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: