QC Analyst II

AVEVA DRUG DELIVERY SYSTEMS INCMiramar, FL
Onsite

About The Position

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 Miramar. Participates in testing to support Analytical Development method validations.

Requirements

  • Bachelor's degree (B.S.) in chemistry or related field
  • 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)

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 heighten 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 guidance of Supervisor
  • Coordinates testing schedules and monitors 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
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