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Manager Packaging

134570811RT0001 Patheon Inc · Mississauga, Canada

Imported listingfull-time1 day ago

About The Role

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

Summary

  • Accountable for the packaging of pharmaceuticals to meet quality standards (e.g. full cGMP, health, safety
  • and environmental compliance), cost targets, delivery dates, while ensuring proper staffing levels, including
  • hiring and training of staff and the continuous development of existing associates. Work with internal and
  • external auditors, clients, equipment vendors, component suppliers and other internal and external
  • contracts as needed. Reviews / approves master production documents, validation reports and SOPs.

Essential Functions

  •  Work with leadership to determine resources required to meet the production schedule (e.g. hiring of
  • staff, shift structure, etc.).
  •  Monitor daily production outputs (e.g. output quantity, etc.) and efficiencies.
  •  Identify, lead and complete all projects (PPI, Quality, CAS, Morale) within established timelines and
  • budget.
  •  Prepare quotations for existing products and future prospective clients, maintain product routings and
  • annual costing.
  •  Develop and implement a succession plan and career path for all key individuals.
  •  Outline clearly key staff roles and expectations, as required.
  •  Ensure the necessary training is provided to individuals such that they are able to excel in their position
  • and monitor the performance of those who require assistance or direction.
  •  Support cross training of individuals thus achieving a flexible work force, as required.
  •  Hire staff and administer performance improvement plans, up to and including termination when
  • appropriate.
  •  Ensure responses to client, Good Manufacturing Practices, safety and CAPA follow-up actions are
  • completed in a timely manner, as required.
  •  Support CEM program. Develop culture of customer service and centricity.
  •  Instill a culture of professionalism and respect for co-workers, clients and the products.
  •  Participate in annual budget creation and monthly tracking of spend.
  •  Promote a safe working environment, report potential hazards and ensure all direct reports follow
  • Environmental Health and Safety procedures.
  •  Select, develop and evaluate staff to ensure the efficient operation of the function. Works with and
  • advises staff on administrative policies and procedures.

REQUIRED QUALIFICATIONS

Education

  • Diploma in related field.
  • Bachelor’s degree in industrial engineering, industrial technology, science or a related field is preferred

Experience

  • Minimum of 5 years of experience in manufacturing or similar operations role, quality, supply chain, or
  • technical operations preferably in pharmaceutical or consumer product packaging environment.
  • Minimum 3 years previous supervisory experience.

Equivalency

Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills and Abilities

  • Understanding of Manufacturing Operations and Plant operations is required. Proven ability to coach and
  • develop staff as well as the technical ability to coordinate departmental business activities. Full knowledge

Manager Packaging Page 2 of 3

  • of Good Manufacturing Practices requirements and pharmaceutical processing regulations. Strong
  • leadership, team building and organizational skills. Demonstrated computer proficiency with Microsoft
  • Office programs including the ability to develop spreadsheets, presentations and reports. Proficiency with
  • the English language.

Standards and Expectations

  • Follow all Environmental Health & Safety Policies and Procedures. Work harmoniously with fellow team
  • members, modelling positive team principles and partnering to meet project and departmental objectives.
  • Carry out all duties within strict compliance to Patheon quality systems SOP's and Good Manufacturing
  • Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to
  • departmental systems in order to maintain a smooth and efficient workflow (visual management, scheduling
  • systems, etc.). Be client and patient centric at all times. Understand Key Performance Indicators and strive
  • to improve the performance of the team by identifying areas for system improvements and engage in
  • problem solving. Models positive thinking and is open to change, motivating the team to adapt to shifts in
  • priorities and new ways of working. Proactively identify areas for improvement in the execution of
  • procedures. Communicate risks to timelines of deliverables in a proactive manner. Consistently strives to
  • improve skills and knowledge in related field.

Physical Requirements

  • Light physical effort and fatigue. Walks, sits or stands for limited periods. May require occasional equipment
  • operation including keyboard equipment. Lifts light items for limited duration. Typically located in a
  • comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as
  • dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal
  • Protective equipment may be required and may include any of the following: safety glasses, safety shoes,
  • lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.

Compensation

The estimated annualized pay range for this position in Ontario is $77,000.00–$115,475.00.

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