Showing posts with label Regulatory Affairs. Show all posts
Showing posts with label Regulatory Affairs. Show all posts

Apply as Manager - Regulatory Affairs at Roche @ Click Here for more details

Post : Manager - Regulatory Affairs
Job Description:
To execute the regulatory strategy by providing guidance to the team for dossier preparation, ensuring timely submission of dossiers, respond to queries from regulatory authorities and keeping one’s self updated with changes to the regulatory environment With the objective of ensuring that the organization obtains approvals and licenses in a timely manner
Regulatory Plan Creation:
Collaborate with global teams during early stages of product development; Share inputs on regulatory requirements in the country from development and data perspective;
Understand timelines of availability of various documents for filing the application and the supply chain of the new product for which regulatory strategy being created; 

Create regulatory strategy for the products assigned and share the same with the manager
Dossier preparation, review and submission:
Request documents from global and local teams for filing the application well in advance; Co-ordinate with team members for accurate collation of the documents for filing the application; Proactively, work with the liaison person to track the submission; Understand likely queries and keep documents ready in advance to either share the same to prevent the query or to have short lead time in submitting the response
Lifecycle Management:
Review and maintain the trackers for registration certificates, import licenses, post marketing commitment, package insert submission so as to facilitate timely submission of the applications as well as for maintaining regulatory compliance at high level; Plan renewal filing well in advance to avoid any delays in submission due to non availability of the documents; Evaluate and submit variations in a timely manner
Regulatory Environment updates:
Keep a track on the development activities of competitors and communicate to the team members on real time basis
People Management:
Set objective goals and evaluate performance of team members; Recommend for promotions; Recommend recognition programs for team; Coach and mentor the team; Provide opportunities to the team to develop their capabilities; Conduct regular team meetings to guide team on departmental issues; Resolve issues faced by team
Functional Competencies
Roche high performance competencies
Decision making
Influencing /persuasion skills
Driving collaboration and team work
Technical knowledge
Organization and planning skills
Negotiating skills
Communication Skills
Presentation Skills
Proven ability to interact well in a multifunctional team setting
Accuracy and attention to detail
Behavioral Competencies
Strategic Agility
Achieving results
Team work and Collaboration
Inspiring and Influencing
Interpersonal Skills
Adaptability
Patient centricity in decision making
Feedback and coaching
.
Additional Information
Location : Maharashtra, Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Medical Affairs
End Date : 26th January, 2019

Apply for Junior Regulatory Affairs Associate at PAREXEL @ Apply Now

Post : Junior Regulatory Affairs Associate
Job Description
1. To support the ongoing clinical trial application project.
2. To support all regulatory activities based on project requirement.
Candidate Profile
1) A master degree in a relevant educational field - life science, pharmacy, others.
2) 0 to 6 months experience with Pharmaceutical industry or CRO with general understanding of Regulatory Affairs.
3) Good communication skills, quick learner and computer savvy.
4) Willing to work preferably in EU shift or as per project requirement
Additional Information:
Location: Bengaluru, Karnataka, India
Education: M.Pharm, M.Sc 

Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
End Date: 20th February, 2019

Apply for Regulatory Affairs Executive at AstraZeneca @ Apply Now


Post : Executive- Regulatory Affairs
Job Description
Position Purpose: 

For assigned products: gain rapid and high quality approvals and ensure high standard of regulatory compliance, in order to achieve the company’s business objectives. Developing India specific Artwork, Support to Regulatory dossier preparation and Submission like New drug application, Site registration and Import licence. Managing Registration sample right from dispatch of samples till the report. As part of New drug application, ADC sample testing. Also follow up for reports, Licence Life cycle management. Coordinating with Clinical Trail team and Global team for GCT application.
Key Result Areas:
• Adherence to AZ and industry codes of conduct, ethics and good regulatory practices
• Ensure that all licensing for assigned products is complete in accordance with relevant norms
• Develop and implement action regulatory plans for allocated products to achieve requisite approvals rapidly and facilitate rapid launch
• Provide Leadership and direction within project teams
• Assist in Issue Management
• Maintain the awareness of, and shape the regulatory environment relevant to the assigned products portfolio
• Competitive Intelligence and analysis
Candidate Profile
• Qualification- Master’s in science/Master’s in Pharmacy preferred.
• Proficient in oral and written communication (English).
• 2-4 years’ experience in Regulatory function, knowledge of dossier compilation
• S/He should be conversant with Indian regulations related to new drugs and clinical trials.
Additional Information
Qualification M.Sc, M.Pharm

Experience : 2-4 years
Location : Bangalore
Industry Type : Pharma
Functional Area : Regulatory Affairs
End Date : 30th January, 2019

Regulatory Affairs Associate at PAREXEL

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post : Regulatory Affairs Associate

Regulatory Affairs Specialist at PPD Pharmaceuticals

PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients.
Post : Regulatory Affairs Specialist

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