Quality Assurance Specialist
vor 3 Wochen
SciPro is seeking a highly skilled Quality Specialist to join our team. As a Quality Specialist, you will play a critical role in ensuring that our pharmaceutical products meet the highest quality standards and regulatory requirements.
Key Responsibilities:- Ensure compliance with Good Manufacturing Practice (GMP) regulations, including audits, inspections, and regulatory submissions.
- Review and approve batch records, change controls, deviations, CAPAs, and validation protocols.
- Conduct and participate in internal audits to ensure compliance with company standards and regulatory requirements.
- Maintain and review Standard Operating Procedures (SOPs) and ensure proper documentation of all quality-related processes.
- Support risk assessments and manage quality risk in processes and production.
- Provide quality-related training to staff to ensure compliance and awareness of quality standards.
- Collaborate with procurement and suppliers to manage supplier quality audits and ensure raw materials meet company standards.
- Assist in the investigation and resolution of customer complaints regarding product quality.
- Identify and implement process improvements in quality assurance and control systems.
- Stay up-to-date with local and EU regulations affecting pharmaceutical manufacturing, ensuring company compliance.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related field.
- Minimum of 3-5 years of experience in Quality Assurance in the pharmaceutical or biotech industry.
- Strong knowledge of GMP, EU regulations, and quality systems.
- Experience with audits and regulatory inspections.
- Excellent organizational, communication, and interpersonal skills.
- Proficiency in German and English (both written and spoken).
- Experience with quality management systems (QMS).
- Familiarity with electronic document management systems (EDMS).
- Strong analytical and problem-solving skills.
- Experience with root cause analysis and risk assessment tools.
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