Sr Research Associate, Analytical Operations
- Edmonton, AB
- On-site
- Posted Sep 18, 2026
- 1 position
Opens an external site
- Employment type
- Full-time
- Experience level
- Mid-level · 2+ years
- Minimum education
- High school
- Posting language
- English
- Working hours
- 40 hours per week
Job summary
Develop and execute analytical methods to support the characterization and process development of novel small-molecule drug substances. Collaborate with cross-functional teams to analyze data, investigate anomalous results, and ensure documentation meets quality and safety standards.
Job details
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description We are seeking a Sr Research Associate in Analytical Development to develop and champion innovative analytical methods and technologies supporting the characterization and process development of novel small-molecule drug substances. Job Responsibilities Develop and execute analytical methods and experiments supporting characterization, process development, and project objectives for novel small-molecule drug substances. Analyze and interpret data, assess quality, investigate anomalous results, and recommend scientifically sound solutions. Produce clear, traceable documentation and communicate results and conclusions through reports, discussions, and presentations. Collaborate across Analytical Development, Process Development, Quality, and Manufacturing to solve technical problems and meet project goals. Perform work in accordance with applicable procedures and quality, safety, and environmental standards while supporting continuous improvement. Basic Qualifications High School and Five Years’ Experience OR Associate Degree and Four Years’ Experience OR Bachelor's Degree and Two Years’ Experience OR Masters' Degree Preferred Qualifications Previous experience with UPLC/HPLC, GC, KF titration, LCMS, GCMS, NMR, DSC/TGA, particle size analysis, XRPD, or related chromatographic and characterization techniques. Knowledge of analytical testing in a regulated laboratory environment. Knowledge of organic synthesis and reaction mechanisms. Experience with coding, data modelling, or digital tools supporting analytical method development and innovation. MSc with 0+ years or BSc with 2+ years of industry experience in chemistry, natural product chemistry, biochemistry, or a related discipline. Knowledge of chromatography and modern chromatography systems. Strong laboratory, data interpretation, problem-solving, and decision-making skills, with the ability to guide experimental design. Clear written and verbal communication, including concise presentation of analytical results. Strong organization, time management, and interpersonal skills; able to work semi-independently and collaboratively to meet deadlines. For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.
What you’ll do
Develop and execute analytical methods to support the characterization and process development of novel small-molecule drug substances. Collaborate with cross-functional teams to analyze data, investigate anomalous results, and ensure documentation meets quality and safety standards.
Requirements
Requires a minimum of a high school diploma with five years of experience, an associate degree with four years, a bachelor's degree with two years, or a master's degree. Candidates should possess strong laboratory skills, knowledge of chromatographic techniques, and the ability to work collaboratively in a regulated environment.
Listed skills
- Problem solving · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Analytical methods
- Small-molecule drug substances
- UPLC
- HPLC
- GC
- LCMS
- GCMS
- NMR
- DSC/TGA
- Particle size analysis
- XRPD
- Chromatography
- Data interpretation
- Problem-solving
- Organic synthesis
- Analytical development
- Natural Product Chemistry
- Titration
- Data Interpretation
- Analytical Testing
- Small Molecules
- Ability To Meet Deadlines
- Analytical Method
- Research
- Chemistry
- Biochemistry
- Decision Making
- Continuous Improvement Process
- Data Modeling
- Design of Experiments (DOE)
- Leadership
- High-Performance Liquid Chromatography
- Innovation
- Interpersonal Communications
- Problem Solving
- Liquid Chromatography Mass Spectrometry
- Nuclear Magnetic Resonance
- Organic Synthesis
- Particle Size Analysis
- Presentations
- Process Development
- Time Management
- Verbal Communication Skills
Job areas
- Science & Research
- Manufacturing
- Healthcare
- Operations Research Associate
- Scheduler / Operations Coordinator
- Stock Clerks
- Production, Planning, and Expediting Clerks
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