Neuland Laboratories – Walk-In-Interview for Production / Quality Control / AQA / Plant Engineering / EHS on 10th Nov 2023

Neuland Laboratories – Walk-In-Interview for Production / Quality Control / AQA / Plant Engineering / EHS on 10th Nov 2023

Neuland Laboratories – Walk-In-Interview

Neuland Laboratories Limited was established in 1984 and today is a publicly listed company headquartered in Hyderabad, India. Neuland is a leading manufacturer of active pharmaceutical ingredients (APIs) and an end-to-end solution provider for the pharmaceutical industrys chemistry needs. We provide solutions across the full range of the pharmaceutical industry’s chemistry requirements, from the synthesis of library compounds to supplying NCEs and advanced intermediates at various stages in the clinical life-cycle, as well as commercial launch. Our strength is our expertise in manufacturing of APIs and advanced intermediates from our US FDA approved facilities. 

  • Department: Production / Quality Control / AQA / Plant Engineering / EHS

  • Role: Chemist / Officer / Executive

  • Qualification: B.Sc / M.Sc / B.Tech / Diploma / Any Degree

  • Experience: 02-08 years

  • Job Location: Hyderabad

    • Date & Time: 10th Nov 2023 Between  9.30AM to 4.00PM

    • Interview Location: Neuland Laboratories Limited, Unit-III Gaddapotharam, Hyderabad, Sanga Reddy District, Telangana

    Work Location:Neuland Laboratories Limited

    Unit-III Gaddapotharam, Hyderabad,

    Sanga Reddy District, Telangana

    Who are unable to attend walk-In can share your CV swetham@neulandlabs.com

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 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

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