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Head - Production - Manufacturing Plant

15.00 to 18.00 Years   Indore   19 Jan, 2023
Job LocationIndore
EducationNot Mentioned
SalaryNot Disclosed
IndustryRecruitment Services
Functional AreaProduction
EmploymentTypeFull-time

Job Description

    We are looking for Production head for Pharma and healthcare industy which has plant in Indore, MP. This position is based our IndoreStrategic management, production operation, audits and quality management, subordinate development, process enhancement, team development, technical support, analytical approach, productivity improvement, projects/new initiatives, cost reduction initiative, safety health and environment, product costingRole & Responsibilities :- Thorough knowledge of National and Global Regulatory GMP requirements and full-fledged exposure of OSD (Tablets, Capsules) and Ointment products mfg. unit; - Strong knowledge and experience with interpersonal skills required to set-up and maintain new OSD and Ointment products mfg. unit using optimum resources;- Responsible and accountable for strict adherence to GMP implementation at mfg. unit and maintaining consistent quality outputs;- Responsible and accountable for maintaining overall expenses within permitted budget and implementation of cost-effective and quality conscious deliverables; - Strong interpersonal abilities to build, manage and retain team of expert, well trained technical and non-technical staff;- Thorough knowledge and experience of preparation, review and implementation of qualifications of mfg. equipments; - Responsible and accountable for preparing and maintaining harmonized documentation for OSD and Ointment products mfg. unit as per GxP requirements; - Responsible and accountable for planning, organization, co-ordination, prioritization, and execution of mfg. schedules within minimal time-frame to achieve optimized utilization of available resources and to increase consistent quality deliverables, for development, scale-up, exhibit, Commercial scale batches; - Responsible for maintaining ongoing activities as per cGMP and EHS standards and to impart training and continuous evaluation and upgradation wherever required;- Responsible and accountable for production planning and timely execution as per marketing requirements; - Responsible and accountable for effective utilization of available resources (men, material, machine) to meet quality driven production outputs;- Responsible and accountable for co-coordinating with other departments / vendors / service providers for ensuring timely fulfillment of calibrations/qualification/preventive maintenance etc. of process equipment/instruments;- Responsible and accountable for ensuring compliance to audits (internal and external/Vendors/Regulatory), staff development, investigations (including Market complaints), change control and CAPA implementation through QMS in production department; - Should have strong vision for quality in all aspects and should be responsible to execute technology transfer, process optimization, validations alongwith regular commercial scale production activities; - Thorough knowledge, experience and interpersonal skills for troubleshooting and new developments;- Responsible to prepare, review and approve documents (SOP/MFR/MPR/BMR/BPR/PDR/ Qualifications/Validations/QRM/Trainings/QMS etc.) with strict adherence to compliance of 21 CFR part 11 requirements or other strict measures to maintain data integrity requirements;- Responsible for timely reporting through available MIS at plant (Department reports, Plant performance, Capacity utilization, Periodic production reports etc.)- Any other responsibilities allotted by plant head and company management for ensuring total GMP compliance- Coordination with General / Private external agenciesSkills and requirements :- Any relevant master degree- 15+ years of relevant experience from Pharma and Healthcare manufacturing industry- Good experience in plant headInterested candidate may call directly on +91 99hidden_mobile5 for quick call,

Keyskills :
technical supportchange controlstaff developmentcontinuous improvement facilitationteam developmentcost reduction21 cfrdata integrity

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