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Serialization Manager information

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$25.1K

$61K

$118.8K

How much do serialization manager jobs pay per year?

As of Jul 13, 2026, the average yearly pay for serialization manager in Raritan, NJ is $60,956.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,000.00 and $70,100.00 per year, depending on experience, location, and employer.

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 cities near Raritan, NJ are hiring for Serialization Manager jobs? Cities near Raritan, NJ with the most Serialization Manager job openings:
Serialization Manager jobs near you
Infographic showing various Serialization Manager job openings in Raritan, NJ as of July 2026, with employment types broken down into 82% Full Time, 15% Part Time, 1% Temporary, and 2% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $60,956 per year, or $29.3 per hour.
Senior Manager, Packaging and Serialization

Senior Manager, Packaging and Serialization

Acadia Pharmaceuticals Inc.

Princeton, NJ • Hybrid

Other

Re-posted 10 days ago

Job description

Seeking talent near: Princeton, NJ; San Diego, CA

Position Summary:

Responsible for coordination of packaging (package design), artwork, and serialization with commercial Drug Product Contract Manufacturing organizations (CMO's), and other third party suppliers for products as identified. Subject matter expert in the field of serialization to oversee our CMOs running commercial and Acadia data management and integration.

Experienced in the technical aspects of product introduction into the EU and other global markets as related to serialization, package design, and local requirements.

Primary Responsibilities:

  • Develops and maintains good working relationships with both internal stakeholders and contract manufacturers.
  • Acquires and maintains scientific and technological knowledge and background of existing and new pharmaceutical (surface) serialization technologies to ensure our CMOs are aligned. Verifies CMO serialization technologies and ensures compliance with pharmaceutical regulatory requirements (EU FMD and DSCSA).
  • Coordinate periodic CMO Manufacturing meetings preparing minutes and tracking completion of action items.
  • Maintains and follow through a consolidated Acadia Manufacturing action log to ensure all manufacturing related actions are completed on time.
  • Work with CMOs and Acadia participants to schedule and coordinate Steering Committee Meetings.
  • Works with Quality Group and Acadia Manufacturing SMEs to ensure Quality Events are managed and communicated appropriately to ensure timely resolution and closure.
  • With Quality Assurance, ensures CMOs remain current and compliant with all GMP related requirements, guidelines and procedures.
  • Provide onsite process coverage as person-in-plant as needed
  • Develops, collects appropriate internal and external metrics to measure CMO and Acadia performance.
  • Communicates manufacturing or technology related issues and information to Manufacturing production team members, department stakeholders, and other members of the project team.
  • Supervise, train and mentor personnel as needed.

Education/Experience/Skills:

BS in Engineering/Chemistry or equivalent combination of relevant education and applicable job experience.  Scientific advanced degree a plus.  A minimum of 8 years of progressively responsible experience within the pharmaceutical/biotechnology or equivalent industry.

Must possess:

  • Contract service provider experience.
  • Strong understanding is required of the biopharmaceutical serialization and packaging process
  • Demonstrated experience with preparing/reviewing annual product review/product quality review reports.
  • Extensive knowledge of current Good Manufacturing Practices (cGMPs)
  • Able to operate effectively and with a strong sense of urgency in a fast-paced environment.
  • Outstanding communicator: direct, effective, clear, concise, well organized and appropriate.
  • Domestic and International travel is required for this role.
  • Experience in a cGMP environment
  • Capability to communicate efficiently and effective about issues of a complex (technological and scientific) nature
  • Attention for detail

Physical Requirements:

While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, see, talk or hear in a standard office environment and independently from remote locations. Employee must occasionally lift and/or move up to 20 pounds.   Ability to travel by car or airplane independently up to 25% of the time and work after hours if required by travel schedule or business issues.

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