Senior Quality Analyst

At-a-Glance:

Are you ready to build your career by joining a global pharmaceutical company? If so, our client is hiring a Senior Quality Analyst!

What You'll Do:

• 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.
  
  
  

What You’ll Bring:

• 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.

Position Type: Contract

Get in Touch:

We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Rishaw at (862) 895-5483 to learn more.

Who We Are:

Since 1986, Hired by Matrix, Inc. has improved our candidates' lives with exciting job opportunities that provide outstanding career advancement. Hired by Matrix offers our contract professionals competitive salaries, benefits after 60 days, and a 401k option with a company match after one year. Hired by Matrix is an Equal Opportunity Employer and proud to be certified as both a Woman-Owned Business Enterprise and a Woman-Owned Small Business.

Connect with us on LinkedIn today and learn more about how HbM can change your career: https://www.linkedin.com/company/hired-by-matrix-inc/

Check out our Career Center: https://www.hiredbymatrix.com/find-work/open-positions/

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