Role at a glance
- Salary
- Not yet verified Check the description for pay details; an amount or pay period has not been verified.
- Location
- Mississauga, Canada
- Work arrangement
- On-site
- Employment
- Full-time
- Education
- Equivalent combinations of education, training, and relevant work experience may be considered.
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Role Summary
This manager role is accountable for packaging pharmaceuticals to meet quality standards, cost targets and delivery dates while ensuring proper staffing, including hiring and training of staff. The role works with internal and external auditors, clients, equipment vendors and component suppliers, and reviews and approves master production documents, validation reports and SOPs.
What You'll Do
- Work with leadership to determine resources required to meet the production schedule, such as hiring of staff and shift structure.
- Monitor daily production outputs and efficiencies.
- Identify, lead and complete projects within established timelines and budget.
- Prepare quotations for existing and prospective clients and maintain product routings and annual costing.
- Develop and implement a succession plan and career path for all key individuals.
- Hire staff and administer performance improvement plans, up to and including termination when appropriate.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
A diploma in a related field plus at least 5 years of manufacturing or operations experience, including 3 years of supervisory experience.
Required
- Diploma in related field
- Minimum of 5 years of experience in manufacturing or similar operations role, quality, supply chain, or technical operations
- Minimum 3 years previous supervisory experience
- Understanding of manufacturing operations and plant operations
- Proven ability to coach and develop staff and technical ability to coordinate departmental business activities
- Full knowledge of Good Manufacturing Practices requirements and pharmaceutical processing regulations
- Strong leadership, team building and organizational skills
- Demonstrated computer proficiency with Microsoft Office programs including spreadsheets, presentations and reports
Preferred
- Bachelor's degree in industrial engineering, industrial technology, science or a related field
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, OfficeJob Description
Job Summary:
This position is 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 of
Manager Packaging 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.About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.