QUALITY CONTROL DOCUMENTATION OFFICER

Job Description

Our Client is looking for a QC Documentation Officer within their company who will be responsible for preparation, review, and issue of QC documentation, in full compliance with cGMPs and company procedures. Moreover, the selected candidate will be required to perform QC related functions according to the exigencies of the Company.

REQUIREMENTS:

• Writing/preparing analytical methods and specifications, including but not limited to status of analysis docs, chromatographic proformas and analytical records.
• Support in documentation related to method validation, process validation, cleaning validation, and stability studies.
• Issuing of COAs for QC Management approval.
• Assisting the QC Manager in drafting/revising SOPs relevant to QC operations.
• Ensuring that all pharmacopeial standards are in compliance with current pharmacopeias and are reflected in internal documents.
• Participate in the management, co-ordination and timely execution/closure of change controls, deviations and CAPAs.
• Creation of specifications and master of tests in the MRP system.
• Co-ordination and management of client sample requests

Selected Person Will Be:

• In possession of a higher qualification in Chemistry or Pharmaceutical science.
• A minimum of two years experience in a pharmaceutical QC environment.
• Extremely organised and possess excellent communications skills.
• Able to work independently as well as in a team environment.
• Self-motivated and have excellent attention to detail.
• Results oriented and will display an attitude that reflects our Company values.

What Does The Company Offer You:

• Continuous opportunity for professional growth and training.
• A competitive salary.
• Health insurance.
• Medical check-ups.
• A culture where teamwork is priority.
• A positive working environment with an employee focused approach.
• Job security.