Job Description:
The QA Operations Specialist will play a pivotal role in ensuring the quality and compliance of oral solid dose production by reviewing batch manufacturing documentation, preparing QP releases, investigating deviations, and implementing corrective actions.
Key Responsibilities:
1. Documentation Review: Conduct thorough reviews of batch manufacturing documentation to ensure accuracy and compliance.
2. QP Release Preparation: Prepare documentation for timely QP release, adhering to regulatory requirements.
3. Deviation Investigation: Investigate and close out deviations in collaboration with other departments, identifying root causes and implementing corrective actions.
4. CAPA Implementation: Identify and implement corrective and preventative actions to prevent future occurrences.
5. Quality Risk Management: Participate in and lead Quality Risk Management Assessments to mitigate risks and ensure quality systems are effective.
6. Audit Participation: Participate in internal and external audits as required, maintaining confidentiality and contributing to continuous improvement.
Requirements:
* Education: Degree in Chemistry, Analytical Science, Pharmaceutical Science, or Forensic Science.
* Skills: Strong IT skills, attention to detail, initiative, self-motivation, discipline, good communication skills, and a strong positive attitude.
Benefits:
* Pension
* VHI
* Paid Holidays