Analyst, Quality Control
Help us build the health of tomorrow
Groupe PARIMA has been a contract development and manufacturing organization (CDMO) since 1994. Over the years, we have developed extensive expertise in the development and manufacturing of non-sterile pharmaceutical products in liquid, semi-solid, and suspension dosage forms.
Position Overview
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Independently perform chemical and physical analyses according to the established schedule, following specifications, methods, procedures, and Good Manufacturing Practices (GMP) at Groupe Parima.
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Participate in laboratory and instrument maintenance, reagent and inventory management, and the training of junior analysts.
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Work in compliance with health and safety regulations and report health and safety risks to management.
Responsibilities
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Good knowledge of USP and EP/BP Pharmacopoeias.
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Independently perform the following physical tests: pH, density, specific gravity, viscosity, deliverable volume, particle size, particle size distribution (PSD), and loss on drying.
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Independently perform assay testing using manual and automated titration methods.
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Independently perform testing using UV-Visible spectrophotometry.
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Prepare mobile phases, diluents, and dissolution media.
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Independently perform dissolution, assay, and related substances testing using HPLC.
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Analyze results with critical thinking and ensure compliance with established procedures and standards.
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Enter analytical results into the LIMS using sound judgment and by comparing them against trending data.
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Ensure data integrity and quality within the QC laboratory.
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Assist in and participate in the training of junior analysts.
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Perform maintenance and calibrations of laboratory instruments used in physical testing.
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Participate in maintaining inventories of reagents, solvents, and consumables required for analyses and laboratory operations.
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Actively participate in laboratory investigations.
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Contribute to problem-solving activities and continuous improvement initiatives within the laboratory.
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Follow health and safety regulations and report health and safety risks to management.
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Occasionally perform selected Lead Analyst tasks based on operational needs.
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Carry out any other duties required for the efficient operation of the laboratory.
Required qualifications and experience
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Good knowledge of USP and EP/BP Pharmacopoeias.
-
Independently perform the following physical tests: pH, density, specific gravity, viscosity, deliverable volume, particle size, particle size distribution (PSD), and loss on drying.
-
Independently perform assay testing using manual and automated titration methods.
-
Independently perform testing using UV-Visible spectrophotometry.
-
Prepare mobile phases, diluents, and dissolution media.
-
Independently perform dissolution, assay, and related substances testing using HPLC.
-
Analyze results with critical thinking and ensure compliance with established procedures and standards.
-
Enter analytical results into the LIMS using sound judgment and by comparing them against trending data.
-
Ensure data integrity and quality within the QC laboratory.
-
Assist in and participate in the training of junior analysts.
-
Perform maintenance and calibrations of laboratory instruments used in physical testing.
-
Participate in maintaining inventories of reagents, solvents, and consumables required for analyses and laboratory operations.
-
Actively participate in laboratory investigations.
-
Contribute to problem-solving activities and continuous improvement initiatives within the laboratory.
-
Follow health and safety regulations and report health and safety risks to management.
-
Occasionally perform selected Lead Analyst tasks based on operational needs.
-
Carry out any other duties required for the efficient operation of the laboratory.
What we offer
- Group retirement savings plan
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Employee recognition program and social activities
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Personal days
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Employee Assistance Program and telemedicine services
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Complimentary hot beverages (hot chocolate, coffee, and mocha)
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Easy access by public transit or free parking
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Employee referral program
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Subsidized meal program
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The use of the masculine gender is intended solely to simplify the text and facilitate readability.
*The use of the masculine gender is intended solely to simplify the text and facilitate readability.
*Our company operates in an international business environment, and proficiency in English is required to communicate with suppliers and clients.