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92,000+ live jobsValidation and Qualification Technician
On-site in León·Full-time·Added 24 days ago (last checked 30 Oct)
Our summary
- Work mode
- On-site, León
- Contract
- Fixed-term, full-time hours
- English
- Required
- Education
- University degree
Visa options
The ad doesn’t mention sponsorship
Not a refusal, but not a yes. Worth asking in your first message.
Skills
This job advert was originally written in Spanish.
Pay & benefits
What you'll get
1 Permanent contract + 1 Replacement contract
Full-time and flexibility options.
Competitive salary, according to the sector agreement.
Continuous training and internal capacity building.
The role
Participate in equipment qualification and process validation according to GMP regulations, performing the following functions:
What you'll do
- Execute and monitor validation master plans.
- Design and implement qualification and validation procedures and protocols.
- Execute validations and qualifications in all their phases: design, installation, operational, and process qualification.
- Participate in the design and preparation of the technical qualification report.
- Preparation of risk analyses.
- Elaborate Standard Operating Procedures.
- Provide support during audits and inspections.
- Any others assigned to them based on their category due to Department needs.
Requirements
Result orientation, proactivity, and teamwork.
Knowledge of GMP regulations, knowledge in quality and risk analysis, as well as qualification and validation techniques and methods.
University degree related to Health Sciences, Chemical Engineering, or similar.
Medium - high level of English.
Demonstrable one year of experience in a similar position within the pharmaceutical industry.
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