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Scientist, Drug/Device Combo Products
full-timeUnited States$87k - $137k

Summary

Location

United States

Salary

$87k - $137k

Type

full-time

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About this role

Job Description

Scientist - Container Closure Integrity Development

Our company’s Device Product & Process Development (DPPD) Team focuses on the design, development, and commercialization of novel biologic/drug/vaccine-device combination products for safe and effective delivery to their intended sites of action. The DPPD Team oversees the development of the device constituent within our pipeline of combination products, spanning various therapeutic areas and routes of administration, including inhalation, implantation, and injection.

The DPPD within our Company Research Labs is seeking a talented, self-motivated, and highly collaborative Scientist with knowledge of container closure integrity (CCI) technology and experience with test method development, testing, and method validation for various product images (vials, syringes, cartridges, and injectors) and secondary packaging.

The candidate will develop methods for our company’s device and combination product pipeline, inclusive of small molecule, biologics, and vaccine products.

 

Key Responsibilities

  • Function as an analytical subject matter expert (SME), troubleshooting and optimizing analytical methods, with a focus on container closure integrity methods

  • Provide technical leadership and mentorship to junior scientists and team members.

  • Develop, validate, and execute feasibility container closure integrity (CCI) studies for complex combination devices & delivery systems

  • Author technical reports and testing protocols

  • Review technical data to ensure compliance with cGMP standards

  • Collaborate with cross-functional teams to ensure successful tech transfer of analytical methods between QC labs

 

Minimum Education Requirement

  • B.S./M.S in Mechanical Engineering, Biomedical Engineering, Industrial & Systems Engineering, Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field/discipline with a minimum of 1 year of relevant work experience in the pharmaceutical, biotechnology, or medical device industries

Required Experience | Knowledge | Skills:

  • Relevant analytical execution, development, validation, and/or quality control (QC) for container closure integrity as it pertains to small molecule, biologics, and vaccine products.

  • Ability to learn new techniques, troubleshooting assays, author and review technical documents

  • Excellent organizational skills to manage multiple projects

 

Preferred Experience | Knowledge | Skills:

  • Hands-on experience in container closure integrity technology (CCIT) method development, validation, and troubleshooting for injectable therapeutics. Candidate should be familiar with the following CCIT technologies for this purpose: dye ingress, high voltage leak detection, vacuum and pressure decay, laser headspace analysis

  • Good technical understanding of USP <1207>

  • Good technical, communication (oral and written), interpersonal, and teamwork skills. 

  • Ability to effectively identify and communicate risks.

  • Experience with other analytical methodologies

#eligibleforERP

AR&D

Required Skills:

Accountability, Accountability, Analytical Chemistry, Biocompatibility, Biomedical Engineering, Biomedical Sciences, Biopharmaceutical Industry, Biotechnology, Clinical Supply Chain Management, Combination Products, Cross-Functional Planning, Data Analysis, Human Factor Engineering, Innovation, Interpersonal Relationships, Machine Learning (ML), Manufacturing Processes, Materials Science, Mechanical Engineering, Mechanical Testing, Medical Device Technologies, Medical Product Development, Pharmacology, Production Process Development, Prototyping {+ 4 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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 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

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

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.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. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$87,300.00 - $137,400.00

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

25%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

01/28/2026

*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.

Other facts

Tech stack
Analytical Chemistry,Biomedical Engineering,Combination Products,Data Analysis,Human Factor Engineering,Machine Learning,Medical Device Technologies,Pharmacology

About MSD

At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing

What you'll do

  • The Scientist will function as an analytical subject matter expert, focusing on troubleshooting and optimizing analytical methods related to container closure integrity. They will also provide technical leadership and mentorship to junior scientists and collaborate with cross-functional teams.

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Frequently Asked Questions

What does MSD pay for a Scientist, Drug/Device Combo Products?

MSD offers a competitive compensation package for the Scientist, Drug/Device Combo Products role. The salary range is USD 87k - 137k per year. Apply through Clera to learn more about the full compensation details.

What does a Scientist, Drug/Device Combo Products do at MSD?

As a Scientist, Drug/Device Combo Products at MSD, you will: the Scientist will function as an analytical subject matter expert, focusing on troubleshooting and optimizing analytical methods related to container closure integrity. They will also provide technical leadership and mentorship to junior scientists and collaborate with cross-functional teams..

Why join MSD as a Scientist, Drug/Device Combo Products?

MSD is a leading Pharmaceutical Manufacturing company. The Scientist, Drug/Device Combo Products role offers competitive compensation.

Is the Scientist, Drug/Device Combo Products position at MSD remote?

The Scientist, Drug/Device Combo Products position at MSD is based in United States, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Scientist, Drug/Device Combo Products position at MSD?

You can apply for the Scientist, Drug/Device Combo Products position at MSD directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about MSD on their website.