Job Description

Vacancy for Regulatory Specialist at GSK 2023. The Regulatory Submission Assembly – Level 1 role is to co-ordinate between multiple stakeholders/LOC, to obtain regulatory submission documents for preparation of quality dossier in agreed timeline and submissions to respective agencies with high quality. Supports Global Regulatory by producing appropriate components for global regulatory dossiers with minimal input from line manager.

Organization	GSK
Post Name	Regulatory Specialist – Submissions Assembly
Job Location	Bengaluru
Official Website	https://www.gsk.com/

Job Title/Position:

Regulatory Specialist – Submissions Assembly

Job Overview:

Job vacancy for Pharmacy, Regulatory affairs

Job Location:

Bengaluru

What are the Key Responsibilities?

Understanding of regulations, guidelines and developing procedures and policies relating to registration and manufacturing of pharmaceutical products, to expedite submission, review and approval of global regulatory applications

Drive the submission and delivery process with the Global Publishing team to ensure timely dispatch and archival of submissions as per the agreed timelines.
Delivery of submission packages to agreed schedule and technical specification
Advise and assist authors with the preparation of submission content and use of GSK document management systems and procedures
Works across the functions and can work with Stakeholders in development functions in provision of advice interpretation of relevant guidance’s, researching topics and resolving issues.

What are the Educational Qualification(s) for Regulatory Specialist?

Bachelor’s degree or experience within Regulatory Affairs in the Drug development environment Chemistry, pharmacy or other related science or technical bachelors degree.

What is the Experience Required for this Job?

0-6 years of experience in Regulatory Affairs or related responsibilities

What are the Preferred Skills required for this Job/Position?

Excellent organizational skills, attention to detail and commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines
Broad understanding of the pharmaceutical industry, drug development environment, and R&D processes and objectives.
Excellent written and verbal communication skills and ability to present information in a clear and concise manner
Ability to build effective working relationships and work in a matrix environment effectively.
Excellent computer knowledge (e.g. MS Word, MS Excel, Adobe PDF, SharePoint, Internet Explorer etc.) and preferably experience with the use of complex IT tools in a large organization
Ability to think flexibly in order to meet constantly shifting priorities and timelines.
Can communicate effectively in English.
Has strong sense of urgency, able to effectively prioritize such that key issues or emerging high priority matters are handled in a timely and effective way.
Service-oriented attitude and ability to interact effectively with all levels of personnel in an interdisciplinary and matrix environment.
Highly developed interpersonal, presentation and communication skills with established internal and external networks.

Related:

Detailed notice

https://jobs.gsk.com/en-gb/jobs/384715

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