Supervisor, Development and Validation

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

• Supervise analytical Development and Validation activities to ensure the group meets its objectives for quality, regulatory compliance, productivity, and timelines.
  
  
• Act as the subject matter expert (SME) for analytical method development, validation, verification, and transfer activities, and provide scientific support to internal teams and clients.
  
  
• Manage, guide, and develop the D&V team while fostering continuous improvement, proactive problem-solving, and scientific excellence.
  
  
• Main D&V point of contact for clients. Collaborate with project managers and the various departments to ensure effective planning and execution of analytical activities related to development and technology transfer projects.

Responsibilities

• Supervise the day-to-day activities of the Development and Validation group to ensure quality, compliance, and timeline objectives are met;

• Plan, prioritize, and coordinate the team's workload based on operational needs and client projects;

• Review and approve protocols, reports, and other technical documents related to analytical method development, transfer, verification, and validation;

• Act as the subject matter expert (SME) for analytical method development, validation, transfer, and troubleshooting activities;
  
  
• Identify, assess, and recommend the implementation of new technologies, analytical methodologies, and scientific best practices to support innovation, operational efficiency, and the growth of the company's analytical services.
  
  
• Actively participate in resolving complex analytical issues, including investigations, OOS, OOT, deviations, and analytical transfers;
  
  
• Monitor the progress of development and validation activities performed internally or by contract laboratories;
  
  
• Collaborate with project managers, clients, and the various departments to support the execution of analytical projects;
  
  

• Main D&V point of contact for clients: participate in client meetings and provide the required scientific expertise regarding analytical strategies, method validations, and technology transfers;

• Ensure the group's activities are carried out in accordance with GMP, internal procedures, and applicable regulatory requirements;

• Maintain and develop the team's technical skills through coaching, training, and mentoring;
  
  
• Conduct performance follow-ups, evaluations, and development plans for team members;
  
  
• Develop and monitor the D&V group's key performance indicators (KPIs) and identify continuous improvement opportunities;
  
  
• Contribute to the optimization of processes, analytical methods, and laboratory practices;
  
  
• Perform any other related tasks required for the smooth operation of the department.
  
  

Required qualifications and experience

• Minimum of a Master's degree in chemistry from a Canadian university, or a degree recognized by a Canadian accreditation body as equivalent, in a scientific field.
  
  
• Minimum of seven (7) years of experience in analytical method development, validation, transfer, or verification in the pharmaceutical industry or a similar regulated environment.
  
  
• Minimum of two (2) years of experience in supervision, team coordination, or people management.

• Strong knowledge of the principles of analytical method development, validation, verification, and transfer;
  
  
• In-depth knowledge of modern analytical chemistry techniques, including HPLC/UPLC, GC, and other relevant technologies;
  
  
• In-depth knowledge of Canadian, American, and international Good Manufacturing Practices (GMP) applicable to pharmaceutical laboratories;
  
  
• Knowledge of pharmacopoeias (USP, Ph. Eur., BP) and their application in a regulated analytical environment;
  
  
• Experience in the development, validation, or execution of in vitro release testing (IVRT) and/or in vitro permeation testing (IVPT) is a major asset.
  
  
• Excellent skills in investigation, scientific problem-solving, and analytical data interpretation;
  
  
• Ability to supervise, engage, and develop a team in an evolving environment;
  
  
• Demonstrated skills in planning, work organization, and priority management;
  
  
• Ability to manage multiple projects simultaneously while meeting deadlines and client expectations;
  
  
• Excellent oral and written communication skills with internal teams, clients, and external partners;
  
  
• Excellent interpersonal, collaboration, and leadership skills;
  
  
• Strong analytical and decision-making skills, and a sense of initiative;
  
  
• Ability to act as a subject matter expert (SME) and explain complex scientific concepts in simple terms;
  
  
• Proficiency in the Microsoft Office suite (Word, Excel, PowerPoint, Outlook);
  
  
• Experience with computerized laboratory systems (LIMS, CDS, or equivalent systems) is an asset;
  
  
• Professional-level bilingualism in French and English
  
  
• Member of the Ordre des chimistes du Québec

What we offer

• Group retirement savings plan

• Employee recognition program and social activities

• Personal days

• Employee Assistance Program and telemedicine services

• Complimentary hot  beverages (hot chocolate, coffee, and mocha)

• Easy access by public transit or free parking

• Employee referral program

• Subsidized meal program

• 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.