Biotech Consultants in EQ, Cleaning, Quality or Process Validation
Vacancy expired!
Job Description
MEDVACON Life Sciences is a Single Source, Life Sciences/drug & device consulting firm specializing in cGMP Quality, Compliance and Regulatory Services, Talent Acquisition, temp-hire & FT, and Emerging Markets Compliance & Training
We're working with a major Biotech company in San Diego on an Equipment Process Validation project due to start in August/Septand will be approx 6 months. There are no travel expenses included for this project so local consultants preferred
If you're interested, please apply here. If your background aligns with the requirements, a member of Talent Acquisition will reach out to discuss the project details.
EOE/Veteran/Disabled
Qualifications
Bachelor's Degree. Life Sciences field preferred.
5+ years in a BIOTECH setting with hands-on in one or more of the following:
Biotech equipment qualification/validation
Cleaning Validation
General cGMP Quality events
Biotech Process Validation
The following are a
Purification and Fermentation
Chromatography skids
Thin films
Small molecule
mRNA
Additional Information
NO! Agencies or 3rd part C/C. W2 or 1099/C-C directly with a consultant only Please attach a WORD resume to your on-line application. This work would start in Aug/Sept 2020 This is a consulting role NOT an FTE The work is ON-SITE, long term No benefits are available for this assignment. All your information will be kept confidential according to EEO guidelines.