Equipment Specialist
Há 2 dias
The Commissioning, Qualification, and Validation (CQV) Analyst is responsible for ensuring the compliance of equipment and processes within a regulated environment.
- Develop and execute commissioning, qualification, and validation protocols for new and existing equipment and processes.
- Conduct risk assessments and gap analyses to identify areas for improvement in quality and regulatory compliance.
- Perform equipment and process qualifications, including installation, operational, and performance qualifications.
- Review and approve validation documentation, including protocols, reports, and deviations.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards.
- Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related field.
- Fluent in English and Portuguese.
- Minimum of 3 years experience in commissioning, qualification, and validation within the pharmaceutical industry.
- A competitive compensation package.
- Opportunities for professional growth and development.
- A dynamic work environment that fosters collaboration and innovation.
Our ideal candidate will possess a strong understanding of FDA and cGMP regulations, as well as experience with equipment and process validation, including IQ/OQ/PQ, cleaning validation, and process validation. If you are a motivated and experienced professional looking to take your career to the next level, we encourage you to apply.
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Industrial Equipment Specialist
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São Paulo, São Paulo, Brasil beBeeInventory Tempo inteiroJob Title: Equipment Inventory SpecialistKey Responsibilities:">Develop and implement effective inventory management strategies to optimize equipment utilization and minimize losses.Collaborate with cross-functional teams to forecast demand, coordinate logistics, and ensure seamless equipment distribution.Analyze data to identify trends and areas for...
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