Welcome to Aegis Lifesciences

WE ARE HIRING

We Are Hiring

If you are qualified / experienced in a relevant field, and would like to explore a career with Aegis Lifesciences, in a techno-driven, future-savvy, globally oriented environment, send in your CV to: gm@aegis-lifesciences.com , with ‘career ’as the subject title.

Job Openings

Executive- Regulatory Affairs

Product technical specialist

Quality Control- Chemical Analysis

Production Supervisor

Title/Designation: Executive- Regulatory Affairs

Job description
  • To assist in new products registration and license renewal compliance to local regulations, as well as CE and ISO 13485 requirement
  • Have the joint responsibility to develop, facilitate and execute comprehensive regulatory strategies through all phases of development and product life cycle, to accelerate and ensure successful product registrations and provides regulatory assessment and supports Change Control Assessment.
  • Review of SOPs, BPRs, specifications and change control to ensure compliance.

Title/Designation: Product Technical Specialist (class III medical device regulatory)

Job description
  • To lead in new products registration and license renewal compliance to local regulations, as well as GMP, CE and ISO 13485 requirement.
  • To lead the QA/RA team and ensure quality and good standard operating procedures within the company.
  • Have the overall responsibility to develop, facilitate and execute comprehensive regulatory strategies through all phases of development and product life cycle, to accelerate and ensure successful product registrations and provides regulatory assessment and supports Change Control Assessment.
  • Reviewing current accreditation/regulatory requirement, performing gap analysis and ensuring compliance to current requirements
  • Provide product specific Regulatory strategies to mitigate risk; works in conjunction with production & QA team to provide advice on process and labeling changes.
  • Compliance with respect to internal/external audits meeting regulatory/ accreditation requirements

Title/Designation: Chemist Quality Control- Chemical Analysis

Job description
  • Manage overall quality control programs in compliance with all applicable regulation and policies, including CDSCO, safety and environmental.
  • Implementation, maintain GLP & Documentation as per CGMP, ISO13485, CE norms.
  • To carry out sampling and testing of RM, PM, FP & validation program as per laid standards & recording of analysis results into issued analytical protocol & records
  • Stability sample analysis & preparation of report as per laid standar

Title/Designation: Production Supervisor

Job description
  • Execute the production plan as per operations to achieve consistent product quality, quantity and yield.
  • Trouble shooting of process and operational issues on shop floor.
  • Supervise batch charging and verification of RM Quantities and responsible for maintaining Batch Production records.
  • Check equipments and connected accessories and operate them as per the process norms.
  • Monitor and maintain all parameters as per SOPs and ensure strict compliance with c GMP and safety norms.

Executive- Regulatory Affairs

Product Technical Specialist

Quality Control- Chemical Analysis

Production Supervisor