2 meilleures offres (chemical operator, cornwall, on) (à pourvoir)

Chemical Process Operator
Pureoyl Healthcare —Cornwall, ON
- De 20 $ à 25 $ de l’heure
- Temps plein
- Maintenance
- Baccalauréat
- Amélioration continue
Postuler rapidement
Chemical Process Operator
Pureoyl Healthcare —Cornwall, ON
- De 20 $ à 25 $ de l’heure
- Temps plein
- Maintenance
- Baccalauréat
- Amélioration continue
Postuler rapidement

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Chemical Process Operator
Pureoyl Healthcare —Cornwall, ON
The role includes operating equipment, supporting product formulation and optimization, assisting in product development, maintaining accurate documentation,…
De 20 $ à 25 $ de l’heure
Postuler rapidement
Chemical Process Operator
Pureoyl Healthcare —Cornwall, ON
The role includes operating equipment, supporting product formulation and optimization, assisting in product development, maintaining accurate documentation,…
De 20 $ à 25 $ de l’heure
Postuler rapidement

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il y a 10 jours

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Chemical Process Operator

Pureoyl Healthcare
Cornwall, ON

Postuler rapidement

Détails du poste

Permanent | Temps plein
De 20 $ à 25 $ de l’heure

Profil recherché

Actions correctives en contrôle de la qualité
SSE
Politiques de santé et sécurité au travail
Maintenance
Actions correctives et préventives (CAPA)
Bonnes pratiques de fabrication (BPF)
Baccalauréat
Développement de produit
Amélioration continue
Nettoyage
Chimie
Évaluation des risques
Production
Registres
Collaboration interfonctionnelle
Procédures opératoires normalisées (PON)
Amélioration des processus opérationnels

Description complète du poste

Position Title: Chemical Process Operator
Department: Manufacturing / Product Development
Reports To: Production / R&D Manager

Position Summary

The Chemical Process Operator will be responsible for carrying out pharmaceutical and healthcare manufacturing processes in compliance with cGMP, GDP, and regulatory requirements. The role includes operating equipment, supporting product formulation and optimization, assisting in product development, maintaining accurate documentation, and contributing to quality and regulatory compliance.

Key Responsibilities

Manufacturing & Operations

Operate, monitor, and maintain processing equipment such as reactors, blenders, filtration systems, incubators, and distillation units as per SOPs.
Execute batch operations for pharmaceutical and healthcare products according to approved batch manufacturing records (BMRs).
Weigh, measure, and dispense raw materials in compliance with GDP.
Perform routine cleaning and minor maintenance of equipment.

Product Formulation & Development Support

Assist R&D team in new formulation trials, process optimization, and scale-up activities.
Support pilot-scale batches and technology transfer to production.
Provide feedback on process challenges to improve yields, efficiency, and compliance.

Documentation & Compliance

Prepare and maintain accurate records in line with Good Documentation Practices (GDP).
Document and control in-process checks, samplings, deviations, and process observations.
Maintain logbooks, equipment use records, and cleaning validation records.

Quality & Regulatory Compliance

Ensure all operations are performed under Good Manufacturing Practices (cGMP).
Participate in regulatory inspections and internal/external audits (e.g., Health Canada, FDA, EU-GMP).
Follow Standard Operating Procedures (SOPs) and ensure strict adherence to validated processes.
Support Quality Management System (QMS) activities including change control, deviation management, CAPA, and risk assessments.

Safety & Continuous Improvement

Adhere to safety protocols and proper handling of pharmaceutical raw materials and chemicals.
Participate in continuous improvement initiatives to optimize processes and reduce waste.
Ensure compliance with environmental, health, and safety (EHS) standards.

Qualifications

Education: Diploma/Bachelor’s in Chemical/Pharmaceutical Technology, Chemistry, Biochemistry, or related field.
Experience: 1–3 years of experience in pharmaceutical or healthcare manufacturing (entry-level may be considered with strong technical background).
Knowledge of cGMP, GDP, and regulatory compliance is mandatory.
Experience in handling incubators, process equipment, and in-process sampling is an asset.

Skills & Competencies

Strong knowledge of formulation, scale-up, and process optimization.
Familiarity with QMS activities (CAPA, deviations, change controls, audits).
Excellent attention to detail and accuracy in documentation.
Strong problem-solving, troubleshooting, and teamwork skills.
Ability to work under regulated environments with cross-functional teams (R&D, QA, QC, Regulatory).

Work Conditions

May involve shift-based or extended hours depending on production schedules.
Exposure to controlled cleanroom and chemical environments (PPE provided).
Requires standing for extended periods, material handling, and strict adherence to hygiene and gowning procedures.

Job Types: Full-time, Permanent

Pay: $20.00-$25.00 per hour

Benefits:

On-site parking

Education:

Bachelor's Degree (required)

Experience:

Chemical Process operator: 2 years (required)

Work Location: In person

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Chemical Process Operator

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