191 Chemical Processes jobs in Ireland

Job Description
2026 Intern Requisitions

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description
Intern Engineer
Location
Ballydine, Ireland

Duration
Internship (Full-time, fixed term)

Reports to
Assigned Technical Mentor or Team Lead

Our company in Ballydine is a world-class pharmaceutical manufacturing site focused on delivering life-saving medicines. As an intern, you'll be part of a team that values innovation, collaboration, and continuous improvement. This is your chance to gain real-world experience in a cutting-edge facility while contributing to meaningful projects that impact global health.

We're looking for enthusiastic and curious students to join our engineering teams for a hands-on internship. This is a fantastic opportunity to explore your interests, apply your academic knowledge, and learn from experienced professionals in a supportive and dynamic environment.

What You Will Do
As an Intern Engineer, you will

• Support production teams with day-to-day operations and troubleshooting activities.
• Assist in process and equipment improvement initiatives to enhance efficiency and quality.
• Collaborate with cross-functional teams on product development and technology transfer projects.
• Contribute to data analysis and digital tools used in continuous improvement efforts.
• Learn about pharmaceutical manufacturing processes, quality systems, and industry best practices.

What We're Looking For

• Currently pursuing a Bachelor's in Chemical Engineering or a related field.
• A strong interest in learning about pharmaceutical manufacturing and engineering.
• Good communication skills and a collaborative attitude—ready to work as part of a supportive team.
• A curious mindset and willingness to ask questions, explore new ideas, and take initiative.
• An interest in digital tools or data analysis is welcome, but not essential.

Why Choose Ballydine?

• Real Experience Work on impactful projects that contribute to real-world outcomes.
• Mentorship Learn from experienced professionals who are passionate about developing future talent.
• Innovation Be part of a site that embraces new technologies and continuous improvement.
• Culture Join a diverse, inclusive, and collaborative team that values your growth.

Ready to Make a Difference?
If you are passionate about inventing solutions to meet unmet healthcare needs, eager to impact the future of global health, and excited to push the boundaries of science and technology, we want to hear from you.

Apply today
to start your journey with one of the world's leading healthcare companies.

PQ20
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
Intern/Co-op (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
Communication, Database Management, Data Entry, Document Management, Office Applications, Process Improvements, Task Coordination, Technical Support

Preferred Skills
Job Posting End Date
09/17/2025

• A job posting is effective until PM 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
R

Process Chemical Engineer is required by CareerWise recruitment to work with our Limerick based biotech client. 12-month contract position.

Process Chemical Engineer to provide technical process design support for Bioprocess systems on new Process Area CAPEX project.

Responsibilities:

• Generation User Requirement Specification (URS) for assigned systems.
• Reviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs, etc.
• Ensures procurement packages (bill of materials (BOM), datasheets, cutsheets etc) meet Regeneron equipment specifications.
• Tracks HAZOP action items and ensures action items are incorporated into system design.
• Attends 30%, 60% and 90% model reviews ensuring systems meet operational, safety and ergonomic requirements.
• Reviews and approves system lifecycle documentation (FS. SDS, IO lists, etc) and ensures they meet requirements.
• Attends factory acceptance test (FAT) of associated equipment if required.
• Attends automation software bench FAT if required.
• Supervises and executes Site Acceptance Testing (SAT) and commissioning activities.
• Generates FAT, SAT and commissioning protocols for assigned equipment and ensures protocols meet specifications.
• Ensures Vendor Document Requirements (VDR) meet requirements.
• Builds Preventative Maintenance (PM) tasks and spare parts lists on Computerised Maintenance Management System (CMMS)

Requirements:

• Requires BS/BEng in Chemical, Process or Mechanical engineering with 3 - 5 years related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.
• Experience with design and commissioning within biopharmaceutical sector would be desirable.
• Experience with DeltaV would be desirable

Please call James Farrar today for further information email:

CareerWise Recruitment (In Search of Excellence)

Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors.

We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.

By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected.

**Join SPX FLOW as Process Engineer

Dunboyne – Ireland**

About The Role
We are currently seeking a talented and motivated
Process Engineer
to join our team. In this role, you will be involved in both project execution and bid proposal development, taking responsibility for the process design of equipment systems and components. You will contribute to the delivery of high-quality, cost-effective process solutions in line with project timelines and customer requirements.

This is an exciting opportunity to be part of a collaborative, multidisciplinary engineering team, where your technical expertise will directly influence the success of our projects across industries such as Dairy, Food, Beverage, and Pharmaceutical.

Key Responsibilities
As a Process Engineer, your main duties will include:

• Process Design:

• Developing process flowsheets, P&IDs, equipment specifications, and operating instructions.

• Performing process calculations (e.g. pipe sizing, pump selection, thermal balances).

• Defining input/output requirements, utilities, KPIs, and performance metrics.

• Safety & Compliance:

• Ensuring plant designs are safe and environmentally responsible.

• Adhering to applicable legislation (e.g. EU Machinery and PED Directives).

