Global Device Platform Lead, Technology Transfer

GSK; Waltham (MA); Hybrid; USD 143,000 - 238,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive program

Health care benefits

Retirement benefits

Job summary

GSK in the United States seeks a Device Lead for Global MSAT Drug Delivery and Aseptic Technology. You will own the Device platform technically and drive delivery to manufacturing sites worldwide, with flexibility and potential international travel.

You will lead cross-functional teams, ensure regulatory compliance (DHF, MDR, FDA QSR), manage risk, and drive device technology transfer and innovation in manufacturing.

Qualifications

• Bachelor's degree in engineering or a Science Degree (e.g., Process/Mechanical Engineering, Materials Science, Biomedical Engineering/ Chemistry).
• 10+ years' experience in Medical Device Manufacturing environment; OR Masters Degree with 5+ years of experience in Medical Device Manufacturing environment.
• Experience in pharmaceutical/medical device GMP, regulatory environment, ISO standards, plus DHF/MDR/FDA guidance.

Responsibilities

• Be the SPOC technical SME interface between Device/Component suppliers and GSK MSAT site teams and represent MSAT at supplier technical/project meetings.
• Deliver a robust supply strategy of the Device platform by collaborating with Strategy, Procurement, Quality, Logistics, including mold tool & assembly asset validation programmers.
• Lifecycle manage the Device Platform, driving Technology Transfer from R&D and maintaining throughout the life, including post-approval regulatory changes, CPV, and manufacturing efficiency.

Skills

Technical leadership

Cross-functional collaboration

Regulatory knowledge

Problem solving

Data-driven decision making

Risk management

Education

Bachelor's in engineering

Science degree

Master's degree (related field)

Job description

GSK in the United States seeks a Device Lead for Global MSAT Drug Delivery and Aseptic Technology. You will own the Device platform technically and drive delivery to manufacturing sites worldwide, with flexibility and potential international travel.

You will lead cross-functional teams, ensure regulatory compliance (DHF, MDR, FDA QSR), manage risk, and drive device technology transfer and innovation in manufacturing.