ZipRecruiter

Log In

1

Serialization Manager Jobs in Raritan, NJ (NOW HIRING)

Palnar

Sr NetSuite Admin

Cranbury, NJ · On-site

Experience in Serialization process/chain of identity, DSCSA and 21CFR Part 11 compliance are mandatory. * Experience in System Administration, Change Management, Data Integrity, and ALCOA+, SOPs and ...

AditiStaffing

SAP MM Functional

Warren, NJ

Functional capabilities include: - DC Inventory Management - Store Inventory Management and Replenishment - Returns Management - Purchase Orders, Invoicing - Serialization and Cost Tracking - Article ...

next page

Showing results 1-20

All JobsSerialization JobsSerialization Manager JobsSerialization Manager Jobs in Raritan, NJ

Serialization Manager information

See Raritan, NJ salary details

$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.

IS Applications Analyst for Manufacturing Systems

Ferring Pharmaceuticals

Parsippany, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

Job description

Job Description:
As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our 'people first' philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world's oldest enemy: disease.
As the IS Applications Analyst for Manufacturing Systems, you will be responsible for the management and support of Manufacturing Systems including Rockwell PharmSuite Electronic Batch Record system (eBR) and Antares Serialization System. Responsibilities will include front-line application support, project management, validation, and end-user training. In addition, the role will need to support design, implementation, and maintenance of Electronic Batch Records (eBR). This role is critical in ensuring compliance with regulatory standards, optimizing batch manufacturing processes, and enhancing data integrity. The IS Applications Analyst for Manufacturing Systems works closely with cross-functional teams to support production operations and be comfortable analyzing data and looking at opportunities to utilize AI tools to enhance processes.
With Ferring, you will be joining a recognized leader, identified as one of "The World's Most Innovative Companies" by Fast Company, and honored by Fortune with inclusion on its "Change the World List," for addressing society's unmet needs. Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country.
Responsibilities:
  • Provide technical and functional support for Manufacturing applications including Rockwell PharmaSuite EBR, Antares Serialization, along with associated hardware such as tablets, printers, and scanners.
  • Design and configure MES eBR systems based on business requirements to digitize and automate batch record management, ensuring compliance with industry regulations (e.g., FDA's 21 CFR Part 11).
  • Create, manage, and maintain electronic batch records, including recipe management, process steps, electronic signatures, and data capture.
  • Oversee -User -Acceptance Testing of MES recipes to ensure business requirements are achieved.
  • Plan and execute validation tests (IQ, OQ, PQ) to demonstrate compliance with regulatory requirements.
  • Provide training to personnel on how to use eBR and Antares Serialization systems effectively.
  • Analyze batch data and historical records to identify trends, deviations, and opportunities for process improvement.
  • Coordinate changes to Enterprise Resource Planning (ERP) system master data, including, but not limited to, items, specifications, lookups, list of values, recipes, routings, and formulas.
  • Maintain comprehensive documentation of system configurations, validation records, and standard operating procedures (SOPs) related to MES eBR systems.
  • Develop system technical documentation, including but not limited to, functional specifications and UAT test scripts.
  • Collaborate with cross-functional teams, including manufacturing, quality assurance, and regulatory affairs, to gather information and resolve discrepancies.
  • Maintain data integrity by implementing periodic system reviews and audit trails for manufacturing systems.
  • Identify opportunities for process improvements or automation utilizing IT systems.
  • Maintain ThinManager or VDI for deploying software such as eBR.
  • Authoring QMS records including deviations, CAPAs (Corrective and Preventative Actions), and change controls.
  • Co-ordinate with Product Vendor in presenting incidents and follow-up in getting solutions.

Requirements:
  • Bachelor's degree in relevant field (computer science, chemical engineering, or pharmaceutical sciences)
  • Minimum 5 years of experience in Pharmaceuticals Industry.
  • Certificate/ASC/ BS in science-related discipline preferred.
  • Proficiency in MES eBR software platforms, preferably in Rockwell Automation PharmaSuite.
  • Knowledge of data integrity principles and strategies to prevent data corruption and maintain data accuracy and consistency.
  • Strong understanding of regulatory requirements in industries with batch processes, including FDA regulations (e.g., 21 CFR Part 11).
  • Familiarity with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) to ensure compliance.
  • Excellent communication skills to collaborate with cross-functional teams, and auditors.
  • Ability to manage eBR projects, including planning, execution, validation, and documentation.
  • Attention to detail and strong data-entry skills.
  • Strong organizational skills and ability to manage multiple tasks and priorities.
  • Proficiency in Microsoft Office Suite (Word, Excel) or equivalent software.

Physical Requirements:
  • Ability to move around the manufacturing plant, including walking, standing, and sitting for extended periods.
  • Occasional bending, stooping, or kneeling may be required to access equipment or systems in different locations.
  • Prolonged periods of sitting and working at a computer terminal.
  • Repetitive motions related to keyboarding, data entry, and mouse usage.
  • Occasionally lifting and carrying equipment or documents weighing up to 25 pounds.
  • Ability to work in a manufacturing environment, which may include exposure to noise, dust, chemicals, or varying temperatures.
  • Compliance with safety protocols, including the use of personal protective equipment (PPE) as required in specific plant areas.
  • Periodic movement between different sections of the plant to liaise with production staff, review processes, or validate records.
  • May involve climbing stairs or accessing elevated workstations.

Role will be in Parsippany, NJ.
Ferring + you
At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work. From working hours that respect your lifestyle, a culture that is welcoming and equitable, and the chance to work with the industry's most impressive people, these are just some of the ways we live our "People First" philosophy.
Our Compensation and Benefits
At Ferring, base salary is one part of our competitive total compensation and benefits package and is determined using a salary range. The base salary range for this role is $76,831 to $105,000 which is the reasonable estimate of the base compensation for this role. The actual amount paid may differ based on non-discriminatory factors such as experience, knowledge, skills, abilities, education and primary work location. Additional compensation for this role will be provided based on competitive annual incentive compensation targets in the form of an annual bonus - payouts are based on individual and company performance.
Benefits for this role include comprehensive healthcare (medical, dental, and vision) with a premium differential, inverse to base salary, to be paid by employees, a 401k plan and company match, short and long-term disability coverage, basic life insurance, wellness benefits, reimbursement for certain tuition expenses, sick time of 1 hour per 30 hours worked, vacation time for full time employees to accrue up to 120 hours in the first four (4) years of employment, and 160 hours in the fifth (5th) year of employment as well as 15 paid holidays per year. We are proud to offer paid parental leave subject to a minimum period of employment at Ferring.
Ferring is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local laws.
Join our team and your voice will be heard, and your contributions will be valued. If you love to come up with new ways to make a positive difference and see them through, you will fit right in.
We are proud to be an Affirmative Action/Equal Opportunity Employer (including Disability/Protected Veterans). We maintain a drug-free workplace.
Location:
Parsippany, New Jersey

Apply