Associate Director, Manufacturing Operations

Job Description
We aspire to be the premier research-intensive biopharmaceutical company.
We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people .
As a Manufacturing Operations Lead, you will play a critical role in ensuring successful site delivery and achieving our Governance Pillars in People, Safety, Quality, Delivery, and Cost.
Your Core Responsibilities
Develop, communicate, and execute a data-driven cross-enterprise schedule for successful site delivery.
Manage production organization, schedule, and changeovers while conducting audits to optimize plant operations.
You will have the opportunity to coach and mentor a team to enhance performance, foster accountability, and drive continuous improvement.
Collaborate with senior leadership to execute strategic initiatives aligned with company objectives .
Lead safety audits and monitor investigations to achieve zero Lost Time Injuries (LTIs) and Recordable Injuries (RI).
Ensure compliance with Global Policies and cGMP, and drive initiatives to reduce Quality Notifications (QNs).
Lead cross-functional teams to meet tight timelines and challenge the status quo with a continuous improvement mindset.
Support the development of a high- performing site organization through learning and development plans.
Who You Are
You are ready if you have:
Level 8 Degree in Science, Engineering, or Technical field.
Evidence of Continuous Professional Development, such as Lean Six Sigma Green Belt.
Minimum of 6 years' experience in the Biopharma , pharma or experience in a regulatory operations industry.
Strong people management experience, managing managers and people development experience.
Experience with site operations projects, including capital projects and manufacturing operations.
Familiarity with regulatory filings and health authority interactions.
Nice to have, but not essential:
Biologics manufacturing experience.
Current Employees apply
HERE
Current Contingent Workers apply
HERE
Secondary
Language(s) Job Description:
As a company, we are committed to 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.
So, if you are ready to:
Invent solutions to meet unmet healthcare needs,
please apply today
.
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:
Not Applicable
Shift:
Valid Driving License:
Hazardous Material(s):
Required Skills:
Continuous Improvement, Cross-Functional Teamwork, Good Manufacturing Practices (GMP), Manufacturing Operations, People Development, People Management, Strategic Planning
Preferred Skills:
Biologics, Lean Six Sigma (LSS)
Job Posting End Date:
09/18/2025
*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:
R
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