Telangana Document reviewer Jobs – 25 Open Jobs Today

Analytical QA Reviewer
DIFGEN PHARMACEUTICALS PRIVATE LIMITED —Kukatpally, Hyderabad, Telangana
- Full-time
- Analysis skills
- Quality control
- Manufacturing
Associate Managing Editor
ARJ —Hyderabad, Telangana
- ₹15,000 - ₹22,000 a month
- Full-time
- Hybrid work
- English
- Microsoft Office
- Master's degree
- Work from home
Quick apply
12d
HEDIS Reviewer with (EM IP/OP)
Eclat Health Solutions —Hyderabad, Telangana
- Medicine
- Master's degree
- Analysis skills
Quick apply
Business Analyst
Cohere Health —Hyderabad, Telangana
- Google Suite
- Microsoft Office
- Analysis skills
Quick apply
10d
Document Controller
Enviri Global Service Centre —Hyderabad, Telangana
- Full-time
- English
- Communication skills
Quick apply
Project Specialist - ESR (Externally Sponsored Research)
Sanofi —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
SOX Manager
Enfinity Global —Hyderabad, Telangana
- Full-time
- Microsoft Access
- ERP systems
Quick apply
Team Lead - HCP Science Content Hub
Opella Healthcare Group —Hyderabad, Telangana
- Full-time
- Doctoral degree
- Writing skills
- Master's degree
13d
Drug Product Project Leader
Novartis —Hyderabad, Telangana
- Full-time
- Doctoral degree
- Master's degree
- APIs
5d
Accounts Payable
JV Ventures —Hyderabad, Telangana
- ₹4,00,000 - ₹7,00,000 a year
- Full-time
- Microsoft Excel
- Oracle
- ERP systems
- Health insurance
Quick apply
11d
Scientist
Perceptive —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
9d
Fund Services Assistant Manager Hyderabad, India Jul. 31, 2026
Alter Domus —Hyderabad, Telangana
- Analysis skills
- Bachelor's degree
- Accounting
US Tax - Senior / TL ( Individual Tax - Form 1040)
PACIFIC GROUP OF COMPANIES —Hyderabad, Telangana
- ₹30,000 - ₹90,000 a month
- Full-time
- English
- Finance
- Master's degree
Quick apply
Regulatory Labeling Mgr
Amgen —Hyderabad, Telangana
- Master's degree
- Analysis skills
- Bachelor's degree
Sr. Associate Regulatory Affairs
Amgen —Hyderabad, Telangana
- B.Sc
- Project management
- Bachelor's degree
Internal Control Testing Senior Analyst
Opella Healthcare Group —Hyderabad, Telangana
- Full-time
- Spanish
- Microsoft Excel
- Finance
Global Scientific Content Manager HEVA and PDMD
Sanofi —Hyderabad, Telangana
- Full-time
- English
- Project management
- Travel
1d
Senior Staff Product Owner
Palo Alto Networks —Ranga Reddy District, Telangana
- Full-time
- Master's degree
- Product management
- APIs
AI Engineer, Agent/Platform Tracks
Parexel —Hyderabad, Telangana
- Computer Science
- Master's degree
- AWS
Controls Automation & Analytics Specialist
Opella Healthcare Group —Hyderabad, Telangana
- Full-time
- Microsoft Excel
- Computer Science
- Finance

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Analytical QA Reviewer

DIFGEN PHARMACEUTICALS PRIVATE LIMITED -
Kukatpally, Hyderabad, Telangana

Apply Now

Job details

Full-time

Qualifications

Analysis skills
Quality assurance
Quality control
Manufacturing

Full job description

Job Summary:

The Quality Control (QC) Specialist will be responsible for ensuring the quality and compliance of pharmaceutical development study protocols and reports. This role involves the review and approval of documentation related to the development process, acting as a subject matter expert (SME) in the QC function, and coordinating with Contract Manufacturing Organizations (CMOs) to investigate deviations related to testing protocols. The ideal candidate will have extensive experience in quality control within the pharmaceutical industry, with strong analytical skills and a deep understanding of regulatory standards.

Key Responsibilities:

Review and Approval of Study Protocols and Reports:
- Review and approve pharmaceutical development study protocols, ensuring they meet regulatory requirements and company quality standards.
- Critically evaluate study reports to ensure data accuracy, completeness, and compliance with established protocols and industry standards.
- Collaborate with cross-functional teams, including R&D, Quality Assurance, Regulatory Affairs, and Manufacturing, to address any discrepancies or concerns identified during the review process.
Quality Control Subject Matter Expert (SME):
- Act as the SME for the QC function, providing guidance and expertise on quality control best practices, methodologies, and regulatory requirements.
- Lead and support the development and implementation of QC processes, procedures, and standards to ensure consistent quality across all pharmaceutical development activities.
- Provide technical support and training to QC personnel and other stakeholders on QC principles, techniques, and regulatory expectations.
Regulatory Compliance:
- Ensure all reviewed and approved documents comply with applicable regulatory requirements, including FDA, EMA, ICH, and other global standards.
- Stay current with changes in regulatory requirements and industry best practices, ensuring that study protocols and reports are updated accordingly.
- Support regulatory submissions by providing QC-related documentation and expertise as required.
Coordination with Contract Manufacturing Organizations (CMOs):
- Work closely with CMOs’ Quality Control units to ensure that all testing activities are conducted in accordance with approved protocols and regulatory standards.
- Investigate and resolve any deviations to testing protocols that occur at CMOs, ensuring a thorough understanding of the root cause and the implementation of corrective and preventive actions (CAPA).
- Monitor and follow up on the effectiveness of CAPA implemented by CMOs to ensure continuous compliance and quality improvement.
Continuous Improvement:
- Identify opportunities for process improvements in the QC review and approval process, and implement changes to enhance efficiency and effectiveness.
- Participate in internal audits and contribute to the development and refinement of standard operating procedures (SOPs) related to QC activities.
- Lead or support quality improvement initiatives, including root cause analysis and the implementation of corrective and preventive actions (CAPA).
Data Management and Integrity:
- Ensure the integrity of all QC data by implementing robust data management practices, including proper documentation, storage, and retrieval processes.
- Review and approve QC data generated during pharmaceutical development studies, ensuring that it meets the required standards for accuracy, precision, and reliability.
- Support the implementation and maintenance of electronic systems (e.g., LIMS) used for QC data management.
Collaboration and Communication:
- Work closely with cross-functional teams to ensure alignment on quality expectations and requirements for pharmaceutical development projects.
- Communicate effectively with internal and external stakeholders, including providing clear and concise feedback on study protocols and reports.
- Represent the QC function in meetings, discussions, and decision-making processes related to pharmaceutical development.

M. Pharmacy or Post Graduation (6years to 9 years experience)

Apply Now

Refine Your Search

document reviewer jobs in telangana

Analytical QA Reviewer

Associate Managing Editor

HEDIS Reviewer with (EM IP/OP)

Business Analyst

Document Controller

Project Specialist - ESR (Externally Sponsored Research)

SOX Manager

Team Lead - HCP Science Content Hub

Drug Product Project Leader

Accounts Payable

Scientist

Fund Services Assistant Manager Hyderabad, India Jul. 31, 2026

US Tax - Senior / TL ( Individual Tax - Form 1040)

Regulatory Labeling Mgr

Sr. Associate Regulatory Affairs

Internal Control Testing Senior Analyst

Global Scientific Content Manager HEVA and PDMD

Senior Staff Product Owner

AI Engineer, Agent/Platform Tracks

Controls Automation & Analytics Specialist

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