QA Analyst

Responsiblties:

• Confirming and ensuring the compliance of the protocols and reports of method validations / verifications / comparison reports and any other study reports.
• Monitoring and ensuring of current Good Laboratory Practices followed by laboratory personnel during routine operation to ensure adherence to procedure.
• Maintaining all the incoming documents with proper tracking, recording, storage and archival of the documents.
• Reviewing and identifying the gaps within the system during routine monitoring and informing the supervisor for necessary improvements in the identified areas.
• Actively participating in laboratory investigations and incidents as well as ensuring the proper compliance.
• Evaluating and confirming the compliance related to raw materials, inprocess and finished product analytical documents.
• Conducting random internal audits in analytical lab and ensuring the compliance.

Experience:

• Possess a bachelor’s degree in chemistry, Pharmaceutical Sciences, or related field of study from an accredited institution. Master’s degree in the above and/or related fields of study as noted above preferred.
• A minimum of eight (8) years of relevant work experience in a pharmaceutical manufacturing setting within the Quality function.
• Experience using statistical software packages is a plus.
• Must be proficient in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.
• Minimum of five (5) years’ experience in quality assurance in a pharmaceutical manufacturing operation environment.

Key Skills:

• Analytical skills.
• Problem-solving ability.
• Communication.
• Verbal communication.
• Quality standards development.
• Time management.