Job Description

Job Description

Our Graduate Programme will start your journey on a career path within the Pharmaceutical industry. Not only will you learn both technical and professional skills, but work on projects that will contribute towards enhancing people’s lives across the world.

You will be part of a diverse and inclusive, multi-skilled global team of highly motivated individuals. 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, what will you be responsible for?

Over the course of the three-year programme you will bring energy, knowledge, innovation and leadership to carry out the following:

• Operate as part of the Engineering, Operations and MS&T teams, on a yearly-rotation basis, supporting the daily and long-term goals of the teams.
• Participate in troubleshooting meetings and root cause analysis workshops in support of manufacturing activities
• Compile data and trends on batch performance (yield & cadence) and adherence to critical product quality measurements
• Author technical memos and strategies for manufacturing investigations and improvements
• Writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same.
• Peer review documentation, ensuring QC Right First Time KPIs are achieved.
• Participate in daily team meetings and ensure effective communication of testing progress, deviations etc.
• Ensure that all Quality Systems within the department are adhered to on a daily basis.
• Complete all documentation in compliance with GMP and GxP standards.
• Provide support with audit/inspection requirements to ensure department compliance/readiness.
• Collaborating with others by sharing your skill-set and expertise
• Drive continuous improvement, perform root cause analysis on system failures e.g. FMEA, Fishbone diagrams, 5 why's etc.
• Drive compliance with 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, including maintenance of accurate records.

This programme will be completed fully on site (Dunboyne)

The ideal person will have:

• Bachelors or Masters degree in Engineering or Science qualification or relevant discipline

PQ20

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:

Project Temps (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Audit Management, Audit Management, Chemical Engineering, Data Analysis, Engineering Design, Engineering Standards, Estimation and Planning, Global Team Collaboration, GMP Compliance, Industrial Engineering, Ishikawa Diagrams, Key Performance Indicators (KPI), Manufacturing Equipment, Manufacturing Processes, Manufacturing Scale-Up, Peer Reviewing, Pharmaceutical Management, Problem Solving, Process Improvements, Professional Engineering, Project Management, Quality Operations, Regulatory Compliance, Regulatory Requirements, Self Motivation {+ 1 more}

 Preferred Skills:

Job Posting End Date:

09/22/2025

*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.