- Location: Adelaide
- Salary: AUD 0 per year
1st of May - 14th of May / 12 Hour days
South Australia - Open to Australian based candidates
$60/h + Super + Penalties
$100 a night meal allowance + motel accomodation
IRIS inspection of heat exchangers during plant outage.
Will be along side experienced technical leads for day / night shifts
08 6280 2417
- SalaryMarket related
Asset Integrity Engineer$1000/day + Super8 hour days Monday - Friday - Perth BasedWorking for an Oil & Gas operatorInitial 12 Month ContractFebruary StartMechanical or Corrosion Materials Engineering backgroundRBIFFSNDTCSWIPNACE
- SalaryMarket related
We are seeking an experienced Clean Room Supervisor to join our pharmaceutical team in Denmark. The ideal candidate will have a strong background in clean room operations, quality control, and a deep understanding of pharmaceutical manufacturing processes. This position offers the opportunity to work in a state-of-the-art facility and be part of a dynamic team dedicated to producing high-quality pharmaceutical products.Responsibilities: Supervise and lead a team of clean room technicians in the pharmaceutical manufacturing process.Ensure compliance with all regulatory requirements and quality standards within the clean room environment.Oversee the daily operations of clean rooms, including monitoring cleanliness, equipment maintenance, and adherence to safety protocols.Collaborate with cross-functional teams to optimize production processes and achieve production goals.Conduct training and performance evaluations for clean room staff, providing mentorship and guidance.Implement and maintain clean room protocols, including aseptic techniques and gowning procedures.Troubleshoot any issues that may arise within the clean room and implement corrective actions.Keep up-to-date with industry trends and regulatory changes to ensure compliance and best practices. Qualifications: Bachelor's degree in a relevant field (e.g., pharmaceutical sciences, microbiology, or related).Proven experience in clean room operations, ideally within the pharmaceutical sector.Strong understanding of GMP (Good Manufacturing Practices) and regulatory requirements.Excellent leadership and communication skills.Detail-oriented with a focus on quality and safety.Ability to adapt to changing priorities and work in a fast-paced environment.Openness to relocating and living in Denmark.