Home / Job / Enaltec Labs Pvt. Ltd – Walk-In Interviews for Quality Control /Quality Assurance / Production on 20th Dec’ 2020

Enaltec Labs Pvt. Ltd – Walk-In Interviews for Quality Control /Quality Assurance / Production on 20th Dec’ 2020

Enaltec Labs Pvt. Ltd – Walk-In Interviews for Quality Control /Quality Assurance / Production on 20th Dec’ 2020

Walking Interview for Q.C. / Q.A. / Production

Location: Pithampur

Production -Chemist / Officer @ Enaltec labs Private Limited

Experience: 1-3 yrs

Job description

Reporting to Shift-in charge/ Executive & Production officer if available for the status
Execution of production activities as per provided BPCR, ECR, etc. as per instruction
Cleaning of equipment as per respective procedures

Required Candidate profile

Follow good manufacturing practices & documentation practices in production area
Preparation for the next requirement of the ongoing activity
Proper handling of shift status with reliever.

Executive/Officer/Chemist – Q.C. / Q.A.

Experience: 1-5 yrs

Job description:

Candidate should have relevant experience and should be adept with operating principles/techniques of HPLC/GC instrumentation
Review of executed BPCRs and release of batch.
To follow updated guidelines of GMP, IMS systems, & Local FDA regulations.

Required Candidate profile:

He/She should be self-directed and systematic with an ability to perform analysis (i.e. method development & validations) using HPLC/GC instrument.
Handling of Change Control, Deviations and CAPA.

Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm

Date: 20th December , 9.30 AM – 4.30 PM

Venue:

Enaltec Labs Pvt. Ltd.

Plot No. 825 – 827, Sector – 3

Industrial Area, Pithampur,

Dist. – Dhar (M.P.)

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

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