Regulatory Affairs Quality Specialist

6 days ago


Philadelphia, Pennsylvania, United States Disability Solutions Full time

We are seeking a highly skilled Regulatory Affairs Quality Specialist to join our team in Philadelphia, PA.

The estimated annual salary for this role is $80,000-$100,000 based on industry standards and location.

About the Role

This is a full-time position reporting to the QA Manager. The successful candidate will be responsible for ensuring compliance with regulatory requirements and developing and implementing quality procedures. They will also conduct supplier audits and monitor quality performance metrics.

  • Conduct supplier audits and assess their quality performance.
  • Develop and implement quality procedures and training programs.
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
  • Monitor quality performance metrics and identify areas for improvement.
Requirements

To succeed in this role, you will require a Bachelor's degree with at least two years of relevant experience or an Associate's degree with four years of experience. A degree in Regulatory Affairs, Biotechnology, Manufacturing, Operations, Supply Chain, or Engineering is strongly preferred. Proven track record in regulatory compliance and quality assurance is essential.

You will also need strong analytical skills and experience in working with quality management systems.

About Catalent

Catalent is a global drug development and delivery leader that produces over 70 billion doses per year. We offer a dynamic, fast-paced work environment and opportunities for career growth. Our benefits package includes 152 hours of PTO, 8 paid holidays, medical, dental, and vision benefits, tuition reimbursement, and more.



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