Back to Job SearchROLE OVERVIEW
We are currently looking for a Design Transfer Workstream Lead – DHF Remediation to join a leading organization in the Pharmaceutical and Medical Device industries, supporting innovative projects remotely from the US. This is an exciting opportunity for a professional with a strong background in design transfer and remediation initiatives who is eager to contribute to impactful healthcare solutions. Join a company that has been shaping the industry since 1998, with a global footprint spanning Europe, Asia, and the Americas.
As part of our client’s team, you will play a pivotal role in ensuring the seamless transfer of design documentation and supporting manufacturing activities, all while working virtually within a collaborative environment geared towards excellence and innovation.
KEY DUTIES AND RESPONSIBILITIE
Your duties as the Design Transfer Workstream Lead will be varied; however, the key duties and responsibilities are as follows:
• Lead the retrospective review of design transfer documentation to ensure accuracy, completeness, and compliance.
• Assess documentation supporting the transfer of designs to manufacturing processes and identify any gaps or inconsistencies.
• Evaluate manufacturing specifications, procedures, and supporting documentation involved in design transfer activities.
• Develop and support remediation strategies to address documentation gaps and enhance transfer processes.
• Coordinate with Outputs, Verification, and Validation workstream leads to align design and manufacturing documentation efforts.
• As the Design Transfer Workstream Lead, you will ensure timely delivery of documentation review and remediation workflows that support product realization and compliance.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Design Transfer Workstream Lead – DHF Remediation, we are looking to identify the following on your profile and past history:
• A Degree or higher level in a relevant field (e.g., Biomedical Engineering, Medical Device, Quality Assurance, or related disciplines).
• Proven experience supporting design transfer within medical device development, including remediation initiatives involving manufacturing or design transfer documentation.
• Familiarity with product realization and manufacturing documentation requirements, working effectively across engineering, quality, and manufacturing teams.
• Strong documentation, analytical, and project coordination skills to manage multiple stakeholder deliverables.
WHAT’S IN IT FOR YOU?
This role offers the chance to contribute to internationally recognized projects in a innovative and fast-paced environment. You will work remotely with a global leader in healthcare, gaining valuable experience in design transfer processes and remediation strategies that impact patient safety and product quality. Our client values proactive and detail-oriented professionals, providing an excellent platform for career growth within the medical device sector.
Key Words: Medical Device / Design Transfer / Remediation / Manufacturing Documentation / Quality Assurance / Project Coordination / Remote Working / Healthcare Industry
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
