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Serum Biotec Limited – Walk-Ins for QC / Production / Accounts & Administration on 18th – 20th June’ 2020

Serum Biotec Limited – Walk-Ins for QC / Production / Accounts & Administration on 18th – 20th June’ 2020

Walk-In Interviews @ SERUM BIOTEC LIMITED

Approved QC Chemist Executive – OSD, Injection

Experience: 2-7 yrs

Qualification: B.Sc / B.Pharm

Job description:

To perform all the In process, Drug substance, Drug product (Release & stability) related sample analysis, Sound knowledge in Quality management systems (Handling of Change control, Deviations, CAPA & Risk assessments),
Knowledge in LIMS preferable

Required Candidate profile

Approval is mandatory.
Candidate willing to relocate to Baddi

Production Executive- Cephalosporin

Experience: 1-5 yrs

Qualification: B.Sc / B.Pharm

Job description:

Issue of BMR, BPR , Manufacturing of products, Proper staging and segregation of issued materials, Co-coordinating with QA, QC, Stores, PPC, PDL, Maintenance and upkeep of core process and secondary areas, Review of equipment and accessories cleaning

Required Candidate profile

Approval is mandatory.
Work experience with Cephalosporin range mandatory

Accountant & Administration

Experience: 1-5 yrs

Qualification: Any Graduate

Job description

Daily accounting, working knowledge of TDS, GST, etc along with administrative work for a pharmaceutical company

Date & Time: 18th June – 20th June, 2020 10 AM onwards

Venue:

Nootan Pharmaceuticals,

Village Tipra, Barotiwala – Kalka Road,

Barotiwala, tehsil Baddi, District Solan,

Himachal pradesh – 174103

Apply for this position

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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

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