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Quality Control Support Lead (2nd Shift)

Manufacturing and Production

Quality Control Analyst

No

Millburn, New Jersey, United States

766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. <br>We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!<br>Imagine what you could do here at Novartis!<br><br>The Quality Control Support Lead serves as the first point of contact and coordination for the Quality Control department. The Lead will ensure that the quality control program is achieved efficiently within the framework of regulatory compliance and operating with high standards of GMP within the department.<br><br>Your responsibilities include, but are not limited to:<br><br>• Ensure all batch records and applicable data are in compliance with specifications, and effectively communicate any deficiencies as needed.<br>• Author and/or review Standard Operating Procedures that pertain to Quality Control-related activities.<br>• Organize the team for the daily activities and personnel adjustments as necessary. Responsible for motivating the team on a daily basis.<br>• Work closely with the Quality Control Manager to ensure optimal performance of the department and the team members and promote a culture of personal accountability for quality and compliance.<br>• Assist the Manager with communication of on job-related information during daily meetings.<br>• Supervise the training of people who are less experienced to ensure they have the necessary technical skills and knowledge.<br>• Integrate and harmonize best practices within areas of expertise.<br>• Enforce best-in-class cGMP and aseptic behaviors.<br>• As Subject Matter Expert, support any deviation, out-of-specification, and out-of-trend investigations that involve quality control testing.<br>• Accountable for maintaining an “Audit Ready” work environment.<br>• Responsible for supporting facilities and equipment commissioning activities.<br>• Ensure inventory levels are adequate for daily operations<br>• SME capable of working independently with little oversight and qualified to coordinate the team and provide effective guidance to all team members<br><br>Note: 2nd Shift 12PM-10PM Sunday-Wednesday<br><br>The pay range for this position at commencement of employment is expected to be between $84,000.00 and $126,000.00 per year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors<br><br>https://www.youtube.com/watch?v=ggbnzRY9z8w<br><br><br>[#video# https://www.youtube.com/watch?v=ggbnzRY9z8w{#400,300#}#/video#]