Associate Director, Drug-Device Concept & Delivery

GlaxoSmithKline; Upper Providence (Delaware County); On-site; USD 143,000 - 238,000; Full time

Benefits offered by this job

Hybrid work arrangement

Job summary

GlaxoSmithKline in the United States is seeking an enthusiastic Associate Director to integrate technical attributes, patient needs and business requirements for drug-device combination (DDC) products. You will join a multi-skilled team delivering robust devices across the development lifecycle.

This hybrid role requires a Bachelor’s degree in engineering or related technical discipline and 8+ years in design and/or development of medical devices, with experience in design controls, risk

Qualifications

• Bachelor’s degree in engineering, materials science, pharmaceutics or related technical discipline.
• 8+ years of experience in design and/or development of medical devices or drug-device combination products.
• Experience with design controls, risk management, design history file requirements.
• Experience working with suppliers, contract manufacturers or external technology partners.

Responsibilities

• Collaborate with internal teams to develop on-target patient-centric DDC products and ensure integrated product development.
• Identify technical risks and lead mitigation using testing and modelling to support device selection.
• Plan and execute engineering studies, device characterization, design verification and validation.
• Author and review key technical documentation and regulatory submission.

Skills

Design controls

Risk management

Regulatory knowledge

Supplier collaboration

Education

Bachelor’s degree in engineering, materials science, pharmaceutics or related technical discipline

Tools

Modeling

Job description

GlaxoSmithKline in the United States is seeking an enthusiastic Associate Director to integrate technical attributes, patient needs and business requirements for drug-device combination (DDC) products. You will join a multi-skilled team delivering robust devices across the development lifecycle.

This hybrid role requires a Bachelor’s degree in engineering or related technical discipline and 8+ years in design and/or development of medical devices, with experience in design controls, risk