Urgent Requirement For Regulatory Specialist – Chennai Lctn

from 3 to 8 year(s) of Experience
INR 4,00,000 - 8,00,000 PA.
Posted: 18 days agoJob Applicants: 357+Job Views: 1529+

Job Description

Position summary

This role supports the medical legal regulatory (MLR) submissions and artwork production teams. Each tactical element of artwork will require a full examination by this role. This person consults with project management, medical editor, and the production specialist creating the adaptation to ensure that the claims and references are accurate and supported, and that each piece has been created and uploaded as required by brand, style, and MLR file standards.

Job qualifications

Bachelor’s degree in Science/Nursing/Medical Technology, or English/Communications, or related field preferred. A combination of work experience and education can be substituted.

Medical, pharmaceutical, or Life Sciences marketing experience preferred

Minimum 2+ years editing experience

Knowledge of medical/pharmaceutical terminology, and federal regulations governing pharmaceutical advertising preferred

Ability to accurately review complex materials including multimedia graphics, texts, and web sites with excellent attention to detail

Operates effectively in a fast-paced, deadline-driven environment; highly organized and multitasks effectively

Excellent team player with strong interpersonal skills; ability to communicate effectively and work well with others

Working knowledge of Microsoft Office and Adobe Acrobat required

Ad agency experience preferred

Job duties

* Checks quality and accuracy of annotations, tags/links, reference binders/packs, and edits to all advertising, promotional, and non-promotional communication materials to ensure accuracy of text, layout, organization and references; compliance with AMA or AP guidelines; and overall sense, consistency, and clarity

* Work closely with Medical Editors and Production to ensure that jobs are compliant to brand, style and file standards

* Keep submission schedule on track during the transition from medical editing (upload) to submission

* Ensure completed job by the studio meets the exact file standards and brief provided

Help Project Management and Production teams to ensure that all files coming in are of suitable quality and align with file and brand standards at the start

Constant communication with MLR, Production, and Project Management teams


Yamini Singh

Human Resource




Desired Candidate Profile

Please refer to the Job description above

Company Profile

Williams Lea India Private Limited

WilliamsLea Tag

Global Infocity Park

Perungudi, Chennai

View Contact Details+

Contact Company:Williams Lea India Private Limited

Address :Module 0308, Third Floor, Tidel Park, Taramani,, Chennai, Tamilnadu, India


INR 4,00,000 - 8,00,000 PA.

Role Category

Drug Regulatory Affairs/Documentation


Regulatory Affairs Manager

Employment Type

Full Time, Permanent

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