CQV/CSV Validation Engineer: Grow in Pharma Quality

Veristainc; Bloomington (IN); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Competitive pay plus performance-based incentives

Medical, Dental & Vision insurances

401(k) Retirement Plan with Employer Matching

Paid Time Off and Holidays

Tuition Reimbursement

Job summary

Verista, located in Bloomington, IN, is looking for experienced Validation Engineers to join our team. Candidates should have over 3 years of experience in validation engineering within the pharmaceutical industry. The role requires expertise in areas like equipment qualification, GMP compliance, and process validation.

The position offers competitive pay, numerous benefits, and opportunities for professional growth. Join us in delivering quality solutions that ensure patient safety and regulatory compliance in a dynamic work environment.

Qualifications

• 3+ years in validation engineering within pharmaceuticals or biotech.
• Expertise in equipment qualification, Delta V, GMP compliance, CIP/SIP.
• Passion for ensuring quality solutions in the pharmaceutical industry.

Responsibilities

• Ensure quality in pharmaceutical projects.
• Collaborate with teams to implement validation processes.
• Deliver high-quality solutions ensuring patient safety.

Skills

Equipment qualification

Delta V

Upstream/Downstream process validation

GMP compliance

CIP/SIP

HVAC

Utilities

Job description

Verista, located in Bloomington, IN, is looking for experienced Validation Engineers to join our team. Candidates should have over 3 years of experience in validation engineering within the pharmaceutical industry. The role requires expertise in areas like equipment qualification, GMP compliance, and process validation.

The position offers competitive pay, numerous benefits, and opportunities for professional growth. Join us in delivering quality solutions that ensure patient safety and regulatory compliance in a dynamic work environment.