.

• Ability to manage multiple priorities and work effectively across teams.

• Experience supporting change assessments and design updates in a structured quality system.

Pay Range:

Disclosure Statement:

Flex Designation:

Flex Eligibility Status:

In this On-Site designated role you will work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertexs Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Onsite

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry ethnicity disability veteran status genetic information sexual orientation marital status or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager or contact Talent Acquisition at