Job Title: Medical & Scientific Content Quality Analyst (QA)
Experience: 3–5 Years
Location: Pan-India
Department: Medical Affairs / Content Operations
Role Overview:
We are looking for an experienced Medical & Scientific Content QA Specialist to ensure the accuracy, consistency, compliance, and quality of medical and scientific deliverables. This role will play a critical part in maintaining high-quality, audit-ready content aligned with regulatory and client-specific guidelines, especially within pharmaceutical and healthcare domains.
Key Responsibilities:
- Perform end-to-end quality review (QC/QA) of medical and scientific content, including:
- Slide decks, manuscripts, publications, and abstracts
- Medical education materials and promotional/non-promotional content
- Digital assets (web content, emails, infographics)
- Validate scientific accuracy, grammar, consistency, and formatting in line with approved references and source documents.
- Ensure compliance with MLR (Medical, Legal, Regulatory) guidelines and client-specific SOPs.
- Conduct fact-checking, citation/reference validation, and cross-verification against source data.
- Identify and flag risk areas, inconsistencies, and compliance gaps, providing actionable feedback to authors/designers.
- Maintain QA checklists, audit trails, and documentation for regulatory readiness.
- Collaborate closely with medical writers, reviewers, and stakeholders to ensure alignment and timely delivery.
- Support process improvements, standardization, and quality metrics tracking (defect rates, rework, turnaround time).
Required Skills & Competencies:
- Strong understanding of medical/scientific terminology and publication standards.
- Hands-on experience with MLR review processes and compliance frameworks.
- Excellent attention to detail with a strong quality mindset.
- Proficiency in quality control methodologies, proofreading, and editing.
- Familiarity with referencing styles (Vancouver, AMA, etc.) and citation tools.
- Ability to manage multiple projects and timelines in a fast-paced environment.
- Strong communication skills to provide clear, constructive QA feedback.
Tools & Systems:
- MS Office Suite (Word, PowerPoint, Excel)
- Reference management tools (EndNote, Mendeley, etc.)
- Content management / workflow tools (Veeva Vault, Aprimo, etc. – preferred)
Preferred Qualifications:
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, or related field.
- Prior experience in pharmaceutical, CRO, or medical communications environment.
- Exposure to audit processes, regulatory submissions, or inspection readiness.
Key Success Metrics:
- Defect leakage rate / first-time-right quality
- Compliance adherence (MLR readiness)
- Turnaround time (TAT) adherence
- Stakeholder satisfaction
コグニザントについて
コグニザント（NASDAQ: CTSH）は、AI Builderおよびテクノロジーサービスプロバイダーとして、お客様にフルスタックのAIソリューションを構築することで、AI投資と企業価値を結ぶ架け橋となっています。業界、ビジネスプロセス、エンジニアリングに関する当社の深い専門知識を活かし、組織固有のビジネス環境をテクノロジー・システムに組み込みます。これにより、人間の可能性を最大限に引き出し、確かな成果を実現するとともに、急速に変化する世界においてグローバル企業が常に一歩先を行くための支援を行っています。 詳細については、cognizant.ai をご覧ください。
雇用に関する追加情報
本募集に記載されている報酬情報は、掲載日時点で正確なものです。Cognizantは、適用される法令に従い、いつでも本情報を変更する権利を留保します。
応募者は、対面またはビデオ会議による面接への参加を求められる場合があります。また、各面接の際に、現在有効な州政府または政府発行の身分証明書の提示を求められる場合があります。
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