CQV / CSV Specialist

Pinnaql; Greenville (NC); On-site; USD 60,000 - 90,000; Full time

Job summary

A trusted consulting firm is seeking an experienced CQV / CSV Specialist to focus on Automation and Manufacturing Systems at their client site in Greenville, North Carolina. In this role, you will lead Computer System Validation tasks and support FDA-regulated manufacturing operations. Candidates must have a Bachelor’s degree and at least 5 years' experience in CSV and automation validation. This is a 4-month contract with potential for extension.

Qualifications

• Minimum 5 years of experience in CSV, automation validation, and CQV within FDA-regulated environments.
• Hands-on experience with PLC-controlled systems and SCADA systems.
• Experience supporting complex manufacturing systems, including robotic lines.

Responsibilities

• Lead and execute Computer System Validation (CSV) and automation-related qualification activities.
• Assess and document changes to manufacturing lines and automated systems.
• Perform automation validation and support qualification activities for laboratory systems.

Skills

Automation validation

Computer System Validation (CSV)

Strong technical writing skills

Risk assessment

Collaboration with engineering teams

Education

Bachelor’s degree in engineering, computer science, life sciences

Tools

PLC-controlled systems

SCADA systems

Cleanroom Building Management Systems (BMS)

Job description

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness.

We are seeking an experienced and technically strong CQV / CSV Specialist with a primary focus on Automation and Manufacturing Systems to support FDA‑regulated manufacturing operations at a client site in Greenville, North Carolina. This is a 4 month contract position with strong possibility to extend.

POSITION OVERVIEW

This role is CSV and automation‑focused, working directly with the client’s automation and manufacturing systems teams. The individual will be responsible for assessing, validating, and qualifying changes to previously qualified automated manufacturing lines and systems within an FDA‑regulated environment.

Manufacturing lines include:

• Liquid and lyophilized vial lines with RABS technologies
• Fully isolated syringe and vial combination lines
• Highly automated and robotic manufacturing systems

In addition to automation and manufacturing systems, the role may also provide CQV support for laboratory systems when needed.

KEY RESPONSIBILITIES

• Lead and execute Computer System Validation (CSV) and automation‑related qualification activities for manufacturing systems.
• Assess, document, and qualify changes to previously qualified manufacturing lines, equipment, and automated systems.
• Support and validate PLC changes, SCADA changes, and automation system modifications.
• Perform automation validation, including understanding and assessing PLC logic and programming.
• Collaborate closely with automation, engineering, and manufacturing teams.
• Support qualification and validation of:
• Automated manufacturing process equipment
• Cleanroom Building Management Systems (BMS)
• Clean utilities and related control systems
• Select IT‑related systems, as applicable
• Author, execute, and review validation documentation (IQ, OQ, PQ, CSV deliverables) in compliance with cGMP, FDA, EMA, and site requirements.
• Perform risk assessments, discrepancy resolution, deviation investigations, and support change control and CAPA activities.
• Provide clear project status updates and support timely release of systems for manufacturing use.
• Support laboratory systems CQV activities as needed.

QUALIFICATIONS

• Bachelor’s degree in engineering, computer science, life sciences, or a related technical discipline.
• Minimum 5 years of experience in CSV, automation validation, and CQV within pharmaceutical, biotech, or other FDA‑regulated environments.
• Hands‑on experience with:
• PLC‑controlled systems
• SCADA systems
• Automation change management and validation
• Strong understanding of:
• Automated manufacturing process equipment
• CSV principles and lifecycle documentation
• cGMP, 21 CFR Part 11, EU Annex 11, data integrity requirements
• Experience supporting complex manufacturing systems, including robotic or highly automated lines.
• Experience with aseptic manufacturing operations (filling, lyophilization, isolators, RABS).
• Strong technical writing, organizational, and communication skills.
• Ability to work independently in a fast‑paced, on‑site manufacturing environment.
• Candidates must be authorized to work for any employer in the United States without visa sponsorship.

At Pinnaql, people always come first. We believe that when you’re empowered to do your best work, bold ideas thrive and real progress happens. This isn’t just a job — it’s an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose‑driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Pinnaql is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, gender identity, gender identity, sexual orientation, gender identity.