• Participating in design and risk reviews.

• Project Delivery:

• Ensuring timely delivery of design outputs to the required quality and within budget.

• Supporting & leading installation and commissioning teams to ensure design intent is met.

• Assisting with documentation handover and support to Aftermarket teams.

• Collaboration & Communication:

• Working closely with internal teams including Mechanical, Electrical, and Automation.

• Participating in project meetings, design reviews, and technical discussions.

• Providing input to sales teams, feasibility studies, and customer site surveys.

• Documentation:

• Preparing operating manuals and spares lists.

• Supporting technical file compilation in line with relevant regulations.

• Leadership (when applicable):

• Acting as Lead Engineer on selected projects, coordinating multidisciplinary teams.

• Managing schedules, resources, and ensuring consistent design standards.

• Engineering Community Engagement:

• Acting as a subject matter expert and mentor where appropriate.

• Supporting continuous improvement initiatives and knowledge-sharing activities.

Qualifications & Experience

• Degree in Process, Chemical, Mechanical Engineering, or a related discipline
• Engineering design experience in hygienic industries (e.g. Dairy, Food, Beverage, Pharma)
• Understanding of hygienic and CIP (clean-in-place) design principles
• Proficiency in Microsoft Office; AutoCAD and SAP experience a plus
• Full driving license
• Fluent in English (spoken and written)
• Strong communication and interpersonal skills
• Ability to manage multiple tasks and work within a matrix structure
• Self-motivated with strong analytical and problem-solving skills
• High ethical standards and a collaborative mindset

What We Offer

• Competitive salary package with annual performance-based bonuses.
• Recognition and performance incentive programs.
• Opportunities for professional growth within a global, innovative company.
• A supportive work environment committed to sustainability and technological advancement.

Next Steps
Does this opportunity align with your career goals? If you're ready to contribute to innovative solutions with a global impact, we would love to hear from you.

Apply now to join a team that is shaping the future of process systems.

For any questions, please feel free to reach out to the recruiter, Olena Kril at

About SPX FLOW
At SPX FLOW, Inc., we specialize in creating innovative flow components and systems. With over 100 years of experience, we offer 20 brands of pumps, valves, mixers, air dryers, hydraulic tools, homogenizers, separators, heat exchangers, filtration solutions, and more. Our products help produce many of your favorite household goods and snacks

Headquartered in North Carolina, we operate in over 25 countries with 5,000 employees worldwide. We are committed to sustainability, holding over 550 patents globally, with 44% focused on clean technology. Join us and be part of a company that values innovation and sustainability.

FULL TIME

Cork, Ireland

Process Engineer (Validation Engineer)

Réalta Technologies are looking for a Process Engineer (Validation Engineer), this role sits within a specialist engineering team supporting the development and manufacture of innovative medical device solutions.

The Process Engineer will provide technical and validation support across manufacturing and project activities, driving process improvements, ensuring compliance, and supporting the introduction of new products and technologies.

Key Responsibilities

• Lead and support process validation activities (IQ, OQ, PQ) and maintain compliant documentation
• Provide engineering input for new product and process introductions
• Drive continuous improvement initiatives to enhance quality, cost, and efficiency
• Support troubleshooting, root cause analysis, and implementation of corrective actions
• Develop and maintain SOPs, work instructions, and other GMP documentation
• Collaborate with cross-functional teams and external partners to deliver on project goals
• Ensure all work complies with Quality and EHS requirements.

Qualifications & Skills

• Level 7/8 Degree in Mechanical, Process, or related Engineering discipline.
• 2–4 years' experience in a regulated manufacturing or medical device environment.
• Strong understanding of process validation and Six Sigma or problem-solving tools.
• Proven project management and analytical skills.
• Excellent communication and collaboration skills.
• Self-motivated, adaptable, and technically curious.

Job Duties Outline job duties/responsibilities below:

• To ensure that engineering, qualification & validation records are developed and maintained as per the cGMP and GDP requirements & SOP.
• Coordination with design consultant as required and respective user department for the design of process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.).
• Review & approval on detailed design as submitted by vendors (e.g. Manufacturing Vessel, Blender, Filling lines etc.).
• To ensure project execution work and follow-ups with different departments (QA, QM, Operations etc.) to meet the project completion within stipulated time frame.
• Effectively communicate & discuss related to day to day activity and concerns within team for efficiency and performance improvement.
• To prepare, review & update of standard operating procedures at regular intervals to meet cGMP requirements.
• To ensure the compliance of current Good Manufacturing Practices of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.).
• To ensure that Preventive Maintenance is developed for relevant equipment/processes in co-ordination with the relevant departments as per schedule.
• Responsible for development, execution and review of Qualification / Re-Qualification and Validation activity of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.)
• To ensure the compliance of Engineering Department activities as per Quality management system.
• Review & verification of Engineering department standard operating procedures at regular intervals to meet cGMP & Regulatory requirements.
• To carry out FAT/SAT activities as required for newly installed equipment/Systems.
• Installation and Operational qualification activity of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.).
• To ensure the calibration of relevant Engineering Department instruments are performed as per validation requirements and documented as required per cGMP requirements.
• To ensure that all Engineering changes are assessed and implemented as per cGMP and local SOP.

