What are the responsibilities and job description for the QC Analyst II position at Aveva Drug Delivery Systems Inc?
Job Summary:
Performs analytical testing of raw materials, and components.
Job Responsabilities
- Performs testing of analytical assays, including HPLC, GC, UV testing for raw materials.
- Perform raw materials and components ID methods.
- Reviews laboratory data as assigned by Supervisor
- Perform testing following compendial methods (USP, EP, JP)
- Maintains proficiency with data acquisition systems
- Calibrates analytical instrumentation by standard protocol
- Revises STPs and SOPs and Specifications
- Assists the supervisor in training new chemists
- Perform method transfer or method verifications.
- Performs IQ/OQ of analytical instrumentation
- Troubleshoots instrumentation with guidance of Supervisor
- Other general QC laboratory responsibilities as assigned
- Support housekeeping and maintenance activities
- Works as a member of a team to achieve all outcomes
- Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements
- Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion
- All other relevant duties as assigned
- Education
o Master's degree (M.S.) in chemistry or related field
- Knowledge, Skills and Abilities
o Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
o Experience in the testing of raw materials.
o Working knowledge of GC, HPLC, Karl Fisher, FTIR, UV spectroscopic methods, and compendial methods.
o Ability to read analyze, and interpret common scientific and technical journals, specifications, standard operating procedures, and standard testing procedures.
o Knowledge FDA, cGMPs, and SOPs
Experience
o A minimum of two (2) years of QC laboratory experience (Master’s degree)
