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Technical Documentation Specialist

Technical Documentation Specialist

Valuesoft Info Services Pvt Ltd.Bangalore, Karnataka, India
30+ days ago
Job description

We are seeking a skilled Technical Writer with expertise in Hematology to create clear accurate and well-structured documentation for scientific clinical or regulatory audiences. The ideal candidate will have a strong background in hematology medical or laboratory sciences and experience writing for technical or clinical stakeholders in the diagnostics pharmaceutical or healthcare industry.

Key Responsibilities :

  • Develop and edit scientific and technical documentation including SOPs lab protocols manuals white papers training materials and regulatory submissions.
  • Translate complex hematological concepts into reader-friendly content for clinical users lab professionals or regulatory bodies.
  • Collaborate with hematologists lab scientists R&D teams and quality assurance personnel to ensure accuracy and compliance.
  • Write content for hematology analyzers reagents test kits or diagnostic platforms (if applicable).
  • Ensure consistency with medical writing standards regulatory guidelines (e.g. CLIA CAP FDA) and internal branding.
  • Support the creation of training modules product inserts technical bulletins and clinical trial documentation if needed.

Qualifications :

  • Bachelors or Masters degree in Hematology Medical Laboratory Technology or a related field .
  • Minimum 2 5 years of experience in technical / medical writing preferably in a diagnostic biotech or clinical lab setting.
  • Familiarity with hematology testing methods (e.g. CBC ESR flow cytometry) and instrumentation.
  • Strong knowledge of regulatory documentation standards (e.g. ICH GCP GLP).
  • Excellent command of written English and attention to scientific detail.
  • Proficiency in MS Office referencing tools (e.g. EndNote) and document control systems.

    • Preferred Skills :

  • Good working knowledge on Hematology process and reporting.
  • Experience working with LIMS or IVD documentation .
  • Knowledge of ISO 15189 CLSI guidelines or related lab quality frameworks.
  • Familiarity with medical device regulations (e.g. EU MDR FDA 21 CFR Part 820).

    • Key Skills

    Dhcp,SQL,Active Directory,VOIP,VMware,Customer Service,Windows,Trouble Shooting,Java,VPN,Sharepiont,hardware,Dns,Technical Support,Software Applications

    Employment Type : Full Time

    Experience : years

    Vacancy : 1

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    Technical Specialist • Bangalore, Karnataka, India