Senior Coordinator Quality Assurance Contract

Sun Pharmaceutical Industries

  • Brampton, ON
  • Permanent
  • Full-time
  • 11 days ago
Job purposeThe main responsibility for this position is to update various TARO document types to meet SUN's
rebranding requirements.Duties and responsibilities
  • Initiate a Project Plan for update of “Taro” documents according to new SUN's guidelines (replacement of logo, related content, format, etc.) under Management guidance.
  • Prepare and revise documents in accordance with an organized project plan, and with pre-determined target dates as per GMP guidelines.
  • Responsible for obtaining signatures for review and approval in the document revision cycle.
  • Verify and submit documents to the appropriate roles/functions and upload approved documents in the respective Quality Systems folders or directories.
  • Process documents using simple workflow where editorial corrections are required, such as a logo or format change only, and using complex workflow where “Taro” content has to be updated.
  • Liaise with QA Documentation team members and Manager, QA Documentation/Change Control with respect to Document workflow as required.
  • Manage tasks and activities for Documentation Change Control records within the Trackwise System.
  • Provide leadership and support to Department stakeholders in the Re-branding Project activities.
  • Any other duties related to Re-branding Project and Documentation as required.
Additional responsibility (Only applicable to customer facing roles)Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business dayQualifications
  • Bachelor's Degree in Science, or other related discipline preferred
  • Previous Quality Assurance experience (2-3 years) in the pharmaceutical Industry is an asset.
  • Well-developed interpersonal and teamwork skills
  • Ability to establish and prioritize daily work schedules in a fast-paced environment.
  • Proficiency in MS Office -Word, Excel, and PowerPoint.
  • Ability to work independently.
  • Knowledge of Health Canada and FDA regulations
  • Good communication and time-management skills
  • Strong organizational skills and ability to multi-task; detail-oriented.
  • Personable, and able to maintain excellent relations with internal clients
  • Any deviations to procedures or systems are brought to the attention of management.
Working conditions
  • Numerous and varied responsibilities demanding attention and detail
  • Working in general office environment.
Physical requirementsOffice basedDirect reportsNA

Sun Pharmaceutical Industries