Careers

TRENDING OPPORTUNITIES AT BJAIN PHARMACEUTICALS

Urgent Hiring

Position – Microsoft Dynamics NAV 2016 Developer

Location – Noida

JD for Microsoft Dynamics NAV 2016 Developer

  • IT personnel with  experience in Microsoft Navision
  • Should have worked for a manufacturing company/ handled manufacturing companies.
  • Should have a good understanding of Finance, manufacturing, warehousing, sales and other key modules
  • Carry out development activities within NAV 2016
  • 5 +years’ experience with Dynamics NAV 2016 programming.
  • Development and integration work with C/AL.
  • Design and implement interfaces with other software systems (websites, enterprise data warehouse).
  • Develop new and modify existing Microsoft Dynamics NAV C/AL customizations, 3rd party advanced solutions, object merges, application upgrades, and system configuration to use base Dynamics NAV features.
  • Ability to write technical documentation, user test scripts.
  • Create, modify pages, reports and tables or custom logic in C/AL .
  • Should able to create backup and installation
  • Should be able to manage Job Queue

Email – pharmahr@bjainpharma.com

Position – Regulatory & Quality Manager

Location – Noida

JD for Regulatory and Quality Manager Preferred for Female Candidate.

  • Responsible for implementation of Quality Management System as per regulatory requirements.
  • Regulatory Documentation.
  • Management of the Continual Improvement of the Systems, Product Quality Review Process for the Corrective and Preventive Action System.
  • Accountable for the Data integrity and implementation of the SOP and policy.
  • Evaluate & approval of master documents pertaining to various departments.
  • Responsible for preparation and approval of all master documents like BMR, SOP, STP, SPEC, formats and checklist.
  • Accountable for Control Sample Management and Stability Management.
  • Responsible for implementation of QA systems for ensuring that compliance as per sops.
  • Responsible for external & internal audits.
  • Review, evaluation, and approval of Document on behalf of factory department in guidance of technical head.
  • To follow cGMP practices and implementation of the information recorded.
  • Responsible for review and approval of equipment qualification/requalification/ validation protocols, a compilation of summary reports of the products.

Email – pharmahr@bjainpharma.com