Regulatory Affairs Consultant - Head

Golden Opportunities

12 - 20 years

50 Lacs

pune chennai delhi / ncr

Posted:-1 days ago| Platform:

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Skills Required

cmc quality management systems fda project management labeling cmc labeling process ema

Work Mode

Work from Office

Job Type

Full Time

Job Description

Role & responsibilities

Minimum of 10 years of Life Science industry experience, with substantial exposure to regulatory affairs.
Hands on experience and demonstrated expertise in Chemistry, Manufacturing, and labeling processing Comprehensive understanding of global regulatory framework, including FDA, EMA, ICH and other international standards.
Excellent communication skills both written and verbal Meticulous attention to detail and organizational prowess Proficiency in project management and cross-functional collaboration Strong analytical and problem-solving skills
Ability to navigate and interpret complex regulatory landscapes across multiple regions Good understanding of Quality Management Systems in the outsourcing scenarios
Must have skill set CMC labeling process global regulatory frameworks Good Clinical Practice Quality Management FDAEMA ICH
Location: Pune, Chennai, Delhi, Bangalore, Kolkata, Hyderabad, Gurgaon

Contact Person: Maheshwari Balasubramanian

Email ID: maheshwari@gojobs.biz

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