Job Description
Here Is What You Need (Minimum Requirements)
- Graduate or Postgraduate in Pharmaceutical or any Science stream.
- Minimum 08+ years of experience in manufacturing of sterile dosage.
- Ability to facilitate investigation process, proposal and implementation of CAPA. Overall knowledge on DMAIC and ALCOA principles.
- Current equipment, technologies and unit operations involved in manufacturing of liquid injectables process which includes batch fabrication, vial depacking, Via1 washing and drying/depyrogenation, Vial Filling and stoppering, Vial capping, Tray loading filter integrity testing device.
- Engage and inspire the team on performance expectations and coach the team to meet those expectations using Coaching Skill principles.
- Critical area management and governing of clean room behavior and practices.
- Process/cleaning equipment validation principles and practices.
- Facilitate and drive the process development, process simplification, continuous improvement projects and technology transfer activities.
- Practices of upkeep and maintenance of production areas in the desired state of readiness of audits and inspections.
- Production concept s: principles of capacity planning, production scheduling, line balancing and inventory management.
- Practices for management and upkeep of manufacturing areas, with emphasis on environment monitoring, personal health and hygiene.
- Quality management systems, investigations and suggesting CAPA.
- Support human resources function in recruitment and onboarding.
- Strong interpersonal skills
- Be accountable for the Good Data Management and Data integrity understanding and performance of the team.
- Daily shift wise batch execution activity planning with micro scheduling and work allocation.
- Deploy the manpower optimally and conduct/ensure the on job training for new joined employee.
- Focus on minimizing downtime during operation to improve run time efficiency.
- Close supervision of preliminary troubleshooting for entire fill finish line.
Behavioral/Any Other Skills
Courage (Think big, speak up and be decisive)
Excellence (Focus on what matters, agree on who does what and measure outcomes)
Equity (Be inclusive, Act with integrity, )
Joy (Take pride, recognize one another, Have fun)
Empower team to make decisions, proper escalation process, maintaining compliance and data integrity.
Bonus Points If You Have (Preferred Requirements)
- Strong leadership capabilities
- Experience with regulatory compliance and quality assurance
- Proficiency in project management tools and methodologies
- Ability to influence and lead cross-functional teams
- Ability to mentor and develop direct reports
- Ability to foster a culture of safety and continuous improvement
Work Location Assignment: On Premise
Manufacturing
Job Classification
Industry: Pharmaceutical & Life Sciences
Functional Area / Department: Customer Success, Service & Operations
Role Category: Non Voice
Role: Technical Support - Non Voice
Employement Type: Full time
Contact Details:
Company: Pfizer
Location(s): Visakhapatnam
Keyskills:
Fabrication
Manager Quality Assurance
Data management
Project management
Pharma
Line balancing
Scheduling
Troubleshooting
Continuous improvement
Recruitment