Job Description

An exciting opportunity has arisen to join our Quality team in Brinny as Director.

The Laboratory Operations Leader will provide strategic and operational leadership to the Laboratories to test quality pharmaceutical products in meeting the four Manufacturing Division priorities of: Compliance, Supply, Strategy and Profit Plan.

The Laboratory Operations Leader is accountable for the effective and efficient running of all operations in a flexible, cross-functional, multiskilled teamwork environment, collaborating effectively with the IPT and Functional Leaders.

The Laboratory Operations Leader is responsible to mould the culture to one that supports a High-Performance Organisation.

This consists of: personal accountability and responsibility, continuous self- development and colleague collaboration in an open and trusting environment where all colleagues are comfortable to voice their opinions The Laboratory Operations Leader is responsible for prioritization of proposed mitigation plans and/or acceptance of Quality Risks identified as part of the Quality Risk Management Process under the remit of decision maker roles and responsibilities (as required)

Primary activities/responsibilities:

Ensure the highest Compliance standards.Ensure supply of high-quality product in line with testing schedules. A  Integral Member of the Site Quality leadership team (QLT) and the Site Leadership Team (SLT) on key operational and strategic prioritiesWork as a key member of the Site Extended leadership team (ELT)Provide sound financial stewardship, management, and control.Lead a cross-functional management team providing ongoing coaching and support, including the identification and development of key talent.Drive performance and management of individuals and team.

Continuous Improvement: Responsible for driving a culture of Continuous Improvement by deploying our Company Six Sigma tools within the laboratories.

Coaching and Training: Develop an effective, focused, and strong laboratory team by understanding: their abilities and unique contribution. Provide your team with the tools and development opportunities to make them successful.

What Qualifications you will need:

Degree or 3rd level qualification (Science, Engineering, Quality).Desirable project management qualification such as ProjectManagement Professional etc.Desirable Lean Six Sigma Green belt or higher

As a company, 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.  We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.

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.

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):

Required Skills:

Analytical Method Development, Analytical Method Development, Analytical Thinking, Aseptic Manufacturing, cGMP Compliance, Change Management, Coaching, Decision Making, Driving Continuous Improvement, Financial Management, Financial Performance Management, Management Process, Mitigation, Motivation Management, People Leadership, Pharmaceutical Quality Control (QC), Pharmaceutical Systems, Quality Assurance Processes, Quality Management, Quality Risk Assessment, Regulatory Compliance, Regulatory Experience, Regulatory Requirements, Risk Mitigation Strategies, Six Sigma {+ 4 more}

 Preferred Skills:

Job Posting End Date:

07/3/2025

*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:R354799