Senior Manager, AIN Documentation, Content Create and Automation (DCCA)

Amgen; Hyderabad; Hybride; INR 1 800 000 - 3 000 000; Plein temps

Résumé du poste

Amgen seeks a Senior Manager, DCCA to lead the India-based team delivering GMP documentation for DS, DP, or FDP across global sites. You will manage service delivery, capacity, and quality to ensure right-first-time documentation, with cross-time-zone collaboration and ongoing improvement.

The role requires 12–17 years in GMP environments and 2+ years of leadership experience, with a focus on documentation standards, change control, and stakeholder partnership. Hybrid work may be available.

Qualifications

• Bachelor's degree required with 12–17 years of experience and at least 2 years managing people.
• Experience in biotechnology/pharma GMP environment and leading teams, projects, or programs.
• Demonstrated ability to develop and revise controlled GMP documents and manage change control.

Responsabilités

• Lead global GMP documentation service operations for DS, DP, or FDP across sites and time zones.
• Establish intake, triage, prioritization, and escalation practices aligned with SLAs.

Connaissances

People leadership

Technical writing

GMP knowledge

Formation

Bachelor's degree in life sciences, engineering, technical communications, or related field

Outils

Electronic document-management systems

Description du poste

Career Category Manufacturing Job Description Senior Manager, AIN Documentation, Content Create and Automation (DCCA) Location: India | Scope: Global service supporting Amgen sites

Under minimal direction, the Senior Manager, DCCA leads a DS, DP or FDP team based in India that creates and revises controlled GMP documentation for Amgen sites globally. The role owns the service-delivery model that enables reliable, compliant, and accurate documentation support - delivering to agreed service-level agreements while driving right-first-time quality, predictable turnaround, and continuous improvement. Hours for this role may vary based on global time zones, which could include hybrid hours, on call requirements, and flexible working hours.

Role Responsibilities

• Lead the daily operation of the global GMP documentation service for DS, DP, or FDP, ensuring requests are received, clarified, prioritized, assigned, completed, and handed off in accordance with defined service-level agreements.
• Establish transparent intake, triage, prioritization, and escalation practices that balance site criticality, compliance risk, business impact, and available capacity.
• Develop and maintain capacity plans, workload forecasts, staffing models, and recovery plans that enable the team to meet commitments across supported sites and time zones.
• Own performance management routines and dashboards for on‑time delivery, right‑first‑time quality, cycle time, queue aging, rework, customer feedback, and resource utilization.
• Identify service risks early, communicate impacts and options clearly, and escalate constraints with proposed mitigation and recovery actions.

GMP Documentation Quality and Compliance

• Ensure document creation and revision activities comply with applicable global and local GMP requirements, good documentation practices, data‑integrity expectations, controlled‑document procedures, and approved change‑control processes.
• Set and maintain standards for document structure, technical writing, accuracy, traceability, version control, formatting, and review readiness to prevent defects before delivery.
• Oversee authoring and revision of controlled GMP documents, such as SOPs, work instructions, forms, manufacturing and laboratory records, technical reports, and associated attachments, based on approved site inputs and change requirements.
• Oversee the content creation of training materials used in the manufacturing areas including instructional design.
• Implement appropriate peer review, quality checks, training, and escalation mechanisms to improve right‑first‑time acceptance and reduce avoidable rework.
• Support inspection and audit readiness; ensure service records, training, and performance evidence are complete, traceable, and review‑ready.
• Oversee investigational support within the specific manufacturing domain.

Global Partnership and Governance

• Serve as the senior‑manager‑level liaison between the India documentation team and global site stakeholders, including Manufacturing, Quality, Engineering, QC, Regulatory, Supply Chain, and other technical functions.
• Create effective governance forums with supported sites to review demand, priorities, service performance, quality trends, capacity needs, and improvement opportunities.
• Clarify and maintain accountability between the service team and site owners: the service team provides disciplined document development and revision support; site functions retain ownership of technical content, approvals, local requirements, and implementation decisions.
• Resolve complex cross‑functional issues that could affect document quality, approval readiness, delivery timing, or compliance, using a risk‑based approach.

People Leadership and Organizational Capability

• Recruit, develop, coach, and retain a high‑performing team of GMP documentation professionals, technical writers, and/or documentation specialists.
• Establish role clarity, training curricula, performance expectations, career paths, and succession plans that build sustainable technical and leadership capability in India.
• Promote a culture of quality, ownership, collaboration, customer focus, and continuous learning while maintaining an inclusive, respectful, and accountable work environment.
• Partner with Human Resources and functional leaders to maintain an adaptable organization that can respond to changing global demand and business priorities.

Operational Excellence and Strategic Improvement

• Standardize and continuously improve documentation workflows, templates, authoring practices, quality controls, and digital ways of working across the service.
• Lead cross‑site projects and improvement initiatives that increase speed, accuracy, scalability, and customer experience without compromising compliance.
• Manage departmental headcount, training, technology, and operating budgets; optimize resources against the long‑range demand plan.
• Represent the documentation service on global teams, task forces, and quality‑system initiatives as needed.

Service Performance and Quality Measures

• Measure Leadership expectation
• On‑time delivery
• Right‑first‑time quality
• Cycle time and queue health
• Compliance performance
• Customer partnership and capacity

Basic Qualifications

Bachelor's degree and 12 to 17 years of experience 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources.

Preferred Qualifications

• Bachelor's degree in life sciences, engineering, technical communications, business, or a related field.
• 7+ years of directly related experience in a biotechnology, pharmaceutical, medical‑device, or other regulated GMP environment, including 4+ years leading people, technical writers, documentation specialists, projects, or programs.
• Demonstrated experience developing and revising controlled GMP documents, including SOPs, work instructions, forms, manufacturing or laboratory records, and related technical documentation.
• Experience operating a shared service or customer‑facing function across multiple sites, cultures, and time zones, with accountability for service‑level agreements and delivery metrics.
• Experience with electronic document‑management and quality‑management systems, document lifecycles, change control, and inspection or audit support.
• Lean, continuous‑improvement, project‑management, or operational‑excellence experience is preferred.

Core Competencies

• Strong people leadership, coaching, talent development, and capability building for a diverse technical team.
• Expert technical writing, editing, and review skills; sound judgment to distinguish content clarity, document quality, and compliance risk.
• In‑depth knowledge of cGMP, good documentation practices, data integrity principles, controlled‑document requirements, and change‑management processes.
• Service‑management discipline: intake, prioritization, workload planning, capacity modeling, performance dashboards, and timely risk escalation.
• Ability to influence global stakeholders, resolve competing priorities, communicate clearly in writing and verbally, and operate effectively across time zones.
• Analytical problem solving, continuous‑improvement mindset, strong attention to detail, and the ability to manage change without compromising quality while demonstrating a commitment to safety, quality, integrity, and Amgen values.

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen