Compliance Manager(Pharma)- USFDA Expert Lezivia Lifesciences

  • company name Lezivia Lifesciences
  • working location Office Location
  • job type Full Time

Experience: 5 - 5 years required

Pay:

Salary Information not included

Type: Full Time

Location: Madurai

Skills: Communication skills, collaboration, Pharmaceutical Manufacturing, USFDA regulations, conducting regulatory audits, developing compliance documentation, providing compliance training, maintaining compliance program implementation, process improvement tactics, Organizational Skills, proficiency with Microsoft Office, regulatory compliance software

About Lezivia Lifesciences

Job Description

Company Description Lezivia Lifesciences is a reputed company known for its quality pharmaceutical products. Many of our products are manufactured at WHO-approved facilities, ensuring the best quality for patients. We aim to provide high standards in our product deliveries, maintaining trust and reputation within the healthcare sector. Role Description This is a full-time on-site role for a Compliance Manager (Pharma) - USFDA Expert, located in Madurai. The Compliance Manager will be responsible for ensuring that all pharmaceutical practices meet USFDA regulations. Day-to-day tasks include conducting regulatory audits, compliance training, documentation, and process improvement. The role involves developing and implementing compliance programs, staying updated with regulatory changes, and coordinating with various departments to maintain compliance standards. Qualifications Experience with USFDA regulations and compliance requirements Skills in conducting regulatory audits and developing compliance documentation Ability to provide compliance training and maintain compliance program implementation Strong understanding of process improvement tactics and staying updated with regulatory changes Excellent organizational and communication skills Proven ability to work collaboratively across various departments Bachelors degree in Pharmacy, Life Sciences, or related field Proficiency with Microsoft Office and regulatory compliance software Experience in pharmaceutical manufacturing or similar role is a plus,