Posted 13 days ago
Validation & Quality Engineering SME
@ United Pharma
Toronto, Ontario
Overview
United Pharma is hiring a contract Validation & Quality Engineering SME to rebuild its cleaning validation program and support facility, equipment and engineering remediation. The role requires at least five years each in cleaning validation and in validation or quality engineering, with protocol and report review.
Responsibilities:
- Run gap assessment of cleaning validation program
- Write cleaning validation protocols and reports
- Assess facility and equipment condition
- Define clean-down and release evidence criteria
- Review qualification protocols and reports
Requirements summary:
- 5+ years cleaning validation in pharmaceutical manufacturing
- 5+ years validation or quality engineering
- Knowledge of IQ/OQ/PQ, change control and ICH Q9
- Experience with cross-contamination control in multi-product facilities
Source and dates
Source type not verified · apify-linkedin
- Employer posting date
- 2026-10-28
- First seen by our source
- 2026-11-10
- Source record updated
- 2026-11-10
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Quality assurance |
| Experience | 5+ years |
| Work setting | Plant or factory, Laboratory |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Education | Bachelor’s degree (preferred) |
| Fields of study | Chemical engineering, Mechanical engineering |
Summary and details written by AI from the posting; the employer’s posting is the authority.
United Pharma
| Field | Value |
|---|---|
| Open jobs on Jobsy | 2 |
Role overview
Validation and quality engineering professional who rebuilds the cleaning validation program and supports facility, equipment and engineering remediation. Candidates must meet the minimum experience for both cleaning validation and validation / quality engineering.
Key responsibilities
- Run a gap assessment of the cleaning validation program; define cleanability, worst-case matrix, limits (e.g. HBEL/PDE-based) and swab locations
- Write cleaning validation protocols, support execution and write reports; set up periodic review
- Assess facility and equipment condition; prioritize maintenance work orders by quality risk
- Define clean-down and release evidence and room/equipment readiness criteria
- Integrate corporate engineering remediation actions; support process qualification and change management
- Review qualification protocols and reports for technical and GMP adequacy
Mandatory requirements
- 5+ years in cleaning validation strategy and execution in pharmaceutical manufacturing
- 5+ years in validation or quality engineering, including protocol and report review
- Knowledge of equipment qualification (IQ/OQ/PQ), change control and risk management (ICH Q9)
- Experience with cross-contamination control in multi-product facilities
Plus the common requirements listed on page 1.
Preferred qualifications
- Solid oral dosage multi-product facility experience
- Experience with HBEL/PDE toxicological limit setting
- Engineering degree (chemical, mechanical or similar)
Experience supporting facility remediation after quality events (e.g. foreign matter)
Journal
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