Role Summary:

  • Provide leadership and support to operations teams to ensure appropriate standards are met.
  • The chosen candidate will be responsible for the development and implementation of improvement initiatives in all manufacturing and development operation.

Core Duties and Responsibilities:

  • Liaise with external and internal customers, suppliers and agencies to define and improve manufacturing and development operations.
  • Optimisation of manufacturing and development operations
  • Identification & implementation of opportunities for improvements
  • Assist in the implementation of capital projects
  • Act as process lead for inspection development
  • Lead technical problem resolution & RCA for all manufacturing operations, in conjunction with cross functional teams.
  • Implementation and monitoring of performance metrics
  • Lead cycle time reduction initiatives in conjunction with manufacturing teams
  • Implementation of best practice
  • Process development programme design / plant trials, execution and implementation
  • Constantly seeking to challenge operational standards and driving continuous improvement.
  • Ability to multitask and prioritize workload
  • Maintain required quality documents in a current compliant state.
  • Subject Matter Expert for and team resource for new product introductions / enhancement development projects
  • Resource for Clinical supply provision projects
  • Aseptic manufacture or oral dose manufacture context
  • Subject Matter Expert for product quality attributes and process critical parameters
  • Design and execution of experimental programme
  • Operation of process laboratories
  • Scale-up and technology transfer project role
  • Liaison for Clinical supply provision projects
  • Liaison for New formulation and product enhancement programmes
  • Complaints, LCRs, Deviations, CAPAs support ensuring effective RCA Smart CAPA’s and on time closure
  • Attainment of SMART goals.
  • Reduction in process cycle-times.
  • Ensure compliance to cGMP at all times

Minimum Qualifications and Experience:

  • Degree in Chemical, Industrial or equivalent Engineering discipline
  • Advanced degree in Pharmaceutics, Pharmacy or related science discipline considered an advantage
  • Technical knowledge(theory and practice) of aseptic manufacturing including lyophilisation considered an advantage
  • Design of Experiment and associated statistical techniques
  • Pharmaceutical product development project life-cycle
  • Strong report-writing and verbal communication skills
  • Laboratory and pilot plant skills
  • Research skills
  • Innovation and creativity skills
  • Project management skills
  • Structured Problem-solving skills – Statistical

Please note, we do not require agency assistance with this role.


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Role Details:

Job Title: Process Engineers
Location: Waterford
Type: Contract
Date: September, 2026
Image of recruitment specialist

Discuss with:

Sarah Lawlor
sarah_lawlor@prochem.ie
Recruitment Specialist
on 083 830 8107
Share:

Role Details:

Job Title: Process Engineers
Location: Waterford
Type: Contract
Date: September, 2026
Image of recruitment specialist

Discuss with:

Sarah Lawlor

sarah_lawlor@prochem.ie

Recruitment Specialist

on 083 830 8107

Share:

Role Summary:

  • Provide leadership and support to operations teams to ensure appropriate standards are met.
  • The chosen candidate will be responsible for the development and implementation of improvement initiatives in all manufacturing and development operation.

Core Duties and Responsibilities:

  • Liaise with external and internal customers, suppliers and agencies to define and improve manufacturing and development operations.
  • Optimisation of manufacturing and development operations
  • Identification & implementation of opportunities for improvements
  • Assist in the implementation of capital projects
  • Act as process lead for inspection development
  • Lead technical problem resolution & RCA for all manufacturing operations, in conjunction with cross functional teams.
  • Implementation and monitoring of performance metrics
  • Lead cycle time reduction initiatives in conjunction with manufacturing teams
  • Implementation of best practice
  • Process development programme design / plant trials, execution and implementation
  • Constantly seeking to challenge operational standards and driving continuous improvement.
  • Ability to multitask and prioritize workload
  • Maintain required quality documents in a current compliant state.
  • Subject Matter Expert for and team resource for new product introductions / enhancement development projects
  • Resource for Clinical supply provision projects
  • Aseptic manufacture or oral dose manufacture context
  • Subject Matter Expert for product quality attributes and process critical parameters
  • Design and execution of experimental programme
  • Operation of process laboratories
  • Scale-up and technology transfer project role
  • Liaison for Clinical supply provision projects
  • Liaison for New formulation and product enhancement programmes
  • Complaints, LCRs, Deviations, CAPAs support ensuring effective RCA Smart CAPA’s and on time closure
  • Attainment of SMART goals.
  • Reduction in process cycle-times.
  • Ensure compliance to cGMP at all times

Minimum Qualifications and Experience:

  • Degree in Chemical, Industrial or equivalent Engineering discipline
  • Advanced degree in Pharmaceutics, Pharmacy or related science discipline considered an advantage
  • Technical knowledge(theory and practice) of aseptic manufacturing including lyophilisation considered an advantage
  • Design of Experiment and associated statistical techniques
  • Pharmaceutical product development project life-cycle
  • Strong report-writing and verbal communication skills
  • Laboratory and pilot plant skills
  • Research skills
  • Innovation and creativity skills
  • Project management skills
  • Structured Problem-solving skills – Statistical

Please note, we do not require agency assistance with this role.

Image of recruitment specialist

Discuss with:

Sarah Lawlor
sarah_lawlor@prochem.ie
Recruitment Specialist
on 083 830 8107
Share:

Apply Now Mobile

"*" indicates required fields

Full Name*
Accepted file types: pdf, docx, odt, doc, txt, Max. file size: 32 MB.
Accepted file types: pdf, docx, odt, doc, txt, Max. file size: 32 MB.
This field is hidden when viewing the form
This field is hidden when viewing the form
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