Job Description: 

The Pharmaceutical Paralegal provides comprehensive legal and administrative assistance to the Legal, Compliance, and Privacy activities within Eupraxia pharmaceuticals and its related companies. This role focuses upon on matters related to pharmaceutical regulation, intellectual property, contracts, data protection initiatives, and corporate governance activities. The Paralegal role helps ensure the company operates in compliance with applicable healthcare, data privacy, and pharmaceutical laws and regulations across global jurisdictions. It supports the company in managing the company’s legal obligations and risk.

Reports to: Senior Director of Legal Affairs, Privacy & Data Protection Officer

Key Responsibilities:

Contract Management

• Draft, review, and maintain templates for contracts, NDAs, clinical trial agreements, vendor and supply agreements, and research collaborations.
• Manage the contract lifecycle using contract management systems and ensure timely renewals or terminations.

Legal Research and Compliance Monitoring

• Conduct legal research on pharmaceutical laws, data privacy, advertising, and anti-bribery regulations.
• Support the implementation of compliance programs and employee training initiatives.

Litigation and Risk Management Support

• Help prepare discovery materials, summarize documents, and coordinate with litigation counsel as needed.

Privacy & Data Protection Support

• Support the Privacy Office with compliance under GDPR, HIPAA, CCPA, and other applicable privacy laws.
• Assist in managing data processing agreements (DPAs) and vendor due diligence related to data protection.
• Help maintain records of processing activities (RoPA) and privacy documentation.
• Support privacy impact assessments (PIAs) and incident response processes, including documentation of breaches or data subject requests.
• Coordinate privacy training and awareness initiatives across departments.

Qualifications:

• Bachelor’s degree in paralegal studies, Legal Studies, Life Sciences, or a related field.
• Paralegal certificate from an accredited program (preferred).
• 3–5 years of experience as a paralegal, preferably within the pharmaceutical, biotechnology, or healthcare industry.
• Knowledge of FDA regulations, Good Clinical Practice (GCP), and data protection laws (HIPAA, GDPR).
• Experience with contract management systems and document management tools (e.g., DocuSign).
• Excellent written, organizational, and analytical skills.
• Strong attention to detail and ability to handle confidential information.
• Excellent verbal, written and interpersonal communication skills.
• Is able and willing to travel internationally, especially between Canada, US and Europe

Additional attributes:

• Strong analytical and problem-solving abilities
• Detail-oriented with strong organizational skills and the ability to manage multiple priorities
• Self-starter who thrives in a fast-paced, dynamic environment
• Ability to work both independently and collaboratively across teams
• Professional presentation with excellent written and verbal communication skills
• Flexible within a constantly changing environment
• Motivated and adaptable team player with the ability to prioritize and meet deadlines

Salary Range:  CAD$ 100,000 – 115,000 annually

Within the posted range, individual pay is determined by job-related skills, relevant experience, education and/or training. Please note that the range details above reflect the base pay only. A bonus will be available based on performance and remaining in post for the agreed contract duration. We also offer a competitive benefits package.

This is an opportunity to work in a small, entrepreneurial, and highly motivating environment, with a strong emphasis on work/life balance and a supportive company culture.

How to Apply:

Please submit your CV and cover letter at link below.

While only short-listed candidates will be notified, we thank each applicant for their submission.

Job Description:

The Process Development Scientist will be responsible for developing manufacturing processes for novel solid and viscous liquid formulations in the Vancouver, Canada laboratory, including responsibilities for process scale-up and tech transfer to contract manufacturing facilities. This is a laboratory-based position, and it is expected that 80% of work time will be spent on-site, rather than working remotely.

Reports to: Director, CMC

Location: Vancouver, BC

Key Responsibilities:

• Design, plan and execute experiments in the Vancouver Laboratory to support the development of novel solid and viscous liquid formulations.
• Develop and/or evaluate appropriate sterilization procedures, including sterile filtration or terminal sterilization by heat and gamma irradiation.
• Scale up manufacturing processes from laboratory to >100L scale for transfer to contract manufacturer sites.
• Engage in technology transfer and production troubleshooting at contact manufacturer sites.
• Identify and procure equipment required for scale-up and for laboratory operations.
• Perform physical characterization of samples as required. Methods may include rheology, viscoelastic analysis, NMR, SEM, and thermal analysis. Ability to operate HPLC/UPLC systems and develop analytical methods is an asset.
• Provide training and supervision to co-op and intern students.
• Interpret and present research findings in a clear, concise manner at company meetings and via written reports.
• Support writing of appropriate sections of regulatory filings, including an IND or IMPD.
• Comply with required Quality Management System procedures, including maintenance of a laboratory notebook.
• Maintain laboratory equipment in a functional status and perform other laboratory duties as needed.
• Assist with CMC group operations as requested.

