R&D Job Opening for Chemistry & Pharma Candidates @ Johnson & Johnson | Apply Online

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stify">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.

  • Requisition ID – 1700159694W
  • Job Title (India Specific): Executive
  • Department: R&D
  • Job Location: Greater Mumbai, India 
Overview:

The Pharmaceutical Development & Manufacturing Sciences Organization (PDMS) of Janssen R&D, constituting of around 1200 people across the globe, aims to develop and bring products to the patients in a timely manner without delays. With a vision of ‘One passionate team transforming molecules to medicines for patients worldwide’ the PDMS Organization covers Active Pharmaceutical Ingredient (API) – Small Molecules, API – Large Molecules, Drug Product Development, Analytical Development, Portfolio Management, Clinical Supply Chain and Strategic Operations.

Small Molecule Method Development (SMMD) is a department of PDMS within the Janssen R&D organization. The department is responsible for the Analytical Method Development/ Validation of assay and related compounds evaluation/ characterization test methods of small molecule drug substance, drug product, intermediates from early development through the lifecycle for commercial products; analytical transfer of these methods to internal and/ or external clinical and commercial testing sites; supporting all regulatory filings (CTA/IND, NDA/MAA, post approval submissions), inspections and investigations. It is also responsible for In-vitro Dissolution Method Development/ Validation and Method Transfer across sites for new as well as marketed products

Job Description:

Responsibility

  • Analytical Method Development and Validation mainly Assay, RS, CU, water content by Karl Fisher, Assay by Titration, LC-MS analysis etc..
  • Instrument calibration / qualification activities.
  • Performs activities following the GMP/ safety requirements.
  • GMP data review, protocol and report preparation for various analytical activities
Qualifications:
  • Masters in Science or Pharmaceuticals (in Analytical Chemistry or equivalent from reputed University
  • At least 8 years of industrial experience in  reputed pharmaceutical company

Functional competencies (Skills, Knowledge and Attributes):

  • Experience with different types of formulations and API analysis with prior experience in Method Development, Validation and Transfers as per regulatory guidelines.
  • Hands on experience in variety of Analytical techniques e.g. HPLC, GC, and UPLC, KFT, and their troubleshooting.
  • Exposure to empower software for HPLC/UPLC data processing preferred.
  • Good analytical data interpretation skills.
  • Hands on computer system validation (CSV) system
  • Experience of working in a regulated environment is a must.

Behavioral Competencies (/Leadership Imperatives): 

  • Analytical thinking
  • Good team player
  • Result Orientation
  • Ethics and values
  • Communication skills (able to write and speak English fluently)

Primary Location
India-Maharashtra-Greater Mumbai
Organization
Johnson & Johnson Private Limited (8080)
Job Function
R&D

Click here to Apply Online

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