Key Responsibilities:

• Plan/schedule, execute, supervise, and review in-process, development, validation, and release testing on samples while working with cross-functional stakeholders to meet company quality standards and timelines.
• Support and manage tracking and trending systems, and programs which assist in the testing, evaluation and monitoring of quality, assay performance and efficiency.
• Author, review, and approve Quality documents (i.e., protocols, reports, SOPs, test methods, technical documents, and risk assessments)
• Contribute, support, and lead writing of OOS/OOE/OOT and deviation investigations. Drive CAPA outcomes.
• Support internal and external audits.
• Assists in the evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards.
• Trains and educates employees and promotes adherence to quality control procedures, policies, standards, and best practices to foster a culture of quality awareness and accountability.
• Analyze quality data and metrics to identify trends, patterns, and areas of improvement.
• Promote a culture of continuous improvement, fostering innovation, and implementing Lean techniques to optimize quality control processes and enhance overall operational efficiency.
• Play a key role in the development and growth of direct reports, providing guidance, coaching, and support to enhance their performance and career progression within the organization.

Essential Requirements:

• Bachelor's degree in scientific disciplines such as Biochemistry, Biology or related field
• 5 years of experience in pharmaceutical industry or equivalent industry experience
• Proven experience as a quality control supervisor or similar leadership role within a quality laboratory environment
• Extensive knowledge of GLP and GDP principles. Understanding of quality management systems (QMS), regulatory requirements (FDA/EMEA), and industry standards.
• Possess a strong understanding of QC testing methods, tools, and techniques.
• Strong analytical and problem-solving skills, with the ability to make data-driven decisions and implement effective solutions.
• Excellent communication and interpersonal skills, with the ability to collaborate with cross-functional teams and effectively communicate quality requirements and findings.
• Experience with leading/supervising people preferred
• Detail-oriented and organized, with the ability to manage multiple priorities and meet deadlines

The salary for this position is expected to range between $85,400.00 - $158,600.00/year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.