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Serialization Manager Jobs in Massachusetts (NOW HIRING)

RadNet

Technical Support Engineer, PACS

Somerville, MA · On-site

$73K - $100K/yr

Collaborate with IT, Product, Engineering, and Project Management teams to escalate and resolve ... Familiarity with scripting, data serialization, and reporting tools such as SSRS. * Strong ...

RadNet

Technical Support Engineer, PACS

Somerville, MA · On-site

$73K/yr

Collaborate with IT, Product, Engineering, and Project Management teams to escalate and resolve ... Familiarity with scripting, data serialization, and reporting tools such as SSRS. * Strong ...

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Serialization Manager information

What does a Serialization Manager do?

A Serialization Manager oversees the process of assigning unique serial numbers to products, typically in the pharmaceutical or manufacturing industries, to ensure traceability and compliance with regulatory requirements. They manage serialization systems, coordinate with IT and production teams, and ensure all products are properly serialized and tracked throughout the supply chain. Their role is crucial for preventing counterfeiting, supporting product recalls, and meeting government regulations.

What is the job description of a serialization?

A Serialization Manager oversees the process of assigning unique serial numbers or codes to products to ensure traceability and prevent counterfeiting. This role involves implementing serialization systems, managing compliance with industry regulations, and coordinating with manufacturing and quality teams. Knowledge of serialization software, regulatory standards, and supply chain processes is essential.

What jobs can I get with a level 4?

A Serialization Manager with a level 4 qualification can typically qualify for supervisory or specialized roles in manufacturing, logistics, or quality assurance that require advanced knowledge of serialization processes. These roles often involve overseeing serialization systems, ensuring compliance with regulations, and managing teams or projects. Relevant skills include familiarity with serialization software, regulatory standards, and process optimization.

How does a Serialization Manager typically interact with cross-functional teams to ensure compliance with global pharmaceutical regulations?

A Serialization Manager regularly collaborates with quality assurance, IT, supply chain, and regulatory affairs teams to ensure all serialized products meet global regulatory requirements. This includes coordinating system integrations, aligning on data standards, and troubleshooting issues that could impact product traceability. Effective communication and project management skills are essential, as the role often requires leading cross-functional meetings, providing training, and ensuring any changes in regulations are quickly implemented across all departments involved in the serialization process.

What is the role of a supply manager?

A supply manager oversees the procurement, storage, and distribution of materials and products within an organization. They coordinate with suppliers, manage inventory levels, and ensure timely delivery to support production and operations. Strong organizational and negotiation skills, along with knowledge of supply chain management tools, are essential for this role.

What are the highest paying industrial jobs?

In industrial settings, roles such as industrial engineers, plant managers, and maintenance managers tend to have the highest salaries. Serialization Managers, responsible for overseeing product serialization processes, can also earn high wages, especially with experience and relevant certifications in manufacturing or quality assurance. These positions often require technical skills, industry knowledge, and sometimes specialized software proficiency.

What are the key skills and qualifications needed to thrive as a Serialization Manager, and why are they important?

To thrive as a Serialization Manager, you need in-depth knowledge of pharmaceutical supply chain regulations, serialization processes, and compliance standards, typically supported by a degree in a scientific, engineering, or related field. Familiarity with serialization software (such as SAP ATTP, TraceLink), data management systems, and regulatory compliance tools is crucial. Strong project management, problem-solving skills, and effective communication enable successful cross-functional collaboration and issue resolution. These skills and qualifications are vital to ensure products meet regulatory requirements, prevent counterfeiting, and maintain supply chain integrity.
What are popular job titles related to Serialization Manager jobs in Massachusetts? For Serialization Manager jobs in Massachusetts, the most frequently searched job titles are:
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What cities in Massachusetts are hiring for Serialization Manager jobs? Cities in Massachusetts with the most Serialization Manager job openings:
Serialization Manager jobs near you
Director, Quality Assurance (Operations)

Director, Quality Assurance (Operations)

