Senior Quality Analyst at Hired by Matrix

Pay Rate: 44.28-46.42 $/Hour

• Responsible for the analysis and characterization of raw materials, ensuring their quality and suitability for production processes.
• Role involves working closely with cross-functional teams to develop and implement testing protocols, troubleshoot material issues, and support continuous improvement initiatives.
• Essential Functions:
  • Conduct detailed analysis of raw materials using Raman spectroscopy and other analytical techniques.
  • Develop and validate testing methods to ensure the accuracy and reliability of material characterization.
  • Collaborate with R&D, quality assurance, and production teams to address material-related challenges.
  • Maintain accurate records of all analyses and prepare comprehensive reports.
  • Stay updated with the latest advancements in Raman spectroscopy and material science.

• Education and Experience:
  • Bachelor’s or Master’s degree in Chemistry, Material Science, or a related field.
• Requirements:
  • Proven experience in using Raman spectroscopy for material analysis.
  • Strong understanding of material properties and their impact on production processes.
  • Excellent problem-solving skills and attention to detail.
  • Ability to work effectively in a team-oriented environment.
  • Training within a regulated Pharmaceutical/biotech/medical device environment.
  • Understanding and application of cGMP’s (EP, JP, USP).
  • Detailed knowledge and application with electronic Quality Systems and Data Integrity.
• Strong attention to detail as demonstrated through consistent quality of work.
• Excellent written and verbal communication skills.
• Computer proficiency in MS Word and Excel, MS Access required.
• Demonstrates process orientation—thinks through required steps and sequencing to ensure quality work output.
• Function as change agent to ensure accurate and timely facilitation of global and department, GMP, etc. changes
• Timely follow up to ensure satisfactory resolution to issues.
• Knowledge of CGMPs (relevant laws, guidance, directives, and industry practice), and demonstrated ability to apply learnings appropriately in a controlled environment.
• Ability to:
  • Anticipate potential problems and take proactive action to avoid/minimize impact.
  • Anticipates consequences of actions and how they impact other areas.
  • Utilize project management skills to independently prioritize, plan and schedule workflow.
  • Interpret and apply GMPs, relevant laws, guidance’s, and directives to extremely complex pharmaceutical situations.
  • Work and coordinate activities across multiple functional groups with a sense of professionalism and urgency.
  • Work collaboratively with internal and external team members and customers/contacts.
• Self-motivated; able to work with minimal supervision.
• Exercises independent judgment in evaluating compliance.