Hyderabad Telangana Pharmaceutical quality control Jobs – 164 Open Jobs Today

Manager, QA Operations
Azurity Pharmaceuticals - India —Hyderabad, Telangana
- Quality control
- Manufacturing
Quick apply
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Sanofi —Hyderabad, Telangana
- English
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Amgen —Hyderabad, Telangana
- Night shift
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QA Specialist
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- ₹30 - ₹40 an hour
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Amgen —Hyderabad, Telangana
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Recruise —Hyderabad, Telangana
- ₹7 - ₹15 an hour
- Full-time
- English
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- Bachelor's degree
Quick apply
Lifecycle Management (LCM) Systems & Support Manager
Amgen —Hyderabad, Telangana
- Software troubleshooting
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AP Accountant
Azurity Pharmaceuticals - India —Hyderabad, Telangana
- Microsoft Excel
- Oracle
- Customer service
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4d
Sr Associate - Contracts & Pricing
Amgen —Hyderabad, Telangana
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Global Scientific Content Manager HEVA and PDMD
Sanofi —Hyderabad, Telangana
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Amgen —Hyderabad, Telangana
- Data analysis skills
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Manufacturing Engineer II
Medtronic —Nanakramguda, Hyderabad, Telangana
- Full-time
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Sr Associate Global Product Supply Planning
Amgen —Hyderabad, Telangana
- Master's degree
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Contract Development & Mfg Mgr Person in Plant
Amgen —Hyderabad, Telangana
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Amgen —Hyderabad, Telangana
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Eli Lilly —Hyderabad, Telangana
- Full-time
- B.Sc
- Project management
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Software Engineer - SAP security/Authorizations first level support
MULTIVAC Sepp Haggenmüller SE & Co. KG —Hyderabad, Telangana
- Hybrid work
- Computer Science
- Engineering
- English
- Health insurance

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Manager, QA Operations

Azurity Pharmaceuticals - India
Hyderabad, Telangana

Quick apply

Job details

Qualifications

Quality management
Quality assurance
Quality control
QA/QC
Pharmacy
Chemistry
Manufacturing

Full job description

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company's patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.

Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

About the Role

Azurity is seeking a Manager to execute QA Operations internationally to ensure full compliance with US FDA, EU GMP, Health Canada, PIC/S and GDP regulations and guidelines. As part of these core responsibilities, this role will support Global Quality Operations including deviation/OOS assessment, CAPA management, change control, PQR reviews, product complaints, performance of vendor audits, and technical batch release, as applicable.

Key Responsibilities

Execute QA oversight for assigned CMOs, 3PLs and other types of vendors based Internationally, including deviation/OOS assessment, change control, and CAPA evaluation.
Perform technical documentation for batch disposition (e.g. batch record reviews, CoAs, deviation/OOS investigation reports, stability data) to support in-market product release.
Ensure quality processes align with international standards and local market requirements.
Collaborate with Supply Chain, Regulatory, Technical Operations, for the supply of medicinal products to the various markets.
Manage assigned vendors for Quality Systems - deviation investigation, CAPAs, change control management, product quality reviews (PQRs), compliance risk assessment, self-inspections, and Quality Technical Agreements.
Support inspections from the local Health Authorities and follow-up actions.
Support GMP/GDP audits of CMOs, 3PLs, and other vendors, if required.
Participate in local risk management and escalation processes aligned with global procedures.
Execute continuous improvement and training of QA personnel related to regulatory/compliance requirements.

Required Skills and Experience

Minimum 5 years in pharmaceutical Quality Assurance / QA Operations (QC experience would be eligible)
Previous experience in managing external pharmaceutical manufacturing partners (CMOs).
Working knowledge of Veeva Quality Vault (Quality Management System) is beneficial.

Preferred Qualifications

Degree in pharmacy, chemistry, or biology or any other related science background.

By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

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Refine Your Search

pharmaceutical quality control jobs in hyderabad telangana

Manager, QA Operations

Manager - Project Controls Analytics & Bid Review

Associate People Partner

Senior Associate Supply Chain Compliance Management (Amgen External Planning)

Associate Manager Medical Supply Operations

Manager, Lab Systems

QA Specialist

Business Analyst

Analytical Trending Scientist

Lifecycle Management (LCM) Systems & Support Manager

AP Accountant

Sr Associate - Contracts & Pricing

Global Scientific Content Manager HEVA and PDMD

Sr Associate Supply Chain Execution (Amgen External Planning)

Manufacturing Engineer II

Sr Associate Global Product Supply Planning

Contract Development & Mfg Mgr Person in Plant

Biostatistics Manager, Centralized Statistical Monitoring (CSM)

Principal TSMS - APIEM

Software Engineer - SAP security/Authorizations first level support

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