Job Description
We are excited to invite applications for the role of Manufacturing Operations Director at our state-of-the-art facility in Dunboyne, a cutting-edge space that fosters collaboration and integrates advanced technology. It provides biologics drug substance and cell banking manufacturing for clinical supply, registration, and commercial launch. This is a unique opportunity to lead clinical and commercial Biologics manufacturing while ensuring operational excellence.
Bring energy, knowledge, innovation to carry out the following:
* Managing operations in a modern facility, ensuring efficient staff movement across various manufacturing processes.
* Planning and directing production activities to align with established policies and objectives.
* Serving on the Site Leadership Team to drive site and organizational priorities.
* Ensuring smooth technology transfers and stable start-ups for clinical and commercial batches.
* Promoting a strong compliance culture, focusing on safety, quality, and adherence to regulatory standards.
* Maintaining permanent inspection readiness and achieving production milestones through effective planning.
* Establishing and delivering key performance indicators (KPIs) related to production efficiency and quality.
* Applying Lean principles to foster a culture of continuous improvement.
* Developing and empowering a diverse operations team to become strong leaders.
* Staying updated on emerging technologies to enhance manufacturing processes.
* Managing financial forecasts and resource needs to optimize departmental performance.
What skills you will need:
In order to excel in this role, you will more than likely have:
* General Competencies
o Strong leadership and interpersonal skills to foster a high-performance culture.
o A commitment to continuous learning and team development.
o Innovative thinking with excellent decision-making and problem-solving abilities.
o Experience in leading cross-functional teams and building diverse talent.
o Ability to influence across various organizational levels and external partners.
o Strong communication skills and a proven track record of delivering results.
* Technical Competencies
o Experience in manufacturing and technical operations, with a focus on Operational Excellence, Six Sigma, and Lean methodologies.
o Knowledge of Biologics drug substance manufacturing, particularly upstream processes.
o Familiarity with global health authority regulations and Good Manufacturing Practices (GMP).
o Experience engaging with regulatory agencies and managing inspections.
* Minimum Education and Experience
o A degree in Science, Engineering, or a related field.
o At least 5 years of leadership experience in a cross-functional environment, including direct or indirect people management.
o Relevant experience in biotech, vaccines, or pharmaceutical manufacturing.
Current Employees apply HERE
Current Contingent Workers apply HERE
Secondary Language(s) Job Description:
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.
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:
Adaptability, Adaptability, Analytical Thinking, Business, Clinical Manufacturing, Driving Continuous Improvement, Emerging Technologies, Employee Development, Good Manufacturing Practices (GMP), Lean Six Sigma (LSS), Maintenance Supervision, Management Process, Manufacturing, Manufacturing Equipment, Manufacturing Processes, Operational Excellence, People Leadership, Pharmaceutical Process Development, Process Manufacturing, Production Operations, Project Management, Project Scoping, Regulatory Compliance, Resource Management, Results-Oriented {+ 3 more}
Preferred Skills:
Job Posting End Date:
06/21/2025
*A job posting is effective until 11:59:59PM on the day BEFOREthe 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:R351198
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