Operations Director at Merck Sharp & Dohme Corp. /Netherlands

Dunboyne, The Municipal District of Ratoath, Ireland -

Full Time

Start Date

Immediate

Expiry Date

04 Aug, 26

Salary

0.0

Posted On

06 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

People Leadership, Operational Excellence, Lean Manufacturing, Six Sigma, Project Management, Regulatory Compliance, Biologics Manufacturing, Technology Transfer, Financial Forecasting, Risk Mitigation, Production Scheduling, Data Analysis, Decision Making, Process Optimization, Manufacturing Quality Control, Sterile Manufacturing

Industry

Pharmaceutical Manufacturing

Description

Job Description A fantastic and hugely exciting opportunity has arisen for an Operations Director for Biologics clinical and commercial manufacturing at our single-use, multi-product commercialization facility in Dunboyne. Reporting to the Operations Lead, this position will drive capacity realization and operational excellence to deliver all components of stable manufacturing teams and processes for a diverse and complex biologics pipeline. This role will have leadership for one of the manufacturing areas (Upstream/Cell Banking, Downstream, and Solution Prep) spanning multiple facilities across the site, enabling standardization and simplified ways of workings for optimal utilization and resource agility. This position will provide leadership and operations support for manufacturing and release in addition to technology transfer, PPQ, inspection readiness and approval of new products. This position will include leadership across the organization, including days and shift teams. Our facility in Dunboyne joined our network in September 2020. Our Dunboyne site is our Company’s first Biologics Drug Substance Single Use Commercialisation Facility, playing a significant role in helping to commercialise key medicines. The innovation and collaboration between our Company’s research and manufacturing teams will significantly accelerate the time it takes to bring a medicine to market for the benefit of patients around the world. Key responsibilities Responsible for all Manufacturing Operations used for clinical and commercial manufacture Prep activities. Plans and directs all aspects of production activities associated with manufacturing or technology transfer and ensures that all projects, initiatives, and processes are in conformance with established policies, standards, and objectives. Develop and delivers toward site and organizational priorities and strategy. Ensure right-first time and stable start-up, including through technology transfer leadership, execution of clinical, PPQ and commercial batches, change management and implementation of process improvements. Drive a strong compliance mindset within the organisation, including initiative-taking safety and quality culture, and adherence to all regulatory expectations. Ownership for ensuring permanent inspection readiness is in place. Ensure production and project milestones are achieved through planning and execution of integrated overall program schedule. Establish and deliver on KPI’s in a timely manner, including schedule adherence, training, hiring, uptime, change controls, investigations, CAPAs, capital/expense targets, sustainability targets, yield/volume/cadence/operational availability, Right First Time, and timely documentation closure. Drive standardization, execution, and operational excellence by applying Lean principles to foster continuous improvement mindset to deliver a productive and cost-efficient operating model. Manage and develop operations team personnel toward strong, empowered leaders. Build, inspire, reward, and develop diverse talent with the capabilities necessary to succeed in manufacture. Develop facility and resource capacity model across areas within scope. Resolve resource and prioritisation constraints and support resource needs and changes. Drive a strong technical and digital mindset within the department, staying up to date with emerging technologies that will benefit the organization and manufacturing processes. Resolve issues and identify risks in a timely fashion to the relevant on-site and above-site stakeholders. Responsible for prioritisation of proposed risk mitigation plans and/or acceptance of Quality Risks identified as part of the Quality Risk Management Process. Provide clear direction and definition of any new project scope, goals, and deliverables, to the site and cross-functional sub-teams on an on-going basis. Resolve issues and identify risks in a timely fashion to the relevant on-site and above-site stakeholders. Manage financial forecasts and workload to achieve departmental headcount and cost improvements. Your profile Minimum Education/Experience: Degree qualification or equivalent (Science, Engineering, Technical or other relevant studies). Demonstrated leadership with at least 10 years leading in a cross-functional manufacturing environment, including indirect or direct people management experience. Demonstrated Biologics manufacturing and technology transfer experience. Technical/General Competencies: Strong leadership and interpersonal skills, including leading and coaching direct team to drive a high-performance organizational culture that accommodates rapid growth & highly dynamic operating execution. Inspirational leader that leverages data to set the vision and drive outcomes. The desire to continuously learn, improve and grow, and cultivate continued development within the team. Innovative thinker, with excellent decision-making and problem-solving skills. Ability to participate in and lead highly effective cross functional teams, build diverse talent, with a passion to build the future of our site in Dunboyne. Ability to influence across organizational layers, as well as outside the site and externally with partners and based on industry benchmarking. Ability to rapidly understand complex business & technical issues including multi-option scenarios to mitigate risk and ensure continuity of supply as well as strategic initiatives. A great communicator, decisive decision maker with a proven ability to deliver excellence. Proven capabilities in site manufacturing and technical operations, experience of Operational Excellence, Six Sigma and Lean Methodologies and a proven track-record in project management. Proven capabilities and knowledge of Biologics Drug Substance manufacturing, particularly in downstream processes Set clear performance standards; overcome obstacles; hold ourselves and others accountable for achieving results. Knowledge of global and company health authority regulations and applicable systems & GMP requirements. Experience engaging with regulatory agencies including in on-site inspections. Sound judgment and comfortable operating in a challenging, fast-paced, and sometimes ambiguous environment. 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. So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today. Required Skills: Adaptability, Adaptability, Business Agility, Data Analysis, Decision Making, Driving Continuous Improvement, Financial Forecasting, Lean Design, Lean Manufacturing, Manufacturing Processes, Manufacturing Quality Control, Mitigated Risks, Operational Excellence, Operations Support, Organizational Culture, People Leadership, Process Optimization, Production Scheduling, Project Management, Regulatory Compliance, Results-Oriented, Risk Mitigation Strategies, Six Sigma, Sterile Manufacturing, Strategic Initiative {+ 2 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE 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): Job Posting End Date: 05/13/2026 *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. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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Responsibilities

Lead biologics clinical and commercial manufacturing operations to drive capacity realization and operational excellence. Oversee technology transfer, PPQ, and inspection readiness while managing diverse manufacturing teams across multiple facilities.