Assistant Manager or IPQA for PHARMACY COMPANY 72 views

Job Profile

-To direct and Control Manufacturing process to meet agreed with production with in planned levels of cost and product quality.

-Spearheading the engineering requirement and identifying the key areas for efficiency/improvement in productivity, automatic etc.

-Prepare and gain agreement for, and implement capital expenditure plans with acceptable cost limits.

-Ensure that the appropriate GMP practice is implemented throughout the factory to ensure that it routinely passes all local and international regulatory audits with respect to quality, safety, Health and Environment protection.

-Develop and maintain effective internal working relationships with all employees teams (Both companies employed and contract casual Labour) in order to promote good industrial relations.

-Build and maintain effective working relationships with all local civilian bodies, and various regulatory authorities in order to ensure high levels of local PR and minimal interference in our operations.

-Ensure that all levels of staffs are recruited, developed and motivated to maintain and improve departmental and over all productivity performance.

-Manage employees and hands-on operations of the plant manufacturing functions

-Develop and manage budgeting and budget execution of factory expansions both Opex & Capex

-Direct all production control, production process development, quality systems with Six Sigma and lean manufacturing principals.

-Planning, directing, and coordinating the manufacturing of products in compliance with company goals and objectives

-Should have thorough technical knowledge of products under manufacturing and to be manufactured in the pipeline with working knowledge of inventory management.

-Drive continues improvements to deliver operational efficiency and in handset compliance standards

-Planning and implementing the preventive and predictive maintenance schedules for improving the overall reliability and safety of plant Equipment.

-Ensuring compliance of various quality measures such as cGLP /cGMP (Good Manufacturing Practices) by the maintenance of appropriate requisite documentations/records.

-Using process, quality and productions improvements methodologies, planning, implementation and maintenance of manufacturing methods for new or existing products and technologies.


-Internal: with cross functional team members

-External: Vendors


-B.Pharm/M.pharm-FDA Approved – Tablet and capsules

-Experience between 03 to 07 years in Pharma packing Environment with WHO GMP norms

-Should have worked with ERP systems have expertise in using computers

-Working knowledge of product costing cost controls principals & measures.

-Should have process knowledge/machine knowledge/computer literacy, Vast vision long term goals for the carrier.

-Should have production management skill.

-strong knowledge of pharmaceutical packing technology (Capsules, Tablets) and its machinery.

-Has in depths knowledge and experience of the classical packing KPI’s and performance efficiency measures.

-Skilled in work and process flow mapping and has delivered productivity improvements through industrial engineering initiatives.


-Performance Driven

-Self-starter and energetic with excellent organizational skills.

-Analytical, conceptual strategic and planning abilities.

-Excellent interpersonal skills. Ability to maintain a healthy relationship with both internal and external stakeholders

-Positive mind-set with a can-do attitude in a dynamic growing Environment.

More Information

  • Salary ₹300,000.00 to ₹600,000.00 /year
  • Education B.pharma/M.pharma
  • No. of Vacancy 1
  • This job has expired!
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  • Address Noida,Utter Pradesh , India
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