Regulatory Affairs Specialist
il y a 7 jours
Job Summary
PHARMAXYOM, a leading consulting firm in the life sciences industry, is seeking a highly skilled Quality Assurance Manager to join our team. As a key member of our quality assurance department, you will be responsible for ensuring the highest standards of quality and regulatory compliance across our client's operations.
Key Responsibilities
- Develop and implement quality management systems to ensure compliance with regulatory requirements and industry standards.
- Conduct regular audits and assessments to identify areas for improvement and implement corrective actions.
- Collaborate with cross-functional teams to develop and implement quality policies and procedures.
- Provide training and support to employees on quality-related topics.
- Investigate and resolve quality-related issues and incidents.
- Develop and maintain quality metrics and reports to track performance and identify areas for improvement.
Requirements
- Bachelor's degree in a relevant field, such as quality assurance, regulatory affairs, or a related field.
- Minimum 5 years of experience in quality assurance or regulatory affairs, preferably in the pharmaceutical industry.
- Strong knowledge of regulatory requirements and industry standards, including GMP and ISO 13485.
- Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
- Strong analytical and problem-solving skills, with the ability to identify and resolve quality-related issues.
What We Offer
- A competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.
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