Job Summary

We are seeking a skilled QC Analyst for sampling and testing for in-process, release, validation and stability purposes while following internal and external (GPP/GMP) requirements for routine quality control testing. The incumbent partners with different departments of all sites of Aleafia as well as external partners. The QC Analyst participates in continuous improvement activities and innovation in the Quality Control space.

Key Responsibilities

- Sample intermediates, bulk product, finished product and materials
- Test samples for in-process, release, validation and stability purposes by chemical, microbiological and pysical techniques
- Inspect incoming raw and packaging materials and finished goods
- Support the Cultivation department by testing cannabis at various points during growth stages and curing.
- Document test results as per SOP and external requirements (GPP/GMP)
- Recognize OOS or OOT results and executes lab investigations.
- Interpret and review data and complete written reports and certificates.
- Participate in deviation investigations
- Data entry, trending and analysis of historical test data
- Initiate and follow through with actions of historical test data
- Initiate and follow through with actions required to close Change Controls and CAPAs
- Evaluate methods and procedures and suggest improvements and changes as required
- Perform method development testing

Qualifications

- Degree or technical diploma in a relevant field (i.e. pharmaceutical, biotechnology, science, chemistry, microbiology and biology)




- Minimum 1-3 years experience in pharmaceutical laboratory environment (GMP compliant)
- Vast experience using chemical, microbiological and physcial test methods and instrument and method troubleshooting
- Experience with active compound and plant material testing is preferred
- Proficiency in various chemical, microbiological and physical techniques and operation of instrumentation and associated software (e.g. pH meter, viscosity and density measurement, Karl Fisher apparatus, Chromatography instruments)
- Ability to work effectively in a team-based environment
- Solid computer skills
- Strong organizational, analytical and multi-tasking ability
- Excellent written and verbal skills
- Understanding of GMPs
- Familiar with international pharmacopoeia and ICH guidelines
- Ability to organize and prioritize workload

Working Conditions

- Mixture of standing and walking, some light lifting
- Generally fast-paced
- Occasional exposure to higher than normal noise levels, frequent exposure to various chemicals used in the testing of raw materials, components and finished products.
- Occasional exposure to strong odours resulting from testing and production procedures.
- On occasion flexible hours of work may be required

Compensation & Benefits

- CA $22.50 per hour
- Health, dental, and LTD benefits
- Paid time off and holidays
- Ongoing training and development opportunities

Job Types: Full-time, Permanent

Pay: $22.50 per hour

Benefits:

- Dental care
- Life insurance
- On-site parking
- Paid time off
- RRSP match

Work Location: In person

📌 QC Analyst (Paris)
🏢 Important Group
📍 Paris