Elusav Recruitment have an excellent opportunity for a Process Engineer to join a leading Global Biopharma company in Waterford.

Reporting to the Team Lead, the Process Engineer will play an integral role within the Product Supply Unit's team, ensuring reliable supply of syringe and vial products to our patients globally.

Responsibilities:

• Provide process engineering support to the Product Supply APU.
• Support delivery of continuous improvement projects to existing equipment.
• Work closely with various departments, such as MSAT, Technical Development, Quality Assurance, and Supply Chain.
• Lead and coordinate elements of an automated inspection project and contribute to process engineering activities related to the development of new and existing manufacturing capacity.
• Utilisation of knowledge gained from existing manufacturing technologies to aid in the development of new technologies with the goal of implementing higher output and yield.
• Ensure safety compliance, providing technical and engineering support for process and equipment failures, identifying, and implementing process and product improvements, supporting qualification of new products/processes, analysing machine performance data, and managing improvement projects within budget and time constraints with a distinct focus on AVI inspection.
• Support new product introductions and capacity expansions, including new vendor selections, maintenance planning, design changes, change controls, OEE improvement, yield improvement, etc.
• Lead systematic technical root cause investigations.
• Support all company safety and quality programs and initiatives.

Requirements:

• Experience in a highly regulated GMP environment.
• Degree in an Engineering discipline.
• Strong documentation/protocol generation and execution skills.
• Automation experience with vision systems is desirable.

Contact:

If you would like to learn more about the vacancy, apply now, or contact Stephen O'Brien on or

Global Biotechnology company, based in south Dublin, Ireland - looking for
Process Engineer Scientist.
The candidate will be responsible for supporting small and large molecule drug product manufacturing at company facilities. As part of our global Process Development organization, they will be key in ensuring the highest standards of process performance, while providing process and product support to inspected drug product operations.

The Job:

• Independently perform design and qualification activities.
• Author and / or reviewer of protocols, reports and technical assessments.
• Supports make-a-batch exercises to determine facility fit and identify gaps in the Visual Inspection process.
• Supports New Product Introduction with visual inspection method development and AVI characterization for new inspection lines.
• Provides expertise on defects identified during batch inspection and supports defect library updates.
• Supports in the development of visual inspection team members by allowing new members to shadow them.
• Support in the characterisation and qualification of AVI vision recipes as part of process improvements.
• Provides support for manufacturing and commercial activities.

Have You:

• Bachelor's degree in Science, Engineering or relevant discipline with 2- 3 year's experience in a similar role OR Master's degree & 2 years of directly related experience.
• Experience in a regulated and or vision related work environment
• 3+ years of drug product process development experience in the pharmaceuticals/biotechnology industry.
• Knowledge of/hands-on experience with end-to-end development for liquid and lyophilized drug products in various presentations.
• Should be interested in working in a team of like-minded inquisitive people who serve the operations team by providing solutions to their inspection needs.
• Independent thinker with demonstrated skills working in teams.
• Strong Interpersonal and communication skills.

The successful candidate must have eligible working VISA in Ireland or European Union (EU) passport.

Berkley Life Science & Engineering is a specialist consultancy, recruiting professionals for organizations throughout Ireland, UK & Europe; for more information go to

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone Aleksas Kremenskas at or send your profile to -

Purpose
New exciting opportunity now exists for a Process Engineer to join the Process Engineering Group on site and report to the Technical Engineering Manager.

Our new team member will serve as technical support for new product introduction (NPI) and commercial manufacturing and will participate and/or lead cross functional or single function teams including liaising with vendors or above site groups. You will typically have prior related work experience; ideally in manufacturing, preferably GMP Setting but we will consider applicants from other working environments as long as they have technology transfer experience.

Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessity for this role.

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

Responsibilities

• Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in line with the standard approval process
• Design/Author/Review/Approve/Execute Execution/development of change controls
• Contribution to Kaizen events as appropriate
• Technical input into quality notification by authoring/reviewing/approving investigations
• Execution of equipment/qualification validation programs; including requalification and re-validation
• Support continuous improvement through Lean Six Sigma methodologies
• Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues
• Serve as technical engineering representative for internal technical group discussions and represent technical Operations Carlow at global technical forums
• Drive 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.
• Accountable for compliance via documentation completion, risk assessments, closing out corrective action, participate in audits and inspections and proactively highlighting any issues around compliance
• May be required to perform other duties as assigned

Qualifications

• Bachelor's Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
• Min 3 years experience ideally in manufacturing, preferably GMP Setting Demonstratable experience of leading technical related projects
• Evidence of continuous professional development is desirable
• Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessity
• Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices
• Report, standards, policy writing skills required
• Equipment and process validation
• Sterile filling processes and equipment
• Proficiency in Microsoft O