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* Collaborate with QA, IT and engineering teams to
ensure compliance with regulatory standards (FDA,
EMA, MHRA, etc).
* Support audits and inspection by preparing
validation deliverables.
* Perform periodic reviews and risk assessments on validated systems.
* Participate in change control processess and
deviation investigations related to computerized
systems.
Requirements:
* Bachelor's degree in Engineering, Life sciences,
Computer science
* 2-3 years of experience in CSV, preferably in a
GMP- regulaed industry (pharma, biotech,
med devices).
* Strong communication, analytical and organizational skills.
Job Type: Full-time
Pay: $4,000.00 - $6,500.00 per month
Schedule:
- Monday to Friday
Work Location: In person