Production Supervisor
AX Pharmaceutical Corp
- Vaughan, Nova Scotia, Canada
- Vaughan, Nova Scotia, Canada
About
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.
- 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.
Languages
- English
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