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Pharmaceutical Serialization Jobs (NOW HIRING)

Packaging Supervisor

Fall River, MA · On-site

$72K - $93K/hr

Strong knowledge of pharmaceutical packaging machinery and cGMP protocols. * Familiarity with serialization tools like Systech and ERP systems like SAP. * Proficient in Microsoft Office tools (Excel ...

... InvaGen Pharmaceuticals, Inc., a Cipla subsidiary is on the search for experienced Packaging ... Responsible for working with Systech serialization system and SAP. * Reducing time spent preparing ...

Manager, Trade & Distribution

Boston, MA · On-site

$135K - $155K/yr

About Servier Pharmaceuticals Servier in the U.S. is a Boston-based, commercial-stage ... You are responsible for ensuring Right of Sale by maintaining serialization integrity, system ...

Packaging Technician

Wilson, NC · On-site

$14.75 - $18.25/hr

Experience in OSD pharmaceutical packaging . * Experience with serialization equipment and processes. * Previous manufacturing or packaging experience in a regulated industry. Physical ...

$76K - $120K/yr

... InvaGen Pharmaceuticals, Inc., a Cipla subsidiary is on the search for experienced Packaging ... Responsible for working with Systech serialization system and SAP. Reducing time spent preparing ...

Manager, Trade & Distribution

Boston, MA · On-site

$135K - $155K/yr

About Servier Pharmaceuticals Servier in the U.S. is a Boston-based, commercial-stage ... You are responsible for ensuring Right of Sale by maintaining serialization integrity, system ...

At least one year of work in a Pharmaceutical cGMP environment is required for consideration ... Serve as SME for packaging systems and serialization processes * Troubleshoot packaging and ...

... pharmaceutical companies producing high volumes of approved, widely used medicines. By combining ... Serve as the site technical expert for packaging and serialization systems, including packaging ...

... pharmaceutical companies producing high volumes of approved, widely used medicines. By combining ... Serve as the site technical expert for packaging and serialization systems, including packaging ...

... serialization systems. * Deep knowledge of cGMP, validation principles (GAMP 5 - Risk Based approach to compliant GxP design and systems), and pharmaceutical regulatory requirements. * Experience ...

... serialization systems. * Deep knowledge of cGMP, validation principles (GAMP 5 - Risk Based approach to compliant GxP design and systems), and pharmaceutical regulatory requirements. * Experience ...

Showing results 41-60

Pharmaceutical Serialization information

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$14

$19

$25

How much do pharmaceutical serialization jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for pharmaceutical serialization in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What are the main responsibilities and challenges faced in pharmaceutical serialization?

In a Pharmaceutical Serialization role, your primary responsibility is to implement and manage systems that uniquely identify and track pharmaceuticals across the supply chain, ensuring data integrity and regulatory compliance. Common challenges include keeping up with evolving global serialization requirements, integrating diverse technologies across manufacturing sites, and troubleshooting data mismatches or system errors. You’ll often collaborate with IT, quality assurance, packaging, and regulatory teams to ensure smooth operations. Success in this role relies on attention to detail, proactive problem-solving, and effective teamwork.

What are the key skills and qualifications needed to thrive in pharmaceutical serialization?

Excelling in Pharmaceutical Serialization requires knowledge of regulatory compliance, supply chain logistics, and pharmaceutical manufacturing processes, often supported by a degree in life sciences or engineering. Familiarity with serialization software platforms (such as SAP ATTP or TraceLink), barcode/RFID technologies, and regulatory standards (like DSCSA or EU FMD) is crucial. Strong attention to detail, analytical thinking, and effective cross-functional communication are valuable soft skills in this field. These competencies ensure that pharmaceutical products are accurately tracked through the supply chain, maintaining product integrity and regulatory adherence.

What is pharmaceutical serialization?

A Pharmaceutical Serialization job involves managing and implementing track-and-trace systems to ensure compliance with regulations like the Drug Supply Chain Security Act (DSCSA) or EU Falsified Medicines Directive (FMD). Professionals in this role oversee serialization processes, ensuring that each drug package is assigned a unique identifier to prevent counterfeit medications from entering the supply chain. They work with regulatory bodies, IT systems, and production teams to maintain data accuracy and integrity. This role is critical for enhancing patient safety and improving supply chain transparency.

More about Pharmaceutical Serialization jobs

What cities are hiring for Pharmaceutical Serialization jobs?

Cities with the most Pharmaceutical Serialization job openings:

What are the most commonly searched types of Pharmaceutical Serialization jobs?

The most popular types of Pharmaceutical Serialization jobs are:

What states have the most Pharmaceutical Serialization jobs?

States with the most job openings for Pharmaceutical Serialization jobs include:

Infographic showing various Pharmaceutical Serialization job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Packaging Supervisor

Artius Solutions

Fall River, MA • On-site

$72K - $93K/hr

Full-time

Re-posted 4 days ago


Job description

Job Title: Packaging Supervisor – 2nd Shift
Location: Fall River, MA
Work Authorization: Must be authorized to work in the U.S.
Duration: Full-time, Onsite
Compensation Range: *,800 – *,600 (Based on experience)
Work Schedule: Monday to Friday | 2nd Shift | Some weekends as per business needs
FLSA Classification: Exempt


Job Summary:

We are seeking a Packaging Supervisor for a leading pharmaceutical manufacturer to oversee 2nd shift packaging operations. This role ensures strict adherence to cGMP, SOPs, and FDA regulations, while leading floor activities, supporting line leaders, and driving operational excellence in a fast-paced, highly regulated environment.


Key Responsibilities:
  • Supervise packaging shift operations and support floor-level execution.

  • Ensure compliance with cGMP, safety, and cleanliness protocols.

  • Support serialization (Systech) and SAP-based operations.

  • Perform pre-checks, in-process entries, and machine inspections.

  • Coordinate with line leaders for efficiency and changeover reduction.

  • Maintain documentation and equipment logs per SOP and regulatory standards.

  • Act as a point of contact for team guidance and SOP interpretation.

  • Train team members and uphold documentation practices.

  • Perform daily checks and enforce safe work practices.

  • Participate in audits and contribute to SOP updates.


Required Qualifications:
  • Experience:

    • 3–15 years in pharmaceutical packaging (generic pharma preferred).

    • Minimum 2 years of work experience in a cGMP-regulated environment.

  • Education:

    • High School Diploma or GED (required).

    • Bachelor's in Pharmaceutical Sciences or a related field (preferred).


Technical Skills:
  • Strong knowledge of pharmaceutical packaging machinery and cGMP protocols.

  • Familiarity with serialization tools like Systech and ERP systems like SAP.

  • Proficient in Microsoft Office tools (Excel, Word).

  • Troubleshooting and compliance support capabilities.


Preferred Skills:
  • Bilingual (Spanish) a plus.

  • Strong leadership, documentation, and training skills.

  • Ability to manage audits and regulatory inspections.

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