cGMP Quality & Validation Specialist (Contract/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

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.