Senior Quality Assurance Professional
5 days ago
Job Overview:
We are seeking a skilled Quality Assurance professional to join our team as an Associate Quality Systems Manager. In this role, you will be responsible for the control, operation, and maintenance of our Quality Documentation Control Systems.
Your Key Responsibilities:
- Ensure the accuracy and integrity of quality documentation, including procedures, job descriptions, and reports.
- Develop and implement effective document control processes to ensure compliance with regulatory requirements.
- Collaborate with cross-functional teams to support site regulatory inspections and provide expert guidance on quality management systems.
- Generate and communicate quality metrics to stakeholders, and participate in quality projects as needed.
- Maintain high-quality standards by training new users, ensuring data integrity, and continuously improving site procedures and forms.
Requirements:
- Bachelor's degree in Science or related discipline.
- 1-3 years' experience in Quality Assurance within the Pharmaceutical industry.
- Strong document control experience, with expertise in Veeva Vault an advantage.
- Proficiency in MS Office tools, particularly Word, Excel, and PowerPoint.
- Familiarity with EU/US quality-related pharmaceutical regulations, especially Data Integrity requirements for GMP documentation.
- Excellent written and oral communication skills, with ability to interact effectively with diverse groups.
About Us:
We are Merck Gruppe - Msd Sharp & Dohme, a leading healthcare company committed to 'Inventing for Life.' We prioritize patient needs and strive to find innovative solutions to complex healthcare challenges.
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