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Production Supervisor
Production SupervisorAX Pharmaceutical Corp • Vaughan, York Region, CA
Production Supervisor

Production Supervisor

AX Pharmaceutical Corp • Vaughan, York Region, CA
Il y a 15 jours
Type de contrat
  • Temps plein
  • Permanent
Description de poste

Position : Permanent Full-Time Production Supervisor.

Location : On site.

Salary : $42.50 hourly / 40 hours per week.

Start : As soon as possible.

Working hours : 09 : 00 to 17 : 00.

Benefits : Health benefits, Financial benefits, Other benefits.

Vacancy count : 1.

Languages

  • English.

Education

  • Secondary (high) school graduation certificate.

    • Experience

  • 2 years to less than 3 years.

    • Location

  • On site. (Work must be completed at the physical location. No option to work remotely.)

    • Responsibilities

  • 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, coordinate and schedule (and possibly review) activities of workers.
  • Establish work schedules.
  • Prepare production and other reports.
  • 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 structure, 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.

    • #J-18808-Ljbffr

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