Gachibowli Hyderabad Telangana Pharmaceutical industry Jobs – 463 Open Jobs Today

Supply Chain Compliance Sr Associate AXP
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Training Content Developer
Dr. Reddy's Laboratories —Hyderabad, Telangana
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- Full-time
- Microsoft Powerpoint
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- Bachelor's degree
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Manager-Analytical & Data Verification
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
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Head of Quality Services
Lonza —Hyderabad, Telangana
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Healthcare Marketing Coordinator
Parkmed healthcare —Hyderabad, Telangana
- ₹25,000 - ₹35,000 a month
- Full-time
- Microsoft Powerpoint
- Nursing
- Microsoft Excel
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8d
Head of Quality Systems Office
Lonza —Hyderabad, Telangana
- Full-time
- PMP
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- Bachelor's degree
Data Analyst 1
Certara —Hyderabad, Telangana
- Full-time
- Remote
- Data analysis skills
- Master's degree
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Sr. Associate Regulatory Affairs
Amgen —Hyderabad, Telangana
- B.Sc
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Manager, C&Q Document Preparation (Drug Substance)
Amgen —Hyderabad, Telangana
- Full-time
- Engineering
- Master's degree
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Business Development Executive – B2B Pharma and Medical Devices
A&C Pharma Specialities LLP —Hyderabad, Telangana
- ₹60,000 - ₹85,000 a month
- Full-time
- Sales
- B.Sc
- Business development
- Work from home
- Flexible schedule
Quick apply
Study Delivery Associate
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
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Sr. Scientist Pharmacovigilance Operations Oversight and Strategy
Haleon —Hyderabad, Telangana
- Full-time
- Medicine
- Doctoral degree
- Project management
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Bussiness Development -Pharma
Amogen pharma pvt ltd —Madhapur, Hyderabad, Telangana
- ₹35,000 - ₹50,000 a month
- Full-time
- Sales
- Business development
- In-person
- Health insurance
- Food provided
Quick apply
Scientist II, Verification Programs
The U.S. Pharmacopeia (USP) —Hyderabad, Telangana
- Full-time
- Laboratory experience
- Master's degree
- Analysis skills
- Paid time off
6d
Team Member Analytical QC
Dr Reddy's Laboratories Limited —Hyderabad, Telangana
- Full-time
- Master's degree
- Manufacturing
- Health insurance
Quick apply
2d
DEPUTY MANAGER-GAS DETECTION HYDERABAD
Bluefence Systems Pvt Ltd —Hyderabad, Telangana
- ₹30,000 - ₹70,000 a month
- Full-time
- CRM software
- Sales
- Salesforce
Quick apply

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Supply Chain Compliance Sr Associate AXP

Amgen -
Hyderabad, Telangana

Apply Now

Job details

Qualifications

Supply chain
Microsoft Office
Project management
Quality assurance
Agile
Quality systems
Document management systems
Communication skills

Full job description

India - Hyderabad

JOB ID: R-248451 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Aug. 31, 2026 CATEGORY: Supply Chain

Senior Associate, Compliance Management (Amgen External Planning)

What you will do
Let’s do this! Let’s change the world! In this vital role you will be part of the External Planning and Delivery
Team, which is responsible for strategy and execution of all aspects of supply chain supporting our
external manufacturing network.

The Senior Associate Amgen External Planning (AXP) reports to the Business Performance Manager of
Supply Planning at the Amgen India, Hyderabad site. In this role, the Senior Associate Supply Chain
Compliance is responsible for leading and maintaining compliance infrastructure for the External Planning
organization ensuring that all GMP and non-GMP documentation, training, and procedural requirements
are established, maintained, and continuously improved to support operational excellence. This individual
will serve as the compliance lead for the External Supply team, owning Standard Operating Procedures
(SOPs), Deviation and Change Controls, training governance, inspection readiness support, and
adherence to internal Amgen policies and global regulatory requirements. This role will require a
close partnership with Amgen External Supply, Global / Regional / Site Supply Chain, Global Distribution,
and External Quality.

