Mgr Scientific Writing

Teva Pharmaceuticals

10-12 years

Not Disclosed

Bangalore

10 Dec. 18, 2025

Job Description

Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager – Scientific Writing
Location: Bangalore, India (560064)
Employment Type: Full-Time | Permanent
Industry: Pharmaceuticals | Scientific Communications | Medical Writing
Experience Required: 10–12 years
Company: Teva Pharmaceuticals
Job ID: 64972
Posted Date: December 17, 2025

Job Overview

Teva Pharmaceuticals is seeking an experienced Manager – Scientific Writing to lead and deliver high-quality scientific communication projects supporting global medical and publication strategies. This role is ideal for a senior medical writer with deep expertise in publication planning, peer-reviewed manuscripts, and congress deliverables, combined with strong project management and cross-functional collaboration skills.

The successful candidate will translate complex clinical and scientific data into clear, compliant, and audience-appropriate content for healthcare professionals, patients, and internal stakeholders, while ensuring adherence to Good Publication Practices and global regulatory standards.

About Teva Pharmaceuticals

Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making high-quality healthcare more affordable and accessible worldwide. Operating in nearly 60 countries, Teva’s portfolio includes many medicines listed on the World Health Organization’s Essential Medicines List, impacting the lives of over 200 million patients daily.

Key Responsibilities

Scientific & Therapeutic Expertise

Develop a strong understanding of assigned therapeutic areas and product strategies to meet scientific communication objectives.
Rapidly acquire knowledge in new therapeutic areas and adapt content across multiple disease domains.
Translate complex clinical trial data and scientific concepts into clear, accurate, and impactful medical content for diverse audiences.

Medical Writing & Publication Management

Author and manage high-quality scientific deliverables, including abstracts, congress posters and presentations, and manuscripts for peer-reviewed journals.
Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure content alignment with evolving clinical data and global strategies.
Maintain rigorous document tracking, version control, and audit readiness using Teva’s publication management systems.
Adapt writing style for varied audiences, including specialist healthcare professionals, nurses, patients, caregivers, and other stakeholders.
Monitor scientific literature and assess its impact on existing publications and communication assets.

Cross-Functional Collaboration

Build effective relationships with authors, external experts, and clinical investigators to support timely and high-quality publication development.
Work closely with Medical Affairs, Clinical Development, Safety, and other internal and external partners to gather inputs and secure approvals.
Support localization and regional adaptation of global scientific content to meet market-specific regulatory and cultural requirements.

Quality, Compliance & Review

Apply Good Publication Practices, including ICMJE guidelines, across all scientific communication deliverables.
Ensure strict adherence to internal SOPs, style guides, and established workflows.
Conduct peer reviews of scientific content to maintain consistency, accuracy, and high editorial standards.

Innovation & Continuous Improvement

Contribute to initiatives aimed at enhancing content development through structured content libraries, AI-enabled tools, and digital asset management systems.
Support the creation of derivative assets such as field medical materials, congress preparation content, and digital scientific communications.

Qualifications & Experience

Education:

Advanced degree required (PharmD, PhD, MD, or Master’s in Life Sciences or related discipline).

Experience:

10–12 years of experience in medical writing, scientific communications, or medical information within the pharmaceutical, biotech, or medical device industry.
Proven experience in medical publication writing, scientific literature analysis, and congress content development.
Strong working knowledge of Good Publication Practices and ICMJE guidelines.
Experience using publication management and tracking systems such as Datavision, Pubstrat, or Komodo.

Language Skills:

Professional-level proficiency in written and spoken English.

Why Join Teva

At Teva, you will contribute to impactful scientific communications that support global healthcare outcomes while working in a diverse, inclusive, and innovation-driven environment. The organization values expertise, collaboration, and continuous improvement, offering opportunities to shape global publication strategies and advance your career in scientific writing.

Equal Opportunity Statement

Teva Pharmaceuticals is an equal opportunity employer and is committed to fostering a diverse and inclusive workplace. Employment decisions are made without regard to age, race, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status.

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