Corona Remedies Limited- Walk-Ins for Production / Packing on 23rd December 2023

Corona Remedies Limited- Walk-Ins for Production / Packing on 23rd December 2023

CORONA Remedies Private Limited-Walk-In-Interview
Production/Packing (OSD Facility)
Designation: Officer/Sr. Officer
Qualification: B. Pharm
Experience: 02 to 04 Years
Job Description:• Execution of batch process as per batch processing record in Granulation, Compression, Coating and Inspection area.
Execution of equipment operation & cleaning activities as per SOP. • Documentation of batch processing record & other related record as per SOP.
⚫ Line clearance activities & compliance status. 
• Monitoring of production yield as per standard.
Production/Packing (OSD Facility)
Designation: Operator

Qualification: ITI
Experience: 02 to 06 Years
Job Description:
• Operate and monitor OSD manufacturing equipment of
Granulation, Compression, Coating and Packing. (Elmach)
• Perform in-process checks and inspections.
• Maintain accurate and up-to-date records of production activities.
• Contribute ideas for process improvement and operational efficiency

Date of Interview: – 23rd December, 2023 (Saturday) Time: 10:00 AM to 02:30 PM
Interview Venue
Plot No.: 503, Village – Bhayla, Near Super Gas,
Bavla Bagodara Highway, Taluka – Bavla, District – Ahmedabad-382220. Interested candidates who are unable to attend walk in may share CV on sagart@coronaremedies.com/sonalv@coronaremedies.com

SMS Pharmaceuticals Ltd- Interview on 22nd Dec 2023

Job Category: pharma
Job Type: Full Time
Job Location: Ahmedabad

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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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