CQV Engineer

Position: CQV Engineer )
Responsibilities   Responsible for providing direct services to site Technical Services management, aiding to increase the throughput of commissioning and qualification activities through the department and across the site.
Will work with Technical Services management but be expected to perform required activities related to validation independently.
This position will support C&Q; activities across the site as directed by site Technical Services management.
Review site commissioning and qualification documentation for accuracy, technical soundness and compliance to both site and regulatory guidelines.
Projects may include new facilities/equipment startup, commissioning, FAT, manufacturing equipment qualification, laboratory equipment qualification and computerized and automation systems including FMS and BMS systems.
Provide support for the development of user requirements and functional specifications.
Support the generation and execution of all commissioning and qualification documentation related to demonstration batches, thermal studies, validation studies for equipment, facilities, utilities, engineering test runs, development studies, software validation and final reports.
Recommendations to management as to the acceptance and release of qualified systems.
Actively participates during all phases of validation projects. Evaluates projects, provides technical information to others.
Review technical and quality system documents such as SOPs, Change Control and Deviation Reports, Batch Production Records, Technical Manuals, P&IDs, construction, as-built, flow diagrams as they relate to validation principles and regulatory compliance issues.
Review various documentation and drawings to ensure any document changes, meet quality and validation requirements and are in full compliance with regulations and standards.
Provide technical assistance during investigations of process/equipment/cleaning/validation issues and aid in the resolution of validation deviations, protocol discrepancies and non-conformances.
Support, investigate and troubleshoot problems and determine possible solutions.
Provide effective solutions for the management of system deviations and non-conformances.
Qualifications   Bachelor's degree in technical field (engineering, biology, chemistry, pharmacy)
Two (2) to five (5) years of applied technical experience within the CQV space of the pharmaceutical, health sciences, or biotech industries.
Hands on commissioning, qualification and validation experience in at least two (2) of the following disciplines is preferred:
Facilities (including design, flow analysis, HVAC), Utilities (including WFI / RO/ purified water, clean steam, clean air, compressed air and gases, process waste systems), major equipment, process / cleaning and equipment validation / qualification or computer software validation.
Firm understanding of cGMP validation requirements / guidelines and current industry practice.
Benefits   Comprehensive benefits package & competitive wages.
A supportive environment where employee growth is promoted.
Paid holidays.
Other great incentives.
Why Pharm Eng Technology?  Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world‑class organizations in North America, Europe, and Asia. At Pharm Eng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors.

It is the growth of our staff that continues to grow our company globally.
EEOC Statement  At Pharm Eng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. Pharm Eng Technology is proud to be an equal chance workplace.

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