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• Device Technical and Engineering Lead
• Inhalation Programs (Director Equivalent) Rahway, NJ Posted 2 days ago Apply Now Job Description Principal Scientist
• Device Technical and Engineering Lead
• Inhalation Programs (Director Equivalent) Our company's Device Product Platforms (DPP) Team designs, develops, and commercializes novel biologic/drug/vaccine
• device enabled combination products to achieve safe and effective delivery to their intended site of action.

The DPP Team manages the development of the device constituent of our company's pipeline of combination products across a variety of therapy areas and routes of administration, with this role focused primarily on inhalation drug-device combination products, including dry powder inhalers, nebulized therapies, and other respiratory delivery platforms. Job description 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 inhalation drug-device combination product programs they lead to ensuring high quality products, robust manufacturing processes and appropriate integration of formulation, device, aerosol performance, patient use, and regulatory considerations. This position interacts extensively with subject-matter experts on the DPP 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 their 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 inhalation combination product development and launches, including device-platform selection, drug-device interface definition, aerosol performance strategy, and patient-centric usability considerations. Principal Responsibilities Provide inhalation subject-matter leadership across dry powder inhaler, nebulized and other respiratory delivery programs, including assessment of device-platform options, drug-device compatibility, dose delivery performance, aerosol characterization strategy, device usability, clinical supply readiness and transition to commercial manufacturing. Lead and set direction for the device development strategy for multiple inhalation drug-device combination product development programs ranging from concept generation/selection, platform assessment, feasibility, development, verification, validation, and clinical/commercial launch readiness: Lead the cross-functional Device Working Groups to ensure full integration of the inhalation product drug/device development activities with the clinical, regulatory, formulation, commercial, human factors, quality and manufacturing functions, including alignment on device selection, aerosol performance, dose delivery, and patient-use requirements. Lead the Device Development Engineering Core teams focused on development of design requirements for the inhalation combination product and engineering execution against established requirements, including device performance and through-life stability, emitted dose, aerodynamic particle size distribution, robustness, usability, and manufacturability. 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 external specialist inhalation CDMOs, inhalation device designers/developers, component suppliers and manufacturing partners for drug-device combination product development, clinical supply, commercial manufacturing, and device technology platform activities. undefined Oversee and serve as a technical integrator of inhalation drug-device combination product development activities, including CDMO and/or site selection, formulation-device compatibility, device-platform assessment, manufacturing unit operations definition, clinical and commercial readiness, device engineering design, aerosol performance testing, engineering analysis, drug-device combination product design controls, risk management, inhalation-specific test method development, design verification and validation, component manufacture, automated assembly, container closure/device interface considerations, and human factors analysis. Proactively anticipate and resolve project obstacles and effectively communicate complex inhalation product technical challenges, including device performance, formulation-device compatibility, aerosol delivery, manufacturability, usability, regulatory expectations, 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, including content related to device description, design controls, risk management, human factors, aerosol performance, manufacturing process, and control strategy. Lead/support/oversee clinical supplies production with respect to drug-device combination product and/or 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, ensuring inhalation-specific user needs, design inputs, aerosol and inhalation device performance requirements, risk controls, verification evidence and validation strategy are appropriately captured. Stay current with new inhalation delivery technologies, respiratory device platforms, relevant worldwide regulations, standards, regulatory expectations and industry developments for orally inhaled and nasal drug products, and effectively share this knowledge with others. Enhance our Company's professional image and competitive advantage through publications, presentations, patents, and professional activities. Qualifications

REQUIREMENTS

B.A./B.S in Pharmaceutical, Science, Biomedical or Engineering-related subject plus a minimum of 10 years of combined experience in, (bio)pharmaceutical, medical device and combination product development. Advanced degree is preferred. 5+ years of leadership experience with deep working knowledge of device, biologic/drug product and process development including regulatory submission and approval processes. Experience with development of inhalation drug products, inhalation drug-device combination products, or respiratory device components is strongly preferred. 5+ years of leadership experience of managing complex device or combination product development programs and leading cross-disciplinary project teams. Has broad knowledge of medical device development, design controls and risk management, alongside deep knowledge of inhalation device design, requirements management, device and aerosol performance verification, automation/process development, design validation, human factors and control strategy. Knowledge of U.S. and global drug-device combination product and 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. Knowledge of regulatory expectations and guidance for orally inhaled and nasal drug products, inhalation combination products, device performance, aerosol characterization, and patient-use considerations is strongly preferred. Proven track record of applying analytical and technical judgment to inhalation product and/or manufacturing process design, development, validation and lifecycle management, including interpretation of device, aerosol, formulation, and process performance data. Self-motivated with ability to work independently Proven ability to lead team members of different 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 Excellent communication, presentation, negotiation, project management, and organizational skills Experience with leading complex development projects at an enterprise level Willing to travel Able to multi-task continuously

Required Skills:

Aerosol, Aerosol, Biomedical Engineering, Biopharmaceutical Industry, Biopharmaceuticals, Combination Products, Cross-Functional Communications, Design Controls, Detail-Oriented, Device Development, Dry Powder Inhalers (DPI), Engineering Analysis, Extensive Traveling, Finite Element Analysis (FEA), Human Factor Engineering, Manufacturing Systems Development, Mechanical Testing, Medical Device Quality Systems, Process Development Engineering, Process Manufacturing, Product Risk Management, Pulmonary Drug Delivery, Risk Control, Risk Management, Self Motivation {+ 1 more}

Preferred Skills:

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US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)

EEOC GINA

Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/) The salary range for this role is $156,900.00

• $247,000.

00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. 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 . You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:

We will consider qualified applicants with arrest and conviction records for employment in compliance with the

San Francisco Fair Chance Ordinance Los Angeles Residents Only:

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular Relocation:

Domestic VISA Sponsorship:

No Travel Requirements:

10%

Flexible Work Arrangements:

Remote Shift:

Not Indicated Valid Driving License:

No Hazardous Material(s): n/a

Job Posting End Date:

09/5/2026

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Requisition ID:

R410988 Apply Now Active Filters Principal Scientist•... Rahway, NJ Clear All Powered By Cookie Policy We use cookies to improve your experience on our site. To find out more, read our privacy policy Accept Cookies Decline Cookies