About the role
Job Title :Technical Writer
Department:Quality Assurance
Job Type - Full time
Location : Bangalore
Bachelor/Master degree
Experience :3-6 years
Position Summary :-We are seeking a detail-oriented and experienced Technical Writer with a background in life sciences to join our dynamic team. The ideal candidate will have 3 to 6 years of experience in technical writing, specifically in creating Standard Operating Procedures (SOPs) and work instructions. This role is crucial in ensuring the accuracy, clarity, and compliance of our documentation processes in the rapidly evolving field of precision medicine. Key Responsibilities:-
Document Development:
1.Author, review, and revise Standard Operating Procedures (SOPs), work instructions, and other technical documents.
2.Ensure that all documentation is accurate, clear, concise, and compliant with regulatory standards.
3.Collaborate with subject matter experts (SMEs) to gather necessary information and translate complex technical processes into user-friendly documents. Cross-Functional Collaboration:
1.Work closely with R&D, quality assurance, regulatory, and other departments to understand and document their processes.
2.Participate in meetings and discussions to stay informed about project developments and upcoming documentation needs.
3.Act as a liaison between technical teams and non-technical stakeholders to ensure clear communication and understanding of SOPs and work instructions.
Training and Support:
1.Develop training materials and guides to assist in the implementation and usage of SOPs and work instructions.
2.Provide training sessions and support to staff to ensure proper understanding and compliance with documented procedures.
3.Assist in audits and regulatory inspections by providing necessary documentation and clarifications.
Preferred Skills:-
1. Excellent writing, editing, and proofreading skills with a strong attention to detail.
2. Ability to understand and document complex technical processes and concepts.
3. Proficiency with document management systems and version control.
4. Strong organizational and project management skills.
5. Ability to work independently and collaboratively in a fast-paced environment.
6. Familiarity with regulatory requirements and standards in the biotechnology or pharmaceutical industry is a plus
Working Condition Office environment with potential for remote work