Experience- Tablet, Capsule, Ointment, Beta LactamSection.
Should have worked at WHO GMP approved plant and have exposure to EU GMP audit also.
Executes the shift production schedule for deputed area and ensures strict compliance to the Standard Operating Procedures, cGMP norms and productivity standards to produce quality product as per plan.
Managing production activities in cost effective manner and Budget adherence
Lead the team in achieving production target related to Quality, compliance, production and cost targets.
Co-ordination with planning and purchase department for availability of material as per planning.
Ensures reduction in wastages and maximises efficiencies (Avoiding reprocess of any batch).
Planning and its execution, Coordination with cross functional teams and utilisation of available resources
Effective implementation of production planning with CGMP norms.
Ensure online documentation on shop floor.
Co-ordinates with Engineering to promptly attend to breakdown / preventive maintenance during the shift.
Supervises the production/ packaging activity to ensure maximum productivity.
Prepares online documentation and generates shift reports; Prepares updated MIS reports and makes available to management as and when required.
Ensures completion of process and equipment validation on a periodic basis.
Ensures safety, statutory and housekeeping standards are adhered to during each shift.
Ensures compliance to Company policies and values.
New ideas for optimising efficiency & flow.
Desired Candidate Profile:
I will be excited to receive your call at 9392631*** or share your CV je**********[email protected]*********r.in
Company ProfileIntegra Software Services Pvt. Ltd.Founded in 1994, Integra Software Services Private Limited is among the largest e-publishing houses across the globe servicing prestigious customers who are among the biggest names in the publishing arena in US & Europe. With team strength of 600 pro...