CQV Consultant

As a Commissioning Qualification Validation Engineer (CQV), you will play a pivotal role in ensuring the successful commissioning, qualification, and validation of critical systems.

Your expertise will be integral in qualifying systems such as Autoclaves, Glassware Washers, Clean Compressed Air, Clean Steam, Clean-in-Place (CIP), Water for Injection (WFI), Heating, Ventilation, and Air Conditioning (HVAC), and Plant Steam systems.

In addition to Facility and Manufacturing equipment, a background in qualifying and validating Lab Equipment is essential for a CQV Engineer.

Commissioning : Lead or support commissioning activities for cleanroom systems and

equipment, ensuring proper installation and functionality according to design

specifications.

Qualification and Validation : Develop and execute qualification and validation

protocols for QC Lab Equipment (examples are HPLC, CTUs, Balances, BacT Alert,

ViCell Blu), cleanroom systems including autoclaves, glassware washers, and clean

utilities such as compressed air, steam, and water systems.

Documentation and Reporting : Maintain comprehensive documentation of

commissioning, qualification, and validation activities. Generate protocols, execute tests,

and prepare final reports ensuring compliance with regulatory requirements and company

standards.

Troubleshooting and Optimization : Identify and resolve technical issues during

commissioning and validation activities. Optimize system performance through

troubleshooting, root cause analysis, and process improvements.

Compliance Assurance : Ensure all commissioning and validation activities adhere to

regulatory requirements such as FDA, cGMP, and ISO standards. Stay abreast of

regulatory updates and industry best practices to maintain compliance.

Requirements

Bachelor’s degree in Engineering, Life Sciences, or related field. Advanced degree

preferred.

Proven experience in commissioning, qualification, and validation of QC Lab Equipment,

cleanroom systems and equipment, in a biopharmaceutical or biotechnology

environment.

Strong understanding of regulatory requirements and guidelines including FDA, cGMP,

ALCOA+, and ISO standards.

Proficiency in developing and executing validation protocols, and protocols and

documenting validation activities in a regulated environment and creating

final protocol packages and final reports.

Required technical expertise in QC Lab environments, cleanroom systems including

autoclaves, glassware washers, clean utilities (compressed air, steam, water), HVAC, and

steam systems.

• Analytical mindset with excellent problem-solving skills and attention to detail.
• Effective communication and interpersonal skills, with the ability to collaborate across

Benefits

• Health Care Plan (Medical, Dental & Vision)
• Retirement Plan (401k, IRA)
• Life Insurance (Basic, Voluntary & AD&D)
• Paid Time Off (Vacation, Sick & Public Holidays)

Azzur Group is an equal opportunity employer and promotes a diverse culture in our workplace. We believe that promoting diversity plays an important role in developing top-quality talent, fostering greater innovation and creativity, and enhancing our relationships with customers and the communities in which we operate.

All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.