Validation Specialist
Anasco, PR, US
Engineering
Bachelors Degree
Full Time, Temporary
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Anasco, PR, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Engineering
Bachelors Degree
First Shift (Day)
Job details
Requirements:
• Fully bilingual (English and Spanish). • Availability to work extended hours in a day and weekends as required. Education and/or experience: • BS in Science or Engineering, preferably Mechanical, Industrial, Electrical, Chemical, or Biomedical. • Hands-on experience with ISO11607 remediation projects, compliance projects, process validation and/or packaging validation projects required. • Experience with managing documents within electronic PLM system. • Experience with working with cross functional team. • Minimum of 5 – 7 years of experience in the medical device and/or pharmaceutical manufacturing environment; with at least five (5) years in manufacturing process, quality or validation engineering position and preferably with exposure to Packaging Validations, Design Control and Product/Process Transfer.
9776677
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