Job for M.Pharm, B.Pharm, M.Sc in Quality Control at Johnson & Johnson

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. Our over 125,000 employees in 60 countries are united in a common mission: To help people everywhere live longer, healthier, happier lives.

Post : Executive - Quality Control

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Job Description
Finished Goods:
• To review and approve finish goods reports & certificate of analysis.
• To review dosimeter certificate of external vendor.
• Ensure online testing entry in test data sheet & logbook during testing & Engaged team in laboratory activity and ensure data integrity and compliance.
• Sample management Send the sample to outside lab for testing and review outside testing certificate.
• Plan the stability testing in coordination with stability coordinator and provide the report to stability section.
• To ensure the proper functioning of the equipment’s and machinery used for the testing purposes in the Quality Control Department.
• To ensure that the right type of samples, from the right Batch and ensure the follow right sampling procedure of the production process reach for testing so that the quality tests give reliable results and thus the specified quality is achieved for the finished goods, Raw material and Packaging material thus produced for further process.
• To act a Record Coordinator for Finished goods testing record.
Microbiology
• To perform and review routine microbiological analysis i.e. Water testing, Bioburden, sterility, & environment monitoring.
• To check all the routine activity related to microbiology is planned as per their scheduled plan.
• To perform & review trend data analysis for water analysis, environments monitoring & Bioburden test.
• To perform and review of microbiological validation activity related to i.e. Sub dose study, cleaning validation, water validation & CME area  validation.
• Review test report and certificate of external vendor i.e. sterility, EO residual test & Water test.
• Review and approved include - Sterility Test, Sub dose study, Environments Monitoring, Microbial Limits Test, Raw Material, Packaging Material, stability test and finish good.

Candidate Profile
• Education: Graduate/Post graduate in Chemistry/Microbiology/Pharmacy.
• Experience: 8 to 10 years of experience in microbiology section from a pharmaceutical /Medical device industry.
• Himachal Pradesh FDA approval (preffered)as Approved microbiologist and Chemical.
• Sound Knowledge  and hands on experience of LIMS .(Laboratory information Management system)

Additional Information:
Experience: 8-10 years
Qualification: B.Sc, B. Pharm, M.Pharm, M.Sc
Location: Himachal Pradesh
Functional Area: Quality Control
Industry Type: Pharma
End Date: 30th April, 2018

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