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AX Pharmaceutical Corp
Production SupervisorAX Pharmaceutical Corp • Vaughan, Ontario, Canada
Production Supervisor

Production Supervisor

AX Pharmaceutical Corp • Vaughan, Ontario, Canada
Il y a plus de 30 jours
Salaire
42,50 $CA par heure
Type de contrat
  • Temps plein
  • Permanent
  • Quick Apply
Description de poste
Position: Permanent Full-Time Production Supervisor.
On site.
Salary: $42.50 hourly/40 hours per week.
Starts as soon as possible.
Working hours from 09:00 to 17:00.
Benefits: Health benefits, Financial benefits, Other benefits.
1 vacancy.

Overview:

Languages: English.

Education:
  • Secondary (high) school graduation certificate.

Experience:2 years to less than 3 years.

On site.

Work must be completed at the physical location. There is no option to work remotely.

Responsibilities:

Tasks:
  • Recommend measures to improve productivity.
  • Resolve work problems, provide technical advice and recommend measures to improve productivity and product quality.
  • Investigate deviations in yield associated with critical process steps , determine their impact or potential impact on the result quality of affected batches.
  • Supervise, co-ordinate and schedule (and possibly review) activities of workers.
  • Establish work schedules.
  • Prepare production and other reports.
  • Recommend measures to improve productivity and product quality.
  • Provide information for maintenance plans to ensure that maintenance and production objectives are met.
  • Co-ordinate work activities with other departments, including but not limited to:
    • Review Batch Production Record, deviation, investigation and OOS reports before the batch is released by quality team.
    • In charge of production documents control before quality team review and Health authorities on site audit.
    • Coordinate with quality control team to qualify hoods and cleanrooms based on SOP, put air samples into cleanrooms, mapping the worst and best spot for microbial sampling.
  • Train staff/workers in job duties, safety procedures and company policies, including but not limited to:
    • Train and supervise operators to clean the hoods and cleanrooms based on approved and validated cleaning procedures from quality assurance team and document it.
    • Train and supervise operators to sample from specific batch and document it into master batch record.
    • Supervise operators for daily calibration of standard weights, scales and document it.
  • Requisition or order materials, equipment and supplies.
  • Set up machines and equipment.
  • Good Manufacturing Practices (GMP), including but not limited to:
    • Good knowledge of different APIs chemical structurer , density, particle size to determine the primary and secondary packing size.
  • Knowledge of licensing regulations, including but not limited to:
    • Proficient in ICH guidelines Q7 for Active Pharmaceutical Ingredients ( APIs ).
    • Proficient in FDA eCFR 21 regulations for APIs.
    • Proficient in Health Canada Drug Establishment License requirement for APIs sampling, re-labelling and re-packaging activities.
  • Label, file and retrieve documents, including but not limited to:
    • Verify all the critical information from master batch record during the re-packaging process.
  • Document and report deviations from specifications and tolerances.
  • Supervise and investigate any label damages, package damages, APIs spillage, document it and report to quality team for review.

Supervision:
  • 3-4 people.

Additional information:

Security and safety:
  • Criminal record check.

Transportation/travel information:
  • Valid driver's licence.

Work conditions and physical capabilities:
  • Attention to detail.

Personal suitability:
  • Organized.
  • Team player.

Benefits:

Health benefits:
  • Dental plan.
  • Health care plan.

Financial benefits:
  • Registered Retirement Savings Plan (RRSP).

Other benefits:
  • Deferred Profit Sharing Plan (DPSP).
  • Free parking available.


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