Merck & Co, Inc

Associate Principal Engineer, Drug-Device Combination Products

Merck & Co, Inc$142K — $224K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • B.S. Degree in Mechanical Engineering or related field with a minimum of 15 years in regulated industry.
  • Proven expertise in combination product assembly process and equipment development.
  • Skilled in authoring design/process FMEA for risk management.
  • Experience designing automated combination product assembly equipment.
  • Hands-on experience in manufacturing site readiness and equipment qualification documentation.

Responsibilities

  • Develop detailed assembly process plans and strategies for combination products.
  • Author design/process FMEA to mitigate design-related risks.
  • Document and validate processes for compliance through IQ, OQ, PPQ and other activities.
  • Create protocols, reports, and specifications in line with SOPs.
  • Manage relationships with equipment suppliers for both large and small-scale devices.
  • Support process and technology transfer to manufacturing facilities.
  • Collaborate with cross-functional teams to achieve project goals.

Benefits

  • Comprehensive medical, dental, vision insurance for employees and families.
  • Retirement benefits including a 401(k) plan.
  • Paid holidays, vacation, and compassionate/sick days.
  • Eligibility for annual bonuses and long-term incentives.
Full Job Description

Job Description

This position is in our organization’s Device Development & Technology (DD&T) group in our Research division.  Our organization’s DD&T group is responsible for the development of devices, combination products, processes, testing and assembly equipment from conception through product launch. Products include autoinjectors, inhalers, implants, infusion pumps, vaginal rings and connected devices/apps. The person in this position contributes to high impact, complex, cross-functional, and cross-divisional teams, initiatives and will provide input to achieve project goals.  Effective collaboration with teams is essential to meet our company's goals/objectives.  The group also plays a key role in supporting commercially launched products.  

Our company's DD&T Team is seeking a hands-on medical device product manufacturing and assembly engineer.  This position will be responsible for hands-on factory floor work and collaboration, via interfacing with our company's internal sites, medical device suppliers and sub-suppliers.  This includes working with both small to large scale medical device assembly equipment suppliers, integrated manufacturing equipment component suppliers and purchased device component suppliers.  In addition, this position shall interrogate device supplier processes as they relate to our company's combination product process specifications and critical quality attributes to support our company's combination product quality control strategy and preserve essential performance requirements.

Education Minimum Requirement:

  • B.S. Degree in Mechanical Engineering or related field with a minimum 15 years of regulated industry experience

Required skills and key responsibilities for this position include:

  • Can develop detailed plans and strategies for combination of product assembly process and equipment development and lead technical team to deliver a qualified process and equipment for clinical or commercial use

  • Author design/ process FMEA to capture design related risks and identify appropriate risk controls to ensure robust and efficient device functionality.

  • Design and author Process validation activity and documentation like IQ, OQ, PPQ etc.

  • Author protocols, reports, create drawings and specifications to ensure proper documentation of development activities in accordance with relevant SOPs.

  • Experience in designing automated combination product assembly equipment and experience in managing equipment suppliers

  • Experience in developing, implementing and troubleshooting combination product assembly equipment processes including vision systems, ultrasonic welding and automated component and glass feeding and handling systems

  • Experience and the ability to manage all aspects of manufacturing site readiness including equipment qualification requirements and all associated documentation

  • Understanding of device and combination product DFM/DFA principles and design and failure modes in relation to assembly processes

  • Excellent oral and written communication skills and the ability to present complex information in a clear and concise manner to partner group stakeholders 

  • Mechanical aptitude and hands-on troubleshooting skills, with the ability to work independently in a laboratory setting and manufacturing floor setting.

  • Strong interpersonal skills with an ability to collaborate in a team environment

  • High level work ethic

  • Support process and technology transfer to our company's manufacturing facilities

Preferred Experience and Skills:

  • CAD design, including knowledge of SOLIDWORKS and

  • 3D printing and the ability to prototype and fabricate custom fixtures for assembly and testing

Required Skills:

CAD Modeling, Combination Products, Computer-Aided Design (CAD), Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Human Factor Engineering, Machine Learning (ML), Medical Device Management, Medical Device Manufacturing, Medical Device Quality Systems, Medical Devices Design, Quality Management Systems (QMS), Risk Control, Test Method Validation

Preferred Skills:

Current Employees apply

Current Contingent Workers apply

US and Puerto Rico Residents Only:

The salary range for this role is

$142,400.00 - $224,100.00

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 .

You can apply for this role through (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:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

08/15/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

Merck & Co, Inc Careers

Join the visionary team at Merck & Co, Inc, a global leader in healthcare dedicated to advancing the world of medicine. As part of our professional community, you'll find dynamic job opportunities that foster innovation and leadership across various fields. Merck & Co, Inc is not just a company; it's a place where you can make a difference.

Work You’ll Do

At Merck & Co, Inc, we are committed to improving global health through groundbreaking research and innovative healthcare solutions. Our team is at the forefront of developing new therapies and vaccines that significantly impact public health worldwide. By joining us, you will collaborate with some of the brightest minds in the industry, using your skills to contribute to projects that save and improve lives around the globe.

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Whether you're seeking an internship, a graduate opportunity, or a professional position, Merck & Co, Inc offers a range of career paths in environments that promote rapid professional growth and development. Explore job opportunities in research, digital transformation, manufacturing, and more, all while benefiting from a culture that supports diversity and inclusion.

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Merck & Co, Inc is an ideal environment for those who lead with curiosity and the drive to innovate. Our leadership is committed to fostering a culture where inventive thinking and collaboration are encouraged, making it a perfect place for professionals who seek to make an impact through their work.

Develop Your Skills

With Merck & Co, Inc, you are not just getting a job; you're gaining access to unparalleled career development opportunities. Enhance your skills through diverse training programs, workshops, and continuous learning courses designed to help you grow at every stage of your career.

Benefits and Culture

We understand that our employees are our greatest asset, which is why we offer competitive benefits designed to support the health and well-being of you and your family. From comprehensive health care coverage and retirement plans to flexible working conditions and wellness programs, our benefits package is designed to meet the diverse needs of our team members.

Join Our Team

Ready to advance your career at Merck & Co, Inc? Search open positions that match your skills and interests. We are continuously hiring and looking for passionate, creative, and solution-driven team players. Prepare your resume, sharpen your interview skills, and become part of a company that's dedicated to making a difference.

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Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ

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