5953 - Senior CQV Engineer / Senior Validation Engineer

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

Senior CQV Engineer Responsibilities:

• Draft protocol templates, media fill summaries, and standardized reports
• Populate bracketing documentation tables and support protocol generation
• Maintain central trackers for protocol reviews, approvals, and interventions
• Coordinate feedback cycles across site/global stakeholders and update documents accordingly
• Provide day-to-day execution support to ensure delivery remains on schedule
• Support documentation drafting and onsite coordination cross-functionally with Validation and QA leads

Requirements:

• Bachelors Degree in an industry-related field
• Minimum 5 years industry experience, including direct experience with Media Fill Validation
• Demonstrated experience in Commissioning & Validation activities
• Demonstrated experience authoring and executing protocols, drafting media fill summaries and standardized reports
• Experience in a pharmaceutical / FDA-regulated manufacturing environment
• Working knowledge of cGMP and facility/equipment validation requirements
• Ability to write clearly, concisely, and persuasively in a professional environment
• Demonstrated ability to interact effectively with all levels of the organization
• Ability to work as part of a cross-functional team
• Strong problem-solving, critical thinking skills, and attention to detail
• Ability to work on-site, full-time, in Greenville, NC

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