Walk in Drive API Regulatory Affairs Dept

Walk In Drive for API Regulatory Affairs Dept (RA) @ R&D CenterWork/Interview Location :- MSN R&D Center, Pashamylaram, Isnapur, TelanganaInterview Date: @FridayInterview Time :- 9AM TO 2PMVenue Details :MSN Laboratories Pvt. Ltd.,MSN R&D center, Pashamylaram, Isnapur, Patancheru, SangareddyContact : Regulatory Affairs Specialist to join our API Division....

Role & responsibilitiesWalk In Drive for API Regulatory Affairs Dept (RA) @ R&D CenterWork Location :- MSN Laboratories Pvt. Ltd.MSN R&D center, Pashamylaram, Isnapur, Patancheru, SangareddyInterview Date: @Saturday & @SundayInterview Time :- 9AM TO 5PMVenue Details :Quality Inn RamachandraWard No- 58, 31-41/10/1, Duvvada, Revenue, Visakhapatnam, Andhra...

Walk In drive for Formulation Research & Development - Department FR&D - MSN R&D Center Pashamylaram on Saturday )Formulation R&D Department ( Formulations R&D) in Formulation Division - R&D Center.Key Responsibilities:Formulation Development: Lead the formulation development process for new pharmaceutical products, including solid oral dosage forms,...

Company DescriptionMorulaa HealthTech Pvt. Ltd. was founded to assist in the commercialization of bio-science technologies and the growth of healthcare companies. Based in Ohio and collaborating with Cleveland Clinic, University Hospitals, and Case Western Reserve University, Morulaa specializes in the Registration of Medical Devices and Distributor...

SKILL SET REQUIRED: 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...

Job Summary We are seeking a detail-oriented Specialist in Regulatory Affairs primarily focusing on Oligonucleotides typically has a role that involves ensuring compliance with regulatory requirements for these products. Responsibilities include managing chemistry, manufacturing, and controls (CMC) documentation for DMF submission, addressing deficiency...

We're Hiring – Regulatory Affairs ExecutiveAre you a regulatory professional looking to grow your career?We're looking for a Regulatory Affairs Executive with 2 years of experience to join our team.What you'll do: Prepare and review regulatory submissions and documentation Ensure compliance with national/international regulatory standards Coordinate with...

We seek a seasoned Regulatory Affairs Head to lead and drive the global regulatory strategy for our formulation-based pharmaceutical products across Europe and Rest of World (ROW) markets at Evertogen Life Sciences. As the Regulatory Affairs Head, you will play a crucial role in overseeing all regulatory submissions, compliance management, and lifecycle...

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...

Job Description Let's change the world. Amgen is searching for a Manager for the Submission Process, Planning, and Management (SPPM) team within Global CMC & Device Regulatory Affairs in Amgen India (AIN). The mission of SPPM is to support productivity across the organization and stakeholders by: - Driving continuous improvement of processes and tools. -...