Level

Sanofi

Qualification & Validation expert, Report Issuance

Sanofi is hiring a Qualification & Validation expert, Report Issuance in Hyderabad, India. Level rates it ; you can apply on Level.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • The posting mentions Veeva Cms, Kneat and technical writing among its tools and skills.
  • Level classes it as a mid-level role.
  • Sanofi has 995 other open roles on Level.
  • This posting went up within the past week.

AI in this role

Author and review pharmaceutical facilities, utilities, and equipment qualification documents and reports.

veeva-cmskneat
technical-writingdocumentationcompliancequality-assurance

Job title: Qualification & Validation Expert, Report Issuance

 

  • Location: Hyderabad

 

About the job

 

Global Manufacturing & Supply (M&S) Services is responsible for delivering and supporting Global M&S teams in partnership with Business and Digital, and drive priority and transformative initiatives across M&S services. The team members of Global M&S Services (Report Issuance) will act as partners in carrying out tasks and fulfilling responsibilities to support identified and established Global Quality processes from the hubs. The Qualification & Validation Report Issuance team is responsible for authoring facilities, utilities, and equipment (FUE) qualification documents, including initial qualification protocols, reports, and requalification reports, quality review reports. This includes comprehensive activities such as data collection, analysis, drafting, document control, review, approval, sign-off, and preparation for inspections and audits.


Main responsibilities:


  • Perform comprehensive content and technical writing and reviews to ensure accuracy, completeness, and compliance against approved Templates, protocols and guidelines for facilities, utilities, and equipment (FUE) qualification documents, including initial qualification protocols, reports, and requalification reports, quality review reports.
  • Review for accuracy and completeness of all data in protocols & reports. Align documentation standards with global Quality requirements and maintain consistency across all qualification and validation team deliverables. Verify accuracy of all data, references, and citations included in protocols, reports to ensure regulatory compliance.
  • Ensure equipment qualification activities comply with Quality regulations and pharmaceutical practices. Summarize key findings and provide clear, protocol-aligned interpretation of results. Perform report signing in Veeva CMS or Kneat.
  • Perform comprehensive content and technical writing and reviews to ensure accuracy, completeness, and compliance against approved Templates, protocols and guidelines for facilities, utilities, and equipment (FUE) qualification documents, including initial qualification protocols, reports, and requalification reports, quality review reports.
  • Review for accuracy and completeness of all data in protocols & reports. Align documentation standards with global Quality requirements and maintain consistency across all qualification and validation team deliverables. Verify accuracy of all data, references, and citations included in protocols, reports to ensure regulatory compliance. Ensure equipment qualification activities comply with Quality regulations and pharmaceutical practices. Summarize key findings and provide clear, protocol-aligned interpretation of results.
  • Translate and adapt protocol, report communications for sites, hubs ensuring clarity and alignment using appropriate Tools. Monitor and track execution of activities against defined timelines to achieve established KPI targets, escalating delays as necessary. Ensure to complete all training in a timely manner. Provide training and guidance to team members on compliance topics and best practices.
  • Ensures full compliance with GxP principles, regulatory requirements, and Sanofi Quality standards throughout equipment qualification and validation processes. Manage Quality Management System (QMS) records, address discrepancies, and ensure timely closure of all related documentation. Support internal audits and inspections if any by providing required equipment Qualification and validation documentation.
  • Drive continuous improvement initiatives through standardization, simplification, and digitalization of equipment qualification processes. Perform all tasks in compliance with Good Manufacturing Practice (GMP) and Health, Safety, and Environment (HSE) requirements, following established instructions, procedures, and records. Execute additional duties as assigned by the manager or team lead, as needed, beyond the responsibilities outlined above.

About you:

  • Experience: >5 years’ professional experience in qualification
  • Soft skills: Proficient in problem-solving, attention to detail, and good organizational skills. Ability to work collaboratively with cross-functional teams in a flexible and proactive manner. Strong analytical skills. Agile thinker and learner, adaptable to complex & dynamic environments
  • Technical skills: Quality systems (e.g., Veeva, Kneat), Word, Excel, Power Point
  • Education: Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related field. Advanced degrees (e.g., MSc, PhD) preferred
  • Languages: Excellent English communication and writing, French or other Languages in addition preferred

 

Why choose us?

  • Bring the miracles of science to life alongside a supportive, future-focused team.
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave.
  • Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas. 




           

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

How we rate this

Qualification & Validation expert, Report Issuance at Sanofi rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Technical WritingDocumentationComplianceQuality AssuranceVeeva CmsKneat

Questions you could be asked

  1. Tell me about a project where technical writing was part of your work. What did you do?
  2. Tell me about a project where documentation was part of your work. What did you do?
  3. Tell me about a project where compliance was part of your work. What did you do?
  4. Tell me about a project where quality assurance was part of your work. What did you do?
  5. Walk me through how you've used Veeva Cms in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Technical Writing, Documentation, Compliance, Quality Assurance, and Veeva Cms. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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