...Responsibilities:-
To have a clear understanding of regulatory guidelines and data requirement for... ...closely with marketing teams and factory head and ensure 100% compliance in the product... ...or full-time course in regulatory affairs
Note :- Ideal Candidate should be from...
...them.
Job Description
Join our global team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating... ...and business development requests
Supervise Regulatory Affairs staff in the country
Qualifications
~ University degree
~...
Rs 10000 - Rs 25000 per month
...We are hiring for Regulatory Affairs Executive. Qualification: B.pharm/M.pharm
Age criteria: below 30
Experience - 0 to 2 years only
Location - Sola, Ahmedabad
Work mode - on site
:
Should have worked in Regulated Market (ROW).
Dossier Submission, Dossier...
...Job Description
Job Title: Regulatory Affairs Manager I
Career Level - D
Introduction to role:
Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management...
...exploring candidates with a less traditional background.
Job Description
Job Summary
We are looking for a seasoned Head Regulatory Affairs to lead the regulatory strategy, ensuring compliance with health product regulations and fostering organizational growth...
QUALIFICATIONS:-
B.PHARMA / M.PHARMA
PHARMA REGULATORY
Skills
Analytical
~ Time management
Presentation skills .
Interpersonal... ....
Experience-- 4-5 Years of Experience in Pharma Regulatory Affairs
Job Summary
Core understanding of technical requirements...
JOB DESCRIPTION
Job Title
Regulatory Affairs Manager
Job Description
Job Description
Business Title: Manager - Regulatory affaire... ...) Regulatory team. Reporting line of this position is to Head RA, ISC. You will have exposure to a multitude of medical...
...combination of this will lead to a truly differentiated experience for you.
If this excites you, then apply below.
Lead Regulatory Affairs
You will be responsible for :
Responsible for Regulatory intelligence dissemination and coordination, this includes
-...
...stakeholders
Compiling variation packages
Experienced in managing, regulatory database and Trackwise.
Your experience and qualifications... ....
Experience:
~2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market
~ Knowledge on...
...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...
...DESCRIPTION: MAIN PURPOSE OF ROLE
Specialist professional individual contributor with comprehensive knowledge in the area of Regulatory Affairs.
Ability to execute highly complex or specialized projects.
Adapts precedent and may make significant departures from...
...Job Summary:
We are seeking a dedicated and knowledgeable Regulatory Specialist to ensure our medical devices meet local and... ...scientific discipline.
- 4 to 5 years’ experience in regulatory affairs within the medical device industry.
- In-depth knowledge of CDSCO...
...Pharmacy, pharmacology, Biotechnology, engineering, or medical technology.
Minimum 5 years of experience in Medical devices regulatory affairs and 7-8 years of working
experience in a Medical devices/Pharmaceutical company.
Good working knowledge of MS-EXCEL and PowerPoint...
...Regulatory Affairs Associate
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...
...Responsibilities
To have a clear understanding of regulatory guidelines and data requirement for... ...closely with marketing teams and factory head and ensure 100% compliance in the product... ...chemical structures.
Any certification or full-time course in regulatory affairs...
...artwork of packaging materials as per current rules and regulations.
Must have worked on ASEAN, CIS, and AFRICA markets.
Review all regulatory agency submission materials for accuracy, comprehensiveness, or compliance with regulatory standards
Evaluation of change...
...approval changes for US, EU, Canada, CEP and other markets
Use of eCTD softwares and submission gateways like ESG & CESP
Providing regulatory inputs in early development phase of APIs
Review of change controls and technical data required for DMF submissions
Collection...
...We are hiring for Regulatory Affairs Analyst IVD Expert
Your Role:
The Regulatory Affairs Analyst IVD Expert supports assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products.
Independently...
...We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard...
...Regulatory Affairs Consultant:
Around 7-10 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologicals) in various markets.
Good understanding of regulatory framework, including regional...
...opportunities, support and rewards that will take you further.
Regulatory Compliance
As part of Global Risk, Regulatory Compliance... ...Role Purpose :
The role of the Vice President Regulatory Affairs involves following responsibilities:
Scan for legal and regulatory...
...MS Excel Good communication in English Hindi, Marathi.
Good with legal drafting Good knowledge of labor laws, licenses & Factory Act.
3)2-3 years work experience in managing regulatory affairs in Pharma, Chemical, Agro industry or firms managing legal work outsourcing.
...This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ+ business community.
Regulatory Affairs Consultant.
~8 years' experience in handling life cycle management of approved drug products (small molecules) in various markets.
~ Good...
...ensure the timely submission of the labels to health authority.
Job Responsibilities
Responsible for coordination & preparation of regulatory submissions and strategies.
Prepare and submit all the supporting documents for labelling submissions as per the type of...
Dear Candidates, Greetings from Randstad India ! We have an opening for the role of Assistant Manager - Regulatory Affairs with a leading pharma company in India. Interested candidates can drop your resume to the mail id ****@*****.*** The details are below...
...Job Description
Job TitleAssociate Director Regulatory Affairs MoSJob Description Associate Director Regulatory Affairs MoS
Critical RA leader of the IGTS MoS Category (Image Guided Therapy Systems Mobile Surgery). Also, a member IGTS MoS Leadership Team and advise...
...Position Overview:
~ Handling assigned activities in the regulatory department.
Experience:
~5-8 years
Qualification:
~ B. Pharm, M.Pharm preferred.
Responsibilities:
Compilation of ANDA submissions in accordance with the latest guidances...
...We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.
Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory Affairs
Experience: 3 to 9 years
Location: Andheri...
...event in Delhi 2022.
Responsibilities
Support in creating regulatory and quality policy plan as needed internally and externally
Work... ...Requirement
Good understanding of the latest regulatory affairs
Ability to quickly prioritize and execute tasks
Strong analytical...
Job Description
JOB DESCRIPTION
Regulatory Affairs 3-4 years Experience Medical Devices & Drug productsSummary:
Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical...