- Sample of Raw materials and Purified water for Analysis
- Arranging retain samples for raw materials and finished products
- Performing daily analytical balance verification- as required
- Performing calibration of pH meters and Fluoride Ion meters as required
- Preparation and standardization of Volumetric solutions and test solutions as required
- Arranging chemicals in the lab and checking for their expiration dates as required
- Arranging quality control documents as needed as required
- Performing wet analysis for raw materials and finished products, which includes Loss on drying, Viscosity, pH and water content etc.
- Performing chart replacement for all chart records which monitor temperature and humidity as required.
- Perform analysis using HPLC/UV-Visible spectrophotometer for raw materials, finished products and stability samples.
- Other duties as required by Management.
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
- The requirements listed below are representative of the knowledge, skill and/or abilities required.
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Ability to apply comprehensive knowledge of pharmaceutical cGMP's and quality system controls, procedures, and records to ensure ongoing quality compliance.
- Ability to perform all requirements independently with limited managerial oversight.
- Excellent organizational abilities to meet accelerated timelines, manage multiple shifting priorities and maximize efficiencies in a dynamic customer-focused environment.
- Superior attention to detail to ensure accuracy of work product.
- Superior critical-thinking and problem-solving skills; ability to recognize and resolve discrepancies and issues.
- Minimum 2 years industrial experience in Quality Control laboratory functions.
- Degree (BS or BA) in Biology, Chemistry, Biochemistry, or relevant related field. Or sufficient technical depth or professional experience will be considered in lieu of technical degree.
- Experience in quality systems, including validation, documentation, compliance department preferred. HPLC analytical experience is a plus
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QC Chemist - Philadelphia, United States - Onsite Personnel LLC
Description
Job Description
Job DescriptionJOB TITLE: Junior QC ChemistESSENTIAL DUTIES AND RESPONSIBILITIES:
QUALIFICATIONS:
EDUCATION AND/OR EXPERIENCE:
Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment. Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws.
