Pharmaceutical, Quality Assurance Analyst Ii

As the world’s leading provider of “green” Plant Cell Fermentation (PCF®) Technology, Phyton Biotech produces paclitaxel and docetaxel and offers comprehensive development and manufacturing services of other plant-based molecules, extracts, and recombinant products for use in the Pharmaceutical, Traditional Chinese Medicine (TCM), Cosmetic, Agricultural and Food Ingredient industries.

Phyton’s cGMP certified facility in Canada specializes in the purification and chemical conversion of natural active ingredients, improving the quality of life for patients and consumers while respecting our environment. With more than 25 years experience in product/process development, production, and commercialization, we manufacture safe, reliable, and high-value ingredients for customers around the world. Our site has the capacity to meet more than ⅓ of global demand for paclitaxel and docetaxel, commonly used active pharmaceutical ingredients (API’s) in chemotherapy medications.

Phyton Biotech is adding to its Pharmaceutical Quality Assurance Department. This team supports the manufacturing of Phyton Biotech’s API’s and Intermediates at development and commercial scale which meet cGMP and Phyton’s quality and safety requirements, while supporting customers and regulatory authorities.

**What Phyton Biotech will offer you**:
Phyton Biotech determines an individual’s pay based on multiple factors including experience, education, job-related skills, and equity within the team or organization. The compensation range for this role is $61,000 - $68,000.

We encourage a progressive team environment with a work home balance by offering an innovative organization wide schedule of 9-day work rotation every two weeks, to afford our employees with additional rotational time off to spend with family.

**We are eager to connect with you, if**:

- You are detail-oriented with an eye for quality and accuracy
- You have strong analytical skills, with capability to evaluate information, and make appropriate decisions in response to challenges
- You thrive in collaborative environments with strong interpersonal skills, but comfortable working autonomously
- You possess the ability to prioritize and multi-task in a fast-paced environment
- You are a reliable and dependable team member

**A day in the department would include**:

- Assist with ensuring Phyton’s quality system remains compliant with regulatory requirements and industry standards
- Supports the continuous improvement of the quality system and procedures to maximize efficiencies and safety, and minimize deviations/incidents/investigations
- Provides quality support for internal departments
- Performs reviews of quality documents, such as SOPs, test methods, non-conformances, OOS’s/OOT’s, CAPAs, change controls, incidents, Certificates of Analysis, protocols, reports and risk assessments
- Performs reviews of QC, Operations, Logistics and Engineering quality records, such as analytical data, completed batch records, completed forms, executed qualification/validation protocols and reports
- Perform document control activities
- Assist with internal, customer and regulatory audits

**Qualifications & Experience**:

- BSc in a life-sciences, chemistry/biochemistry or related discipline required
- Minimum of 3 years hands-on experience in a pharmaceutical, biopharmaceutical/biotech industry
- Experience in a regulated manufacturing environment is an asset, including food, nutraceutical, or pharmaceutical production
- Knowledge of a Quality Management Systems (QMS) an asset

Pay: $61,000.00-$68,000.00 per hour

Additional pay:

- Overtime pay

**Benefits**:

- Casual dress
- Company events
- On-site parking

Schedule:

- Day shift
- Monday to Friday

Work Location: In person

Expected start date: 2025-07-07