Job Description

*WE\xe2\x80\x99RE HIRING!* *OUR MISSION* At Alberta Veterinary Laboratories/Solvet (\xe2\x80\x98AVL/Solvet\xe2\x80\x99), our multi-faceted team is dedicated to promoting the health and welfare of animals. Built on the values of INNOVATION, QUALITY, PEOPLE/ANIMALS, ACCOUNTABILITY, PASSION, and SAFETY, AVL is a Canadian company searching for new solutions to old problems through the development and world-wide distribution of products that bring great comfort and ease to both owners and animals. Founded in 2009, this Calgary-based, family owned and operated company has provided quality animal health products to thousands of farmers, vets, and pet owners. At AVL/Solvet our mission is simple \xe2\x80\xa6 we listen to our customers and deliver solutions to problems they face daily. Let\xe2\x80\x99s help you launch your career with AVL/Solvet! We are looking for an experienced and energetic new team member to join our Quality team on-site in our Calgary head office as a Quality Assurance Analyst (evening shift - 2:30-11:00pm) who can drive our pharmaceutical manufacturing operations. *IMPORTANT NOTES* - Candidates MUST have their own RELIABLE transportation to the facility as Calgary Transit DOES NOT operate an evening route
- The successful candidate will be required to provide a satisfactory Police Background Check, work references, and current Confirmation of Medical Health *THE ROLE* Under the direction of the QC Manager with oversight from the VP, Quality & Regulatory Affairs, you will be responsible for sampling and testing within the pharmaceutical industry for in-process/finished, release, validation, and stability while following internal GMP requirements for routine quality control testing. You will also be assisting with method development and validation including exercising data integrity principles in managing laboratory data. All activities will be undertaken and completed in the dedicated on-site lab according to Good Manufacturing Practices. *DAY-TO-DAY* - Implement of Good Manufacturing Practices (GMP) in the pharmaceutical industry
- Participate in the authoring, review and implementation of clear and concise Policies and Standard Operating Procedures (SOPs), Procedures, Work Instructions, Reports, and other technical documentation
- Sample raw materials, intermediates and finished product
- Test samples for in-process, release, validation, and stability purposes using chemical, microbiological, and physical techniques
- Inspect incoming raw and packaging materials and finished goods
- Document test results as per SOP procedures and Good Documentation Practices (GDP)
- Interpret and review data, and complete written reports and certificates
- Recognize Out of Specification (OOS) test results and participate in executing lab investigations
- Participate in deviation investigations
- Participate in R&D activities related to testing
- Participate in method development and validation
- Data entry, analysis and trending
- Initiate and follow through with actions required to open/close Change Controls and Corrective and Preventative Actions (CAPAs)
- Evaluate methods and procedures and suggest improvements and changes as required
- Calibrate, validate, or maintain laboratory equipment
- Maintain lab cleanliness and safety standards participating in weekly rotation of safe waste chemical disposal
- Effectively collaborate and work with other departments to complete these tasks
- Perform other duties as requested *IDEAL FIT* Education & Experience - Minimum of a BSc in Chemistry (Analytical preferred) or Biochemistry, or a Degree in Chemical Engineering or related field of engineering (completion of critical coursework to be verified)
- Minimum of 3-years of related work experience in pharmaceutical laboratory, or related GMP/ISO compliant laboratory environment
- Demonstrated lab skills experience and the ability to use chemical and physical test methods
- Previous related experience with HPLC (high performance liquid chromatography), GC (gas chromatography), IC (ion chromatography) including trouble shooting, along with analytical method development and validation according to ICH (International Council for Harmonisation)
- Some experience with microbiological methods considered an asset
- Understands the content and implementation of Policies, SOPs, Work Instructions, and other technical documents
- Up to date with current trends in analytical chemistry for the pharmaceutical industry, as well as Health Canada regulations and GMP guidelines
- Experience working with various with computer programs, instrument software programs (i.e., Empower), databases and electronic data records Skills and Attributes - Excellent interpersonal and communication skills (both written and spoken) (professional level of English required)
- Reliable, punctual and thrives as part of a busy team
- Highly detail-oriented, hands-on, resourceful, and proactive in preventing and solving problems
- Proven organizational and time-management skills with the ability to prioritize to meet deadlines
- Able to rigorously apply, follow and maintain rules, regulatory requirements, procedures and processes
- Curiosity driven with the motivation and ability to troubleshoot challenging processes and solve complex technical problems
- Able to work both independently with minimal oversight and as an integral part of the team
- Comfortable with multi-tasking and adaptable to changing priorities within a team-oriented entrepreneurial environment
- Consistently demonstrates initiative and willingness to go above and beyond
- Able to remain calm under pressure *WHAT\xe2\x80\x99S IN IT FOR YOU* At AVL/Solvet, we are committed to keeping our team healthy and motivated, so they can do the best work of their lives. We\xe2\x80\x99ve built a company where people love to come to work, and we think you will too! AVL/Solvet team members benefits include: - Full-time Monday-Friday (2:30-11:00pm)
- Casual dress
- Company-provided PPE (note \xe2\x80\x93 this position may be exposed to some hazardous chemicals within a controlled environment)
- Paid time off (including vacation, sick and personal days)
- Life insurance and comprehensive healthcare benefits
- Opportunities for professional growth through learning & development initiatives
- A dynamic, inclusive, and collaborative work environment *NEXT STEPS* If this opportunity sounds like a great fit and you want to stand out from the crowd, apply by providing a COVER LETTER explaining your interest in AVL and how you can bring immediate value to this position, along with a current copy of your RESUME. We appreciate the interest from all candidates in our career opportunities. If you have the qualifications we are looking for, can rise to the challenge of living AVL/Solvet values, and can demonstrate how you will be a valuable team member, we will be in touch to schedule an interview. The collection, use, and retention of personal information will be in accordance with AVL/Solvet privacy policies and practices. By submitting your resume and personal data to AVL/Solvet and participating in a personal interview, you acknowledge and consent to collecting, using, and disclosing your personal information by AVL/Solvet to determine your suitability for employment opportunities. Job Type: Full-time