Regulatory Officer/QA Supervisor

A Licensed Pharmacist who will ensure that regulatory requirements issued by FDA are updated and maintained. He/she is also responsible to ensure compliance to requirements of Good Distribution Practices issued by WHO – World Health Organization and International Standards for Pharmaceutical Industry.

• Secures Regulatory licenses from FDA and ensure that these licenses are updated and maintained.

• Keeps an up-to-date copy of legislation, regulations and guidelines and industrial goods practice and ensure to fully comply with said changes as soon as they become effective.

• Handles all necessary arrangement, reporting and coordination during External Audit by Regulatory Body and Client.

• Coordinates, consolidates, reviews and submits Root Cause Analysis and CAPA – Corrective Action and Preventive Report for audit findings during External Audit by Regulatory Body and Client within the timetable set by the auditors.

Qualifications:

• Licensed Pharmacist
• At least one (1) year of experience in Warehouse, Manufacturing, or
  Logistics operations.
• Strong knowledge of Good Distribution and Warehousing Practices
• Familiar with Quality Audit standards and audit preparation.
• Possesses strong analytical and problem‑solving skills.

Maersk is committed to a diverse and inclusive workplace, and we embrace different styles of thinking. Maersk is an equal opportunities employer and welcomes applicants without regard to race, colour, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, pregnancy or parental leave, veteran status, gender identity, genetic information, or any other characteristic protected by applicable law.
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