Position Responsibilities:

Processing Tasks

Work within the current GMP and Health Canada guidelines and adhere to all regulatory standards within the Company.
Ensure that all aspects of local manufacturing plasma operations are performed according to the company standards.
Ensure that safety regulations are followed and maintain a clean and safe work environment at all times.
Perform activities related to the registration, processing and freezing of plasma units, and complete related documentation in a timely manner.
Perform activities related to the serum and plasma sample collection.
Ensure that labelling, packaging, and storage of all samples and plasma units are done according to regulations and procedures.
Perform activities related to the shipment and the arrival of plasma samples to testing facilities and manage communication with transporters when required.
Ensure that all sample shipments are assembled according to the requirements of the customers and the standards.
Maintain the storage of plasma units organized with all supporting and updated documentation required in all Production department areas.
Perform activities related to plasma unit packaging.
Assist the Plasma Processing Supervisor with plasma units’ shipment preparation and loading.
Monitor all temperature and humidity-controlled areas in the production department. This includes the freezers and the production department areas.
Complete properly equipment logbooks.

Supplies management

Perform activities related to the receipt and registration of materials and supplies
Assist the Plasma Processing Supervisor in maintaining an updated soft good inventory
Communicate with suppliers to obtain required documentation in a timely manner, to manage the delivery of items or to address any complaints or questions.

Documentation and Procedures management

Maintain proper records and documentation that complies with GDP/GMP guidelines and internal Standard Operating Procedures and ensure they are easy to access.
Report quality issues and procedural deviations to the Plasma Processing Supervisor.
Assist the Plasma Processing Supervisor in performing Corrective and Preventive actions (CAPA) plans related to the production department so they can be closed in a timely manner.
Identify defects, batches recall, standards storage conditions failures, or any Quality Assurance specification that can potentially affect plasma units during their shelf life.

Other

Participate in continuing education when presented with the opportunities, and take the lead in the education of other staff when necessary.
Maintain a consistent and regular attendance record.
Train new Plasma Processing staff if required in all aspects of their function, including Good Manufacturing Practice (GMP) principles, adherence to procedures and protocols, and any software/hardware that is necessary to complete their duties.
May be required to work weekends, evenings and some holidays.
Perform other duties as assigned, including but not limited to, cleaning of all areas of the Center, receiving and shipping of products and materials.

Required Skills, Qualifications and Experience:

1. Bachelor's Degree in Science or related field preferred

2. Certification or qualification in recognized courses related to laboratory work or medical laboratory sciences is an asset.

3. At least 1 year of related experience in the industry or medical/research laboratory is an asset.

4. Demonstrated analytical/problem-solving abilities

5. Proficient in usage and handling of computers and related peripherals

Job Types: Full-time, Permanent

Pay: $35,776.00 per year

Benefits:

Flexible language requirement:

Schedule:

Application question(s):

Were you referred by a current Grifols employee (Formally known as Canadian Plasma Resources)? If so, please indicate their name.
Are you available to work evenings AND weekends?

Education:

Work Location: In person

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