Teva Pharmaceuticals Hiring 2023.Teva Pharmaceuticals Notification full details below..Interested and eligible candidates can Apply Now.Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day.
Vacancy details:
- Post Name: Regulatory Affairs Associate II
- Qualification: M Pharm/ MSc/B Pharm/BSc
- Overall Pharma industry experience: 4-7 years
Job Description: Greeting from Teva Pharmaceuticals !!!!
Important Details :
- Location: Navi Mumbai, India,
- Post of date:05/10/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
The opportunity
Providing regulatory support for European and International Markets by completing the designated projects and tasks, in line with the internal Work Instructions and within the defined timeframes, in order to achieve regulatory compliance.
Prioritizing, planning and monitoring the tasks related to regulatory support, documenting and informing the involved parties of the status and progress.
Maintaining the related documentation and associated electronic databases, in line with in-house procedures.
Communication with other Teva departments across Europe and International Markets, 3rd Parties and the related Agencies.
Maintaining and developing awareness of the current/pending regulatory legislation and guidelines.
Fulfilling other allocated department duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel.
How you’ll spend your day
To coordinate and communicate with the various business units for the tasks and with agencies regarding regulatory submissions.
To organize and perform the required regulatory activities/tasks in order to maintain the databases in line with the requests received from the different EU and International Markets.
To ensure high quality standards are followed to support the market functions.
To give regulatory support to project teams, stakeholders and other sites, as required.
To enforce and improve the defined processes within the Regulatory Affairs department.
Maintain and develop awareness of current/pending regulatory legislation and guidelines.
Support the defined processes within the department and provide input where improvements can be made.
To work as a team player and provide adequate support to the manager and team.
To conduct effective trainings to new team members and providing required assistance in getting them on-the-job.
Participate in team meetings and give feedback to the manager from time to time about the task progress.
Your experience and qualifications
Qualifications:
M Pharm/ MSc: 4-5+ years of experience
B Pharm/BSc: 5-6+ years of experience
Experience:
Overall Pharma industry experience: 5-7 years
Minimum of 5 years’ experience in the Pharmaceutical Industry, within Regulatory Affairs.
Experience of regulatory documentation within Europe and/or International Markets.
Working within project teams and interaction with other function in the Pharmaceutical Industry.
Knowledge:
Experience and knowledge of European and/or other regulatory legislation and procedures.
CMC filing experience w.r.t. Modules 3 and 5
CPP Filings
Regulatory databases
Understanding of processes and departments within a pharmaceutical company.
French language proficiency will be an added advantage.
Skills
Excellent oral and written communication
Ability to work under pressure and to tight time deadlines.
Effective time and organization management
Negotiation
Initiative
Analytical (Data and Documentation)
Computer literacy
Presentation skills
Reports To
Manager- Regulatory Affairs
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