Pharmaceutical Guidance Complete Pharma Solution
Gland Pharma Limited – Urgent Requirement for Freshers & Experienced in Microbiology / QA Validations
Urgent requirement for Microbiology
Greetings from GLAND PHARMA!!!!!
We have urgent requirement in Microbiology department, interested candidate can share their profiles to hrd.pmy@glandpharma.com & hanumanthrao.rasike@glandpharma.com.
JOB DESCRIPTION:
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Sterility testing of the finished products, In-process, starting and Packing materials.
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Daily Observation of the Sterility test canisters/ tubes.
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Sterility method validations as per the Pharmacopoeia guidelines.
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Disinfectant Preparation and filtration as per the schedules.
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Environment monitoring in the Sterility testing areas.
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Culture prepartion by using the Bioballs, In house isolates and ready to use cultures.
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Maintaining Good laboratory practices and Good Documentation practices.
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Tasks to be performed as instructed by the HOD/ Department In-charge.
Experience: 0-3 yrs
Qualification: B.Sc / M.Sc- Microbiology
Urgent requirement for – QA Validations
Interested Candidates, please share us your updated profile (with Photo) along with CTC Letter to hrd.pmy@glandpharma.com & hanumanthrao.rasike@glandpharma.com
Description:
1. Performing all calibration and validation activities.
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Involving in HVAC qualifications & airflow study.
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Preparation of qualification protocols and execution of process equipments (Autoclave, Washing machine, Tunnel, Filling machine, sealing machine), HVAC and utilities (waster system, Compressed air, Nitrogen, etc…)
Qualification: B.Pharm / M.Pharm / B.Tech / B.E / M.Tech
Experience: 1 to 3 Years (Injectable Experience)
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube
