Brundavan Laboratories walk-in interviews on 27th – 31st May 2024

Brundavan Laboratories walk-in interviews on 27th – 31st May 2024

Brundavan Laboratories Pvt. Ltd is a reputable manufacturer and exporter of Bulk Drugs & Intermediates, adhering to cGMP standards. Founded in 2005 by seasoned professionals with extensive industrial expertise, the company boasts a highly skilled research and development as well as manufacturing team.

Walk-In Interviews @ Brundavan Laboratories Pvt. Ltd

Job Role: Production Chemist

Qualification Required: B.Sc / B.Com /Inter
Experience Required: 1 to 5 years in API/Bulk drug industry, communication skills must.
Work Location: Survey No.60 to 62, V: Yellagiri, M: Choutuppal, D: Yadadri Bhongiri
No of Positions: 10
Job Description:

Production Manufacturing activity

Responsible for the shift handling

Handling of reactors & Related log books

Keep all documentation such as records and log books updated.

Creating pleasant working conditions by maintaining good housekeeping safety norms and discipline.

Follow GMP & SOP’s in manufacturing areas.

Production Documentation.

Related Jobs  Job opportunity for Research Scientist at Zydus Lifesciences | Apply Now

Walk-In Interview Details: 

Interview Date:   27th May 2024 to 31st May 2024,
Time:  10:00 a.m to 04:00 p.m.
Interview Venue: Survey No.60 to 62, V: Yellagiri, M: Choutuppal, D: Yadadri Bhongiri, Telangana State.
Contact Person: A. Ramesh
Contact Details: Mobile: 8367099933 / 8019191906
Send CV to: hr@brundavanlabs.com

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

Apply for this position

Allowed Type(s): .rtf

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

Check Also

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE PURPOSE: To describe microbiological test controls …