Additional Attributes:

• Highly self-motivated
• Able to work independently and as part of a study team
• Detail-oriented with a view to the overall scope of the project
• Organized
• Accountable
• Self-directed learner

Requirements:

• At least 5 years of experience in the pharmaceutical industry.
• PhD in chemistry, biochemistry, or pharmaceutical sciences. Candidates with an MSc or a BSc and industry experience will be considered.
• Experience with viscous liquids compounding techniques.
• Experience with sterile filtration and terminal sterilization by autoclave is an asset.
• Experience with aseptic techniques is an asset.
• Knowledge and experience with GMP practices is an asset
• Excellent verbal and written communication skills.
• Ability to multitask and work well in a team, especially in a fast-paced environment.
• A life-long learner mindset.
• A critical thinker.

Salary Range: CAD$120,000 – 130,000 annually

Within the posted range, individual pay is determined by job-related skills, relevant experience, education and/or training. Please note that the range details above reflect the base pay only. A bonus will be available based on performance and remaining in post for the agreed contract duration. We also offer a competitive benefits package.

This is an opportunity to work in a small, entrepreneurial, and highly motivating environment, with a strong emphasis on work/life balance and a supportive company culture.

How to Apply:

Please submit your CV and cover letter at link below.

While only short-listed candidates will be notified, we thank each applicant for their submission.

Eupraxia is seeking an experienced Lab Manager to oversee the daily operations of our R&D laboratory. The successful candidate will ensure safe, efficient, and compliant laboratory operations while managing equipment and inventory. This role requires technical knowledge of chemistry, as well as proficiency in equipment maintenance, and a commitment to upholding the highest standards of laboratory safety and quality.

Location: Vancouver, BC, Canada

Reports to: Associate Director, Pharmaceutical Development

Responsibilities:

• Maintain compliance with federal, provincial, and local safety regulations including the BC Occupational Health and Safety Regulation, and WorkSafeBC standards
• Develop, implement, and enforce laboratory safety protocols and standard operating procedures
• Conduct regular health and fire safety training and maintain accurate safety documentation
• Perform safety inspections and hazard assessments; address identified risks promptly
• Manage chemical inventory, storage, and disposal in accordance with regulations
• Order laboratory consumables and manage supplier relationships
• Oversee shipping and receiving of chemicals and samples, including international shipping documentation and compliance
• Monitor and maintain laboratory facilities, including HVAC, and coordinate services as required
• Implement plan for any future facility renovations
• Track operating budget and expenditures to ensure financial accountability

Requirements:

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, Chemical Engineering, or related scientific field with 3-5+ years (Bachelor’s) or 2+ years (Master’s) of laboratory management or senior technical laboratory experience
• Proven experience with international shipping logistics and import compliance
• Experience with analytical chemistry or biological assays would be advantageous

Additional attributes:

• Highly motivated self-starter with strong initiative in identifying operational improvements
• Proactive problem-solver who can troubleshoot equipment issues and safety concerns independently
• Attention to detail in maintaining compliance records, inventory management, and safety documentation
• Excellent organizational and time management skills to juggle multiple laboratory priorities
• Continuous learner committed to staying current with laboratory regulations and best practices
• Clear communicator capable of explaining safety procedures and technical requirements to diverse audiences
• Strong vendor and supplier relationship management skills
• Experienced with high potency compound handling and associated safety protocols
• Enthusiastic about pitching in on experimental work when needed, working closely with researchers alongside lab management duties

Salary Range: CAD$70,000-130,000 annually

Within the posted range, individual pay is determined by job-related skills, relevant experience, education and/or training. Please note that the range details above reflect the base pay only. A bonus will be available based on performance and remaining in post for the agreed contract duration. We also offer a competitive benefits package.

This is an opportunity to work in a small, entrepreneurial, and highly motivating environment, with a strong emphasis on work/life balance and a supportive company culture.

How to Apply:

Please apply at link below. While only short-listed candidates will be notified, we thank each applicant for their submission.