Tolmar · 1 day ago
QC Analyst II (Onsite)
Tolmar is a pharmaceutical company seeking a QC Analyst II to perform routine testing of raw materials and finished products according to regulatory protocols. The role involves prioritizing tasks, conducting analyses, and contributing to team objectives while ensuring quality and consistency.
BiotechnologyHealth CareManufacturing
Responsibilities
Prioritizes tasks and performs job duties with minimal guidance from management. Works to complete tasks in an efficient manner, and is a productive member of the department
Performs analyses on a variety of samples using intermediate preparation techniques and analysis methods. Employee will be trained and become proficient in the intermediate preparation techniques and analysis methods
Actively contributes to short-term team objectives, focusing on routine tasks while ensuring consistency and quality
Develops and implements strategies to overcome daily challenges and improve workflows
Applies intermediate technical skills and a foundational understanding of cGMP, organizational structure, and departmental processes to complete standard work assignments
Takes the initiative to support projects and actions demonstrating a continuous improvement mindset
Delivers high-quality work on a consistent basis, meeting deadlines and maintaining reliability in daily tasks
Proactively develops actionable solutions based on an understanding of the problem, collaborating with team members when necessary to ensure the solution is effective and aligns with organizational goals and regulatory requirements
Demonstrates strong focus and concentration to complete tasks with minimal mistakes, maintaining quality under pressure, and ensuring focus during work to support infrequent preventable errors
Takes responsibility for individual contributions and accepts accountability for performance
Actively participates in team activities, challenges, and shared responsibilities (such as T-cards, archival, etc.), showing enthusiasm and a can-do attitude to inspire others, while maintaining professionalism
Overcomes challenges with a positive attitude, staying focused on the goal even in the face of setbacks Models good laboratory stewardship by maintaining a clean, orderly and safe work environment and proactively restocks low inventory items and routine lab supplies
At the direction of management, trains junior analysts in analysis methods and lab techniques
Accountable for documenting all activities and maintaining records according to good documentation practices
Accountable for proper use, care and maintenance of instrumentation
Provides detailed accounts of testing performed to investigators. Under the direct supervision of an investigator, may perform investigational testing
Makes scientific recommendations to management/technical writers regarding QC procedures
Completes tasks on time and works to eliminate repeat errors. Follows all procedures applicable to job functions to ensure high quality of work
Responsible for ensuring that company and regulatory data integrity guidelines are consistently followed
Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers and is willing to assist co-workers in the completion of tasks
Performs intermediate method transfers
Represents the department by providing accounts of testing performed and results of method transfer activities and assists with troubleshooting aberrant method transfer results, if necessary
Interacts respectfully with all other employees both inside and outside of the department and members of management and shows interest in others' input and reasoning. Appropriately resolves differences of opinion
Upon delegation, may be responsible for representing the QC chemistry laboratory when communicating with outside departments and vendors
Identifies issues and escalates those issues to the department senior leadership or management as appropriate
Participates 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
Performs additional duties as assigned
Qualification
Required
Knowledge of a government regulated pharmaceutical laboratory environment, preferably for drugs or medical devices including cGMP, GLP and ICH and their application to laboratory testing and review processes and procedures
Intermediate understanding of the use of USP, NF and other compendia
Ability to use and maintain analytical laboratory instruments such as HPLC, FTIR, GPC, GC, Dissolution and UV-Vis spectrophotometers
Effective written and oral communication skills
Knowledge of computer systems for sample tracking, laboratory equipment, chromatography, raw data handling and storage
Ability to interpret, understand and follow analytical procedures/calculations and scientific principles
Bachelor's degree in scientific discipline, preferably in Chemistry or Biochemistry
Two or more years of experience in a QC analytical laboratory position in the pharmaceutical industry
Experience with chromatography software
Benefits
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.
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 StageRecent News
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