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Job Description
Senior QA Associate role involves leading quality initiatives, ensuring compliance, and promoting safe practices in a pharmaceutical production environment.
We are seeking a highly skilled professional to provide quality leadership, direction, and governance for our organization. Key responsibilities include reviewing and approving GMP documents, monitoring quality systems, and ensuring data integrity.
Essential qualifications include a degree in a relevant field (e.g., Pharmacy, Chemistry, Engineering, Quality) and a minimum of 2 years of relevant experience. Strong organizational skills, critical thinking, and problem-solving abilities are also required.
Key Responsibilities:
- Review and approval of GMP documents, including standard operating procedures, raw material specifications, and validation documents.
- Monitoring of quality systems, including data integrity and systems.
- Evaluation and contribution of regulatory information to regulatory documents.
Key Attributes:
- Excellent attention to detail.
- Experience working in cross-functional teams and proven ability in decision making.
- Demonstrates ability in critical thinking, data analysis, problem solving, and experience in root cause analysis.
- Strong organisational skills, including ability to follow assignments through to completion.
- Understanding of Data Integrity and its applications.
- Self-motivated, positive, and ability to work under pressure.