CGMP Equipment Qualification & Process Validation - Biotech

CGMP Equipment Qualification & Process Validation - Biotech

Vacancy expired!

Job Description

MEDVACON Life Sciences is working with a

major Biotech company in San Diego on an Equipment Process Validation project.

The project is due to start in August 2020 and will be approx 6 months. There are no travel expenses included for this project.

This is Biotech Equipment Qualification involving:

• Process Consulting
• Equipment Qualification protocol writing and executing

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.

REQUIREMENTS:

Bachelor's Degree. Life Sciences field preferred.

5+ years in a BIOTECH setting

5+ years hands-on experience with biotech equipment qualification OR process flow

The following are a

• Purification and Fermentation
• Chromatography skids
• This films
• Small molecule
• mRNA

EOE/Veteran/Disabled

Qualifications

REQUIREMENTS:

Bachelor's Degree. Life Sciences field preferred.
5+ years in a drug or device setting
5+ years hands-on experience working on biotech process validation


EOE/Veteran/Disabled

Additional Information

Please attach a WORD resume to your on-line application.

This is a consulting role NOT an FTE

The work is ON-SITE starting mid to late August

No benefits are available for this assignment.

W2 or 1099

directly with a consultant only

NO! Agencies or 3rd part C/C. Please do not submit your candidates.

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