Qc Laboratory Analyst I - Littleton, United States - Adventure Ready Brands
Description
:Purpose and Scope
The Quality Control Laboratory Analyst I is primarily responsible for daily performance of the testing of all raw materials, batches, and finished goods.
Essential Job Functions
- Test and release applicable raw materials.
- Test and release bulk batches.
- Complete finished goods testing.
- Complete stability testing.
- Ability to preform analytical and microbial testing.
- Preparing as needed and shipping samples for outside microbiological and analytical testing.
- Prepare and execute inhouse microbiological testing for environmental and production samples.
- Prepare and execute analytical methods based on Approved Laboratory Methods.
- Assist in ordering and maintaining stock of all laboratory equipment and chemical standards.
- Assist QC Manger and QA/RA Manager in developing and maintaining laboratory GLP's.
- Monitor work activities to ensure adherence to Standard Operating Procedures, QA Manuals and programs.
- Assist with developing new testing validations and methods on Analytical Equipment
- Provide QC assistance and support to managers, supervisors, and manufacturing personnel.
- Undergo training on SOP's as listed on the accompanying Training Matrix.
- Participate and interact in internal and external training programs.
- Other duties as assigned
Requirements:
Requirements:
- 03 years laboratory experience or the equivalent combination of education (associate degree, or relevant life science courses and experience).
- Understanding or Previous experience in a GMP and GLP environment.
- Proficiency with Microsoft Office (Excel and Word)
- Understanding and knowledge of pharmaceutical cGMP, FDA guidelines and industry standards.
- Must be well organized.
- Ability to work effectively in a team.
- Technical writing skills.
- Multitasking and attention to detail.
- Must be able to work independently.
- Ability to handle confidential company data, projects, information, etc.
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