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Work as QC Officer @ Johnson & Johnson

Janssen, the pharmaceutical division of Johnson & Johnson, is dedicated to addressing and solving some of the most important unmet medical needs of our time in India, in oncology, immunology, neurosciences & analgesia, dermatology, infectious diseases and metabolic diseases in India. Driven by a strong commitment to the health and well-being of patients, Janssen India brings innovative products, services and solutions to people throughout the world. Janssen recognizes the impact of serious conditions on people’s lives, and aims to empower people through disease awareness, education and access to quality care in six therapeutic areas.

Job Title – Officer (QC)

Requisition ID – 1600122471W

Location – Mumbai

Position Summary

Janssen Supply Chain (JSC) is a global organization responsible for supplying medicines to markets around the world. With Quality as their primary focus, this group strives to provide access to and affordability of medicines through innovation and strong collaboration with their R&D and commercial partners to deliver life changing solutions for patients in need. Stability Operations is a department within the JSC, responsible for the management of stability testing of pharmaceutical products and active pharmaceutical ingredients manufactured in the different manufacturing sites.

Job Responsibilities:

  • Perform and document stability analyses and investigations on drug substance  and drug product for various techniques (HPLC, Dissolution, Titiration, CE, etc)  according to protocol, specifications, analytical methods and procedures
  • Ensure proper planning for execution of analysis within window so as to ensure first pass analysis avoiding human errors.
  • Adequate knowledge on regulatory requirements for stability testing
  • To ensure immediate escalation of issues not in conformity with applicable procedures /policies etc.
  • Results reporting into the LIMS or any other applicable system
  • Maintenance and qualification/calibration of lab equipment
  • Technical/scientific support to other  labs within the premises
  • Participate in project teams as analytical technical team member
  • Comply with the analyst responsibilities according to various procedures
  • Training of colleagues
  • Initiate, document and coordinate deviations and events in applicable Event Tracking System
  • Implement CAPAs
  • Compilation of work instructions and standard operating procedures
  • Initiate applicable change requests according to the procedures
  • Execute the tasks according to the cGMP guidelines.
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Skills, Knowledge and Attributes:

  • Experience with sample analysis (Formulations and bulk drugs)
  • Expertise with a variety of analytical techniques e.g. HPLC, GC, UPLC, dissolution, KF, DSC, etc.
  • Exposure to empower software for HPLC data processing preferred
  • Experience of working in a regulated

Qualifications:

Education & Certifications: Bachelors / Masters in Science (Analytical chemistry or equivalent).

 Approximate Years of Industry experience: At least 4 years of experience in a Pharmaceutical Industry (Quality Control).

Apply Online 

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