Jobs Companies Excelya Quality Control Specialist (Medical Writing)

À propos de ce poste Quality Control Specialist (Medical Writing) chez Excelya

Excelya · Sur site · Bengaluru, Karnataka, India

Redefine Medical. Empower Innovation. Build with Audacity.

Join Excelya as Our Next Medical Star!

At Excelya, we don’t just work—we Excelyate. Across 24 countries, 900+ passionate professionals are shaping the future of healthcare with one bold ambition: to become Europe's leading mid-size CRO, offering the best employee experience.

Now, we’re calling on curious minds and courageous spirits to step into a career-defining role in Medical Affairs. Ready to make an impact that travels the globe? Let’s talk.

 

About the Job

We are seeking a Quality Control Specialist (QCS), for a full-time role, to provide quality control review of medical writing deliverables, ensuring accuracy, consistency, scientific integrity, and compliance with client requirements, internal procedures, and applicable regulatory guidelines.

 

Your Mission:

  • To perform quality control activities, ensuring the accuracy of all information, data, and references for the documents/tables/figures/listings produced, also reviewing spelling, grammar, appropriateness of language, correct mention of links to other parts of the document or other documents, and compliance with industry guidelines.
  • To check information in the document against the data source (internal consistency within a document and across documents).
  • To deliver documented quality review comments or checklists to the document’s author through resolution, while interacting with the Medical Writers and other team members to resolve QC findings.
  • To liaise with internal groups such as Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical, and Quality Assurance to gather necessary information.
  • To ensure timely completion of quality control activities and keep the Medical Writer (MW) informed of document status in relation to quality and timelines.
  • To maintain familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing and quality control.

Requirements

What You Bring to the Table:

We are looking for candidates who embody our values of Audacity, Care, and Energy and also:

  • Degree in Life Sciences.
  • At least 2-4 years of experience in medical writing or content QC.
  • Experience in reviewing protocols, CSRs, CTDs, ICFs and IBs.
  • Fluent in English.

Benefits

Why Choose Excelya?

At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger.

So, if you're ready to excel with purpose, let’s write the next chapter together.

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À propos de Excelya

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.

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