Quality Assurance Associate

3 weeks ago

Simcoe, Canada Thrive Cannabis Full time

**QUALITY ASSURANCE ASSOCIATE**

**Job Location**: Thrive Cannabis

**Employment Type**: Full-time permanent employment onsite

**Division**: Operations, Quality

**Hours**: 40 hours per week

**JOB SUMMARY**

Thrive Cannabis is seeking a self-motivated individual to support the Quality team. The Quality Assurance Associate will be responsible to:

- Represent Quality as an ambassador for regulatory compliance regarding GMP, Cannabis Acts & Regulations, and company policies and procedures.
- Work in collaboration with the Quality Assurance Manager to perform delegated QAP duties (as required).
- Prepare and review quality-related documentation, including batch records, master specifications, logbooks, and all follow-ups.
- Investigate, review, and track QMS (customer complaints, non-conforming reports, CAPA, MOC, DEV, risk assessment, OOS, OOT, etc.).
- Participate in new initiatives, new product development, in-house quality projects as required.
- Support, participate in, and assist with materials and inventory management activities (receipt, return, adjustment, investigation, release, etc.).
- Provide support for the implementation of quality procedures, processes, and programs.
- Work closely with the operation and other stakeholders to ensure site compliance.
- Provide training to personnel as needed.
- Work with site and multidisciplinary teams to ensure cross-functional quality requirements are met.
- Assist/backup the Quality team on-site and off-site as needed.
- Participate in APQR, internal, and external audits as needed.
- Other duties as requested

**KNOWLEDGE, SKILLS AND ABILITIES**:

- Knowledge of health & Safety and Quality standards and compliance.
- Ability to work in a team as well as independently.
- Ability to take initiative and drive improvements.
- Strong interpersonal, communication, and computer skills.
- Ability to multitask, prioritize activities, and adapt to changing priorities in an evolving environment.
- Ability to write technical documents (SOPs, Investigation Summaries, etc.).
- Work extended hours and/or weekends to support product and quality activities.
- ERP experience is an asset.

**REQUIREMENTS**:

- Bachelor of Science or diploma in a science-related field (chemistry, biochemistry, biology, microbiology, medicine, horticulture, pharmaceutical, food, natural health product and medical laboratory science).
- Minimum of 2-5 years' experience in quality assurance, quality, and document control.
- Experience working in a regulated environment, pharmaceuticals, cannabis, chemical, food or natural health product manufacturing environment is preferred.
- Understanding of Quality Management Systems including batch record review, batch release, document control, change requests, deviations, investigations, and CAPA
- MS Office proficiency is required
- Effective verbal and written communication in English

**DIVERSITY AND INCLUSION**

We are proud to foster and celebrate a diverse community of professionals We take pride in nurturing an inclusive culture that empowers our people to be their authentic selves, celebrate their differences and love where they work.

If you require accommodation (including, but not limited to, an accessible interview site or alternate format of job posting) during the recruitment and selection process, please do not hesitate to let our team know We are here to help.

**Benefits**:

- Extended health care
- On-site parking
- Paid time off

Flexible Language Requirement:

- French not required

Schedule:

- 8 hour shift

Ability to commute/relocate:

- Simcoe, ON N3Y 4K3: reliably commute or plan to relocate before starting work (required)

Work Location: One location

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