MEDVACON Life Sciences is a consulting and talent placement firm specializing in ensuring the safety of the drug and device supply chain.  We design and implement Quality Systems for our clients to ensure the safe manufacture, holding and distribution of drug products.  Our core services include cGMP Quality, Compliance, Regulatory & Validation Services. 

The pharmaceutical industry moves quickly ...and we're always interested to meet professionals with a solid background in the drug/device, FDA regulated setting. 

Our Talent team is always working a high volume of consulting and perm needs for our clients.  If you're open to something new now or in the future - we can help! 

APPLY here and a member of the Talent team will reach qualified candidates to explore job opportunities.

We look forward to working together!

Bachelor's Degree 

5+ in pharma/biopharma or medical device industry

5+ in an FDA, regulated setting

Solid knowledge in one or more of the following:

• GMP Validation
• CSV/Data Integrity
• Program/Project Management
• Regulatory Compliance
• Audit/Inspection Readiness
• CAPA/Remediation
• QMS
• IT Quality Management
• Process Improvement
• Quality Systems Implementation
• Risk Management 
• Medical Device
• Manufacturing Process
• QA Positions

The ability to travel for consulting assignments

US work authorization

Willing to complete a background check

Work on W2 or 1099 

Please attach a WORD resume to your submission

All of your information will be kept confidential according to EEO guidelines.