Rx Group
Direct message the job poster from Rx Group
Founder at Rx Group
Helping biotech’s bring safer medicines to patients, by finding them the best quality assurance talent. Engagement:
Contract (6–12+ months)
Start:
February 2026 onwards
Pay:
Market rates (all-in hourly)
Rx Group is supporting a major greenfield manufacturing build and we're expanding the CQV team significantly from early next year. We're looking for CQV Engineers at a range of levels to support qualification and validation activities across a new Oral Solid Dose (OSD) facility, associated labs, utilities and computer systems.
This is a long-term, high-impact project covering full CQV lifecycle activities on a large, newly constructed campus. Most work can be done remotely, with periodic on-site time as the project moves through IQ/OQ/PQ execution.
Key Responsibilities
Develop and execute CQV documentation (IQ/OQ/PQ) for:
OSD process equipment
Analytical and QC lab instruments (HPLCs are a plus)
Facility systems and clean utilities (water systems, HVAC, EMPQ)
Computer systems / IT / OT systems
Support classifications, assessments, protocol generation and reporting
Execute validation activities on-site as required
Work according to the Project Validation Master Plan and site procedures
Collaborate with senior SMEs across equipment, facilities and CSV workstreams
Experience Required We’re looking for a mix of profiles and levels, including strong juniors through to experienced engineers.
Experience in CQV, Validation or Engineering within pharma/biotech
Hands‑on experience with IQ/OQ/PQ authoring and execution
Strong documentation skills and familiarity with GMP expectations
Ability to travel for on-site work when needed
Nice to Have
Utilities CQV (HVAC, PW/WFI, EMPQ)
CSV / IT/OT validation
Greenfield or large capital project experience
How to Apply If you have CQV or validation experience and are available from February 2026 onwards, feel free to apply with your resume, location, availability and your all‑in hourly rate.
Seniority Level Mid‑Senior level
Employment Type Contract
Job Function Quality Assurance, Engineering, and Manufacturing
Industries Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Founder at Rx Group
Helping biotech’s bring safer medicines to patients, by finding them the best quality assurance talent. Engagement:
Contract (6–12+ months)
Start:
February 2026 onwards
Pay:
Market rates (all-in hourly)
Rx Group is supporting a major greenfield manufacturing build and we're expanding the CQV team significantly from early next year. We're looking for CQV Engineers at a range of levels to support qualification and validation activities across a new Oral Solid Dose (OSD) facility, associated labs, utilities and computer systems.
This is a long-term, high-impact project covering full CQV lifecycle activities on a large, newly constructed campus. Most work can be done remotely, with periodic on-site time as the project moves through IQ/OQ/PQ execution.
Key Responsibilities
Develop and execute CQV documentation (IQ/OQ/PQ) for:
OSD process equipment
Analytical and QC lab instruments (HPLCs are a plus)
Facility systems and clean utilities (water systems, HVAC, EMPQ)
Computer systems / IT / OT systems
Support classifications, assessments, protocol generation and reporting
Execute validation activities on-site as required
Work according to the Project Validation Master Plan and site procedures
Collaborate with senior SMEs across equipment, facilities and CSV workstreams
Experience Required We’re looking for a mix of profiles and levels, including strong juniors through to experienced engineers.
Experience in CQV, Validation or Engineering within pharma/biotech
Hands‑on experience with IQ/OQ/PQ authoring and execution
Strong documentation skills and familiarity with GMP expectations
Ability to travel for on-site work when needed
Nice to Have
Utilities CQV (HVAC, PW/WFI, EMPQ)
CSV / IT/OT validation
Greenfield or large capital project experience
How to Apply If you have CQV or validation experience and are available from February 2026 onwards, feel free to apply with your resume, location, availability and your all‑in hourly rate.
Seniority Level Mid‑Senior level
Employment Type Contract
Job Function Quality Assurance, Engineering, and Manufacturing
Industries Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr