Sr Exe/ AM - Documentation & QA Cell (DQA)

Kredd Scientific Nascence

Mumbai

On-site

INR 900,000 - 1,200,000

Full time

36 hours ago
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Job summary

Kredd Scientific Nascence is seeking a Sr Exe/AM - Documentation & QA Cell (DQA) for a full-time on-site role in the Mumbai Metropolitan Region. You will prepare, review, and maintain scientific, technical, and clinical documentation aligned with quality standards and regulatory requirements.

Daily duties include document control, version accuracy, coordinating approvals, and supporting audits with complete, compliant records.

Qualifications

  • Experience in scientific or regulated documentation (clinical, lab, or pharma).
  • Proficient in converting complex data into clear, structured documents.
  • Strong analytical ability to verify accuracy and completeness.
  • Familiarity with GMP/GLP or similar quality standards.
  • Detail-oriented with excellent organizational skills and deadlines.
  • Clear written and verbal communication; on-site collaboration with teams.

Responsibilities

  • Prepare, review and maintain scientific, technical and clinical documentation.
  • Manage document control systems, ensuring version accuracy and approvals.
  • Support audits and inspections with complete and compliant documentation.
  • Collaborate with R&D, QA and operations to capture processes clearly.
  • Develop and update templates, SOPs and documentation guidelines.

Skills

Clinical Documentation
Technical Writing
Analytical Skills
Regulatory QA
Attention to Detail
Communication
Cross-functional teamwork

Education

Bachelor's/Master's in Chemistry/Pharma/Life Sciences/Engineering

Job description

Company Description

Kredd Scientific Nascence is focused on transforming the future of health and industry through advanced chemical innovation. The team combines curiosity, rigorous science, and cutting-edge chemistry to deliver breakthroughs that aim to improve lives and set higher standards across sectors. Kredd fosters a culture of forward-thinking and boundary-pushing, encouraging bold ideas and practical implementation. The organization is committed to challenging the status quo and turning complex scientific concepts into impactful solutions. Prospective team members join a mission-driven environment dedicated to synthesizing a healthier, more innovative future.

Role Description

The Sr Exe/ AM - Documentation & QA Cell (DQA) is a full-time, on-site role based in the Mumbai Metropolitan Region. The role involves preparing, reviewing, and maintaining scientific, technical, and clinical documentation in alignment with internal quality standards and regulatory requirements. Daily responsibilities include managing document control systems, ensuring version accuracy, coordinating approvals, and supporting audits and inspections with complete and compliant documentation. The position collaborates closely with R&D, quality assurance, and operations teams to capture processes and outcomes clearly and consistently. The role also includes developing and updating templates, SOPs, and documentation guidelines to enhance quality, traceability, and regulatory readiness.

Qualifications
  • Strong expertise in Clinical Documentation and Documentation for scientific, laboratory, or regulated environments.
  • Proficiency in Technical Documentation and Technical Writing to translate complex data and processes into clear, structured documents.
  • Well-developed Analytical Skills to review, validate, and interpret technical information for accuracy and completeness.
  • Experience working within QA or regulatory frameworks, including familiarity with GMP, GLP, or similar quality standards.
  • Bachelor's or Master's degree in Chemistry, Pharma, Life Sciences, Engineering, or a related technical discipline.
  • Attention to detail, strong organizational skills, and the ability to manage multiple documents and deadlines simultaneously.
  • Comfort working on-site in cross-functional teams, with clear written and verbal communication skills.
  • Prior experience in a chemical, pharmaceutical, biotech, or research-intensive environment is highly beneficial.
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