cGMP Quality Compliance Validation contract and perm

MEDVACON; Edison (NJ); Hybrid; USD 70,000 - 100,000; Full time

Job summary

MEDVACON in Edison, New Jersey is seeking contractors for cGMP Quality Compliance Validation roles in a pharmaceutical setting. The company collaborates with leading pharmaceutical firms and offers positions available for W2 or direct 1099.

Candidates with prior consulting experience in cGMP environments focused on Quality, Compliance, Validation, and CSV are encouraged to apply. Flexibility for hybrid or remote work may be available.

Qualifications

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

Responsibilities

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

Skills

cGMP Quality

Compliance

Validation

CSV

Consulting Experience

Job description

cGMP Quality Compliance Validation contract and perm

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.

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.