The Validation Engineer/ Specialist will be responsible of all validation activities for the assigned project. This project include the validation of multiple autoclaves and Temperature controllers. Validation Scope may include: Validation Life Cycle Execution Technical Documentation Process GAP Analysis Risk Assessment C&Q activities among others.
Qualifications :
- Bachelor degree in Engineering or Science
- 5 to 10 years of experience required in the medical device biotechnology or pharmaceutical industry (liquid dosage a PLUS).
- MUST have experience validating autoclaves
- Experience with Validation Life Cycle (Process Packaging and Cleaning).
- Experience and knowledge in regulations including GMP.
- Experience developing and conducting efficient processes to meet production demands.
- Excellent technical writing and verbal communication skills are required.
- Excellent detail oriented individual who can identify milestones.
- Great interpersonal and communications skills.
- Able to interact with all areas and clients.
- Proficiency utilizing MS Office Suite (Word Excel and PowerPoint) is required.
- Available to work extended hours holidays if require.
- Must be available to travel and work non-standard shifts if necessary.
- Only candidates who qualifies with all requirements will be evaluate.
- Bilingual (Spanish & English) a plus but not necessary.
Additional Information :
Validation and Engineering Group USA Inc. is an Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
The Validation Engineer/ Specialist will be responsible of all validation activities for the assigned project. This project include the validation of multiple autoclaves and Temperature controllers. Validation Scope may include: Validation Life Cycle Execution Technical Documentation Process GAP An...
The Validation Engineer/ Specialist will be responsible of all validation activities for the assigned project. This project include the validation of multiple autoclaves and Temperature controllers. Validation Scope may include: Validation Life Cycle Execution Technical Documentation Process GAP Analysis Risk Assessment C&Q activities among others.
Qualifications :
- Bachelor degree in Engineering or Science
- 5 to 10 years of experience required in the medical device biotechnology or pharmaceutical industry (liquid dosage a PLUS).
- MUST have experience validating autoclaves
- Experience with Validation Life Cycle (Process Packaging and Cleaning).
- Experience and knowledge in regulations including GMP.
- Experience developing and conducting efficient processes to meet production demands.
- Excellent technical writing and verbal communication skills are required.
- Excellent detail oriented individual who can identify milestones.
- Great interpersonal and communications skills.
- Able to interact with all areas and clients.
- Proficiency utilizing MS Office Suite (Word Excel and PowerPoint) is required.
- Available to work extended hours holidays if require.
- Must be available to travel and work non-standard shifts if necessary.
- Only candidates who qualifies with all requirements will be evaluate.
- Bilingual (Spanish & English) a plus but not necessary.
Additional Information :
Validation and Engineering Group USA Inc. is an Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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