AXP is a critical component of Amgen’s Global Supply Chain, responsible for enabling reliable, efficient,
and agile planning and delivery operations for Amgen’s CMO-sourced products. The Senior Associate,
based at Amgen’s Hyderabad site, will be a key member of this team and a foundational contributor to the
External Planning work center, supporting the business performance and continuous improvement of
planning operations. The role requires strong knowledge of GMP environments, document management
systems, and cross-functional collaboration within a highly regulated biopharmaceutical supply chain.

Responsibilities:
Compliance & SOP Governance

Own and manage all team SOPs (GMP and non-GMP), work instructions, and guiding documents.
Lead periodic SOP reviews, revisions, and lifecycle management in alignment with Amgen quality systems.
Ensure alignment of team procedures with global policies, regulatory requirements, and CMO oversight standards.
Coordinate cross-functional reviews and approvals of procedural documents.
Maintain document control and ensure inspection readiness at all times.
Monitor and report performance metrics (e.g., cycle time, aging, on-time closure); escalate overdue items.
Monitor and report (SOP, training, regulatory commitments, deviations and change
management) trending and provide leadership with insights and action plans for
improvement.

Training Management

Own and track all team training requirements (GMP and non-GMP).
Manage training completion, driving closure of overdue items.
Partner with Quality and HR to ensure accurate training curricula and assignment.
Develop training materials and support onboarding of new team members.
Prepare compliance dashboards and periodic status reports.
Regulatory & Audit Support
Support internal and external audits and inspections related to External Supply operations and documentation practices
Track and manage compliance commitments, CAPAs, and action items for the team.
Ensure proper documentation and archival of audit-related records.
Partner with Quality Assurance to ensure inspection readiness across the External Planning function.
Deviation & Change Control Management
Own and manage deviations and change control records across AXP supply chain
operations.
Ensure timely initiation, routing, and closure in accordance with procedures and timelines.
Maintain accurate, complete, and compliant records within quality systems.
Support workflow execution through coordination, tracking, and documentation updates.
Ensure audit readiness with complete, accurate, and inspection-ready records.
Continuous Improvement
Monitor adherence to established procedures and identify compliance gaps.
Drive process improvements to simplify documentation, training tracking, and governance workflows.
Support risk assessments and change management activities impacting External Planning.
Key Skills & Competencies
Strong attention to detail and compliance mindset
High level of ownership and accountability
Ability to manage multiple priorities in a fast-paced environment
Proactive problem-solving skills
Strong stakeholder management and collaboration skill
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.
Basic Qualifications:
Any degree and 5-9 years’ supply chain experience in GMP-regulated pharmaceutical / biotechnology industry, or related business fields
In addition to meeting above requirements, you must have at least 2 years’ experience working in teams, projects, and programs. This experience may run concurrently with the required GMP-regulated

Preferred Qualifications:

Experience in Supply Chain, External Manufacturing, or Quality within a GMP environment.
Strong knowledge of GMP documentation practices and quality systems.
Experience managing SOPs and document control systems.
Familiarity with document management systems and training compliance tracking.
Experience supporting audits or regulatory inspections.
Strong organizational and project management skills.
Excellent written and verbal communication skills.
Ability to operate independently while partnering cross-functionally.
Proficiency in MS Office and document management systems.

Apply Now

Refine Your Search

pharmaceutical industry jobs in gachibowli hyderabad telangana

Supply Chain Compliance Sr Associate AXP

IMS Forecast Specialist II

Quality Assurance Associate - Drug Substance ( Supervisor )

Scientific Writer

Reporting and Analytics Manager

Training Content Developer

Manager-Analytical & Data Verification

Head of Quality Services

Healthcare Marketing Coordinator

Head of Quality Systems Office

Data Analyst 1

Sr. Associate Regulatory Affairs

Manager, C&Q Document Preparation (Drug Substance)

Business Development Executive – B2B Pharma and Medical Devices

Study Delivery Associate

Sr. Scientist Pharmacovigilance Operations Oversight and Strategy

Bussiness Development -Pharma

Scientist II, Verification Programs

Team Member Analytical QC

DEPUTY MANAGER-GAS DETECTION HYDERABAD

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