Quality Control Supervisor

Prollenium Medical Technologies Inc.; Aurora; Presencial; CAD 80.000 - 110.000; Jornada completa

Descripción de la vacante

Prollenium Medical Technologies Inc. is seeking a QC Supervisor to lead the QC laboratory at its Aurora site and support testing aligned with ISO 13485. The role reports to the Director of Quality and collaborates with QA, manufacturing, and regulatory teams.

The ideal candidate has a Master’s degree in a scientific discipline and 3–5 years of QC supervisory experience in GMP/ISO environments, with hands-on use of HPLC and other analytical tools.

Formación

• MSc in a scientific discipline (Chemistry, Biology or related).
• 3–5 years of supervisory QC experience in GMP/GLP/ISO environments.
• Experience with analytical equipment (HPLC, spectrometers, GC, Mass Spec) and QA records.

Responsabilidades

• Oversee QC laboratory operations at two locations (Aurora and Richmond Hill).
• Ensure testing complies with ISO 13485 and regulatory audits.
• Lead staffing, training, and performance reviews in QC.
• Coordinate qualification, calibration, and validation programs.
• Review trending data and present to Quality leadership.

Conocimientos

Leadership

Teamwork

Written communication

Problem solving

Organization & planning

Flexibility

Educación

M.Sc. in Chemistry/Biology or related

Herramientas

HPLC

Spectrometers

Mass Spec

Chromatography

Inventory management systems

Descripción del empleo

Company Overview:

Prollenium Medical Technologies Inc. is a fast-growing Canadian developer, manufacturer, and international distributor of premium hyaluronic acid (HA) dermal fillers and cosmetic products. We are proud to address all of our client's needs through streamlined 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. With regulatory approvals from the US FDA and Health Canada, Prollenium has sold over 5 million syringes from its Revanesse® product line across more than 80+ countries worldwide. Prollenium was the first 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 QC Supervisor is the point person for all staff in the QC laboratory on items related to testing. This important role assists in achieving a smooth workflow, while fulfilling the requirement of ISO 13485. This position reports to the QC Manager.

MAJOR RESPONSIBILITIES:

The QC Supervisor is the point person for all staff in the QC laboratory on items related to testing. This important role assists in achieving a smooth workflow, while fulfilling the requirement of ISO 13485. This position reports to the Director of Quality.

• Scope of Responsibilities: Responsibilities include QC laboratory operations at both locations of Prollenium Medical Technologies (Aurora and Richmond Hill) including raw materials testing and retain programs, in-process and finished product release testing, stability programs and equipment calibration and validation programs.
• Audit Participation: The QC Supervisor will be expected to participate in regulatory audits and represent the QC Department when auditors / inspectors raise questions about departmental activities.
• Management Reviews: The QC Supervisor will participate in scheduled management reviews and present the relevant trending, successes, obstacles faced over the relevant period time covered by the management review activities.
• Staffing, Resources and Training: The QC Supervisor role will include periodic meetings with the Director of Quality Assurance to relay requests related to staffing, resources and training (internal or external) which will in turn be brought to the attention of upper management (ie Director of Human Resources, Logistics Supervisor, Director of Business Operations or President and CEO) on a case by case basis.
• Coaching and Mentoring: The QC Supervisor role will include the responsibility of interacting with the QC chemists and encouraging individual interests as they relate to learning new QC tests or addressing correcting human error in the performance of a test. This role will also (ie Director of Human Resources, Logistics Supervisor, Director of Business Operations or President and CEO) on a case by case basis.
• Staff Performance: The QC Supervisor role will involve input related to QC staff performance reviews which will be discussed with the Director of Quality Assurance and brought to the attention of upper management (ie Director of HR, President and CEO) on a case by case basis.
• QC Testing and Record Keeping: The QC Supervisor role will be expected to participate in routine QC testing activities when other duties are not being conducted. The priority is to find a balance in the fulfilment of the requirements of the ISO13485 quality system and the need to efficiently supervise the QC laboratory.

MINIMUM QUALIFICATIONS:

Technical Knowledge/Experience

• M.Sc. University Degree in a Scientific Discipline (Chemistry, Biology, or related).
• Knowledge of Chemistry and Chemical test methods.
• Experience with Analytical Equipment (HPLC, Spectrometers, Chromatography, Mass Spec, etc).
• Inventory management systems, set-up and management.
• 3-5 years supervisory experience in a QC function in a GMP/GLP or ISO compliant environment.

Behavioural

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

• Leadership: Effectively manage, coach and mentor QC Associates
• Teamwork: Working effectively and productively with others. Willing to assist in laboratory testing.
• Written Communication: Writing clearly, succinctly and understandably
• Problem Solving: Anticipating, analyzing, diagnosing and resolving problems
• Organization and Planning: Utilizing logical, systematic and orderly procedures to meet objectives
• Flexibility: Agility in adapting to change

PREFERRED QUALIFICATIONS:

• Experience in Microbiological Testing
• Experienced in Validation Protocol Development and Report Writing
• Experience in Stability Protocol Development and Report Writing
• SOP writing experience
• Training experience

The position is based in Aurora.

Note: We use AI-enabled tools to support certain aspects of our recruitment process.