About this role
The team is seeking a Quality Assurance Deputy Manager/Manager to oversee quality assurance processes and ensure compliance with industry standards. The successful candidate will play a crucial role in maintaining high-quality standards and regulatory compliance within the organization.
Key Responsibilities:
- Lead the preparation, review, and maintenance of the Validation Master Plan (VMP) to ensure alignment with industry standards and regulatory requirements.
- Review and approve Qualification/Validation protocols to ensure compliance with CGMP standards.
- Ensure all quality systems are maintained according to CGMP requirements and monitor compliance across all departments.
- Develop and implement standard operating procedures (SOPs) related to quality assurance.
- Conduct regular audits and assessments to identify areas for improvement and ensure adherence to quality standards.
- Collaborate with cross-functional teams to address quality-related issues and implement corrective actions.
Required Skills & Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, or a related field.
- Proven experience in quality assurance within the pharmaceutical or biotechnology industry.
- Strong knowledge of CGMP regulations and validation processes.
- Excellent analytical and problem-solving skills.
- Strong communication and interpersonal skills to work effectively with various stakeholders.
Experience:
- A minimum of 5-8 years of relevant experience in quality assurance or a related field.
What we offer:
- Opportunity to work in a dynamic and innovative environment.
- Professional development and career growth opportunities.
- Collaborative and supportive team culture.
Applications are read by our talent team, usually within two working days.
If you look like a fit we will call you, and you will hear from us either way.