Neuland Laboratories Ltd – Walk-In Interviews for Multiple Positions (30 Openings) on 28th Nov’
API – Production Chemist (Only Male Candidates Preferred)
Date: 28 November , 10.00 AM – 4.00 PM
Venue: Hotel Grand Orchid, Near Miyapur Allwyn “X” Roads, Hyderabad
Contact – Sushma Nadimpalli ( 9550258000 )
Education : B.Sc (Chemistry) / Dip.Chem Engg
Experience : 1- 3 Years in API Production
Documents : Latest CV & Last 2 pay slips
Reports to Shift Production Officer / Executive.
Responsible for carrying out all the production activities pertaining to his section in the shift following the standard operating procedures and safety norms.
Receiving batch manufacturing sheets / formats / records from QA department.
Conducting the process operations and recording the process parameters progressively in BMS.
Maintaining that the process equipment and surrounding areas are always clean and hygienic.
Observing and reporting the need for calibrations.
Records the data in the batch manufacturing sheets, formats and other related records properly.
Handed over the production documents and records to the quality assurance department
Responsible for maintaining discipline in the shift and also for keeping the production area in an orderly manner.
Reporting any deviations / abnormalities in time to the shift production officers or executive.
Co-ordinates with maintenance people in the shift for the smooth completion of routine and preventive maintenance jobs.
Attending the training programs periodically to improve knowledge and working skills to the desired levels.
To maintain discipline and follow the company rules and regulations
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