Stability Associate II

Tolmar CareersWindsor, CO
1d$26 - $29Hybrid

About The Position

Responsible for maintaining the following systems and/or databases: Stability System II Software, stability database, stability variances, stability environmental chambers, assistance in writing stability protocols and reports, data auditing and stability records.

Requirements

  • Knowledge of cGMPs and ISO9001, with commitment to following written procedures.
  • Proficient in use of Word and Access software programs, and ability to learn new software programs quickly.
  • Effective oral and written communication.
  • Organized, with high accuracy of work and attention to detail.
  • Ability to work independently with minimal supervision to meet scheduled deadlines.
  • Ability to work well with employees at all levels.
  • Ability to audit data, review data and write reports.
  • Valid driver’s license and acceptable Motor Vehicle record required.
  • Bachelor’s degree in scientific discipline, math or science preferred, or equivalent experience.
  • Two or more year’s experience in the pharmaceutical or medical device industry.

Nice To Haves

  • Experience with quality or stability is desired.

Responsibilities

  • Requisition, label and place stability samples into appropriate storage conditions according to approved protocols.
  • Enter new lots into the Stability System II Software and stability databases.
  • Pull samples at appropriate time points and deliver to the QC, AD and Microbiology Labs, as appropriate.
  • Monitor chamber storage conditions per electronic monitoring systems and follow-up on any excursions.
  • Audit stability data after data entry for accuracy & compliance to protocols.
  • Review stability data to monitor product performance.
  • Ensure that variances, aberrant results and incident reports are documented.
  • Print graphs and data as required for investigations.
  • Write stability protocols and reports for regulatory submissions.
  • Accurately process Document Change Requests (DCR’s) and Product Change Orders (PCO’s) as required.
  • Approve PCO’s after assessing impact to the stability program.
  • Transport stability samples between company locations.
  • 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.
  • Perform other related duties as required.

Benefits

  • Benefits summary: https://www.tolmar.com/careers/employee-benefits
  • Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package.
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