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Azelis Canada Inc., among the leaders in the distribution of active ingredients and specialty chemicals, offers a wide range of distinctive services and customized solutions throughout Canada. We provide specialty ingredients and chemicals to the Personal Care, Pharmaceutical, Food & Health, CASE as well as Chemical specialties markets such as lubricants, HI&I, oil & gas and Pulp & Paper. Regulatory expertise and specialized warehousing/logistic capabilities completes our ability to provide a one-stop solution for our clients and global supply partners.
We are certified under Responsible Distribution Canada and also are ISO 9001:2000 registered which proves our commitment to quality and ethics.
Job Overview:
Under the supervision of the SHEQ Manager, Azelis Canada, the employee is primarily responsible for compliance with quality and regulatory standards supporting Azelis operations (ex. ISO, RD, TDG, GMP, WHIMIS / EC GHS.) and the ISO procedures. It provides the link between the department, customers and suppliers to meet the specific needs. It ensures the proper functioning of the quality system to meet the standards and maintain Azelis’s certifications and ensures that all internal units know and apply current rules of SHEQ.
Responsibilities and Duties:
Ensure compliance with the standard and quality of the overall system in order to maintain certifications and offer services that meet the quality standards of Azelis and needs of customers and suppliers, among others doing:
Performing internal audits in accordance with established procedures and deadlines.
Performing the external audits for service providers according to established procedures and deadlines.
Addressing the demands of non-compliance and complaints of customers and suppliers and to do the required follow-ups until the closing of the files.
Establishing or proposing corrective actions and / or preventive actions, depending on the targeted issues during audits, requests for non-compliance or complaints.
Ensuring and monitoring the efficiency of the implementation of the chosen corrective and / or preventive actions.
Prepare updates to internal and external procedures that support the standards.
Ensuring internal and external communications and the implementation of changes to procedures.
Validating Certificates of Analysis (CofA) versus the specifications for all products and processes the problems when required.
Identifying how to dispose of quarantined products (quarantine warehouse).
Establish the import limits of the products.
Requesting the permits required by various regulations and performing the follow up if there are any changes in permits and import.
Contributing to the development and maintenance of the ERAP plan «emergency response assistance plan»
Contributing to the development of the emergency plan in regard to the building, transport and hazardous goods and applying it when necessary.
Proceeding with nominations and notifications of products
Identifying the impact of changes or added regulations on Azelis operations
Understand and resolve common situations by interacting with customers and suppliers and the different departments and bring to the attention of his superior all situations at risk to grow, to ensure at all times a high quality and proactive customer service.
Develop expertise in relation to products and the different industries by developing and maintaining current knowledge about the products and services of suppliers in order to, at all times, provide updated information and respond quickly and accurately to customer requests.
Develop expertise in relation to the regulations by developing and maintaining current knowledge about the laws and regulations in order to, at all times, provide updated information and respond quickly and accurately to customer requests and suppliers.
Ensure the development of internal knowledge of quality and regulatory affairs, including the systems used, by offering information sessions to members of other units to ensure that all have a common understanding of processes related to quality, know how to apply them and can support the operations of the quality and regulatory affairs department.
Standardize and document the procedures for carrying out the work to ensure consistency in the execution of tasks and facilitate the substitution.
Support other internal departments in handling customer requests and suppliers to offer excellent customer service and develop and maintain a privileged customer relationship that supports the vision of Azelis.
Support the Quality and Regulatory Affairs Manager in the implementation of standards relating to health and safety.
Support the Quality and Regulatory Affairs Manager in various projects or folders by performing various tasks in meeting deadlines, to facilitate the compliance of the operational management and allow Azelis to achieve its objectives.
In case of the absence of the Quality and Regulatory Affairs Manager, the responsibility is transferred to the agent on the activities of Good Manufacturing Practices (GMP).
Providing internal support by performing all other responsibilities assigned to it, including the occasional replacement of his colleagues, to allow Azelis to respect its services and / or meet its objectives.
Qualifications:
DEC or AEC in an appropriate discipline: quality management, regulatory affairs, chemistry, environmental science, engineering
Experience of 1-2 years in a chemical products company (nutri, pharma, etc) in the quality sector or in a laboratory.
Already performed internal and external audits
Excellent time management skills and priority setting skills.
Strong analytical skills, attention to detail and accuracy
Demonstrated ability in solving various issues
Excellent ability to work in teams in a dynamic environment.
Strong ability to adapt and evolve in a dynamic and constantly evolving environment
Negotiation skills and political savvy to interact with the various authorities as well as with employees
Languages: French; English
Computer Skills: Word; Excel; PowerPoint; Outlook; ERP; SharePoint; Quality Software