Pharmaceutical Validation Engineer

Evolve Scientific · Carole Park QLD 4300 · Casual/Holiday
Posted 58d ago

Pharmaceutical Validation Engineer

Evolve Scientific
Carole Park QLD 4300

·

Casual/Holiday

~$99k - $119k pro rata(Estimated)
$50 - $60 per hour
KEY POINTS WE FOUND
  • Join a leading pharmaceutical manufacturing company as a Validation Engineer.
  • Support validation and qualification activities in a GMP-regulated environment.
  • Develop and execute validation documentation and provide technical support.

About the Role
Our client, a leading pharmaceutical manufacturing company based in Brisbane's western suburbs, is seeking an experienced Validation Engineer to join their team on a casual ongoing basis for 6-12 months, working Monday to Friday, 38 hours per week.

This role will support validation and qualification activities across maintenance/Engineering, Production and Packaging, providing technical expertise for equipment, facilities and systems within a GMP-regulated manufacturing environment.

Please note: Applicants will be required to successfully complete a medical assessment, drug screening and police check.

Key Responsibilities

  • Execute equipment, facility and system validation and qualification activities.
  • Develop and execute validation documentation, including URS, FS, Risk Assessments, IQ, OQ, PQ and validation reports.
  • Support new equipment/system installations, upgrades and lifecycle management.
  • Provide technical support for equipment changes and risk-based change management.
  • Investigate and report deviations and support Continuous Improvement initiatives.
  • Ensure activities comply with GMP/cGMP, company procedures and health and safety requirements.

Skills & Experience
The successful candidate will have:

  • A Bachelor's degree in Engineering, Science or a related discipline.
  • Hands-on experience with equipment, facility and/or system validation and qualification.
  • Experience with validation lifecycle documentation such as URS, FS, DS, IQ, OQ, PQ and Traceability Matrices.
  • Experience working in a GMP manufacturing or highly regulated environment.
  • Understanding of risk-based change management/change control.
  • Strong technical writing, communication and organisational skills.
  • Experience in Manufacturing and working with Project Management Systems.

Apply Now
If you think this could be the role for you, please apply now with a cover letter and detailed resume in Word format.
For further information, please contact Simon Taylor at ************************************.

With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

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Skills

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Change managementEquipment validationGmpGmp environmentProject management systemsQualification activitiesTechnical documentationTechnical writingTradingValidation

Evolve Scientific