Regulatory Affairs Executive

Hyderabad, India **Job ID** R0000012328 **Category** Regulatory / Consulting **ABOUT THIS ROLE**: **Regulatory Affairs Associate** Must have experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. - To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned...

Looking for a full time Regulatory Affairs executive with 1-3 years experience in APIs (Active pharmaceutical ingredients). No freshers. **Job Types**: Full-time, Regular / Permanent **Salary**: ₹200,000.00 - ₹980,116.12 per year **Benefits**: - Paid time off - Provident Fund Schedule: - Day shift Supplemental pay types: - Yearly bonus Ability...

**We are hiring an Executive in Regulatory Affairs** **Qualification **:B. Pharmacy/M. Pharmacy (Pharmaceuticals) **Experience**: 3- 4 yrs. **Location **:Balanagar (Hyderabad) **Date**: 28/08/2023 TO 05/09/2023 (Mon to Fri) **Time ** : 10 AM TO 4 PM **Skills Required**: 2) Update the registration dossiers, evaluate queries received from respective...

Hyderabad, IndiaJob ID R Category Regulatory / ConsultingABOUT THIS ROLE:Regulatory Affairs AssociateMust have experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned deliverable(s) including:Submission...

Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...

Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...

Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...

Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. You will help make an impact on people’s lives and change futures every day. We are equally committed to bringing out your best and fostering a collaborative workplace built on trust and respect. We empower our people to take charge of their potential. We offer...

About Us SteriMax is the largest privately-owned injectable company in Canada. Our foundation rests upon the principles of providing high quality products, maintaining a reliable product supply, and supporting the needs of Canadian patients. For more details, please visit our website Detailed Responsibilities · Manages and provides leadership to an...

About UsSteriMax is the largest privately-owned injectable company in Canada. Our foundation rests upon the principles of providing high quality products, maintaining a reliable product supply, and supporting the needs of Canadian patients. For more details, please visit our website www.sterimaxinc.comDetailed Responsibilities· Manages and provides...

Regulatory Affairs Consultant.8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute...

Regulatory Affairs Consultant.8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute...

Regulatory Affairs Consultant.8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional...

1. Preparation of technical documents like, Specs, COA, Method of analysis of raw materials and finished products and stability summary sheet etc. 2. Co-ordinate with different departments in plant to arrange the data for documents preparation. 3. Provide the required technical documents of the products to the regulatory team in corporate office. 4. Takes...

POSITION DESCRIPTIONReporting to the Team Leader of Post-Approval Regulatory Affairs, the Regulatory Affairs Associate will prepare regulatory submissions for Health Canada and actively participate in the management of submissions under regulatory agency review in order to fulfill regulatory jurisdiction requirements. The Regulatory Affairs Associate is...

Regulatory Affairs AssociateAround 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of  drug products (small molecules as well as biologics) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresContribute to preparation...