First seen by our source: 25 days ago
CQV engineer - US and Canada
@ Project Delivery Partners
Ontario
Overview
Project Delivery Partners is hiring a junior to senior Commissioning, Qualification & Validation (CQV) Engineer for pharmaceutical and biotech manufacturing projects across the US and Canada. The field-based role covers commissioning, IQ/OQ qualification and validation of utilities, process equipment and automation systems under GMP. The posting states full-time or contract employment with no pay or schedule given.
Responsibilities:
- Prepare, execute and review commissioning and IQ/OQ protocols
- Perform walkdowns, verifications and functional testing
- Develop turnover packages and traceability matrices
- Document and escalate deviations
Requirements summary:
- Bachelor's degree in engineering, life sciences or related field
- 5+ years CQV experience in GMP facilities
- Proficiency with Kneat or similar validation tools
- Ability to read P&IDs and engineering drawings
Tools & skills
Source and dates
Source type not verified · manatal
- Employer posting date
- Not provided
- First seen by our source
- 2026-10-12
- Source record updated
- 2026-10-12
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Mid level |
| Department | Quality assurance |
| Experience | 5+ years |
| Hours per week | 40 (estimated) |
| Travel | air: minimal · ground: moderate |
| Work setting | Plant or factory, Laboratory |
| Position | Sitting and standing |
| Physical demands | physical moderate · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | Engineering, Life Sciences |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Project Delivery Partners
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Now part of the Efor Group | Committed To Excellence
Full company description
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players. Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges. At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs. Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
- LinkedIn followers
- 41,286
- People associated on LinkedIn
- 211
- Reported office locations
- 23 Lesmill Road, Suite 410, Toronto, Ontario M3B 3P6, CA
- 2475 Northwinds Parkway, Suite 200, Alpharetta, Georgia 30009, US
- 2500 Regency Pkwy, Cary, North Carolina 27518, US
- 866 Yuhangtang Road, Hangzhou, CN
- 116c 2F Quang Trung Street, Haoni City, VN
- Ruko Citra Garden 6, Jakarta, ID
- 8/F. Park Sun Building, Hong Kong, HK
- Jland Biz Centre – Menara JCorp, Kuala Lumpur, MY
- 1 Fusionopolis Place, Singapore, 13, SG
- Hua Yin Street Taipei, Taipei, TW
- Monahan Road, Cork, IE
- Av. Diagonal 409, Barcelona, ES
- Av. Eng. Antonio de Goes, 60 Sala 702, Recife, BR
- 1 Tw Alexander Dr, Durham, North Carolina 27703, US
- Business categories
- Information Technology
- Consulting
- Pharmaceutical
- Other recorded names
- Project Delivery Partners
- PharmEng Technology
- Specialties
- Consulting
- Pharmaceuticals
- Biotechnology
- Validation
- Medical Devices
- Engineering
- Regulatory Affairs
- Commissioning & Qualification
- automation
- project management
- quality systems
- training
- thermal mapping
- and Toxicology
- Profile identifies a recruitment agency
- No
- Reported total investment
- 0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. As part of Efor’s global network of 3,000 experts…
| Field | Value |
|---|---|
| Industry | Pharmaceutical Manufacturing |
| Company size | 201-500 employees |
| Headquarters | Toronto, Ontario |
| Organization type | Privately Held |
| Specialties | ConsultingPharmaceuticalsBiotechnologyValidationMedical DevicesEngineeringRegulatory AffairsCommissioning & Qualificationautomationproject management |
| Open jobs on Jobsy | 5 |
| View page |
Job Title: CQV Engineer (Jun - Mid - Senior Level)
Location: North America (Canada and U.S.A)
Industry: Pharmaceutical / Biotech Manufacturing
Employment Type: Full-Time or Contract
Position Summary
We are seeking a jun -, mid- to senior-level Commissioning, Qualification & Validation (CQV) Engineer to support project execution in pharmaceutical and biotech manufacturing facilities. This role is field-based and execution-oriented, focused on delivering commissioning, qualification, and validation activities across multiple systems and equipment.
The ideal candidate will have solid hands-on experience in GMP-regulated environments, with proven expertise in supporting CQV deliverables for utilities, process equipment, and/or manufacturing systems.
Key Responsibilities
- Support the preparation, execution, and review of commissioning, qualification (IQ/OQ), and validation protocols.
- Perform walkdowns, verifications, functional testing, and support equipment/system handover.
- Participate in FAT/SAT, installation verification, punchlist management, and issue resolution.
- Develop turnover packages (TOPs), traceability matrices, and associated documentation.
- Collaborate with QA, Automation, Engineering, and Construction teams to ensure delivery per GMP and project standards.
- Document and escalate deviations, supporting investigation, resolution, and closeout.
- Ensure compliance with cGMP, ASTM E2500, and risk-based CQV methodologies.
Systems in Scope (examples)
- Utilities: Purified water, WFI, clean steam, HVAC, compressed air and gases, CIP/SIP.
- Process Equipment: Bioreactors, filtration systems, chromatography skids, formulation tanks, centrifuges, filling and packaging equipment.
- Support Systems: Automation platforms (DeltaV, SCADA, BMS), cleaning systems, lab or analytical equipment.
Qualifications
- Bachelors degree in Engineering, Life Sciences, or related technical field.
- 5+ years of experience in CQV within GMP-regulated facilities (pharmaceutical or biotech).
- Strong knowledge of utilities, process equipment, or manufacturing systems.
- Proficiency with Kneat or other electronic validation tools.
- Ability to read and interpret P&IDs, engineering drawings, and technical documentation.
- Strong understanding of cGMP requirements, validation practices, and risk-based approaches.
- Excellent communication, organization, and technical writing skills.
- Team-oriented with the ability to work in cross-functional, fast-paced environments.
Preferred Experience
- Participation in greenfield, brownfield, or expansion projects.
- Familiarity with automation and building management systems.
- Experience using commissioning tracking tools or turnover documentation systems.
About Efor Group
Efor Group | The Global Leader in Life Science Compliance Engineering
Founded in 2013, Efor Group is today the world leader in compliance engineering for the Life Sciences industry. We support pharmaceutical, biotech, and medtech companies in securing production compliance and accelerating the market launch of safe and effective drugs, vaccines, and medical devices.
With 3,200 experts across three continents, Efor delivers recognized excellence in quality engineering and regulatory compliance to the worlds largest healthcare players.
Our mission is clear: to remove technical and regulatory barriers so that innovation turns into accessible therapiesfaster, safer, and worldwide.
Ready to transform healthcare with us? Join the journey.
www.efor-group.com
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