QA Technician

at  Prime Health Ltd

QUALITY ASSURANCE (QA) TECHNICIAN

Our Organization Prime Health Ltd. is a fastest growing NNHP (Natural and Non-prescription Health Product) manufacturing company based in Maple Ridge, BC having presence in North America, Asia, Middle East and Latin American countries. We are passionate in delivering result and customer satisfaction. To boost our growth, we are looking for a “Quality Assurance Technician” with the following job description and requirements:

MINIMUM REQUIREMENTS

• Minimum 2-3 years of experience in Quality Assurance in the pharmaceutical industry or a similar role.
• University Degree (Post graduate degrees and Health Professional degrees are preferred)
• Basic knowledge in CFIA FSEP Manual and HACCP System preferred.
• In-depth understanding of quality systems
• Knowledge of Natural Health product formulation is an asset.
• Ability to work independently and as a member of a team.
• Excellent written and verbal communication skills
• Able to manage multiple projects and deadlines.
• Ability to identify compliance risks.
• Proficiency with computer applications such as Word, Excel, PowerPoint, and Outlook
• Excellent scientific knowledge
• Ability to interpret complex Regulatory documents such as Health Canada guidance documents to provide guidance to internal and external stakeholders.
• Ability to multi-task and to work in a fast-paced environment.
• Attention to detail.
• Strong organizational skills, troubleshooting skills, time management skills.
  Salary: $20 to $21 hourly
  Job location: Maple Ridge, BC
  Job type: Full time permanent
  Benefits: After probationary perio

• Preparing, reviewing, finalizing and maintaining general and operational SOPs file.
• Conducting periodic SOP reviews and scheduling training to all concerned departments.
• Reviewing work orders/Batch manufacturing records and associated logs and checklists for any errors.
• Assisting the Regulatory department in preparation of Quality Technical Agreements with the Clients and third-party laboratories.
• Reviewing, managing and helping to prepare Investigation Reports for market complaints.
• Reviewing, preparing, and implementing change control & deviation reports for any new changes in documentation as well as deviation in actual manufacturing.
• Reviewing, finalizing, and releasing of all finished product work orders.
• Maintaining files or record of internal and external calibration.
• Preparing and maintaining all required documents and files for customer audit and regulatory authority audit and attend all audit process to make it successful.
• Designing the formatting for quarterly departmental audit and annual audit and perform to evaluate gaps in processes and remove the gaps and give training to staff members
• Monitoring finished products to confirm the compliance as per quality standard, preparing deviation report if any and give training to responsible team to remove future noncompliance.
• Meetings to be attended: I. Health and Safety II. Third party audit III. General management meeting (as per requirement) IV. Production meeting (As per requirement).
• Preparing and sending detailed weekly report including suggestions for improvements.
• Time to time duties as assigned by management.