Sr Production Manager/Chemist in BENNET PHARMACEUTICALS LIMITED

Job Posted on Jul 4, 2021

Recruiter Type:	Company
Company Name:	BENNET PHARMACEUTICALS LIMITED
Address:	204 B Vardhman COMPLEX, SUBHANPURA MAIN ROAD Vadodara, Gujarat 390023 India
Contact Person:	SIDDHARTH JAIN
Phone:	09825110437
Email Address:	bennetjain@gmail.com
Required in:	Formulation Unit
Job Department(s):	Production
Job Title:	Sr Production Manager/Chemist
Qualification:	B.PHARM, M.Pharm
Job Details:	The Role of the Sr. Production Chemist will be hard core equivalent to Technical Manager-Formulations. He/She will be responsible for Day to day production of all OSD's (Tablet/Capsules/Oral Liquid/Oral Powders and Softgel Capsules). The basic understanding of the soul of any Formulation is a core requirement. Production Manager is responsible for the selection of most optimum cost effective process with highest quality is desirable, considering Pharmacopoeial requirements. New Product Development shall not be a challenge, and should be able to read- and understand the Research Literatures for practical applicability. Should be through with logical reasoning and practicality and Most Important is Progressive Positive approach. He should be able to manage complete Plant activities Like QA/QC/Engineering and all supporting departments. The knowledge of floor is must, and should be able to go on the floor for every desirable issue. Team Builder and Team Building activities. Should be able to solve the problem not create the problem. For him the quality of the product should be top most, and efficient production should be top most priority, by safeguarding the quality of the products by leading the development and coordinating the production activities. Directly reporting to the CEO, this position presents the right individual the opportunity to grow to director level. Your responsibilities: Manages day-to-day operations of multidisciplinary deptt to ensure performance within stipulated timelines. Supervises and Monitors performance of Plant, his team members and lead the projects. Coordinates the activities within the Manufacturing and Quality Department to manage production schedules ensuring the highest quality standards, and safety issues Communicate with all relevant inter-company contacts: provide adequate information, consult the appropriate persons in case of problems and contribute to the decision making process supervise together with the Quality department / QA Deptt in controlling and production activities to ensure GMP compliance and other regulatory compliances. Should be able to handle audits of any regulatory level, with greatest interpersonal and speaking ability.
Regulatory Exposure*:	Required
Audit Experience:	WHO
Experience*:	5 years minimum
Vacancies:	2
Last Date*:	15/07/2021

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