August 2026

The role holders effectively manage the production of Chemistry, Manufacturing and Control (CMC) documentation for designated product ranges (synthetics/biologics) to deliver the needs of both the AZ business and the customer. AstraZeneca

Bachelors degree in pharmacy or similar medical education. Pharma experience with regulatory focus in a multi-national. Regulatory Affairs Manager, you will play a critical role in ensuring patients continue to have access to innovative healthcare solutions. Boehringer Ingelheim

Awareness about the FDA recommendation on the commercial marketing status notification submission in terms of content and time frames and submissions.

Coordinate with cross-functional teams, including Clinical, Quality, and Manufacturing, to gather necessary regulatory documentation.

Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections.

According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix. Thermo Fisher Scientific

Review and assess local country labels to identify deviations from the core labeling and propose topics for further cross-functional assessment during the periodic core labeling review process

Experience in Media Preparation, MLT, BET, sterility method validations, execution, documentation preparation, and review.  NATCO - Walk-In Interview. Production, Engineering, QC, Microbiology and QA

Your focus will be on coordinating pharmacovigilance and drug safety delivery, resolving issues, and developing team capability.