Job Description

A new and exciting opportunity has come for a Validation Senior Engineering Specialist(s) on our Carlow Site with Technical Operations.

The successful candidate will be responsible for:

• Leadership of validation activities within the Recovery and Cleaning qualification team and across other validation teams.

• Maintaining compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made.

• Compliance via documentation completion, risk assessments, closing out corrective actions, participation in audits and inspections and proactively highlighting any issues around compliance.

• Supporting regulatory audits and submissions as required.

What you will do:

Bring energy, knowledge, innovation, and leadership to carry out the following:

• Planning, scheduling and oversight of Periodic Revalidation & Initial Qualification studies.

• Responsible for setting and delivery of validation strategies.

• Lead and supports complex & critical investigations associated with validation and commercial activities.

• Co-ordinate multiple complex projects in parallel including but not limited New Product Introductions, Process Improvements and Investigations.

• Execution of Periodic Revalidation, Cycle Development & Initial Qualification studies as required.

• Technical review and approval of Periodic Revalidation, Cycle Development & Initial Qualification protocols & reports.

• Authoring and reviewing standard operating procedures and technical reports.

• Engage in the early stages of projects.

• Act as validation SME on the equipment within the area assigned

• Serving as a key member during internal audits and external inspections/audits.

• Implementing the requirements as outlined in the site & project Validation Master Plan(s) and periodic revalidation plan.

• Supporting regulatory submissions.

• Lead and promote various organizational initiatives as needed (examples include EHS, workload forecasting, work standardisation, etc).

• Providing technical and validation oversight to process, design and project delivery teams.

• Represent the site in internal collaborations through Manufacturing Division Communities of Practice for Validation to include imparting of best practices in Validation and investigation activities.

• Maintain continuous focus on quality and safety compliance and unflinching focus on the customer.

• Within the role you will be acting as a validation engineer reporting within the Validation Engineering Team.

What skills you will need:

In order to excel in this role, you will more than likely have:

• Proven history of leadership skills within current and previous roles.

• Relevant technical qualification(s) in Applied Pharmaceutical / Biological / Computer / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.

• A minimum of 4-5 years directly related experience in academia, pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.

• SME in Cleaning Validation for reusable parts and process vessel washing and using Automated COP and CIP systems

• Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable

• Experience of coaching, mentoring and leading a team in the validation department in the past is desirable

• Prior experience in drug product processing equipment, PQ, Process Performance Qualification and Validation, site readiness, authoring documents subject to regulatory inspection.

• Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices ​

• Experience in working in other validation areas such CTU, Isolator and Filling Lines, Sterilisation (SIP & Autoclaves), Ancillary Qualification (Filters, CCI, Shipping) is considered advantageous but not mandatory.

Our facility in Carlow site broke ground in 2008 and is a filling site for the launch and commercial supply of vaccines,biologicsand small molecule drug product. Since itsinitiallaunch, the site has attracted significant internal investment and is now home toa number ofstate-of-the-artproduction facilities,laboratoriesand temperature-controlled warehousing units. The Carlow site is a significant employer in theSouth Eastregion and attracts high performing talent through close collaborations with universities and colleges in the region

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.

Pleasedon'thesitate 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, Data Analysis, Deviation Management, Equipment Qualification, GMP Compliance, Good Manufacturing Practices (GMP), New Product Introduction Process, Regulatory Audits, Sterile Manufacturing, Troubleshooting

Preferred Skills:

Standard Operating Procedure (SOP), Validation Activities

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:

No relocation

VISA Sponsorship:

Yes

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

06/8/2026

*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.