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Pharmaceutical Serialization Jobs in California (NOW HIRING)

Kaav Inc

SAP Project Manager-CA

La Verne, CA · On-site

... client in the pharmaceutical manufacturing domain. The ideal candidate will have extensive ... Nice to Have: * Experience with Pharma serialization, SAP ATTP , or other compliance-related ...

Grifols

Packaging Technician I/II 1st Shift

Clayton, CA · On-site

$18.25 - $22.25/hr

Qualified to set up and operate Packaging equipment (e.g. serialization equipment , vial labelers ... pharmaceutical or biotech environment. Work is performed in a manufacturing environment with ...

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Pharmaceutical Serialization information

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How much do pharmaceutical serialization jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for pharmaceutical serialization in California is $19.52, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $21.59 per hour, depending on experience, location, and employer.

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.

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 are the most commonly searched types of Pharmaceutical Serialization jobs in California?

The most popular types of Pharmaceutical Serialization jobs in California are:

What are popular job titles related to Pharmaceutical Serialization jobs in California?

For Pharmaceutical Serialization jobs in California, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Serialization jobs in California look for?

The top searched job categories for Pharmaceutical Serialization jobs in California are:

What cities in California are hiring for Pharmaceutical Serialization jobs?

Cities in California with the most Pharmaceutical Serialization job openings:

Pharmaceutical Serialization jobs near you
Infographic showing various Pharmaceutical Serialization job openings in California as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $40,600 per year, or $19.5 per hour.

SAP Project Manager-CA

Kaav Inc

La Verne, CA • On-site

Contractor

Re-posted 26 days ago

Job description

Job Title: SAP Project Manager

Location: La Verne, CA (ZIP: 91750)
Start Date: Immediate
Type: Contract
Work Mode: Onsite (Local candidates only)

Job Description:

We are seeking an experienced SAP S/4HANA Upgrade Project Manager to lead a high-impact SAP upgrade project for our client in the pharmaceutical manufacturing domain. The ideal candidate will have extensive experience in SAP S/4HANA upgrade projects, preferably in regulated industries like pharma, ensuring compliance with GxP, FDA, and other regulatory standards.

Key Responsibilities:

  • Lead and manage SAP S/4HANA upgrade projects from planning to go-live and post-implementation support.
  • Develop and maintain detailed project plans, schedules, budgets, and resource allocation for SAP upgrade initiatives.
  • Coordinate with cross-functional teams (IT, QA, Manufacturing, Supply Chain, Finance) to ensure seamless integration and compliance.
  • Drive risk management, change control, and issue resolution for upgrade projects.
  • Ensure all project deliverables meet regulatory and quality requirements, including GxP compliance and validation protocols.
  • Communicate project progress, risks, and mitigation plans to executive stakeholders.
  • Collaborate with vendors and system integrators for technical upgrade execution.
  • Oversee test planning, execution, and validation documentation in line with FDA and GMP regulations.

Required Skills & Experience:

  • 10+ years of experience as an SAP Project Manager, with specific focus on SAP S/4HANA upgrades.
  • Proven track record of managing at least 5 SAP upgrade projects in pharmaceutical manufacturing environments.
  • Strong understanding of GxP, FDA validation, and CSV (Computer System Validation) processes.
  • Experience in SAP modules relevant to manufacturing and supply chain (PP, MM, WM, QM).
  • Excellent knowledge of project management methodologies (Waterfall, Agile/Hybrid) and tools (MS Project, Jira).
  • Exceptional stakeholder communication, team leadership, and vendor management skills.
  • Ability to manage budget, scope, and timelines under strict compliance standards.
  • PMP or equivalent Project Management certification is highly desirable.

Nice to Have:

  • Experience with Pharma serialization, SAP ATTP, or other compliance-related modules.
  • Familiarity with 21 CFR Part 11 compliance and electronic records/e-signature requirements.