Stelis Biopharma – Urgent Hiring for Quality Control Department

Are you passionate about upholding the highest standards of quality in biopharmaceuticals? Stelis Biopharma is dedicated to delivering life-changing drugs with unwavering quality. We are currently seeking talented individuals to join our Quality Control department in Bengaluru, India.

Details About Stelis Biopharma Limited Hiring

  • Website: https://www.stelis.com/
  • Department: Quality Control
  • Role: Associate/Senior Associate
  • Education: Master’s degree in Biochemistry/Biotechnology/Chemistry
  • Experience: 0 – 4 Years
  • Batch: NA
  • Salary: NA
  • Job Location: Doddaballapura, Bengaluru
  • No Of Vacancies: NA
  • Opening Date: 30th Apr’ – 4th May’ 2024

About Company

Stelis Biopharma Limited (Stelis) is the biopharmaceutical division of Strides Pharma Science Limited (Strides), a global pharmaceutical company headquartered in Bangalore, India. Strides provides affordable high quality generic medicines in over 100 countries supported by its  global manufacturing footprint spanning eight facilities spread across four continents, including multiple sites with Stringent Regulatory Authority approvals such as USFDA, EMA and others. To know more about Strides.

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Job Descriptions

Technical Skills:

  • Proficiency in HPLC and GC method analysis
  • Experience with QC equipment calibration (HPLC, GC), analytical method validation, and method transfer
  • Competence in balance and pH meter calibration and handling
  • Experience in handling raw materials
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Primary Responsibilities:

  • Preparation of quality system-related SOPs, specifications, STPs, GTPs, raw data sheets, and certificates of analysis
  • Preparation/review/execution of method transfer and method validation protocols and reports
  • Initiation and implementation of change controls in routine analysis
  • Handling of deviations and out-of-specification issues and managing corrective and preventive actions (CAPA)
  • Estimation of proteins through UV-Spectrophotometer
  • Analysis of DS (Drug Substance), DP (Drug Product), and stability study samples using HPLC Chromatography
  • Maintaining data integrity and traceability in all activities
  • Instrument/equipment qualification in Quality Control
  • Ensuring activities are performed in compliance with GMP, company SOPs, and health and safety policies
  • Handling and sampling of raw materials
  • Coordinating with regulatory bodies, internal and external customers, vendors, service providers, and conducting internal and external trainings
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Apply Now:

Email your resume to: J.DhanaVignesh@stelis.com | Email subject: Quality Control – Stelis
Or apply here: Stelis Quality Control Job Application

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