Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Statistician

Sanofi
Sanofi
2-5 years
upto 5 LPA
Hyderabad
3 April 23, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Statistician

Location: Hyderabad, India
Company: Sanofi
Job Type: Full-Time | Regular
Application Deadline: 15 May 2026
Experience Required: 2–5 Years (Not suitable for freshers)


About the Company

Sanofi is a leading global healthcare organization dedicated to transforming scientific innovation into life-changing therapies. With a strong presence across vaccines, oncology, rare diseases, immunology, and cardiovascular care, Sanofi is at the forefront of advancing data-driven pharmaceutical manufacturing and quality excellence worldwide.


Role Overview

The Statistician will be part of the Global MSAT (Manufacturing Science and Technology) Statistical Support team, playing a critical role in enhancing manufacturing efficiency, product quality, and regulatory compliance through advanced statistical methodologies.

This position offers global exposure, working closely with manufacturing sites, quality teams, and process development experts to drive data-driven decision-making across the pharmaceutical value chain.


Key Responsibilities

  • Perform statistical analysis aligned with business and manufacturing needs across global sites

  • Design and implement statistical process control (SPC) charts for monitoring manufacturing and quality control processes

  • Conduct process capability studies to evaluate performance and identify optimization opportunities

  • Lead statistical comparability assessments for technology transfers and supplier evaluations

  • Perform stability analysis using linear and non-linear modeling techniques, including thermokinetic models

  • Support analytical method validation through robust statistical design and interpretation

  • Design and analyze experiments (DOE) to optimize product quality and process parameters

  • Apply advanced statistical techniques including mixed-effects models, multivariate data analysis (MVDA), and equivalence testing

  • Deliver clear, actionable insights from complex datasets to cross-functional stakeholders

  • Ensure compliance with statistical SOPs, regulatory guidelines, and global quality standards

  • Train internal teams on statistical methodologies and best practices


Required Qualifications

Education:

  • Master’s degree in Statistics or Biostatistics

Experience:

  • 2 to 5 years of experience in statistical analysis within pharmaceutical, biotech, or manufacturing environments

Technical Skills:

  • Strong expertise in statistical tools such as SAS, R, Python, JMP, or Dataiku

  • In-depth knowledge of statistical process control, DOE, and multivariate analysis

  • Understanding of pharmaceutical manufacturing processes and regulatory frameworks

Additional Skills (Preferred):

  • Experience with databases such as MS SQL Server, MySQL, or Snowflake

  • Data visualization skills using tools like Power BI or Streamlit

  • Familiarity with Git/GitHub for version control

Soft Skills:

  • Excellent communication skills to explain complex statistical concepts to non-statistical stakeholders

  • Strong analytical thinking with attention to detail and scientific rigor

  • Ability to work in multicultural, cross-functional global teams

  • Proactive mindset with problem-solving capabilities

Languages:

  • Fluency in English (French is an added advantage)


Why Join This Role

  • Work with a globally recognized pharmaceutical leader

  • Contribute to cutting-edge manufacturing and quality innovation

  • Gain international exposure across multiple manufacturing sites

  • Be part of a high-impact, data-driven scientific environment


Important Note for Applicants

This role requires prior hands-on experience in statistical analysis within pharmaceutical or manufacturing domains. Freshers are advised to apply for entry-level roles such as Junior Statistician, Data Analyst, or Biostatistics Trainee positions before targeting mid-level roles like this.


Equal Opportunity Statement

Sanofi is committed to fostering an inclusive and diverse workplace. All qualified applicants will receive equal consideration regardless of background or identity.


How to Apply

Interested candidates can apply through the official careers portal. For more verified pharmaceutical and clinical research job opportunities, visit ThePharmaDaily.com