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Serialization Jobs in New Jersey (NOW HIRING)

TeamSoft

Warehouse Associate/Serialization

East Windsor, NJ · On-site

$16 - $19/hr

Complete serialization processes and maintain accurate inventory records. * Identify and report damaged, missing, or overage products. * Assist with cycle counts and physical inventory. * Inspect and ...

TeamSoft

Warehouse Associate/Serialization

East Windsor, NJ · On-site

$16 - $19/hr

Complete serialization processes and maintain accurate inventory records. * Identify and report damaged, missing, or overage products. * Assist with cycle counts and physical inventory. * Inspect and ...

Robert Half

Systems Engineer

Bridgewater, NJ · On-site

$38 - $44/hr

Help manage serialization and track-and-trace solutions by supporting compliance with global standards such as GS1 and applicable pharmaceutical supply chain regulations. * Assist with the ...

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$14

$32

$64

How much do serialization jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for serialization in New Jersey is $32.70, according to ZipRecruiter salary data. Most workers in this role earn between $21.49 and $40.00 per hour, depending on experience, location, and employer.

What is the job description of a serialization?

A serialization job involves designing, implementing, and managing systems that assign unique identifiers to products, data, or digital assets to ensure traceability and prevent counterfeiting. It requires knowledge of coding, database management, and industry regulations, often utilizing serialization software and tools. The role may also include quality control and compliance monitoring to meet regulatory standards.

What jobs pay 500,000 a year in the US?

In the field of serialization, high-paying roles such as senior software engineers, solutions architects, or technical leads can reach or exceed $500,000 annually, especially in large tech companies or financial institutions. These positions typically require advanced skills in programming, system design, and experience with serialization tools and frameworks. Compensation at this level often includes base salary, bonuses, and stock options.

What is a Serialization job?

A Serialization job involves managing the processes and systems used to track and trace products, typically in industries like pharmaceuticals, food, and logistics. It ensures compliance with regulatory requirements by assigning unique identifiers to products and maintaining secure data records. Professionals in this role work with serialization software, regulatory guidelines, and supply chain teams to prevent counterfeiting and improve product traceability.

What are the key skills and qualifications needed to thrive in the Serialization position, and why are they important?

To thrive in Serialization, particularly within pharmaceutical or life sciences industries, a strong understanding of regulatory standards, track-and-trace processes, and supply chain operations is essential, often supported by a degree in engineering, life sciences, or a related field. Proficiency with serialization software platforms (such as SAP ATTP, Systech, or TraceLink), as well as familiarity with global regulatory requirements and validation protocols, is highly valued. Excellent attention to detail, problem-solving skills, and effective communication are crucial soft skills in this role. These abilities ensure accurate compliance, seamless product traceability, and efficient collaboration across production, IT, and quality assurance teams.

What is the highest paying pharmaceutical job?

In the pharmaceutical industry, senior roles such as Pharmaceutical Directors, Vice Presidents, or Chief Scientific Officers tend to have the highest salaries, often exceeding $150,000 annually. These positions typically require extensive experience, advanced degrees, and leadership skills, and may involve overseeing drug development, regulatory compliance, or strategic planning.

What types of projects or tasks does a Serialization specialist typically handle on a day-to-day basis?

Serialization specialists are responsible for configuring and maintaining systems that assign, track, and verify serial numbers on pharmaceutical products throughout the manufacturing and distribution process. On a typical day, they may collaborate with IT, quality assurance, and production teams to troubleshoot data integration issues, ensure regulatory compliance, perform system upgrades, and conduct audits or validation of serialized packaging lines. They also work closely with external partners or regulatory authorities to meet evolving serialization requirements. This role requires balancing technical tasks with cross-departmental communication to keep supply chains running smoothly and ensure product integrity.

What jobs in the US pay 300,000 a year?

In the field of serialization, senior roles such as lead engineers, architects, or specialists with extensive experience and advanced skills in programming, data management, and systems design can earn salaries of $300,000 or more annually. These positions often require advanced certifications, a strong understanding of distributed systems, and leadership responsibilities. High-paying roles are typically found in large tech companies, finance, or specialized industries with complex data processing needs.
What are the most commonly searched types of Serialization jobs in New Jersey? The most popular types of Serialization jobs in New Jersey are:
What are popular job titles related to Serialization jobs in New Jersey? For Serialization jobs in New Jersey, the most frequently searched job titles are:
What job categories do people searching Serialization jobs in New Jersey look for? The top searched job categories for Serialization jobs in New Jersey are:
Serialization jobs near you
Infographic showing various Serialization job openings in New Jersey as of July 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $68,006 per year, or $32.7 per hour.

Senior Manager, Packaging and Serialization

Acadia Pharmaceuticals Inc.

Princeton, NJ • Hybrid

Other

Re-posted yesterday

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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