Home / Job / Saurav Chemicals Limited – Walk-In Interviews for Production on 23rd June’ 2021

Saurav Chemicals Limited – Walk-In Interviews for Production on 23rd June’ 2021

Saurav Chemicals Limited – Walk-In Interviews for Production on 23rd June’ 2021

Saurav Chemicals Limited | LinkedIn

Saurav Chemicals Limited is established in the early 90’s SCL offers a wide range of Active Pharmaceutical Ingredients and Intermediates to its customers worldwide. Saurav Chemicals Limited (a USFDA Approved API manufacturing Pharmaceutical company is conducting interviews in Production. 

Walk-In for Production Executive @ Saurav Chemicals Limited

Job description:

PRODUCTION SHIFT INCHARGE (PHARMA API ONLY)

Saurav Chemicals Limited (a USFDA Approved API manufacturing Pharmaceutical company is conducting interviews in PRODUCTION EXECUTIVE experience in Pharma API Required.

For Production Executive/Shift Incharge

  • Vacant Positions- 5

  • Salary: INR 450000- ,650,000 P.A.

  • Industry: Pharma / Biotech / Clinical Research

  • Qualification: M.Sc / B.Sc / Dip. Chemical / BE Chemical

  • Experience in Pharma API required

  • Age limit – 26Y to 42Y

  • B.Tech Min 4 yrs Experience is required

    M.Sc Min 7 yrs Experience is required.

Walk-In Date: 23 June, 2021

Time: 11 AM onwards

Venue:

Saurav Chemicals Limited

Bhagwanpura Unit-3,Barwala Road Derabassi,

Chandigarh ambala Highway

Contact: HR Department:-

Contact – Naveen Saini ( 7988038678 )

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

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

Check Also

SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS) Building And Equipment …