Device Engineering Group Lead

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Job Description

OBJECTIVES/PURPOSE:

Lead mentor and develop the Injection Systems Development device engineering team to strengthen technical capability execution discipline and talent growth.

Drive consistency in the application and evolution of device platforms design standards and Design Control/DHF expectations across programs and partners.

Assure robust compliant device/combination product solutions by guiding risk management and verification/validation strategy and driving data-based technical decisions.

Partner with internal stakeholders and external development/manufacturing partners to align user needs requirements and execution plans ensuring timely delivery of robust platform-based solutions.

ACCOUNTABILITIES:

• Provide functional leadership for the device engineering team (7-10 engineers) including prioritization coaching/mentoring and performance support.
• Provide project and technical leadership to cross-functional teams to progress device/combination product programs through clinical development registration and launch readiness.
• Ensure projects and team deliverables meet Design Control and DHF expectations in accordance with applicable regulations and standards.
• Facilitate consistent application of platform-based design solutions requirements and best practices across pipeline programs by sharing lessons learned and aligning teams and partners on standard approaches.
• Direct development and review of statistically sound design verification protocols/reports and support design validation activities.
• Establish and maintain effective working relationships with external design/development manufacturing and service partners to ensure aligned scope quality and timelines.
• Support continuous improvement of design control processes and documentation practices to maintain compliance with medical device and combination product regulations.

CORE ELEMENTS RELATED TO THIS ROLE:

Leads and develops a team of device engineers to provide injection system combination products for subcutaneous drug formulations.

Provides technical governance and consistency across multiple device/combination programs rather than driving development for a single asset.

DIMENSIONS AND ASPECTS:

Technical/Functional (Line) Expertise

• Recognized device/combination product SME; deep expertise in drug delivery system development from feasibility through qualification and launch readiness.
• Applies and coaches Design Control and DHF deliverables (21 CFR 820 ISO 13485) including requirements/specification development V&V and statistically sound verification protocols and reports.
• Strong working knowledge of risk management (ISO 14971) design validation and Human Factors support and deviation/complaint/failure investigations to drive robust technical recommendations

• Manages the preparation of device/combination product CMC sections for global regulatory submissions.

Leadership

• Provides functional leadership for a team of 10 device engineers; sets expectations prioritizes work across multiple programs mentors and develops capability.
• Leads project and technical direction for cross-functional teams through clinical development registration and launch readiness; communicates clearly to multidisciplinary audiences.
• Drives continuous improvement of design control practices and ways of working; influences internal stakeholders and external partners to adopt agreed standards and deliverables.
• Identifies and leads departmental/functional initiatives.

Decision-making and Autonomy

Makes day-to-day technical and execution decisions across multiple projects (test strategy requirements maturity V&V approach DHF completeness) and escalates high-impact trade-offs as needed.

Evaluates complex drug delivery system issues and data; provides clear go/no-go recommendations defines mitigations and leads/assists investigations to resolve deviations and test failures.

Interaction

Partners closely with internal stakeholders (Quality Manufacturing Regulatory Drug Product development Clinical Legal) to align technical deliverables timelines and compliance expectations.

Establishes and maintains strong working relationships with external design/development and manufacturing partners service providers testing laboratories CROs and CMOs.

Innovation

Develops fit-for-purpose feasibility and verification strategies and encourages technically rigorous data-driven experimentation to retire risk early.

Builds organizational capability by coaching best practices (e.g. applying In-Silico first principles and DFSS where applicable) codifying lessons learned and sharing knowledge across programs and with partners.

Complexity

Manages technical execution across a portfolio of device/combination product programs in parallel balancing competing priorities schedules and resource constraints.

Operates within a highly regulated global standards environment (FDA ISO AAMI/ANSI) and a complex external partner network requiring disciplined documentation and alignment across organizations.

EDUCATION BEHAVIOURAL COMPETENCIES AND SKILLS:

• Bachelors Degree and 12-15 years relevant industry experience or Masters Degree and 10-13 years relevant industry experience or Ph.D. 5-7 years relevant industry experience.
• Demonstrated ability to lead and develop technical engineers (coaching performance feedback delegation and talent development).
• Expert-level competency in Design Control/DHF execution and quality (requirements risk management V&V traceability) and ability to audit/coach teams and partners on expectations.
• Strong stakeholder management and communication skills to influence cross-functional decisions and manage external partner performance (design/development manufacturing labs/CRO/CMO) to schedule and quality.

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees and we strive to be more transparent with our pay practices.

For Location:

U.S. Base Salary Range:

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors including the qualifications of the individual applicant for the position years of relevant experience specific and unique skills level of education attained certifications or other professional licenses held and the location in which the applicant lives and/or from which they will be performing the actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical dental vision insurance a 401(k) plan and company match short-term and long-term disability coverage basic life insurance a tuition reimbursement program paid volunteer time off company holidays and well-being benefits among others. U.S. based employees are also eligible to receive per calendar year up to 80 hours of sick time and new hires are eligible to accrue up to 120 hours of paid vacation.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race color religion sex sexual orientation gender identity gender expression parental status national origin age disability citizenship status genetic information or characteristics marital status status as a Vietnam era veteran special disabled veteran or other protected veteran in accordance with applicable federal state and local laws and any other characteristic protected by law.

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Job Exempt