5 Glp Practices Jobs

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4.0 - 8.0 years

0 Lacs

medak, telangana

On-site

Job Description : Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter ins...

Posted 3 weeks ago

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10.0 - 12.0 years

0 Lacs

hyderabad, telangana, india

On-site

Company Description Helex is a therapeutics company developing a new class of targeted medicines for genetic kidney diseases using its proprietary LNP drug delivery and AI-based drug design platforms. With a world-class team of scientists and drug developers, Helex operates from ASPIRE BioNEST, Hyderabad, India, and New York, USA, and is supported by Bayer Co.Lab Cambridge. Role Description This is a full-time on-site role located in Hyderabad, India. A Senior Scientist in Gene Editing at Helex will be responsible for leading research and development projects to advance the company's gene-editing technologies for renal applications. The day-to-day tasks will include designing and conducting ...

Posted 1 month ago

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2.0 - 8.0 years

0 Lacs

tirupati, andhra pradesh

On-site

You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of experience. Immediate joiners are preferred for this role. As a part of your role, you will be responsible for conducting HPLC analysis of solid orals/nasal products, handling QC activities related to Raw Materials, Packing, In Process, and Finished Products, and ensuring compliance with GMP/GLP Practices. The ideal candidate should have 2-8 years of experience and should have prior experience working in regulated plants approved by USFDA/MHRA. Working in this position will provide you with the opportunity to work in a fully automated world-class manufacturing facility, handle diverse dosage forms in ...

Posted 4 months ago

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2.0 - 8.0 years

0 Lacs

tirupati, andhra pradesh

On-site

The ideal candidate for this role should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of our team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. In return, you will have the opportunity to work in a fully...

Posted 5 months ago

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0.0 - 1.0 years

2 - 2 Lacs

Ludhiana

Work from Office

Freshers can also welcomed for interview. QC Executive To monitor all process steps (physical, chemical & microbiological testing) and control points as per defined parameters and standards. To monitor effectiveness of overall cleaning and sanitation of the plant including all warehouses. To monitor GLP practices in lab, resources needed as per laboratory requirement. To monitor the product quality through compliance of specification for raw material, packaging material & finished products. To monitor testing plan, calendar & standard for inside & outside testing & to ensure outside testing as per schedule. To check and verify the daily deviation report, taking appropriate actions against th...

Posted 5 months ago

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