CSV/DI Computer Systems Validation & Data Integrity [Pharma/Med Device]
Job Description
Company Description MEDVACON specializes in ensuring the safety of the drug and device supply chain in the Pharmaceutical, Biotechnology and Medical Device industries.
Our Life Sciences consultants design and implement Quality Systems to ensure the safe manufacture, holding and distribution of drug products. From concept development through design, installation, start-up, commissioning, qualification and validation, MEDVACON offers single-source responsibility and acts as a point of contact to drive and deliver project-specific needs. From Implementation of Quality Systems Process and Procedures to full-service Commissioning & Qualification to Validation and Compliance consulting services to Engineering, MEDVACON delivers the highest level of quality.
Job Description If you're interested in Pharma, Med Device or Biotech Consulting and your background aligns with CSV IN AN FDA REGULATED SETTING, PLEASE APPLY.
Qualifications Bachelor's Degree in Life Sciences
5+ years experience in CSV life-cycle activites in a related cGMP setting
Additional Information Please attach a WORD resume to your on-line application.
These are contract assignments
1099 OR W2.
Benefits are not offered for consulting positions.
All your information will be kept confidential according to EEO guidelines.