Johnson and Johnson Kenvue
Location
Mumbai | India
Job description
Ensure qualification on assigned analytical technologies and instrumentation for testing capabilities.
Execute the assigned stability testing for shelf-life assessment of stability studies.
Responsible for method validation activities including technical documentation under the guidance of the team leader.
Participate in method transfer process regarding testing activities under supervision.
SUPPORT TO EQUIPMENT MANAGEMENT PROGRAM:
Responsible for assigned calibration activities for lab instrumentation and technology.
TECHNICAL DOCUMENTATION:
Partner with key responsible for providing data in technical documents e.g. stability reports, method transfer, method validation protocol and reports, etc.
LAB PROCESS/QUALITY SYSTEMS MANAGEMENT:
Diligently follow and execute (as required) assigned responsibilities in compliance with critical laboratory processes and quality systems.
Focus on basic lab processes and requirements during work and escalate wherever required.
ENGAGEMENT ON SITE INITIATIVES:
Participate and collaborate with site cross functional teams for assigned deliverables when nominated on such forums.
Qualifications
What We Are Looking For
Required Qualifications
Basic technical expertise related to chemistry, analytical techniques, stability study assessment.
Diligent execution of analytical projects with the right first-time approach.
Basic knowledge of current GMP, quality systems, site specific SOPs, regional/Global technical requirements
Overall awareness related to instrumentation principles and working, good documentation practices, data integrity aspects, etc.
Ability to work with digital tools and software applications.
Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators.
Good oral and written communication skills
Challenges the status quo and brings innovative ideas and suggestions.
Displays technical curiosity and self-initiative to deliver beyond usual activities.
Good interpersonal skills to partner within team
Education: Minimum MSc, B Pharm, M. Pharm, Ph.D. or equivalent science stream
Other Skills: MS office advanced
Work experience: Minimum 1 to 3 years in Analytical development, Quality Control or related functions in healthcare/pharma/FMCG sector with exposure to GMP and Quality environment preferred.
Job tags
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