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Quality Control Associate

4 months ago

Richmond Hill Ontario, York region, Canada Prollenium Medical Technologies Inc. Full time

COMPANY:

Prollenium Medical Technologies Inc. is a fast-growing Canadian developer, manufacturer and international distributor of premium HA dermal filler. We are proud to address all of our client's needs through streamlined medical device innovation. Prollenium is able to ensure a continual flow of creation, unique ideas, and a steady pipeline of new and exciting products that provide safe and effective results. US FDA, Health Canada, and CE approvals, over 4 million syringes in the Revanesse product line have been sold to 70+ countries world-wide. Prollenium is the only manufacturer of Hyaluronic Acid dermal fillers in North America. Join our dedication to innovation.


Prollenium provides competitive compensation, benefits, and development opportunities.


JOB SUMMARY:

The Quality Control Associate, under the direction of the department leader, performs routine and non-routine quality control testing of raw materials and products at various stages. The associate provides support for stability, process validation, method validation, transfer and development activities. This position reports to the Quality Control Supervisor.


MAJOR RESPONSIBILITIES:

  • Overall responsibility to ensure the QC functions are in an ISO compliant state at Prollenium
  • Perform routine raw material, in-process and finished product testing
  • Perform non-routine testing to support production process validation, stability studies or any testing assigned by management
  • Review testing documents and release documents
  • QC Inventory management, including release of raw materials, in process and final products, and chemicals used for testing; Keep track of consumables, testing samples and retention samples
  • Maintain good quality system documentation and record keeping
  • Assist with drafting and revising SOPs, Forms, protocols and reports


ADDITIONAL RESPONSIBILITIES

  • Ordering supplies
  • Receipt and inspection of supplies
  • Maintenance of laboratory equipment
  • Attending meetings
  • Other duties as assigned


MINIMUM QUALIFICATIONS

Technical Knowledge/Experience

  • Four-year university chemistry degree.
  • 1-3 years work experience in a QC function in a GMP/GLP or ISO compliant environment.
  • Excellent written and oral communication skills.

Behavioural

Demonstrated ability to apply the following behavioral competencies on the job:

  • Teamwork: Working effectively and productively with others;
  • Written Communication: Writing clearly, succinctly and understandably;
  • Problem Solving: Anticipating, analyzing, diagnosing and resolving problems under supervision;
  • Organization and Planning: Utilizing logical, systematic and orderly procedures to meet objectives
  • Flexibility: Agility in adapting to change


PREFERRED QUALIFICATIONS:

  • Knowledge of microbiology and polymer chemistry;
  • Experience with wet-chemist testing;
  • Experience with inventory management;
  • Experience with technical document preparation;


WORKING CONDITIONS:

Requirement to work in laboratory setting up to 50% of the time.


Note: This is a 15-months contract position.