Global Regulatory Writing Manager

Biopharma Careers; Hyderabad; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

Amgen in Hyderabad seeks an experienced Regulatory Writer to maintain critical business relationships across cross‑functional product teams and, when needed, lead regulatory writing activities for submissions. The role involves mentoring junior writers, coordinating with contracted writers, and contributing to global regulatory plans.

Ideal candidates have advanced degrees with several years of related experience, a strong grasp of ICH/GCP guidelines, and excellent communication and

Qualifications

• Regulatory writing experience in pharmaceutical/biotech sectors.
• Ability to interpret and apply ICH/GCP guidelines.
• Experience with SOPs, templates, and submission standards.

Responsibilities

• Author regulatory submission documents, including a wide range of reports and addenda.
• Conduct formal review and approvals of authored documents per SOPs.
• Manage regulatory writing activities for submissions under supervision.
• Lead regulatory writing activities on product teams and contribute to Global Regulatory Plans.
• Collaborate with contract/freelance writers as needed and mentor junior writers.
• Generate document timelines with team input and monitor progress.
• Stay updated on regulatory guidance and industry developments.

Skills

Regulatory writing

Leadership

Time management

Communication skills

Project management

Education

Doctorate degree

Master’s degree

Bachelor’s degree

Diploma

Tools

Microsoft Office

SOPs knowledge

ICH/GCP knowledge

Job description

Career Category

Regulatory

Job Description

Let’s do this. Let’s change the world. In this vital role you will maintain key business relationships with appropriate cross-functional product team members. As requested, this role may serve as functional area lead on product teams, manage (with supervision) writing activities for product submissions, train and mentor more junior writers, and assist with departmental activities.

Roles & Responsibilities

• Author regulatory submission documents, as assigned, including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, Pediatric Investigation Plans, and other regulatory documents;
• Conduct the formal review and approval of authored documents, following applicable standard operating procedures;
• With considerable supervision, manage regulatory writing activities for product submissions, including new and supplemental drug applications/biologics license applications;
• Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group);
• May provide functional area input for Global Regulatory Plan and team goals;
• May work with contract and freelance writers;
• May participate in training and mentoring of junior medical writers;
• May participate in departmental and cross‑departmental initiatives, as appropriate.;
• Generate document timelines, with team input;
• Keep abreast of relevant professional information and technology.

Basic Qualifications

• Doctorate degree OR
• Master’s degree and 4 to 6 years of directly related experience OR
• Bachelor’s degree and 6 to 8 years of directly related experience OR
• Diploma and 10 to 12 years of directly related experience

Preferred Qualifications

Functional Skills

• Proficiency with word processing and other Microsoft Office Programs
• Significant knowledge of scientific/technical writing and editing, and of overall clinical development process for new compounds;
• Ability to understand and follow complex standard operating procedures (SOPs), guidance documents, and work instructions;
• Understanding and application of principles, concepts, theories and standards of scientific/technical field.
• Substantial knowledge and understanding of International Council on Harmonization (ICH) and Good Clinical Practice (GCP) guidance’s and requirements.

Soft Skills

• Excellent written/oral communication skills and attention to detail
• Ability to effectively demonstrate leadership in a team environment which requires negotiation, persuasion, collaboration, and analytical judgment;
• Proficient time and project management skills.
• Self-starter with a drive and perseverance to achieve results

What we expect of you

We’re all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications.

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Objects in your future are closer than they appear. Join us.