Telangana Author Jobs – 134 Open Jobs Today

Technical Writer
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- ₹25 - ₹30 an hour
- Writing skills
- Project management
- Bachelor's degree
C&Q Document Preparation Support (Facilities & Utilities)
Amgen —Hyderabad, Telangana
- HVAC
- Organisational skills
- In-person
Internal Job Posting-Software Engineer - III
FactSet Research Systems —Hyderabad, Telangana
- Full-time
- Computer Science
- System design
- Java
9h
Associate Director, Biostatistics
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
- Hybrid work
- Doctoral degree
- Project management
- Travel
React Developer with .Net
Verisk —Hyderabad, Telangana
- Full-time
- Azure
- Computer Science
- Software troubleshooting
Senior Validation Engineer
Amgen —Hyderabad, Telangana
- Public speaking
- Master's degree
- Analysis skills
Senior Product Manager, FinOps
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Computer Science
- Engineering
- Master's degree
3d
Specialist IS Engineer - System Implementation & Development
Amgen —Hyderabad, Telangana
- Azure
- Computer Science
- Public speaking
Technical Solutions Consultant, PDM-PLM
Google —Hyderabad, Telangana
- Full-time
- Computer Science
- Engineering
- System design
Product Manager, Manufacturing Execution & Batch Lifecycle
ValGenesis —Hyderabad, Telangana
- Full-time
- Computer science
- Doctoral degree
- B.Sc
Quick apply
Data Engineer, Global Procurement Technology
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Java
- Databases
- SQL
8d
Specialist Stability
Amgen —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Software Engineer
Zuddl —Hyderabad, Telangana
- System design
- Java
- JavaScript
Quick apply
13d
Principal Product Analyst
Amgen —Hyderabad, Telangana
- Azure
- DevOps
- Public speaking
Lead Software Engineer
HealthEdge —Hyderabad, Telangana
- Full-time
- Azure
- Computer Science
- Databases
Sr Analyst IT
Mattel —Hyderabad, Telangana
- Full-time
- Oracle
- Computer Science
- Master's degree
Quick apply
Associate Director, Triage and Medical Review
Regeneron —Hyderabad, Telangana
- Medicine
- Databases
- Bachelor's degree
- Health insurance
- Paid time off
Senior Specialist ITVS Digital Validation
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
- Hybrid work
- Computer Science
- English
- Databases
2d
IT&D Manager, Demand Planning
Reckitt —Hyderabad, Telangana
- Project management
- Agile
- Analytics
- Health insurance
Senior IBM DOM Developer – Supply chain DTC
Mattel —Hyderabad, Telangana
- Full-time
- Hybrid work
- Azure
- Computer Science
- System design
Quick apply

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Technical Writer

AVEVA DRUG DELIVERY SYSTEMS INC -
Kukatpally, Hyderabad, Telangana

Apply Now

Job details

₹25 - ₹30 an hour

Qualifications

Writing skills
Project management
Quality assurance
Bachelor's degree
Technical writing
Manufacturing
Document management systems
Communication skills
Editing
FDA regulations

Full job description

Job Summary:

The Technical Writer will be responsible for creating, reviewing, and managing documentation related to pharmaceutical testing protocols and reports. This role involves overseeing the approval process of these documents and coordinating with Contract Manufacturing Organizations (CMOs) to ensure the timely and accurate execution of testing activities. The ideal candidate will have a strong background in technical writing within the pharmaceutical or biotech industry, excellent project management skills, and a keen eye for detail.

Key Responsibilities:

Writing and Documentation:
- Develop, write, and revise pharmaceutical testing protocols, including stability, validation, and method development protocols, ensuring clarity, accuracy, and compliance with regulatory requirements.
- Author comprehensive testing reports that summarize the results, analyses, and conclusions of pharmaceutical testing activities.
- Ensure all documents meet the company’s style guidelines and are consistent with industry standards and regulatory expectations.
Approval Process Oversight:
- Manage the review and approval process for testing protocols and reports, coordinating with internal teams such as Quality Assurance, Regulatory Affairs, and R&D to obtain necessary approvals.
- Track the progress of documents through the review cycle, ensuring timely completion and addressing any issues or delays that arise.
- Facilitate meetings and discussions to resolve any concerns or discrepancies during the review process.
Coordination with Contract Manufacturing Organizations (CMOs):
- Act as the primary point of contact with CMOs for the execution of pharmaceutical testing activities.
- Provide CMOs with the necessary protocols and instructions, ensuring they have all required information to perform the testing accurately and in compliance with regulatory standards.
- Monitor the progress of testing at CMOs, addressing any issues or questions that arise and ensuring that timelines are met.
Regulatory Compliance:
- Ensure all documentation complies with applicable regulatory standards, including FDA, EMA, and other global regulatory requirements.
- Stay current with industry regulations and best practices, updating protocols and reports as necessary to maintain compliance.
Cross-Functional Collaboration:
- Collaborate with cross-functional teams, including Quality Control, Quality Assurance, Regulatory Affairs, R&D, and external partners, to gather the necessary information for protocol and report writing.
- Work closely with project managers to align document timelines with overall project schedules.
Document Control and Management:
- Maintain organized records of all testing protocols, reports, and related documents.
- Manage document version control and ensure that all stakeholders have access to the most current versions of documents.
Continuous Improvement:
- Identify opportunities to improve the efficiency and effectiveness of the document creation and approval processes.
- Contribute to the development and maintenance of standard operating procedures (SOPs) related to documentation and testing processes.

Education: Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmaceutical Sciences) or a related field. Advanced degree preferred.
Experience:
- 3+ years of experience in technical writing within the pharmaceutical, biotech, or related industry.
- Experience writing protocols and reports for pharmaceutical testing, including stability studies, method validation, and quality control.
- Familiarity with regulatory requirements for pharmaceutical testing documentation (e.g., FDA, EMA guidelines).
Skills:
- Exceptional writing and editing skills, with the ability to convey complex scientific information clearly and concisely.
- Strong project management skills, with the ability to manage multiple projects and deadlines simultaneously.
- Excellent interpersonal and communication skills, with the ability to collaborate effectively with internal and external teams.
- Detail-oriented with a strong commitment to accuracy and quality.

Preferred Qualifications:

Experience coordinating with Contract Manufacturing Organizations (CMOs) or other external partners.
Familiarity with electronic document management systems (EDMS).
Understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).

Working Conditions:

Office-based position with occasional travel to CMOs or other partner sites as required.
Flexibility to work with teams across different time zones.

Apply Now

Refine Your Search

author jobs in telangana

Technical Writer

C&Q Document Preparation Support (Facilities & Utilities)

Internal Job Posting-Software Engineer - III

Associate Director, Biostatistics

React Developer with .Net

Senior Validation Engineer

Senior Product Manager, FinOps

Specialist IS Engineer - System Implementation & Development

Technical Solutions Consultant, PDM-PLM

Product Manager, Manufacturing Execution & Batch Lifecycle

Data Engineer, Global Procurement Technology

Specialist Stability

Senior Software Engineer

Principal Product Analyst

Lead Software Engineer

Sr Analyst IT

Associate Director, Triage and Medical Review

Senior Specialist ITVS Digital Validation

IT&D Manager, Demand Planning

Senior IBM DOM Developer – Supply chain DTC

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