SMS Lifesciences – Walk-Ins for Freshers & Experienced in Production / Regulatory Affairs / Process Development Lab on 4th & 5th Aug’ 2023

SMS Lifesciences – Walk-Ins for Freshers & Experienced in Production / Regulatory Affairs / Process Development Lab on 4th & 5th Aug’ 2023

SMS Lifesciences India Limited is presently engaged in the business of manufacturing, buying, selling, offering consultancy, importing and exporting, acting as commission agents and generally dealing with of all types of Organic & Inorganic Chemicals, Pharmaceuticals, Active Pharmaceutical Ingredients (API) and Intermediates. It has a strong research and manufacturing team supported by state of the art facilities.

  • Department: Production / Regulatory Affairs / Process Development Lab
  • Qualification: B.Sc, M.Sc, Intermediate
  • Experience: 2-5 yrs / Freshers
  • Designation: Tr. Chemist / Chemist / Sr. Chemist / Officer / Sr. Officer / Fitter
  • Location: Unit-I, Kazipally, Hyderabad
  • Interview Date: 4th to 5th Aug’ 2023
  • Timing: 09:00 am to 1:00 pm
  • VenueSMS Lifesciences India Limited, Unit-I, Kazipally, Hyderabad
  • Candidates those who are unable to attend walk-in interview can share their resumes to careers@smslife.in

Note:

  1. Candidates must carry their updated resume, highest qualification certificates, latest increment letter & pay slip of the last 3 months
  2. As part of Covid-19 safety measures, candidates are requested to sanitize their hands at the entrance, Maintain social distance and ware face mask before entering the venue.
Job Category: pharma
Job Type: Full Time
Job Location: Kazipally Unit-I

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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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