Our highly skilled workforce, with their unwavering commitment to excellence, will be the critical pillar for IMAEC MEDNTEK’s success story. We will achieve our shared goals and organizational objectives by strategically focusing on attracting, retaining and developing the correct talent mix with diversity in relation to gender, age, expertise and geographical heterogeneity. At IMAEC MEDNTEK we provide an opportunity to our employees to share across their innovative ideas and views. We ensure their talent enhancement and career growth with our core development strategy. We are providing an environment for our employees to feel connected at all levels of their personal and social developmental stages. We are here building trust and believing in our people/stakeholders.
- Monitor manufacturing activities in compliance with cGMP
- Ensure the RM, PM availability as per production plan
- Implements operational manuals, production plans and programs
- Ensure conformance of manufacturing process and with organizational objectives and goals
- Ensure the general cleanness and hygienic conditions of the manufacturing area
- Asist in pilot scale batches, ensure the compliance of MFR, BMP & BPR and its record maintenance
- RO EDI Plant Operation & Documentation.
- Ensure all production equipment’s in well maintained and working conditions
- Responsible for internal and external audits and ensure its compliances
- Asist in plant certifications and record maintenance
- Coordinate with QA / QC in daily activities. Ensure record updating as per SOP and compliance
- Team work and on job training activities
- Ensure routine maintenance and calibration activities
- Follow safety practices and work environment
- Monitoring the Production Performance as: Achievement against production Plan Target, Utilized actual man hours against standard man-hours, Capacity utilization of different machines, productive man-hours against non-productive man-hours, and optimum utilization of available resources
- Qualification: B. pharm
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