8 meilleures offres (quality lab, whitby, on) (à pourvoir)

Quality Assurance Associate
TJP Labs Inc. —Pickering, ON
- De 23 $ à 25 $ de l’heure
- Fins de semaine au besoin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Office
- Assurance Dentaire
- Assurance Vision
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RPN - Clinical Data Quality Analyst
Power Staffing Solutions —Courtice, ON
- À partir de 35 $ de l’heure
- Temps partiel
- Soins infirmiers
- Signes vitaux
- Analyse de données
Postuler rapidement
il y a 1 jour
Quality Lab Technician
ProAmpac —Whitby, ON
- 21,52 $ de l’heure
- Expérience en laboratoire
- Amélioration continue
- Contrôle de la qualité
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il y a 1 jour
Quality Analyst/Coordinator
ProAmpac —Whitby, ON
- De 60 000 $ à 65 000 $ par an
- Microsoft Word
- Ingénierie
- Expérience en laboratoire
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il y a 12 jours
Alternate Quality Assurance Person
Cannapiece Corp —Pickering, ON
- De 70 000 $ à 80 000 $ par an
- Systèmes PGI
- Microsoft Office
- Expérience en supervision
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Chemistry Laboratory Manager
Auxilium Health —Oshawa, ON
- De 65 000 $ à 75 000 $ par an
- Fins de semaine au besoin
- Compétences rédactionnelles
- Expérience en laboratoire
- Maintenance
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22 h
QC Inspector (Electrical)
E.S. Fox Limited —Pickering, ON
- De 90 000 $ à 140 000 $ par an
- Ingénierie
- Pas d'expérience requise
- Baccalauréat
- Assurance Dentaire
- Programme d'Aide aux Employés
QC Inspector (Mechanical)
E.S. Fox Limited —Pickering, ON
- De 90 000 $ à 140 000 $ par an
- Ingénierie
- Pas d'expérience requise
- Baccalauréat
- Assurance Dentaire
- Programme d'Aide aux Employés

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RPN - Clinical Data Quality Analyst
Power Staffing Solutions —Courtice, ON
Contribute to the development of more efficient data quality processes, reporting, and documentation standards.
À partir de 35 $ de l’heure
Postuler rapidement
il y a 1 jour
Lab Supervisor
Confidential —Toronto, ON
The successful candidate will oversee laboratory testing, support method development and validation activities, ensure compliance with regulatory standards, and…
De 80 000 $ à 100 000 $ par an
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Quality Assurance Associate

TJP Labs Inc. -
Pickering, ON

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Détails du poste

Permanent | Temps plein
De 23 $ à 25 $ de l’heure

Profil recherché

Microsoft Powerpoint
Microsoft Word
Utilisation de l'équipement de protection individuelle (EPI)
Étiquetage
Politiques de santé et sécurité au travail
Investigation des déviations en contrôle de la qualité
Actions correctives et préventives (CAPA)
Bonnes pratiques de fabrication (BPF)
Microsoft Office
Esprit d'analyse
Baccalauréat
Amélioration continue
Contrôle de la qualité
Gestion des risques
Inspection de la qualité
Réglementation en santé et sécurité du travail (SST)
Pharmacie
Production
Procédures opératoires normalisées (PON)
Compétences en communication
Permis de conduire

Description complète du poste

The QA Associate ensures compliance with GMP standards, established procedures, documentation accuracy, product quality, and regulatory requirements. The role involves close collaboration with production and warehouse teams to maintain control over materials, batch records, retains, and documentation while ensuring operational readiness for audits and inspections.

Responsibilities:

· Maintain an active QA presence on the line, ensuring compliance with GMP, company SOPs, and Health Canada regulations.

· Perform and document line clearances before batch start-up, product, or flavour changeovers.

· Conduct continuous in-process checks (e.g., pouch weight, seal integrity, count accuracy) and record findings in real time.

· Quantify and document rejects and yield losses and reconcile them with batch records.

· Immediately report any deviations, mix-ups, or nonconformances and assist in preliminary impact assessments.

· Ensure all batch records are accurately filled out in real time and signed by responsible personnel.

· Control issuance and reconciliation of batch records, labels, and QA-controlled documents.

· Verify and approve production labels prior to use, ensuring correct product strength and flavor identification.

· Log and maintain retain samples, ensuring proper labelling, storage, documentation, and chain of custody.

· Ensure correct material status (e.g., QA hold, released) and traceability during dispensing and production.

· Receive incoming raw materials; verify identity, label integrity, documentation, and match with Certificates of Analysis (CoA).

· Enforce GMP and hygiene practices on the floor; ensure personnel follow gowning, cleaning, and behavior protocols.

· Support audit readiness and inspection requirements; participate in internal inspections and ensure production areas remain audit ready.

· Identify potential compliance risks or procedural gaps and report them to QA management.

· Assist in investigating deviations, OOS results, and customer complaints related to production or packaging operations.

· Contribute to continuous improvement initiatives and risk mitigation actions across QA and production.

· Perform other quality-related tasks as assigned by QA management.

Additional Requirements:

· Must be legally eligible to work in Canada.

· Flexible availability: able to work various shifts (days, nights, weekends, holidays) and be on-call when required, in accordance with Ontario’s Employment Standards Act (ESA).

· Willing to rotate across shifts as business needs require.

· Must have a valid driver’s license and access to a reliable vehicle for travel between sites.

· Detail-oriented, accountable, able to work independently, and responsive in a fast-paced production environment.

· Adheres to all health and safety practices under the Occupational Health and Safety Act (OHSA).

Physical and Environmental Conditions:

· Must be able to work in continental shifts.

· This role requires standing and walking for extended periods on the production floor.

· Tolerant of strong flavour/odor environments and comfortable wearing respirators and other PPE for full shift durations.

· Employee must be capable of lifting materials up to 20 kg.

· Production areas may operate at varying noise levels; hearing protection is provided when required.

· Work is performed in temperature-controlled environments with frequent interaction between production and warehouse areas.

Qualifications:

· Bachelor’s degree or diploma in Science, Pharmacy, or a related field.

· 1–2 years of experience in a GMP-regulated environment (pharmaceutical or nutraceutical).

· Working knowledge of GMP, GDP, and quality systems (deviation, CAPA, change control).

· Strong analytical and critical thinking skills.

· Good communication skills, both written and verbal.

· Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Job Types: Full-time, Permanent

Pay: $23.00-$25.00 per hour

Benefits:

Dental care
On-site parking
Vision care

Education:

Bachelor's Degree (required)

Experience:

Pharmaceutical manufacturing: 1 year (preferred)

Work Location: In person

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quality lab emplois - whitby, on

Quality Assurance Associate

RPN - Clinical Data Quality Analyst

Quality Lab Technician

Quality Analyst/Coordinator

Alternate Quality Assurance Person

Chemistry Laboratory Manager

QC Inspector (Electrical)

QC Inspector (Mechanical)

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