Document Senior Specialist Job At Bristol Myers Squibb
The Document Senior Specialist position at Bristol Myers Squibb offers a meaningful opportunity to work within Quality Management Systems while supporting life-changing pharmaceutical innovations. Based in Hyderabad, this Pharmacy Job role focuses on procedural document management, compliance, and continuous improvement within a global biopharmaceutical organization. Graduates seeking Pharmacy Jobs and wanting to start their career with Pharmacy Careers can apply now.
Job Details
- Job Title: Document Senior Specialist
- Location: Hyderabad, Telangana, India
About the Company
Bristol Myers Squibb is a global biopharmaceutical company driven by a single vision—transforming patients’ lives through science. The organization offers a culture of innovation, inclusion, and flexibility, enabling employees to work on meaningful projects that impact patient outcomes while growing their careers in an environment uncommon in scale and scope. This Pharmacy Job role plays a significant role in the company.
Educational Requirements for this Pharmacy Job
- Pharmacy degree
- 3+ years of experience in the Biopharma, Pharmaceutical, or Cell Therapy industry
Key Responsibilities for this Pharmacy Job
- Facilitate site procedural documents across QMS frameworks and electronic systems
- Author, review, approve, issue, implement, review, and retire procedural documents
- Assess compliance of site documents against global procedures and policies
- Act as site Subject Matter Expert for QMS procedures and document systems
- Support strategic initiatives and continuous improvement projects
- Synthesize SME feedback to document current and future processes accurately
- Support inspections, audits, investigations, and CAPA activities
- Collect metrics, identify trends, and communicate document status to stakeholders
- Support additional QA systems such as Change Control, Quality Risk Management, and Product Quality Reviews
Skills Required for this Pharmacy Job
- In-depth knowledge of cGMP requirements and global health authority regulations
- Strong procedural document writing skills with excellent grammar and structure
- Experience working in matrixed, cross-functional environments
- Ability to manage projects, timelines, risks, and escalations
- Strong judgment using a risk-based compliance approach
- Fluency in professional English for reading, writing, and speaking
- Ability to work independently with appropriate managerial guidance
Why This Job Role?
This Pharmacy Job role provides the opportunity to work with a globally respected biopharmaceutical leader while contributing directly to quality systems that support patient safety and regulatory compliance. It offers exposure to global initiatives, cross-site collaboration, continuous improvement projects, and a career environment focused on growth, flexibility, and meaningful impact. Graduates seeking Pharmacy Jobs and wanting to start their career with Pharmacy Careers can apply now.
