Job Description
Leading a team of quality professionals ensuring compliance and quality oversight across external manufacturing of p
roducts and devices.
In this role you will be
subject matter expert in EQA and manufacturing quality systems, technology platforms, regulatory expectations, and external manufacturing management, with the opportunity to represent the company in external forums. Leads complex cross-functional initiatives to optimize quality and business processes driving continuous improvement.
Bring energy, knowledge, innovation to carry out the following:
Lead a team of quality professionals accountable for activities at the External Entity (EE) site associated with the manufacturing of Company Products and Devices.
Provide quality oversight over molding, manufacturing, assembly, testing, packaging, storage, and distribution of products manufactured at an EE.
Ensure products are produced or tested following approved processes/methods in conformance to all applicable regulatory requirements, regulatory filings, and company policies.
Act as a subject matter expert for both EQA and our manufacturing division in specific Quality Systems, technology platforms, regulatory expectations, and/or external entity management.
Represent our company in outside forums on areas of expertise, driving complex cross-functional initiatives to develop/optimize Quality/business processes.
Manage and lead a small team of Quality Assurance professionals, holding regular 1-on-1 meetings and Employee Development Plan discussions.
Collaborate with other functions to continuously improve our company's effectiveness and efficiency in quality management and quality systems supporting the external network.
Oversee performance management processes including objectives setting, approval, revision, year-end accomplishment evaluation, and performance discussions with direct reports.
What skills you will need:
In order to excel in this role, you will more than likely have:
Minimum four-year degree in Science, Engineering, or other relevant technical discipline (e.g., BS/MS Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering or equivalent).
Minimum of 12 years relevant experience in the Pharmaceutical and/or Medical Device industry with thorough knowledge of Quality Systems, Quality Assurance, and Quality Control including solid knowledge of global GMP and MDCP regulatory requirements.
Good knowledge and experience with MDCPs.
Strong interpersonal, communication, coaching, motivation, negotiation, and persuasion skills to build strong relationships.
Ability to work across boundaries; demonstrated interpersonal, relationship building, and leadership skills.
Proficiency in English, both verbally and in writing.
Previous experience participating in regulatory inspections.
Familiarity with domestic and foreign regulations and compendia governing plant operations.
We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.
As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.
We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.
Please feel free to speak to us about what flexibility means to you during your application.
So, if you are ready to:
Invent solutions to meet unmet healthcare needs, please apply today.
Required Skills:
Adaptability, Audit Management, Decision Making, Driving Continuous Improvement, FDA Inspections, Motivation Management, People Leadership, Process Improvements, Quality Assurance (QA), Quality Management Systems (QMS), Regulatory Compliance, Sterile Manufacturing, Strategic Thinking, Supplier Quality Management, Training and Development
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
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:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Remote
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
06/17/2026
*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.
Requisition ID:
R398616