Manufacturing Process Engineer

Russell Tobin; Dublin; On-site; EUR 55,000 - 71,000; Full time

Job summary

Russell Tobin is seeking a Manufacturing Projects Scientist Engineer in Dublin for a 12-month contract. The role involves contributing to cross-functional teams across Manufacturing, Engineering, QA, and Regulatory to drive process improvements and new product start-ups.

You're expected to have strong GMP knowledge, be proficient with DeltaV, MES Syncade and SAP, and bring 3–4 years of manufacturing experience, including NPIs, with experience drafting batch records and SOPs.

Qualifications

• Currently completing a Bachelor's/Master’s in science or engineering.
• GMP biologics manufacturing equipment and process automation knowledge.
• Proven ability to support closeout of complex technical investigations.
• Experience with DeltaV, MES Syncade and SAP.
• 3–4 years’ experience in a US or DS manufacturing capacity.
• 3–4 years’ experience with New Product Introductions (NPIs).
• Proficient in writing Paper Batch Records (PBRs) and SOPs.
• Experience with writing MES EBRs is a plus.

Responsibilities

• Contributes to cross functional team (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain, etc.) for process improvement implementations, new product start-ups or other process changes.
• Support new product introduction risk assessments to ensure the appropriate controls are in place to enable manufacturing.
• Support product change over protocols to allow a smooth transition from sustaining to new product manufacturing.
• Represent the Manufacturing at meeting to ensure the end user requirements are represented.
• Supports process technology transfer, and the preparation of manufacturing documentation for development, engineering and PPQ batches.

Skills

GMP Biologics

Process Automation

NPIs

Experience in US/DS manufacturing

Paper Batch Records

SOP Writing

DeltaV

MES Syncade

SAP

Education

Bachelor's or Master's in Science/Engineering

Tools

DeltaV

MES Syncade

SAP

Job description

Manufacturing Projects Scientist Engineer

Join a globally recognised biopharmaceutical organisation known for delivering breakthrough innovations that improve the lives of millions of patients worldwide. With a strong commitment to scientific excellence, cutting-edge research, and patient-focused healthcare solutions, the company offers the opportunity to work on impactful projects within a highly collaborative and inclusive environment. Employees benefit from exposure to world-class technologies, continuous professional development, and the chance to contribute to therapies that shape the future of medicine.

• 12-month contract
• Dublin 15, Ireland
• Monday to Friday: Business Hours

Responsibilities include:

• Contributes to cross functional team (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain, etc.) for process improvement implementations, new product start-ups or other process changes.
• Support new product introduction risk assessments to ensure the appropriate controls are in place to enable manufacturing
• Support product change over protocols to allow a smooth transition from sustaining to new product manufacturing
• Represent the Manufacturing at meeting to ensure the end user requirements are represented
• Supports process technology transfer, and the preparation of manufacturing documentation for development, engineering and PPQ batches.

Qualifications:

• Currently completing a Bachelors/Master’s in science, Engineering, or a related subject.
• In-depth theoretical knowledge of GMP biologics manufacturing equipment and process automation.
• Proven ability to support the closeout of complex technical investigations.
• Strong working knowledge of systems such as Delta V, MES Syncade and SAP.
• 3-4 years’ experience in an US or DS manufacturing capacity.
• 3-4 years’ experience of working on New Product Introductions (NPIs)
• Proficient in writing Paper Batch Records (PBRs) and Standard Operating Procedures (SOPs)
• Experience with writing MES EBRs (This is not a necessity but would be an advantage)

Accommodations

We are committed to providing reasonable accommodations to applicants and employees with disabilities. If you require a reasonable accommodation to participate in the application or interview process, or to perform the essential functions of this role, please contact us.

Russell Tobin is an equal opportunity employer. We do not discriminate on the basis of the race, religious creed, color, national origin, ancestry, physical disability, mental disability, reproductive health decision making, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, sexual orientation, veteran or military status, or any other characteristic protected by applicable federal, state, or local law.

Russell Tobin is a Fair Chance employer. We consider all qualified applicants, including those with criminal histories, in a manner consistent with applicable state and local Fair Chance laws and ordinances, including, the California Fair Chance Act and all applicable local Fair Chance ordinances.