Bloomington CQV/CSV Validation Engineers

Verista, Inc.; Bloomington (IN); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Competitive pay

Benefits

Career growth

Team collaboration

Job summary

Verista is seeking a Validation Engineer for the Bloomington, IN area to ensure quality and regulatory compliance in pharmaceutical processes. The role focuses on equipment qualification and process validation to safeguard patient safety and product integrity.

Ideal candidates have 3+ years in validation engineering within pharma/biotech, with hands-on experience in GMP environments and utilities/HVAC considerations.

Qualifications

• 3+ years in validation engineering within pharmaceuticals or biotech.

Skills

Equipment qualification

Delta V

Upstream/Downstream

GMP compliance

CIP/SIP

HVAC

Utilities

Job description

Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Join Our Team: Validation Engineers Wanted in Bloomington, IN!

Are you a skilled Validation Engineer with a passion for ensuring quality in the pharmaceutical industry? Verista is actively seeking talented professionals to join our team in the vibrant Bloomington, IN area!

Who We’re Looking For:

• Experience : 3+ years in validation engineering within pharmaceuticals or biotech.

• Skills : Expertise in equipment qualification, Delta V, Upstream/Downstream process validation, GMP compliance, CIP/SIP, HVAC, or Utilities.

• Location : Based in or willing to relocate to Bloomington, IN.

• Passion : Dedicated to delivering high-quality solutions that ensure patient safety and regulatory compliance.

What We Offer:

• Exciting projects with leading pharmaceutical companies.

• Competitive compensation and benefits based on proven experience.

• Opportunities for professional growth and development.

• A collaborative, innovative work environment in the heart of the Research Triangle.

#PharmaJobs #ValidationEngineer #Bloomington #Hiring #ExpertsDeliveringSolutions

Benefits

Why Choose Verista?

• High growth potential and fast-paced organization with a people-focused culture
• Competitive pay plus performance-based incentive programs
• Company-paid Life, Short-Term, and Long-Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

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For more information about our company, please visit us at Verista.com