Packaging Manager manages and oversees the packaging staff on designated shift to achieve operational objectives. Observes, analyzes, and researches packaging line operation to develop and implement scientific and efficient process. Being a Packaging Manager implements quality control check to ensure the packaging meets environment, health, and safety regulations. Provides staff with directions on materials and equipment for each package. Additionally, Packaging Manager may require a bachelor's degree. Typically reports to a head of a unit/department. The Packaging Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. Extensive knowledge of department processes. To be a Packaging Manager typically requires 5 years experience in the related area as an individual contributor. 1 to 3 years supervisory experience may be required. (Copyright 2024 Salary.com)
The Role
As the Senior Manager of Visual Inspection, Labeling, and Packaging Operations at Moderna, you will play a pivotal role in overseeing the final stages of production for parenteral drug products within a new state-of-the-art Drug Product cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products in vials and pre-filled syringes. The Sr. Manager will play a crucial role in establishing the operational strategy, implementing best practices, and building a team to achieve excellence in manufacturing operations while adhering to regulatory compliance and quality standards. You will be at the forefront of our mission to deliver mRNA therapies to patients worldwide, using your expertise to ensure the smooth operation of our manufacturing processes. Your work will directly contribute to the production of therapies that have the potential to transform the lives of patients.
Here’s What You’ll Do
In this role, your responsibilities will include:
Develop and execute Operational readiness strategies to ensure the successful launch and ongoing production of drug products,
Establish robust operational readiness plans to transition from the construction phase to full-scale production, ensuring all systems and processes are in place for cGMP compliance,
Oversee the hiring, training, and development of a high-performing operations team capable of executing visual inspection, labeling, and packaging across multiple production lines,
Collaborate with cross-functional teams working in a highly matrixed environment to drive decisions and influence outcomes to enable Moderna’s clinical pipeline,
Drive continuous improvement initiatives to enhance operational efficiency, reduce costs, and improve product quality,
Develop and manage the operational budget, including capital expenditure planning and cost control measures,
Lead risk management activities to identify potential operational issues and implement mitigation strategies,
Ensure adherence to all environmental, health, and safety guidelines, promoting a culture of safety within the operations team,
Establish key performance indicators (KPIs) to measure and report on operational performance, making data-driven decisions to optimize processes,
Foster a culture of innovation and collaboration, encouraging team members to contribute ideas for process improvements and operational excellence,
Serve as the primary point of contact for operations during regulatory inspections and audits.
Here’s What You’ll Need (Minimum Qualifications)
Bachelor of Science degree in Engineering, Pharmaceutical Sciences, or a related technology discipline.
A minimum of 8 years of experience in drug product inspection, labeling, and packaging, with at least 2 years in a leadership role.
Experience working with semi-automated inspection equipment.
Experience working with semi-automated labeling and packaging equipment.
Proficiency with clinical and commercial labeling requirements including med IDs and serialization.
Experience developing Knapp Test Kits and implementing an operator qualification strategy in support of visual inspection.
In-depth knowledge of cGMP regulations, pharmaceutical processing, and cleanroom operations.
Strong leadership skills with the ability to develop and motivate a diverse team.
Excellent project management, organizational, and communication skills.
Demonstrated ability to work cross-functionally and manage complex projects with multiple stakeholders, with the ability to convey complex information in an understandable manner to various stakeholders.
Experience with budget management and cost optimization in a manufacturing environment.
Problem-solving mindset with a commitment to quality and safety.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
Proven track record of successful facility start-ups or major operational projects (e.g., Greenfield or Brownfield projects) within the pharmaceutical industry.
Experience working with difficult-to-inspect products.
Experience working with lyophilized and pre-filled syringe products.
Operational experience with Automated Visual Inspection equipment.
A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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