Hyderabad Telangana Writer Jobs – 130 Open Jobs Today

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CS Writing Scientist

Haleon -
Hyderabad, Telangana

Apply Now

Job details

Full-time
8 hours ago

Qualifications

English
Presentation skills
Agile
Computer skills
Medical terminology

Full job description

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.

Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.

Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

Hello. We’re Haleon . A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re in control of. In an environment that we’re co-creating. And a culture that’s uniquely ours. Care to join us. It isn’t a question

About the role

The CS Report Writing Specialist is accountable for production of safety documentation for all product types in alignment with national reporting requirements to support local, regional and global regulatory submissions.

POSITION PURPOSE

Role is refocused on authoring of safety documents intended for regulatory submissions and other safety reports, Prepare safety writing deliverables, including planning, authoring, contributing to safety strategy and data analysis, coordination with contributing functions, and quality control of assigned safety writing projects from initiation to completion. Support CS Science staff with authoring and development of benefit-risk assessments, safety risk management plans, safety signal evaluations, regulatory submissions and aggregate reports. Produce fit-for-purpose safety documentation across CH categories of high quality and according to defined timelines

RESPONSIBILITIES

Prepare safety writing deliverables, including planning, authoring, contributing to safety strategy and data analysis, coordination with contributing functions, and quality control of assigned safety writing projects from initiation to completion.
Maintain product safety information at active level and ensure consistent use across regulatory reports.

Use appropriate sources of information and database searches to retrieve relevant data for inclusion to safety reports
Review published literature for identifications of safety signals and/or inclusion into periodic reports.
Serve as the principal owner and co-ordinator of the safety deliverables and have responsibility for completion of the deliverable in compliance with Company guidelines.
Produce or contribute to safety documentation for regulatory submissions and to fulfil legal obligations of the MAH. Examples include but are not limited to Safety Risk Management Plans, Periodic Benefit Risk Evaluation Reports, Developmental Safety Update Reports, Medical Device Periodic Safety Update Reports, Cosmetic Undesirable Effects Reports, Canadian Annual Reports, US Periodic Adverse Drug Experience Reports, and Clinical Overviews and Summaries.
Provide safety summaries in support of communication on relevant safety information both, internally and externally.
Assist CS Science team in producing regulatory supporting documentation for labelling updates and in performing routine signal detection activities (e.g. review of ICSRs)
Accountable for maintaining personal readiness in response to internal audit or regulatory inspection
With guidance, contribute to process improvement initiatives within Consumer Safety

QUALIFICATIONS

Degree in Biomedical or Healthcare-related speciality

COMPETENCIES AND SKILLS :

Fluency in English and solid writing/editorial skills
Prior experience authoring clinical, safety or regulatory documents (e.g. PBRERs)
Sound knowledge of MedDRA terminology and familiarity with medical terminology
Ability to prioritize and manage multiple demands and projects within deadline
Good presentation skills, and ability to interpret and present data in a logical manner
Self-starter, flexible in adapting to changing circumstances or new information, able to adapt quickly in a fast-moving environment.
Sound computing skills

Job Posting End Date

2026-09-15

Equal Opportunities

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong.

During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees.

The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.

Adjustment or Accommodations Request

If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.

Apply Now

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About the role

The CS Report Writing Specialist is accountable for production of safety documentation for all product types in alignment with national reporting requirements to support local, regional and global regulatory submissions.

POSITION PURPOSE

RESPONSIBILITIES

Prepare safety writing deliverables, including planning, authoring, contributing to safety strategy and data analysis, coordination with contributing functions, and quality control of assigned safety writing projects from initiation to completion.

Maintain product safety information at active level and ensure consistent use across regulatory reports.

Use appropriate sources of information and database searches to retrieve relevant data for inclusion to safety reports

Review published literature for identifications of safety signals and/or inclusion into periodic reports.

Serve as the principal owner and co-ordinator of the safety deliverables and have responsibility for completion of the deliverable in compliance with Company guidelines.

Provide safety summaries in support of communication on relevant safety information both, internally and externally.

Assist CS Science team in producing regulatory supporting documentation for labelling updates and in performing routine signal detection activities (e.g. review of ICSRs)

Accountable for maintaining personal readiness in response to internal audit or regulatory inspection

With guidance, contribute to process improvement initiatives within Consumer Safety

QUALIFICATIONS

Degree in Biomedical or Healthcare-related speciality

COMPETENCIES AND SKILLS :

Fluency in English and solid writing/editorial skills

Prior experience authoring clinical, safety or regulatory documents (e.g. PBRERs)

Sound knowledge of MedDRA terminology and familiarity with medical terminology

Ability to prioritize and manage multiple demands and projects within deadline

Good presentation skills, and ability to interpret and present data in a logical manner

Self-starter, flexible in adapting to changing circumstances or new information, able to adapt quickly in a fast-moving environment.

Sound computing skills

Equal Opportunities

Adjustment or Accommodations Request

Note to candidates