Scientific Writer I (PSSW) at Bristol Myers Squibb
A rare chance for aspiring Scientific Writers pursuing careers at Bristol Myers Squibb to join Bristol Myers Squibb in Hyderabad. This full-time position focuses on regulatory documentation and offers a unique opportunity to contribute to innovative medicines that transform patients’ lives. Applications are open now.
About the Company
Bristol Myers Squibb is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a strong emphasis on collaboration and accountability, the organization fosters a purpose-driven culture that inspires its employees to engage in meaningful work and provides opportunities for growth in a supportive environment.
Job Details:
- Company: Bristol Myers Squibb
- Location: Hyderabad – TS – IN
- Job Type: Full time
- Posted On: Posted Today
- Job Requisition ID: R1606939
Bristol Myers Squibb Careers: Position Summary
The role offers professionals pursuing Bristol Myers Squibb careers the opportunity to lead document strategy and author message-driven, clear and concise regulatory documents in support of submissions and approvals in key markets and other geographies. The objective is to coordinate and author documents needed for regulatory submissions, ensuring the integration of scientific, medical, and regulatory input from cross-functional team members.
Key Responsibilities
- Coordinate and author complex safety aggregate reports, risk management documents, and regulatory documents, ensuring the integration of scientific, medical, and regulatory input from development team members.
- Participate in relevant document subteam(s) and ensure effective planning and management of timelines for all components of assigned documents.
- Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
- Maintain document prototypes and shells.
- Comply with internal and external processes and guidelines while managing the review process and resolving issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents.
Qualifications
- Minimum of BS/BA degree in science (PhD/PharmD/Master’s degree preferred) with approximately 1-2 years of regulatory documentation or related experience. All PhD in biological sciences and PharmD candidates are considered.
- Strong writing skills in authoring and managing the production of scientific documents (pharmaceutical regulatory documentation and/or publications in peer-reviewed journals).
- Ability to analyze and interpret complex data from a broad range of scientific disciplines.
- Basic understanding of global pharmaceutical drug development.
- Ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team.
- Expertise in MS Office.
Bristol Myers Squibb hires for skills and capabilities, not just credentials. If this role excites you, but doesn’t perfectly match your resume, you are encouraged to apply anyway.
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This Bristol Myers Squibb careers opportunity allows qualified candidates to contribute to vital regulatory documentation efforts. Interested individuals are encouraged to apply before the deadline to join a team that is dedicated to transforming patient lives through innovative solutions.
