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Annora Pharma Walk In 7th May 2022 for Production / Quality Control / Analytical Development

ANNORA Pharma Walk In Interview 2022  M.Sc / M.Pharm / B.Sc / ITI / Diploma   for Production / Quality Control / Analytical Development At Hyderabad. ANNORA Pharma Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.

  • Vacancy details:
  • Post Name: Production / Quality Control / Analytical Development
  • Section: Analytical Method Validation / Microbiology / Granulations / Coating / Compression
  • Qualification: M.Sc / M.Pharm / B.Sc / ITI / Diploma      
  • Experienced:0 to 6 years
  • Openings:NA
  • Salary:NA

Job Description: ANNORA Pharma Hiring For Production / Quality Control / Analytical Development !

  • Important Details :
  • Location: Hyderabad
  • Post of date:05/05/2022
  • Selection Process: The selection will be on the basis of Interview.
  • Walk In Date:7th May 2022
  • Time: 09:00 am to 12:00 pm
  • Venue:Annora Pharma, Sy. no. 261 Plot no. 13 to 14 Annaram Village, Jinnaram Mandal, dist, Hyderabad, Telangana 502313

Job description

Note:

  • Candidates must carry their updated resume, highest qualification certificates, latest increment letter & pay slip of the last 3 months
  • 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.

About Company:

ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements. Spread over in thirty-five acres land, our manufacturing facility close to the city of Hyderabad, India specializes in manufacturing of Tablets, Capsules, Pellets, Liquid Orals, Suppositories and Dry Powder Syrups catering to a diverse therapeutic range. Our state-of-the-art manufacturing facility is designed to meet the standards conforming to Schedule M of Indian Drugs & Cosmetics Act, USFDA and European Regulatory Agency’s Guidelines.

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