HomeProductionProduction Specialist - Officer | Sanofi Healthcare | Toopran Mandal, Telangana

Production Specialist – Officer | Sanofi Healthcare | Toopran Mandal, Telangana


Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain, and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

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With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

“Sanofi, Empowering Life”

Position: Production Specialist – Officer

Location: Toopran Mandal, Telangana

Job Description:

Duties & Responsibilities

  • Responsible for executing Insulin compounding activities.
  • Operate the equipment pertaining to compounding activities.
  • To support or suggestions for continuous improvements pertaining to processes.
  • Responsible for project support and validation support such as effective installation, commissioning, qualification/ validation of equipment in the compounding area.
  • Responsible for executing various operations of the compounding area for the Insulin Project.
  • Support in preparation of Compounding related SOPs, PPTs, training matrix, and consumables list.
  • Ensuring timely cleanliness of the area and equipment of the Compounding area.
  • In-line with the APU concept, follow the instructions from superiors and facilitate in meeting
  • business requirements.
  • Do critical troubleshooting in consultation with the head of the production, i.e. when sterility assurance
  • could be compromised due to breakdown or severe malfunctions.


  • Acquire relevant equipment and process training with respect to the Compounding of Insulin and relevant operations.
  • Responsible to support various regulatory inspections/audits and adhere to GMP compliance.
  • Acquire knowledge and training on internal and external audits.


  • Responsible for coordinating with QA, QC, Validations, Engineering, HSE, and Projects to support in respective relevant activities.
  • Support activities conducted by cross-functional departments such as HSE, Lean management and facilitate the exchange of information.


  • To identify, correct, and promptly report unsafe conditions, behavior’s, or potentially hazardous situations.

Knowledge, Skills & Competencies / Language

  • Act for change: Adapt to changing circumstances in a positive and enthusiastic manner.
  • Cooperate Transversally: Develop and maintain effective cross-functional working relationships and partnerships.
  • Good communication skills.
  • Adaptability to new technologies and techniques.
  • Good levels of confidence and problem-solving capabilities.
  • Knowledge of GMP/ GXP and technicalities involved in manufacturing relevant activities.
  • Language requirements: Fluency in English (reading, writing, and listening).
  • Working in Shifts

Qualification: B.Sc/B.Pharma, MS/M.Sc/M.Pharma

Experience: 2-3 Years of Relevant Pharma Experience

Salary: Negotiable

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At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients, and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences, and provide equal opportunity for all.

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