Walk-ins For Regulatory Affairs- ROW - Hyderabad

We have vacancies in various regions for Regulatory Affairs professionals. · ...

The Regulatory Affairs Manager will be responsible for product registration in ROW regions, coordinating with auditors/customers, preparing dossiers for RoW region in CTD/country specific format, communicating with agents/partners for submission of Dossiers and further updates or ...

To manage and support regulatory submissions approvals lifecycle maintenance of pharmaceutical products in ROW markets ensuring compliance with local regulatory requirements and company timelines. · Prepare review submit regulatory dossiers CTD ACTD country-specific formats for p ...

Prepare regulatory dossiers for submission to authorities and manage drug regulatory affairs within Europe & Row region. · ...

+ Regulatory Affairs Job Opportunity at Biological E Limited. · + Responsible for Regulatory submission to ROW · Experienced in handling management expansion of product portfolios markets/ territories · ...

The role is responsible for analytical method development for injectable formulations and supports method optimization and troubleshooting during formulation development. · M.Sc. in Analytical/Chemistry/Pharmaceutical Sciences or B.Pharm/M.Pharm in Pharmaceutics/Analytical · ...

Lead complex projects, shape product strategy and bring breakthrough medicines to market. · ...

We are seeking a Regulatory Affairs Specialist to join our team at Orbicular Pharmaceutical Technologies Pvt Ltd. · ...

Job Description · We are seeking an experienced Full Stack Developer with expertise in AWS, Ruby on Rails, React.js, JavaScript, and other technologies listed below. · Briefly Describe Your Job Role: · As a Senior Ruby on Rails Developer you will be responsible for building scala ...

We are committed to advancing solutions that improve health outcomes through innovative and specialized scientific approaches. · ...

We are looking for a Regulatory Affairs Specialist – Global Lifecycle Management (LCM) to support and manage post‑approval regulatory activities across global markets, ensuring compliance and timely maintenance of product licenses. · ...

Dr Reddy's is a leading multinational pharmaceutical company looking for a Regulatory Affairs Specialist to support post-approval regulatory activities across global markets. · ...

Prepare submission check-list based on regulatory & product specific requirements Dossier compilation and review of ANDA's for different dosage forms. Review of all technical documents which are required for ANDA compilation (Specifications STP COA's protocols BMR's BPR's Bio rel ...

The company Medifodil Smart Pharma Solutions is expanding its Regulatory Affairs team and seeking an experienced Regulatory Affairs Specialist with 4-6 years hands-on experience. · Bachelor's or Master's degree in Pharmacy Life Sciences or a related discipline. · ...