What are the responsibilities and job description for the QC Analyst III position at Aveva Drug Delivery Systems?
Description
About Us:
Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide.
Job Summary
Performs analytical testing of raw materials, components, standards, intermediate/finished products. Responsible for testing involved with technology transfer from qualified laboratories on or off-site to QC Tamarac. Participates in testing to support Analytical Development method validations.
Key Responsibilities
Education
About Us:
Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide.
Job Summary
Performs analytical testing of raw materials, components, standards, intermediate/finished products. Responsible for testing involved with technology transfer from qualified laboratories on or off-site to QC Tamarac. Participates in testing to support Analytical Development method validations.
Key Responsibilities
- Supports release and stability testing for raw materials, components, standards, intermediate/finished products
- Prepares and executes verification protocols for in-house/compendia test methods
- Executes technology transfer protocols and assists in evaluations
- Analytical support to AD for qualification/validation of test methods
- Reviews laboratory work and approves data packages as designated by the Supervisor
- Maintains a heightened proficiency with data acquisition systems;
- Execute methods for calibration of analytical instrumentation
- Writes and reviews STPs, SOPs, Specifications, and technical reports
- Trains analysts on methods and instrumentation
- Independently troubleshoots instrumentation
- Maintains QC compliance systems with the guidance of the supervisor
- Coordinates testing schedules and monitors the status of sample testing as assigned by the Supervisor
- 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
- Bachelor's degree (B.S.) in chemistry or related field or;
- Master's degree (M.S.) in chemistry or related field
- Ph.D. degree in chemistry or related field
- Ability to apply advances mathematical concepts such as exponents, logarithms, quadratic equations, linear regression, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, and correlation techniques..
- 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.
- Ability to read, analyze, and interpret common scientific and technical journals, specifications, standard operating procedures, and standard testing procedures. Ability to write presentations and articles that conform to prescribed style and form. Ability to effectively present information to middle management.
- Knowledge FDA, cGMPs, and SOPs
- A minimum of five to seven (5)-7 years of QC laboratory experience (Bachelor’s degree)
- A minimum of two to five (2 -5) years of QC laboratory experience (Master’s degree)
- A minimum of two (2) years lab experience (Ph. D. degree)
- Aveva Drug Delivery Systems and DifGen Pharmaceuticals provides a comprehensive benefits plan
- Medical/Dental/Vision Insurance
- Paid Time Off
- 401k with employer match
- Paid Holidays and Floating Holiday