Specialist, Master Batch Record (MBR) Design
Welcome to Novartis, a global healthcare company that is dedicated to improving and extending the lives of patients worldwide. We are currently seeking a highly skilled and motivated Specialist in Master Batch Record (MBR) Design to join our team. In this role, you will be responsible for designing and developing master batch records for our pharmaceutical products, ensuring compliance with regulatory requirements and company standards. We are looking for an individual with a strong attention to detail and a passion for quality in all aspects of their work. If you have the necessary qualifications and a drive to make a difference in the lives of patients, we encourage you to apply for this exciting opportunity.
- Design and develop master batch records for Novartis pharmaceutical products, ensuring accuracy and completeness.
- Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Regulatory Affairs, to gather necessary information and incorporate into master batch records.
- Ensure compliance with regulatory requirements and Novartis standards throughout the design process.
- Conduct thorough reviews and revisions of master batch records to reflect any changes in product specifications or processes.
- Maintain up-to-date knowledge of industry regulations and guidelines related to master batch record design.
- Identify and implement process improvements to enhance efficiency and quality in master batch record design.
- Communicate effectively with internal stakeholders to gather feedback and incorporate suggestions into master batch record design.
- Participate in audits and inspections to demonstrate compliance with regulatory requirements.
- Train and mentor junior team members in master batch record design and related processes.
- Demonstrate a strong attention to detail and commitment to quality in all aspects of work.
- Continuously strive to improve processes and exceed expectations in order to make a positive impact on the lives of patients.
Bachelor's Degree In A Related Field Such As Pharmaceutical Science, Chemical Engineering, Or Industrial Design.
Minimum Of 3 Years Of Experience In Creating And Managing Master Batch Records (Mbrs) In A Pharmaceutical Manufacturing Environment.
In-Depth Knowledge Of Cgmp Regulations And Fda Guidelines For Pharmaceutical Manufacturing.
Proficiency In Using Electronic Document Management Systems And Mbr Design Software.
Strong Attention To Detail And Excellent Organizational Skills To Manage Multiple Mbrs And Ensure Accuracy And Completeness.
Project Management
Data Analysis
GMP Knowledge
Technical Writing
Quality Control
Collaboration
Regulatory compliance
Problem-Solving
Process mapping
Documentation management
Attention
Batch Record Design
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
creativity
Organization
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Specialist, Master Batch Record (MBR) Design in Indianapolis, IN, USA is $45,000 to $65,000 per year. This can vary depending on factors such as experience, education, and company size. Additionally, location can also play a role in salary ranges.
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Novartis AG develops, manufactures, and markets healthcare products. It operates through the following segments: Pharmaceuticals, Alcon, Sandoz, Vaccines & Diagnostics, and Consumer Health. The Pharmaceuticals segment provides patent-protected prescription medicines. The Alcon segment offers surgical, ophthalmic pharmaceuticals, and vision care products. The Sandoz segment provides generic pharmaceuticals. The Vaccines & Diagnostics segment provides human vaccines and blood testing diagnostics.
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