1 - 10 of 43 Bmr Jobs

Opening in Production department for an API Manufacturing unit of Cadila Healthcare Limited based at Ahmedabad location. Designation: Executive / Senior Executive Department: Production ... view more

Job Description: Leading and Management of IPQA team. Performing IPQA activity (Line clearance, in-process checks, sampling, etc.) at shop floor for Dispensing, Manufacturing, and Packing area. Revi ... view more

We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable unit for our SEZ Matoda Plant. INJECTABLE REQUIREMENT 1. Sterile Manufacturing (Injectable/Paren ... view more

1. To do planning for ELISA and Rapid IVD product manufacturing. 2. to Handling and monitoring of manufacturing ELISA and IVD product as manufacturing process flow and maintain the all manufacturing ... view more

  Master & Issuance of SOPs, Formats, Logbooks, GTP, STP, Specification & other documents Preparation & Revision of SOP Handling of Deviation, Incidence, OOS, and Investigation ... view more

Roles and Responsibilities Execution of activities as per scheduled plan, coordination with warehouse, QC and QA for day to day execution of activities, handling of dispensing , manufacturing of sca ... view more

Roles and Responsibilities - To be responsible for batch start up activity, monitoring, yield monitoring and overall coordinating the daily operations for manufacturing & packing operations of T ... view more

Roles and Responsibilities 1. Responsible for all sections of production area and plan and execute production to meet business requirements within timelines. 2. Ensure data integrity and compliance ... view more

Job Location: Baroda, Gujarat Profile: Production Officer/Manager Job details- To monitor the daily activities in the Production area as per the GMP guidelines. (Washing area, Manufacturing area ... view more

Designation : Quality Assurance / QA Manager Description : The candidate should be responsible for product release activities, BMR, BPR SMF, QMS, OOS, OOT, QAMS activities, Review dossier filings, sp ... view more

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