Zevra Therapeutics

Boston, MA • On-site

Full-time

Posted 8 days ago

Job description

About Zevra Therapeutics, Inc.
We are a rare disease therapeutics company leading with science to make life-changing therapeutics available to patients with significant unmet needs. We involve key thought leaders, physicians, patients, care partners, and advocacy groups in all of our clinical and regulatory development strategies.
With a keen understanding that drug development often requires creative solutions, we have the insight and expertise to forge new pathways to success that others have missed. By following the data without bias, our transparent narratives and common-sense perspective have successfully overcome complex development challenges to make much-needed therapies available to patients.
Nimble and dauntless, we push boundaries beyond what is thought to be possible and advance new therapies that have the potential to bring meaningful improvement to patients' lives.
About the role
The Director of Quality Operations has a critical role within Zevra that will provide technical leadership for the administration of Zevra's Quality Management System (QMS). The position is responsible for improving Zevra's QMS and supporting operational processes. This position is further responsible for assuring that all development and commercial operations carried out by Zevra and its contractors consistently comply with Zevra standards and applicable regulations. Key attributes of the incumbent include enthusiasm for building lasting organizational systems suitable capable of growing with the organization. The qualified candidate must have experience building and maintaining sustainable and trusting cross-functional relationships with key strategic internal and external stakeholders. The incumbent must rapidly earn a strong reputation supporting programs from preclinical through commercialization stages. This position requires close cross-functional teamwork, an ability to understand and communicate risk, and a desire to coach and develop cross-functional staff.
What you'll do
  • Performs Quality review and approval of IMP and Commercial Product manufacturing documentation (e.g., master batch records, validation protocols and reports) and provides disposition of drug substance, drug product, clinical trial materials, and disposition of commercial finished goods,
  • In coordination with the Manufacturing team, assures that the serialization system for commercial distribution remains compliant,
  • Responsible for the execution of compliant administration of exception, investigation, CAPA, product complaints management systems pertaining to Zevra and vendor and operations,
  • Supports preparation of content and facilitates conduct of periodic Quality Management Reviews and supports preparation of annual product reviews, • Engages in the day-to-day efforts of Quality Vendor Management,
  • Conducts and/or facilitates internal and external (vendor) audits, self-inspections and regulatory inspection readiness meet company and applicable regulatory standards. This includes, but is not limited to, audit planning and execution, reporting and coordination with external contractors,
  • Supports periodic GxP training and ensure that training requirements are consistently met, as required,
  • In collaboration with Head of Quality and other department heads, prepare, review, approve, and implement SOPs as required,
  • Responsible for Quality Review Boards, providing technical expertise for product quality decisions,
  • Responsible for manufacturing investigations, in collaboration with the Manufacturing Team, ensuring appropriate corrective and preventive actions are taken as required,
  • Support continuous improvement initiatives to optimize Zevra's quality and compliance position,
  • Cross-train and serve as back-up for Quality Systems, as assigned.

Qualifications
  • 10+ years of progressive experience in pharmaceutical/biotech industry with expertise in establishing effective and efficient systems and processes supporting pre-clinical, clinical and commercial programs,
  • 7+ years of Quality leadership experience with a successful track record in vendor oversight and managing relationship with external stakeholders as well as internal QA systems in a virtual environment,
  • 7+ years' experience in the establishing and administering of GCP-, GLP- and GDP compliant systems,
  • Bachelors or Advanced degree in a scientific or related discipline,
  • Understanding of worldwide requirements of GxP compliance and quality systems for clinical and commercial products,
  • Leadership role in the management of regulatory/health authorities inspections,
  • Experience with new product launch and implementation of serialization systems and commercial product complaint processes is a plus,
  • Strong team player that has a customer service approach and is solution oriented,
  • Ability to travel both domestically and internationally as needed, likely to be ~10 15%,
  • The candidate will need to embrace Zevra's mission and core values,
  • Ability to effectively communicate with inspiration, lead and influence individuals from multiple functional departments at all levels of the organization,
  • Strong organizational and time management skills to balance working on multiple projects and initiatives in parallel,
  • A proven self-starter capable of high performance with limited direction and oversight,
  • Excellent people leader with strong mentorship skills. Track record of strong personal performance combined with demonstrated ability to build and lead highly engaged teams in a changing environment,
  • Excellent written communication and oral presentation skills.
  • Proven ability to thrive working in a fast-paced, innovative remote environment while remaining flexible, proactive, resourceful, hands-on and efficient,
  • In-depth knowledge of GxP, 21CFR, EU GMP, ICH, ISO, QSR, EUGDP and other applicable domestic and international regulations, standards, Directives and Guidance.
  • A commitment to collaborative leadership, execution, teamwork and the maintenance of a professional culture based on trust and mutual respect,
  • Excellent interpersonal, reading, writing, negotiation, communication, conflict resolution and public presentation skills, along with exceptional organizational and problem-solving skills,
  • Proven ability to analyze scientific issues and develop relevant and realistic recommendations and plans and take responsibility for implementing,
  • Ability to identify and manage contract/vendor resources to support Quality related goals,
  • Successful track record of working in a matrixed (virtual) organization and building strong relationships with other functions and contractors/vendors,
  • Experience in a virtual manufacturing environment,
  • Ability to work under pressure, meet deadlines and contribute to achieving high level activities as well as tactical and administrative tasks, and
  • Experienced leader in Quality Assurance.

Equal Employment Opportunity Statement
Zevra is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
Notice to External Recruiters
Zevra does not accept unsolicited resumes from agencies or search firms. Recruiters are requested not to contact employees or hiring managers. All candidate submissions must be coordinated through our Human Resources team and require a prior written agreement. Any resumes sent without such an agreement will not create any implied obligation.

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