Publié il y a 13 jours
Shop-Floor QA SME
@ United Pharma
Toronto, Ontario
SIGNAUX
Résumé des exigences :
- Mandatory requirements
- Experience with batch record review, line clearance and in-process QA checks
- Strong working knowledge of good documentation practice and data integrity on the floor
- Plus the common requirements listed on page 1.
- Preferred qualifications
- Solid oral dosage (tableting, encapsulation, coating) and/or packaging experience
Source et dates
Type de source non vérifié · apify-linkedin
- Date publiée par l’employeur
- 2026-10-28
- Première détection par notre source
- 2026-11-11
- Mise à jour du dossier source
- 2026-11-11
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
United Pharma
| Champ | Valeur |
|---|---|
| Offres sur Jobsy | 3 |
Description
Role overview
Embedded QA professional providing routine quality presence on the manufacturing and packaging floor. Strengthens real-time oversight, cGMP behaviors and batch documentation quality during the remediation program.
Key responsibilities
- Provide daily QA presence on manufacturing and packaging lines
- Verify clean equipment and room status; oversee line clearance and batch start-up
- Support batch record review and correct documentation issues at source
- Coach operators on cGMP behaviors and good documentation practice (ALCOA+)
- Identify, escalate and trend floor-level events; support human-error reduction actions
- Contribute to cleaning and line-clearance procedure updates and floor-level training
Mandatory requirements
- 5+ years of GMP manufacturing QA with direct shop-floor support
- Experience with batch record review, line clearance and in-process QA checks
- Strong working knowledge of good documentation practice and data integrity on the floor
- Able to work on-site full time, including flexible shift coverage when approved
Plus the common requirements listed on page 1.
Preferred qualifications
- Solid oral dosage (tableting, encapsulation, coating) and/or packaging experience
- Experience in sites under regulatory remediation
- Experience with electronic batch records and MES
Journal
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