• Associate Principal Scientist – Device Technical and Engineering Lead (Associate Director Equivalent)

This position will be responsible for applying their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs they lead to ensure high quality products and robust manufacturing processes

• This position interacts extensively with subject-matter experts on the DPPD team and members of internal cross-functional product development teams from concept through product launch
• Additionally, the position will ensure products and processes are developed in accordance with applicable regulatory, quality, company, and customer requirements
• This position will lead cross-functional development teams within and external to Device Development & Technology
• The incumbent must be able to work well with all levels of employees and be able to effectively coordinate the execution of device development strategies

This individual will be expected to apply his/her knowledge of product design and development; manufacturing process development, qualification, and validation; and design control and risk management techniques to positively support and influence clinical and commercial combination product development and launches

• Lead and set direction for the device development strategy for multiple drug-device combination product development programs ranging from concept generation/selection, development, verification, and validation to launch readiness:
• Lead the cross-functional Device Working Groups to ensure full integration of the device development activities with the clinical, regulatory, formulation, commercial and other key company functions
• Lead the Device Development Engineering Core teams focused on development of design requirements for the combination product and engineering execution against the established requirements
• Represent Device Development and the project-specific Device Working Groups on cross-functional teams, including the Development and Commercialization Team (DCT)
• Additionally, maintain engagement with Early Development Teams (EDT) and Product Development Teams (PDT)
• Serve as key point-of-contact with potential external device designers, developers, and suppliers for selected device technology platforms

Oversee and serve as a technical integrator of all device development activities including engineering design, engineering analysis and testing, medical device design controls, risk management, test method/fixture development, design verification and validation, injection molding, automated assembly, and human factors analysis

• Proactively anticipate and resolve project obstacles and effectively communicate complex product technical challenges, device development strategy, timelines, milestones, and risks within our Company and with external suppliers
• Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs under your leadership
• Lead/support/oversee clinical supplies production with respect to device component manufacture and final assembly of biologic/drug product with device constituent part
• Lead/support the development, implementation and continuous improvement of Device Development and Device Project Leader processes, procedures, and tools
• Maintain a high level of engagement in the program-specific design controls process and design history file development
• Stay current with new device technologies, relevant worldwide regulations, standards, and effectively share this knowledge with others

This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely

• B.A./B.S in Mechanical Engineering, Biomedical Engineering, Industrial and System Engineering, or other types of engineering plus a minimum of 10 years of combined experience in medical device and combination product development
• Including development drug-device combination product or a medical device component of a combination product
• Leadership experience of managing device or combination product development programs and leading cross-disciplinary project teams
• Proven track record of applying analytical skills in product design, development, and validation
• Self-motivated with ability to work independently
• Proven ability to lead team members of diverse skill sets and backgrounds
• Strong interpersonal skills and a strategic thinker; able to influence without formal authority; ability to influence and present ideas to senior leadership
• Experience with leading complex development projects at an enterprise level
• Willing to travel

Able to multi-task continuously

• Has broad knowledge of medical device development, design controls and risk management, alongside deep knowledge in device design, requirement management, design verification, automation/process development, design validation, and control strategy
• Knowledge of U.S. and global medical device and healthcare regulations, including FDA combination products cGMP, Quality System Regulation, FDA Human Factors guidance, ISO 14971, 11608 and 11040, EN 62366, Council Directive 93/42/EEC, etc
• Excellent communication, presentation, negotiation, project management, and organizational skills

Combination Products, Combination Products, Communication, Computer Science, Cultural Diversity, Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Diversity Awareness, Human Factor Engineering, Injection Moldings, Machine Learning (ML), Manufacturing Processes, Mechanical Testing, Medical Device Quality Systems, Medical Device Regulations, Medical Devices, Medical Devices Design, Negotiation, Process Manufacturing, Product Design, Production Process Development, Project Management, Quality Management Systems (QMS) {+ 4 more}

Enhance our Company’s professional image and competitive advantage through publications, presentations, patents, and professional activities $139,600.00 - $219,700.00 An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs

• The successful candidate will be eligible for annual bonus and long-term incentive, if applicable
• We offer a comprehensive package of benefits
• Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits