...help organizations improve their operations and meet regulatory standards through our expertise in regulatory affairs and project management. Our company is based in... ...This is a full-time role for a Regulatory Affairs Executive. The Regulatory Affairs Executive will be responsible...
Rs 3 lakh p.a.
...Analytical method validation review as per the ICH guideline.
- Drug Master File review
- Technical query response to the various regulatory authorities.
Ideal Profile
~ You have at least 1 year post-qualification experience in a similar role.
What's on Offer?...
...Dear Candidates
Greetings from Randstad India !
We have an opening for the role of Executive Regulatory Affairs with a leading pharma company in India.
Interested candidates can drop your resume to the mail id
The details are below:
Qualification...
RA US injectable JD:
Knowledge on manufacture and testing of sterile products and Knowledge of environmental conditions during sterile product manufacturing.
Review and clearance of pre-exhibit batch R&D documents like formula clearance w.r.t Q1/Q2, IIG, specifications...
#ROW MARKET #CIS #MENA #AFRICA #LATIN #ASIA #EUROPE MARKET
Vacancy - 15
Qualification - B.Pharm/M.Pharm
Job Description :
Sound knowledge of CTD/ECTD/ACTD dossier review of OSD/Parenteral dosage forms.
Excellent knowledge of ICH/Country specific/Variation...
Rs 2.2 - 2.8 lakhs p.a.
...registration Dossier
Registration / Submission certificates updation
Translation files record
Regulatory Affair,Formulation,Pharmaceutical
Designation: Executive - Regulatory Affairs
Vacancies: 1
Experience: 1.0 Year(s) - 2.0 Year(s)
Telephonic Interview...
...launches; private equity fund administration; advisory firm set-up, regulatory registration and infrastructure design; ongoing regulatory... ...Responsibilities
The Senior Associate: Enterprise Risk and Regulatory Affairs will provide support:
to the attainment of the overall...
...Executive - Regulatory Affairs (PLMDS)
at ClinChoice (View all jobs)
Chennai - India
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’...
...We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team.
Positions are: Executive / Sr. Executive / Asst. Manager - Regulatory Affairs
Experience: 3 to 9 years
Location:...
...are seeking a highly skilled and experienced Vice President Regulatory affairs to lead our Regulatory department and contribute to the strategic... ...industry.
VP Regulatory Affairs
Regulatory Affairs Executive with a Ph.D. in Entomology and over 20 years of extensive...
...each day.
Job Description
You will focus on leading regulatory services for global research projects of novel medicinal... ...dossiers for DCGI, including preparation of application forms, Executive Summary, country-specific statement, as well as country-level customization...
Rs 5 - 6 lakhs p.a.
...work frequently with other employees and team members to coordinate complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory Responsibility means a duty or responsibility, assigned to an individual by...
Rs 10 - 12 lakhs p.a.
...joiners/ team members with respect to routine activities and updation.
Any other work assigned by supervisor.
Regulatory Affair,dosseir,submission
Designation: Sr executive/Assistant Manager - Regulatory Affairs
Vacancies: 1
Experience: 5.0 Year(s) - 10.0 Year(s)...
...Regulatory Affairs Specialist
Responsibilities:
Prepare and submit regulatory documentation for new and existing medical products, including drugs, devices, and biologics.
Stay up-to-date on ever-evolving regulatory requirements and guidelines.
Liaise with regulatory...
...Qualification - Energy studies – any field
Competencies / Key Skills Required -
1. Research competencies including writing skills for regulatory submissions to nodal agencies
2. Strong technical and analytical skills
3. Strong written and oral communication skills...
...Everyone at Halma India makes an impact, and so do you when you join us!
Responsibilities:
Have regular meetings with international Regulatory Teams of Halma Companies to understand their evolving business needs wrt Indian market.
Assist them in understanding the India...
...This is a critical and senior position within the global regulatory affairs team at Teva. In this multifaceted role, the incumbent will interface... ...skills – verbal as well as written.
Strong and compelling executive presence.
Assertive and tactful in managing people,...
Rs 10 - 15 lakhs p.a.
...product application (ANDA/EU-MA)/Post approval submission to the regulatory authority (specifically EU/US)
-Hand on experience in... ...hand Ons experience for handling of E-CTD software
Regulatory Affair,RA
Designation: Regulatory Affairs - Pharma
Vacancies: 1...
...the global paints, coatings and inks market, Eastman is looking for a highly motivated individual to join the Product Steward & Regulatory Affairs (PSRA) team. The Product Steward Representative is the key link between the business and technology partners, and the larger Global...
...Medical Device Regulatory Affairs Job duties of a Regulatory Affairs Specialist include:
Developing and implementing regulatory strategies for new and existing products
Preparing and submitting regulatory documentation to regulatory authorities
Liaising with regulatory...
...more connected world.
Job Overview
Regulatory Affairs oversees compliance activities for... ...:
• Support daily Regulatory Affairs function eg; compliance to 21 CFR 820,807... ...organization.
Competencies
SET : Strategy, Execution, Talent (for managers)
ABOUT TE...
...About the job
Key Accountabilities:
Project Execution:
Works effectively within a team environment
Works within broad project guidelines as directed by the Project Lead or Technical SME
With the guidance of the project Technical SME demonstrates the ability...
Rs 2 - 5 lakhs p.a.
...as per current prescribed guidelines of the respective regulatory authority.
~ Well versed with the guidelines of ICH... ...dossiers, samples legal documents.
RA,Regulatory Affairs
Designation: Officer / Executive - Regulatory Affairs
Vacancies: 1
Experience: 2.0...
...GP, Ecosprin AV, Jalra, Tazloc, Glynase and more.
Responsibilities:
For the CMC RA position: Biosimilar Product Development Regulatory support – CMC
For the Clinical RA position Biosimilar Product Development Regulatory support - Clinical
Biosimilar Regulated market...
...About the job
We are looking for an experienced Regulatory Affairs Specialist to join our growing team to assist CMR Senior Regulatory Affairs Specialist (AMEA) in all tasks relating to registrations for new or modified product. We are advertising this role to be based in...
Rs 3 - 5.5 lakhs p.a.
...Description :
Regulatory Compliance:
Stay updated on medical device regulations, standards, and guidelines (e.g., FDA, ISO, CE Marking... .../M.Pharma or Biomedical Engineering or Diploma in Regulator Affairs, Quality Management System.
~3-5 years of experience in Quality...
...Topline:
Documentation of Regulatory product Dossiers, Compliance implementation within different verticals with Process and training
Regulatory Auditing skills for the compliance process strengthening
Legislative aspect of Regulations forming and designing
Advocacy...
...We are hiring for dynamic individuals in Regulatory Affairs Department:
Experience: 3 years up to 12 years
Designation: Senior Exec / Assistant Manager / Deputy Manager
Qualification: M. Sc. / M. Pharma/ B. Pharma
For Below Mentioned roles: -
Role 1: - API...
Rs 3 - 5 lakhs p.a.
...interpret trial data
advise scientists and manufacturers on regulatory requirements
provide strategic advice to senior management throughout... ...and advertising before a product's release.
Regulatory Affairs,Regulatory Compliance,marketing Authorisation
Designation:...
$ 70000 p.a.
...ll meet these challenges. Join us!
The Senior Director, Regulatory Affairs is a leader, who provides vision and direction in a fast-paced... ...competitive drug development environment. They report to the Executive Director of Regulatory Affairs and are responsible for...