Telangana Author Jobs – 133 Open Jobs Today

Technical Writer
AVEVA DRUG DELIVERY SYSTEMS INC —Kukatpally, Hyderabad, Telangana
- ₹25 - ₹30 an hour
- Writing skills
- Project management
- Bachelor's degree
Staff Software Engineer/Data Scientist
The Hartford —Hyderabad, Telangana
- Full-time
- Azure
- Databases
- SQL
Sr Associate Biostatistics
Amgen —Hyderabad, Telangana
- Doctoral degree
- English
- Master's degree
Librarian
Pallavi International School, Sagar Road, Chintapally Guda, Hyderabad —Bongulur, Telangana
- From ₹20,000 a month
- Full-time
- Research
- Master's degree
- Bachelor's degree
- Health insurance
Quick apply
13d
Fullstack Developer- React
Verisk —Hyderabad, Telangana
- Full-time
- Azure
- Computer Science
- Software troubleshooting
On Job Trainee
Pulsus Group —Hyderabad, Telangana
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
C&Q Document Preparation Support (Facilities & Utilities)
Amgen —Hyderabad, Telangana
- HVAC
- Organisational skills
- In-person
Lead QA Engineer - Contract
WPP Production —Hyderabad, Telangana
- Hybrid work
- Computer Science
- Databases
- Bachelor's degree
- Flexible schedule
Quick apply
Senior Product Manager - Tech, Amazon Appstore
ADCI - BLR 14 SEZ —Hyderabad, Telangana
- Full-time
- Bachelor's degree
- APIs
- Analytics
2d
Sr. Product Manager, Amazon Customer Service
ADCI HYD 13 SEZ —Hyderabad, Telangana
- Full-time
- Business development
- Bachelor's degree
- Product management
13d
C&Q Document Preparation Support (Finished Drug Product)
Amgen —Hyderabad, Telangana
- Organisational skills
- In-person
- Manufacturing
8d
Principal Service Engineer
Providence Global Center —Hyderabad, Telangana
- Part-time
- Azure
- Computer Science
- Master's degree
- Health insurance
Sales Manager With Cloud & SMB Sales Focus
GlobalOutlook —Hyderabad, Telangana
- Email
- Microsoft Powerpoint
- Microsoft Excel
- Azure
C&Q Document Preparation Support (Drug Product)
Amgen —Hyderabad, Telangana
- Organisational skills
- In-person
- Manufacturing
8d
Consumer Safety Science Scientist
Haleon —Hyderabad, Telangana
- Full-time
- Agile
- Computer skills
9d
Customer Centric Engineer (APAC Market)
Workato —Hyderabad, Telangana
- Computer Science
- B.Sc
- Java
Quick apply
Prof, Controlled Doc Mgmt
サイネオス・ヘルス —Madhapur, Hyderabad, Telangana
- Travel
SAP FICO BRM
Luxoft —Hyderabad, Telangana
- English
- Banking
Global Regulatory Writing – Senior Manager
Amgen —Hyderabad, Telangana
- Doctoral degree
- Word processing
- Writing skills
Sr. Specialist, IT Validation Services
Bristol-Myers Squibb —Hyderabad, Telangana
- Email
- Hybrid work
- Management
- Computer Science
- English
1d

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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

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