
Specialist, Manufacturing Quality Assurance
Novartis is seeking a highly skilled and detail-oriented Specialist to join our Manufacturing Quality Assurance team. As a global leader in the pharmaceutical industry, we are committed to producing high-quality medicines that improve and extend people's lives. The ideal candidate for this role will have a strong background in quality assurance within a manufacturing environment and a passion for ensuring compliance with regulations and standards. If you are a meticulous and dedicated professional with a strong understanding of quality systems and a desire to make a positive impact, we encourage you to apply for this exciting opportunity at Novartis.
- Conduct quality checks and audits of manufacturing processes to ensure compliance with regulations and company standards.
- Develop and implement quality assurance procedures and policies.
- Monitor and analyze data to identify trends and areas for improvement in manufacturing processes.
- Collaborate with cross-functional teams to maintain and improve quality standards.
- Train and educate manufacturing personnel on quality requirements and procedures.
- Investigate and resolve quality issues and non-conformances.
- Conduct risk assessments and implement corrective and preventive actions.
- Maintain and update quality documentation and records.
- Stay current with industry trends and regulatory changes to ensure compliance.
- Represent the company during regulatory inspections and audits.
- Participate in continuous improvement initiatives to enhance quality systems and processes.
- Identify areas for cost reduction and efficiency improvement within the quality assurance function.
- Mentor and coach junior team members to ensure a high level of performance.
- Communicate quality metrics and performance to upper management.
- Uphold the company's commitment to producing high-quality medicines and improving patients' lives.
Bachelor's Degree In A Relevant Field, Such As Pharmaceutical Sciences, Chemistry, Or Engineering.
Minimum Of 5 Years Experience In Quality Assurance Within A Manufacturing Environment, Preferably In The Pharmaceutical Industry.
Knowledge And Understanding Of Gmp Regulations And Industry Standards, With Experience In Conducting Audits And Maintaining Compliance.
Strong Analytical And Problem-Solving Skills, With The Ability To Identify And Resolve Quality Issues In A Timely Manner.
Excellent Communication And Interpersonal Skills, With The Ability To Work Effectively With Cross-Functional Teams And External Stakeholders.
Data Analysis
statistical analysis
Quality Control
Root Cause Analysis
Process validation
Risk assessment
Documentation management
Compliance monitoring
SOP Development
Audit Preparation
Gmp Regulations
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Adaptability
Problem-Solving
Decision-making
According to JobzMall, the average salary range for a Specialist, Manufacturing Quality Assurance in Cambridge, MA, USA is between $60,000 and $80,000 per year. However, this range may vary depending on the individual's level of experience, education, and specific job duties. Some employers may also offer additional benefits such as bonuses, healthcare, and retirement plans.
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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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