Tolmar · 1 day ago
QC Analyst I (Onsite)
Fort Collins, Colorado, United States
Full-time
Onsite
New Grad, Entry Level
$28/hr - $29/hrTolmar is a company focused on quality control in the pharmaceutical sector, and they are seeking a QC Analyst I to ensure the quality of products through sampling, inspection, and testing. The role involves performing routine testing and maintaining accurate records in compliance with regulatory protocols.
BiotechnologyHealth CareManufacturing
Responsibilities
Complete training and become proficient in basic preparation techniques and analytical methods
Perform analyses on a variety of samples using basic preparation techniques and analytical methods
Inspect and sample materials in accordance with specified requirements. Determine appropriate sampling area and PPE requirements based on material properties
Perform heating, mixing and sampling of raw materials using laboratory and material handling equipment
Ensure proper status, containers, and storage of materials and product
Review SOPs and work instructions using the electronic document management system
Collect and retain samples in accordance with procedures
Perform retest sampling
Pull additional sample requests or inventory requisitions for items in inspection
Perform cleaning and monitoring of rooms and equipment
Document all activities and maintain records in adherence to good documentation practices
Maintain accountability for proper use and care of instrumentation
Complete tasks on time and work to eliminate repeat errors
Follow all procedures applicable to job functions to ensure high quality of work
Prioritize tasks and performs job duties with minimal guidance from management. Work to complete tasks in an efficient manner and serve as a productive member of the department. Contribute to a highly productive environment by avoiding distractions
Follow procedures to determine status or disposition, and properly document results on records and in laboratory notebooks
Ensure that company and regulatory data integrity guidelines are consistently followed
Provide detailed accounts of testing performed to investigators. Under the direct supervision of an investigator, may perform investigational testing
Maintain accountability for promoting an atmosphere of teamwork, cordiality and respect towards co-workers
Provide support to the department leadership with the implementation of new systems, and continuous improvement efforts. Generate new ideas to create efficiencies and improve processes; willingly support new ideas and process enhancements
Participate in required annual hazardous waste training. Hazardous waste involvement may include but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures
Interact respectfully with all other employees both inside and outside of the department and members of management and show interest in others’ input and reasoning. Appropriately resolve differences of opinion
Complete training in accordance with requirements and timelines
Coordinate equipment calibration with Calibration Technicians
Monitor equipment and facilities for proper operating conditions
Participate in monthly quality and safety walkthroughs
Perform various other duties as assigned
Qualification
Required
Bachelor's degree in scientific discipline, preferably in Chemistry or Biochemistry
Valid driver's license and Acceptable MVR may be required
Ability to bend, squat, and lift minimum of 30 pounds required
Ability to pass physical and eye exam required. Ability to see color
Basic understanding of a government-regulated laboratory environment, preferably for drugs and medical devices including GMP, GLP, and ICH and their application to laboratory testing and review processes and procedures
Basic understanding and familiarity in the use of USP, NF and other compendia
Ability to use and maintain analytical laboratory instruments such as HPLC, FTIR, GC, and UV-Vis spectrophotometers
Ability to interpret, understand and follow analytical procedures and calculations
Working knowledge in drug or device cGMP
Knowledge of computer operations, including proficiency with MS Word, Excel and Access. Ability to learn Tolmar's electronic systems
Strong organizational skills and attention to detail
Skill in effective written and oral communication
Ability to work independently and properly prioritize tasks with limited supervision
Ability to work well with employees at all levels and departments
Ability to use critical thinking to address potential areas of concern
Knowledge of computer systems for sample tracking, laboratory equipment, raw data handling and storage
Preferred
Previous experience in an analytical laboratory position preferred
Experience in a high-volume manufacturing environment preferred
Benefits
Shift differential: 18% after training period
Benefits summary: <https://www.tolmar.com/careers/employee-benefits>
Company
Tolmar
TOLMAR is a northern Colorado based pharmaceutical research, development, manufacturing and commercial operations company.
Founded in 2006
1001-5000 employees
H1B Sponsorship
Tolmar has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (3)
2023 (5)
2022 (3)
2021 (7)
2020 (6)
Funding
Current Stage
Late StageLeadership Team
A
Anil D'souza
Chief Executive Officer
Gerald Wallner
Data Integrity Manager
Recent News
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