cGMP Quality Compliance Validation contract and perm

Edison, NJ, us on site Until 8/21/2026 First posted April 21, 2026 Last posted April 21, 2026
Job description

MEDVACON Life Sciences works with many leading pharmaceutical companies to hire contractors for projects & assignments in cGMP Quality, Compliance, Validation and CSV work.

We have a high number of assignments open for pay on W2 or direct 1099.  We cannot work with agencies on c/c 

There may be flexibility on some assignments for hybrid or remote.

 

 

Participate on cGMP Quality and/or CSV roles in a pharmaceutical or biotech setting.

Apply here and a member of our Talent team will reach you.

 

Prior consulting exp in a cGMP setting in pharma or biotech in Quality, Compliance, Validation and/or CSV.

NO AGENCIES!  Please do not submit candidates.

Please attach a WORD resume to your submission

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

 

 

About this role

Summary

Participate in cGMP quality, compliance, validation, and CSV roles in pharma or biotech.

Job title

cGMP Quality Compliance Validation contract and perm

Experience level

Industry

pharmaceutical

Location requirements

Edison, NJ, US; remote/hybrid possible

Salary

Not specified

Management role

No

Skills & keywords

Required skills

cGMPpharmaceuticalbiotechvalidationCSV

Preferred skills

None specified

Specializations

QualityValidationCSVpharmaceuticalbiotech
Locations

Structured locations inferred from the posting.

Edison, NJ, USA

On-site City
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