Caring for the world, one person at a time, inspires and unites the people of Johnson & Johnson. We embrace innovation—bringing ideas, products and services to life to advance the health and well-being of people around the world. We believe in collaboration, and that has led to breakthrough after breakthrough, from medical miracles that have changed lives, to the simple consumer products that make every day a little better.
Post : Scientist
The objective of this position is to execute and coordinate analytical testing for raw material qualification for different projects received from global R&D consumer sites as per established requirements and quality standards. In addition, the responsibility also includes related documentation, laboratory activities, extended analytical support for site queries, collaboration with internal teams and participation in training programs.
Job Description
1. Analysis of assigned samples
2. GMP, EHS and procedural compliance
3. Analytical data review
a. Planning and coordinating assigned analysis for raw material qualifications
b. To coordinate for timely analysis of raw material, release and stability samples as per correct specification and accuracy of data
c. To coordinate with external lab for characterization study and Elemental impurities.
d. To use and maintain the equipment as per requirements for physical testing of stability samples.
e. Address plant queries in time of crisis
f. Provide extended Analytical support to global regions.
g. Maintaining laboratory notebooks as designated by supervisor
h. Preparation of technical documents such as analytical reports, protocols, Technical justifications etc.
i. Participate in handling and resolution of laboratory non-conformances with related documentation
j. Implement corrective actions as required.
a. Ensure compliance to lab discipline and regulations
b. Review of calibration records as required.
c. Participate in internal and external audits as required
d. Preparation of SOPs, test methods, etc.
e. Coordinate for instrument calibration as required
f. Participate in training sessions and inform supervisor of training requirements
k. Review of recommendation, technical feedback etc.
l. Preparation of technical documents such as analytical reports, test methods, etc.
Candidate Profile
Minimum Masters in Chemistry/Pharmaceutical sciences or similar technical discipline
Additional Information
Qualification : M.Sc, M.Pharm
Location : Maharashtra-Greater Mumbai
Industry Type : Pharma
Functional Area : R&D
End Date : 25th December, 2018
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