C&Q Engineer
- Seeking an experienced Commissioning & Qualification (C&Q) Engineer for a high-profile capital project.
- Responsible for delivering commissioning and qualification activities for pharmaceutical processing equipment.
- 12-month casual contract with strong likelihood of extension.
About the company/role:
- We are seeking an experienced Commissioning & Qualification (C&Q) Engineer to join a high-profile capital project
- This is a critical role within the core C&Q project team, responsible for delivering commissioning and qualification activities for pharmaceutical processing equipment to the highest industry and regulatory standards.
- 12-month casual contract with strong likelihood of extension
- Fulltime, standard business hours
Duties include, but not limited to:
- Plan, coordinate and execute commissioning & qualification (C&Q) activities for GMP pharmaceutical equipment
- Develop and execute qualification protocols including FAT, SAT, DQ, IQ, OQ
- Author and review GxP documentation (URS, traceability matrices, protocols, reports, risk assessments, change controls)
- Translate project requirements into detailed test plans across systems within the facility
- Coordinate schedules, resources, and risks to deliver milestones on time
- Lead C&Q execution within your assigned area and provide technical guidance to stakeholders
- Collaborate cross-functionally with Engineering, Validation, QC, R&D, and Project Delivery teams
- Drive problem-solving activities and continuous improvement initiatives
- Support HS&E risk assessments and ensure compliance with cGMP and regulatory standards
- Provide informal leadership to a team of 4–5 indirect reports during execution phases
Skills/experience required:
- Degree in Engineering or a relevant Science discipline (Chemical, Mechanical, Bioprocess or similar)
- 5 years’ experience in commissioning & qualification within pharmaceutical or GMP environments
- Strong experience qualifying automated process equipment and systems
- Solid understanding of cGMP, validation principles, and risk-based qualification
- Ability to interpret technical drawings and engineering documentation
- Excellent problem-solving, communication, and stakeholder management skills
- Proven ability to manage competing priorities and deliver to tight schedules
- Experience with Kneat, Veeva, or similar validation systems (advantageous)
- Knowledge of Siemens PCS / S88 systems (advantageous)
Apply!
If you think this could be the role for you then please apply now! Please send us a cover letterAND a detailed resume in WORD format (PDFs can be corrupted / not processed).
Or, if you have any questions, please contact Linda on ************.
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