Laboratory Analyst
Philip Morris•Aurora, CO
•Onsite
About The Position
Quality Control Laboratory Analyst We are hiring a Quality Control Laboratory Analyst for our Aurora, CO office! As a Quality Control Laboratory Analyst, you will apply validated methods and work instructions to perform routine analyses and technical activities, ensuring that raw materials, semi-finished products, and finished products are analyzed and monitored appropriately.
Requirements
- Bachelor’s degree in Chemistry, Engineering, or a related scientific field with 5+ years of laboratory experience, or a Master’s degree with 2+ years of laboratory experience.
- Experience in quality and laboratory environments within the tobacco, food, pharmaceutical, or other regulated industries.
- Strong experience with HPLC, GCMS, Agilent software, and LabVantage LIMS.
- Advanced knowledge of quality tools, root cause analysis, analytical methods, and statistical techniques.
- Strong data analysis and reporting skills.
- Ability to train, mentor, and share knowledge with junior staff.
- Knowledge of ISO 17025 standards
Nice To Haves
- experience in FDA-regulated industries is a plus.
Responsibilities
- Ensure compliance with PMI standards, legal requirements, and environmental, health, safety, and sustainability guidelines.
- Promote a proactive, safety-first culture using preventive and predictive approaches.
- Perform physical, chemical, and microbiological testing of raw materials, tobacco, semi-finished, and finished products according to approved procedures and methods.
- Maintain the integrity and timely reporting of results within the laboratory management system and support certificate of analysis generation.
- Review and release testing results completed by other laboratory personnel.
- Support method validation, method transfers, and ISO 17025 accreditation activities.
- Participate in the creation and review of procedures, work instructions, and quality documents.
- Operate, verify, and calibrate laboratory equipment in accordance with PMI and ISO requirements.
- Maintain laboratory logbooks and records in compliance with QMS requirements.
- Investigate out-of-specification results, resolve deviations, and contribute to corrective actions using problem-solving tools.
- Provide timely and accurate information regarding products and testing activities.
- Ensure compliance with QMS requirements and ISO 17025 standards.
- Collaborate with colleagues and support teams to ensure efficient quality processes and achieve quality and productivity goals.
Benefits
- Hourly Rate: Starting at $30/hour
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
