The CQV Engineer performs commissioning, qualification, and validation testing on manufacturing process equipment and instruments; authors protocols, initiates controlled documentation, and provides client support for CQV projects either independently or as part of a larger team. Responsibilities may include generation of documents such as master plans, design qualification, equipment, facility and utility commissioning and development and development of final reports. The position requires extensive interaction with clients to identify CQV needs and work towards solutions that meet schedule, cost, and quality expectations and requirements. CQV Engineers take a proactive role in supporting CQV projects and in providing client support. They build a high level of trust with internal and client personnel. This trust is developed through consistently upholding Encova Values and demonstrating Honesty, Integrity, Pride, Accountability, Teamwork, and Commitment.
Performs commissioning, qualification, and validation testing on utilities and manufacturing process equipment and instruments
Authors protocols, initiates controlled documentation in support of CQV projects
Provides project planning, management, execution, and follow up
Reviews equipment specifications, manuals, and develops an understanding of how instruments work; tests equipment accurately to meet requirements for intended use
Investigates failures and deviations; creates reports
Analyses and reviews spare parts lists to ensure they are fit for purpose
Reviews engineering drawings for accuracy and acts to correct errors
Performs system walk-downs and makes changes using the change control of processes
Initiates and resolves client Corrective and Preventative Actions (CAPAs)
Provides analyses and summary reports
Creates and maintains job plans, maintenance and PMs
Provides team leadership.
Acts as a client representative
Provides CQV guidance and Engineering technical support to CQV Engineers and Specialists.
Provides engineering design and construction support.
Expert understanding and work habits compliant with cGMPs and pharmaceutical and biopharmaceutical unit operations
Good understanding and application of commissioning and qualification and willingness to learn
Good analytical, organizational, time management and problem-solving skills
Exceptional writing skills required to author and execute DQ, FAT, SAT, CTPIQ, OQ, PQ, and PV documents, develop SOPs, create final reports and author validation and quality policies, procedures and guidelines
Be familiar with working in a construction environment and possess thorough understanding and knowledge to apply current industry guidelines and standards
Ability to read, interpret and correct P&IDs
A thorough and working knowledge of and ability to apply GMP, GCP, GLP, GAMP and CFR21 Part 11 guidelines to ensure compliance as they relate to qualification of systems and validation of processes
Proficient with Microsoft Word, Excel, and Project
Profincient with Kneat Validation Lifecycle Management Software
Hands-on experience working in a corporate setting as a productive and supportive member of a project team
Validation experience in the following areas: manufacturing and utility systems, CIP & SIP, autoclave validation, qualification of controlled temperature environments, process validation, cleaning validation, equipment qualification, and use of the Validator 2000 and/or Kaye Digistrip
Engineering experience in the following areas: manufacturing process equipment. Manufacturing support systems and utility systems
Detail oriented with superior skills in planning, organizing, and communicating CQV project tasks across a multidisciplinary team
Ability to provide self-direction and work independently or on a team
Project team leadship experience
Analytical, organizational, time management and problem-solving skills
Communication skills with ability to tailor messages for specific audiences such as director and above, operational and entry levels
Experience & Education Required for Associate CQV Engineer:
BS in Engineering, seven years of relevant project experience and four years of applicable (Commissioning, Qualification, or Validation) experience or the equivalent combination of education and experience. Quality System/Life Science manufacture industry experience is required.
MS in Engineering, seven years of applicable (Commissioning, Qualification, or Validation) experience or the equivalent combination of education and experience. Quality System/Life Science manufacture industry experience is required.
PCI is proud to serve pharmaceutical, biotechnology, medical device, and clinical research industries nationwide by providing calibration, commissioning and consulting solutions. At PCI, calibrations are performed by highly technical, cGMP/GLP-trained personnel who are knowledgeable in quality guidelines enforced by the FDA, EPA and ISO/IEC 17025:2005. PCI is an FCX Performance Company and a Subsidiary of Applied Industrial Technologies (NYSE: AIT); a leading industrial distributor that offers more than 6.5 million parts to serve the needs of MRO and OEM customers in virtually every industry.
Applied® provides engineering, design and systems integration for industrial and fluid power applications, as well as customized mechanical, fabricated rubber and fluid power shop services. Applied also offers storeroom services and inventory management solutions that provide added value to our customers.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, ancestry, gender, sexual orientation, age, disability, protected veteran status, marital status, medical condition or any other characteristic protected by law.