Sr. Team Leader

8 - 12 years

0 Lacs

Posted:3 days ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

As an experienced professional in pharmaceutical manufacturing with over 8 years of experience in sterile dosage manufacturing, your role will involve a wide range of responsibilities to ensure the smooth operation of the production process. Here is what you need for this role: **Role Overview:** You will be responsible for facilitating the investigation process, proposing and implementing CAPA, and demonstrating overall knowledge of DMAIC and ALCOA principles. Additionally, you will need to have a strong understanding of the current equipment, technologies, and unit operations involved in manufacturing liquid injectables. **Key Responsibilities:** - Engage and inspire the team on performance expectations and coach them using Coaching Skill principles - Manage critical areas and govern clean room behavior and practices - Validate process/cleaning equipment and drive process development and continuous improvement projects - Maintain production areas in a state of readiness for audits and inspections - Implement quality management systems, investigations, and suggest CAPA - Support human resources function in recruitment and onboarding - Plan daily shift-wise batch execution activities with micro-scheduling and work allocation - Optimize manpower deployment and conduct on-the-job training for new employees - Focus on minimizing downtime during operations to improve efficiency - Supervise preliminary troubleshooting for the entire fill finish line **Qualifications Required:** - Graduate or Postgraduate in Pharmaceutical or any Science stream - Minimum 8+ years of experience in manufacturing sterile dosage - Strong interpersonal skills - Accountability for Good Data Management and Data integrity understanding - Behavioral skills like Courage, Excellence, Equity, and Joy If you have the following preferred requirements, it would be considered a bonus: - 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 Please note that the work location assignment for this role is On-Premise. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.,

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Pfizer logo
Pfizer

Pharmaceutical Manufacturing

New York New York

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