Engineering Graduate - Brinny

MSD Malaysia; Cork; Hybrid; EUR 32,000 - 44,000; Full time

Job summary

Merck & Co., Inc. in Ireland invites applications for our Engineering Graduate Rotational Programme at Brinny, Cork.

This full-time, early-career opportunity develops engineering insight across GMP environments, with exposure to process validation, production support and cross-functional projects. The programme seeks MSc/BSc graduates in Science, Chemical, Mechanical, Electrical or Process Engineering who are eager to learn, collaborate, and drive improvements in safety, quality and efficiency

Qualifications

• MSc/BSc in Science, Chemical, Mechanical, Electrical or Process Engineering.
• Strong problem solving and teamwork skills.
• Experience with GMP environments is desirable.

Responsibilities

• Support process development and scale-up activities.
• Assist with method validation and equipment qualification.
• Provide technical support to manufacturing teams and documentation.

Skills

Chemical Engineering

GMP Compliance

Problem Solving

Project Management

Process Engineering

Data Analysis

Education

MSc/BSc in Science/Chemical/Mechanical/Electrical/Process Engineering (2:1)

Job description

## Engineering Graduate - BrinnyApply: Not Applicable: IRL - Cork - Brinny: Full time: Posted Today: End Date: September 19, 2026 (3 days left to apply): R403749Job DescriptionA fantastic opportunity has arisen to join our **Engineering Graduate Rotational Programme**. This position will contribute to developing and implementing strategic planning in Ireland by providing engineering insight and expert knowledge about the processes supporting the manufacture of product or disease area. The role is designed to strengthen the depth and breadth of technical, analytical, business and leadership capability within the business. It provides opportunities for individuals to excel personally and professionally and impact on the organisation's goals and objectives in Compliance, Supply, Strategy & Profit Plan.**Bringing a collaborative style, energy, knowledge, innovation and leadership to carry out the following:**Knowledge of or experience with some of the following would be an advantage:* Method validations, method transfers and equipment qualifications in a GMP environment.* Protein chemistry, chromatography, immunoassays and Microbiology.* Engineering preventative maintenance, utility supply, wastewater treatment, black utilities, calibrations and production support.* Facilities, plant management, and project management.* Support of new product introductions and technical transfers to and from the site, including new technologies.* Preparation of documentation, including protocols and reports, associated with the projects in accordance with GDP (good documentation practice) and site procedures.* Process and equipment optimisation to sustain and improve product quality, yields and throughput. Making recommendations and implementing measures to improve engineering, facility & production systems, equipment performance, yields and quality of product.* Problem solving to drive results in a cross functional team environment.* Execution of process development on existing products or new late-stage clinical products including scale up to plant equipment.* Identifying continuous improvement activities and leading or participating in cross-functional teams to implement. Supporting activities in the areas of cost reduction, process efficiency and operational excellence.* Providing site and on-the-floor technical support to the engineering and production areas/leaders for process/equipment optimization and troubleshooting.* Ensuring that all safety, quality and environmental compliance goals are achieved, including thoroughly investigating deviations and ensuring appropriate corrective actions are identified and implemented in full.* Responsible for process engineering and safety preparations* Provide technical support for commercial and Commercialisation products, including process and equipment validation.* Responsible for completion of process monitoring during production. **To excel in this role, you will likely have:*** MSc/BSc. qualification 2:1 (Science, Chemical, Mechanical, Electrical or Process Engineering)* High personal integrity, credibility, and energy. Demonstrated ability to work as part of diverse teams in an inclusive manner. Demonstrated ability to be self-driven with respect to driving results and implementing identified improvement initiatives.* Previous experience in pharmaceuticals, as well as an aptitude for problem solving in a technical environment are desirable.PQ20**Required Skills:**Chemical Engineering, Chemical Engineering, Cost Reduction, Cost Reduction Initiatives, Cross-Cultural Teams, Data Analysis, Engineering Design, Engineering Standards, Estimation and Planning, GMP Compliance, Immunoassays, Industrial Engineering, Manufacturing Equipment, Manufacturing Scale-Up, Microbiological Analysis, Operational Excellence, Problem Solving, Process Engineering, Process Improvements, Process Manufacturing, Professional Engineering, Project Management, Protein Chemistry, Self Motivation, Strategic Planning {+ 2 more}**Preferred Skills:**Current Employees apply HERECurrent 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**Job Posting End Date:**09/19/2026**\\*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.