Maintenance Supervisor, Pharmaceuticals
Top Benefits
About the role
Maintenance Supervisor, Pharmaceuticals
-
Responsible for the equipment maintenance team, including coordination of tasks and adherence to the periodic maintenance schedule.
-
Supervise the validation team.
The Maintenance Supervisor, Pharmaceuticals…
Responsibilities:
-
Responsible for the equipment maintenance program, including calibrations.
-
Monitor performance indicators related to equipment compliance activities (maintenance, calibrations).
-
Actively participate in problem solving with employees, making fair and equitable decisions related to productivity, costs, quality and commitment.
-
Manage service providers.
-
Actively participate in the Health and Safety Committee.
-
Provide ideas and solutions to improve efficiency and safety.
-
Manage employee performance and development.
-
Monitor, track and report monthly operating expense variances for department and projects.
Skills and experience required:
-
Technical diploma or bachelor’s degree in engineering from a Canadian university.
-
Minimum of five (5) years’ experience in a highly regulated manufacturing sector, with a minimum of two (2) years in a similar position in the pharmaceutical industry.
-
Good experience with Canadian (Health Canada) and American (FDA) Good Manufacturing Practices (GMP).
-
Management skills with proven ability to manage multiple priorities.
-
Proven customer relations skills
-
Ability to lead people and encourage team participation
-
Strong team player and motivated problem solver
-
Excellent organizational, interpersonal and presentation skills
-
Excellent communication skills
-
Good computer skills (Microsoft Office, Outlook)
-
Bilingual (French and English). Fluency in English is essential.
What we offer :
-
Medical, dental and travel insurance
-
Group pension plan
-
Recognition program and social activities
-
Personal leave
-
Employee support program and telemedicine
-
Free beverages (hot chocolate, coffee, mochaccino)
-
Accessibility by public transit or free parking
-
Referral program
-
Subsidized meal program
About Groupe PARIMA
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. We have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. This strategic focus has allowed us to establish a unique expertise to support your product development and manufacturing needs, which, combined to our operational flexibility and commitment to delivering on time, enables us to operate as an extension of your team. Over the years, we have added specialized capabilities such as handling of low-flash point mixtures, and packaging metered-dose sprays (nasal or sublingual), towelettes and sachet/stick/packs.
Our business is 100% free-for-service and exclusively focused on contract services. We are here to help you meet your company objectives, not to compete with you.
We have been favorably inspected by the European, US, Turkish and Canadian health authorities, and we are manufacturing products for markets in over 30 countries.
Product Development: Formulation Development, Packaging Development, QbD, Process Scale-up, process validation, project management
Analytical Testing: IVRT, HPLC, UPLC, LCMS, Particle Size, Microbiology, Viscosity
Commercial manufacturing for USA, Europe, Canada Turkey, South America, Mexico, Australia, New Zealand, MENA; Serialization, cold-chain
Manufacturing: creams, ointments, lotions, gels, solutions, liquids, suspensions, flammable products (Antiseptic gel), inert atmosphere
Packaging: Bottles, Jars, Sprays, Pumps, Tubes, Airless Pumps Pledgets/towelettes, Nasal Sprays, Sublingual Sprays, Metered-dose delivery, Syringe applicator (non-sterile), sachets and Stick packs, inert atmosphere
Maintenance Supervisor, Pharmaceuticals
Top Benefits
About the role
Maintenance Supervisor, Pharmaceuticals
-
Responsible for the equipment maintenance team, including coordination of tasks and adherence to the periodic maintenance schedule.
-
Supervise the validation team.
The Maintenance Supervisor, Pharmaceuticals…
Responsibilities:
-
Responsible for the equipment maintenance program, including calibrations.
-
Monitor performance indicators related to equipment compliance activities (maintenance, calibrations).
-
Actively participate in problem solving with employees, making fair and equitable decisions related to productivity, costs, quality and commitment.
-
Manage service providers.
-
Actively participate in the Health and Safety Committee.
-
Provide ideas and solutions to improve efficiency and safety.
-
Manage employee performance and development.
-
Monitor, track and report monthly operating expense variances for department and projects.
Skills and experience required:
-
Technical diploma or bachelor’s degree in engineering from a Canadian university.
-
Minimum of five (5) years’ experience in a highly regulated manufacturing sector, with a minimum of two (2) years in a similar position in the pharmaceutical industry.
-
Good experience with Canadian (Health Canada) and American (FDA) Good Manufacturing Practices (GMP).
-
Management skills with proven ability to manage multiple priorities.
-
Proven customer relations skills
-
Ability to lead people and encourage team participation
-
Strong team player and motivated problem solver
-
Excellent organizational, interpersonal and presentation skills
-
Excellent communication skills
-
Good computer skills (Microsoft Office, Outlook)
-
Bilingual (French and English). Fluency in English is essential.
What we offer :
-
Medical, dental and travel insurance
-
Group pension plan
-
Recognition program and social activities
-
Personal leave
-
Employee support program and telemedicine
-
Free beverages (hot chocolate, coffee, mochaccino)
-
Accessibility by public transit or free parking
-
Referral program
-
Subsidized meal program
About Groupe PARIMA
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. We have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. This strategic focus has allowed us to establish a unique expertise to support your product development and manufacturing needs, which, combined to our operational flexibility and commitment to delivering on time, enables us to operate as an extension of your team. Over the years, we have added specialized capabilities such as handling of low-flash point mixtures, and packaging metered-dose sprays (nasal or sublingual), towelettes and sachet/stick/packs.
Our business is 100% free-for-service and exclusively focused on contract services. We are here to help you meet your company objectives, not to compete with you.
We have been favorably inspected by the European, US, Turkish and Canadian health authorities, and we are manufacturing products for markets in over 30 countries.
Product Development: Formulation Development, Packaging Development, QbD, Process Scale-up, process validation, project management
Analytical Testing: IVRT, HPLC, UPLC, LCMS, Particle Size, Microbiology, Viscosity
Commercial manufacturing for USA, Europe, Canada Turkey, South America, Mexico, Australia, New Zealand, MENA; Serialization, cold-chain
Manufacturing: creams, ointments, lotions, gels, solutions, liquids, suspensions, flammable products (Antiseptic gel), inert atmosphere
Packaging: Bottles, Jars, Sprays, Pumps, Tubes, Airless Pumps Pledgets/towelettes, Nasal Sprays, Sublingual Sprays, Metered-dose delivery, Syringe applicator (non-sterile), sachets and Stick packs, inert atmosphere