6245 - Solution Prep Principal CQV Engineer / Lead Validation Engineer

Verista, Inc.; Apex (NC); On-site; USD 108,000 - 168,000; Full time

Benefits offered by this job

Competitive pay

Disability Insurance

Medical/Dental/Vision

401(k)

Paid Time Off

Tuition Reimbursement

Team Activities

Job summary

Verista in Apex, NC is seeking a Solution Preparation Principal CQV Engineer to lead commissioning, qualification and validation activities for solution preparation systems in biopharmaceutical manufacturing.

You will author and execute CQV documentation, ensure compliance with cGMP, support equipment startup and FAT/SAT, and collaborate with engineering, automation, QA, and manufacturing to deliver projects on time; onsite work in Apex, NC is required.

Qualifications

• Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or related technical field.
• 10+ years of role-specific experience.
• Experience supporting CQV activities within GMP-regulated pharma/biotech environments.
• Hands-on experience with solution preparation, buffer prep, or media prep systems.
• CQV lifecycle documentation (IQ/OQ/PQ) knowledge.

Responsibilities

• Support CQV activities for solution preparation systems used in biopharmaceutical manufacturing.
• Author, review, and execute CQV lifecycle documentation including IQ/OQ/PQ protocols and reports.
• Ensure validation documentation complies with cGMP regulations and internal quality procedures.
• Participate in system impact assessments, risk assessments, and validation planning activities.
• Coordinate with engineering, automation, quality assurance, and manufacturing teams to align project deliverables.

Skills

CQV lifecycle experience

CQV validation documentation

Cross-functional coordination

Independent work style

10+ years experience

Technical writing

Education

Bachelor's degree in Engineering, Biotechnology, Life Sciences, or related field

Tools

Kneat

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

We are seeking aCQV Engineer with hands‑on experience supporting solution preparation systems within biopharmaceutical manufacturing environments. This role will focus on solution preparation, buffer preparation, and media preparation unit operations, supporting commissioning, qualification, and validation activities to ensure systems are designed, installed, tested, and qualified in compliance with cGMP and regulatory expectations.

The ideal candidate will have strong experience across the CQV lifecycle, including authoring validation documentation, supporting equipment startup and commissioning activities, coordinating vendor testing, and ensuring systems achieve operational readiness. Experience working within digital validation platforms such as Kneat is highly desirable.

This position requires an individual who can work independently while collaborating cross‑functionally with engineering, automation, vendors, and quality teams to ensure successful project execution.

Solution Preparation Principal CQV Engineer Responsibilities:

Commissioning, Qualification & Validation

• Support commissioning, qualification, and validation (CQV) activities for solution preparation systems used in biopharmaceutical manufacturing.

• Author, review, and execute CQV lifecycle documentation including:

• Ensure validation documentation complies with cGMP regulations and internal quality procedures.

• Participate in system impact assessments, risk assessments, and validation planning activities.

Solution Preparation Process Support

• Provide technical support for solution preparation unit operations, including systems such as:

• Support equipment startup and operational readiness for solution preparation processes.

• Assist with troubleshooting and process verification during commissioning and qualification activities.

Vendor & Equipment Startup

• Support Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) for new equipment.

• Coordinate with equipment vendors and system integrators to ensure systems are installed and functioning according to design specifications.

• Participate in equipment startup, commissioning, and operational testing activities.

Cross-Functional Coordination

• Collaborate with engineering, automation, quality assurance, and manufacturing teams to align project deliverables.

• Assist with deviation investigations, change control processes, and documentation updates.

• Ensure CQV activities align with project schedules and operational readiness milestones.

Digital Validation Systems

• Utilize electronic validation platforms (e.g., Kneat) to develop, manage, and execute validation documentation.

• Maintain data integrity, traceability, and compliance within digital validation systems.

Requirements:

• Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or related technical field

• 10+ years of role specific experience

• Experience supporting CQV activities within GMP-regulated pharmaceutical or biotechnology environments

• Hands‑on experience with solution preparation, buffer prep, or media prep systems

• Strong understanding of CQV lifecycle documentation (IQ/OQ/PQ protocols and reports)

• Ability to work independently while coordinating with cross-functional teams

• Strong technical documentation and communication skills

• Experience using digital validation platforms such as Kneat

• Experience supporting FAT/SAT, commissioning, and equipment startup

• Familiarity with single-use systems and biologics manufacturing processes

• Experience working within biologics or cell culture manufacturing facilities

• Onsite job requirement in Apex, NC

_ For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. _

*Verista is an equal opportunity employer.

National (US) Range

$107,800—$168,011 USD

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