ZipRecruiter

Log In

2

Full Time Pharmaceutical Serialization Jobs (NOW HIRING)

Infosys

SAP ATTP Consultant

Raleigh, NC · On-site

$61.25 - $83.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... full-time Infosys employee you are also eligible for the following benefits: * Medical/Dental ... global pharmaceutical serialization and reporting regulations. • Lead SIT, UAT, deployment ...

Infosys

SAP EWM Consultant

Foster City, CA · On-site

$73.50 - $100.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... full-time Infosys employee you are also eligible for the following benefits: * Medical/Dental ... Pharmaceutical Serialization regulatory knowledge is a plus. • Proven track record of leading ...

Artius Solutions

Packaging Supervisor

Fall River, MA · On-site

$72K - $93K/hr

S. Duration: Full-time, Onsite Compensation Range: *,800 - *,600 (Based on experience) Work ... of pharmaceutical packaging machinery and cGMP protocols. * Familiarity with serialization tools ...

Tjoapack

Packaging Engineer

Clinton, TN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Clinton, TN | Full-time ???? Vacancies: 1 About Tjoapack Tjoapack is a global contract packaging ... At least one year of work in a Pharmaceutical cGMP environment is required for consideration.

Keysource Acquisition

EDI Manager

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

With over 30 years of experience, we are a Fast 55 award-winning, industry-leading pharmaceutical ... In this role, you will be responsible for leading EDI and DSCSA technical teams managing full time ...

Shionogi Inc.

Supply Chain Coordinator

Florham Park, NJ

$70K - $90K/yr

... pharmaceutical products, components, and materials across global sites and partners. This role ... Support serialization activities by coordinating with 3PL providers, packaging partners, and ...

Hatteras

Senior Manager - Fulfillment Center

Tinton Falls, NJ · On-site

$115K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Job Type Full-time Description SUMMARY The Senior Manager, Fulfillment Center holds operational and ... pharmaceutical traceability and serialization, cosmetic GMP practices, client audits, and hazardous ...

Shionogi Inc.

Supply Chain Coordinator

Florham Park, NJ · On-site

$70K - $90K/yr

... pharmaceutical products, components, and materials across global sites and partners. This role ... Support serialization activities by coordinating with 3PL providers, packaging partners, and ...

Tjoapack

Validation Writer

Clinton, TN · On-site

Clinton, TN | Full-time | Onsite ???? Department: Technical Services About Tjoapack Tjoapack is a ... One year of prior experience in a Pharmaceutical cGMP environment is required for consideration.

Tjoapack

Validation Writer

Clinton, TN · On-site

Clinton, TN | Full-time | Onsite ???? Department: Technical Services About Tjoapack Tjoapack is a ... One year of prior experience in a Pharmaceutical cGMP environment is required for consideration.

Aequor

Manufacturing Supervisor | Metered-Dose Inhaler Onsite in Fall River, MA Full-Time The Production ... Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study ...

New

All JobsPharmaceutical Serialization JobsFull Time Pharmaceutical Serialization Jobs

Full Time Pharmaceutical Serialization information

What are the key skills and qualifications needed to thrive in a full time pharmaceutical serialization role?

To succeed in a Full-Time Pharmaceutical Serialization role, you need a solid understanding of pharmaceutical supply chain regulations, serialization processes, and a background in life sciences or engineering. Familiarity with serialization software (such as SAP ATTP or TraceLink), barcode systems, and compliance standards like DSCSA or EU FMD is typically required. Strong attention to detail, problem-solving abilities, and effective communication help ensure accurate data management and cross-functional collaboration. These skills are vital for maintaining regulatory compliance, product traceability, and the integrity of the pharmaceutical supply chain.

What are some common challenges faced in a full time pharmaceutical serialization role, and how can they be addressed?

Professionals in full-time pharmaceutical serialization roles often encounter challenges such as integrating serialization technology with existing manufacturing systems, ensuring data accuracy across global supply chains, and keeping up with evolving regulatory requirements. Addressing these challenges requires strong collaboration with IT, quality assurance, and supply chain teams, as well as ongoing training to stay updated on compliance standards. Proactive communication and meticulous attention to detail are key to minimizing errors and ensuring successful implementation and maintenance of serialization solutions.

What is pharmaceutical serialization?

Pharmaceutical serialization is the process of assigning unique identifiers, such as serial numbers, to each saleable unit of a pharmaceutical product. This system is designed to track and trace drugs throughout the supply chain, helping to combat counterfeit medicines and ensure regulatory compliance. Serialization allows manufacturers, wholesalers, and pharmacists to verify the authenticity of products, improve inventory management, and enhance patient safety. Full time pharmaceutical serialization professionals are responsible for implementing and maintaining these systems within pharmaceutical companies.
More about Full Time Pharmaceutical Serialization jobs

What cities are hiring for Full Time Pharmaceutical Serialization jobs?

Cities with the most Full Time 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 job categories do people searching Full Time Pharmaceutical Serialization jobs look for?

The top searched job categories for Full Time Pharmaceutical Serialization jobs are:

Full Time Pharmaceutical Serialization jobs near you
Infographic showing various Full Time 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.

Senior Manager, Supply Chain

Revolution Medicines

Redwood City, CA • On-site

Full-time

Posted 10 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
Commercial Supplies Packaging Management.
  • Serve as the primary technical point of contact for external contract packaging organizations and packaging component suppliers.
  • Provide technical support for routine commercial packaging operations at external Contract Manufacturing Organizations (CMOs), including management of deviations, complaints, and investigations related to packaging, labeling, and logistics.
  • Drive timely issue resolution to ensure product quality, regulatory compliance, and continuity of supply.
  • Partner closely with Quality, Manufacturing, and external partners to ensure uninterrupted commercial supply.
  • Support department leadership with resource planning and financial reporting activities.
  • Initiate, review and approve internal and CMO specifications for primary, secondary, and tertiary packaging components used for commercial products.
  • Author and maintain Bills of Materials (BOMs) and packaging process instructions for new and existing products.
  • Collaborate with Technical Development to provide input on manufacturability, scalability, and packaging design for Revolution Medicine products.
  • Lead or support technology transfer activities for packaging processes from development to commercial manufacturing.
  • Participate in or lead packaging process validation activities for solid dose products across global manufacturing networks.
  • Maintain awareness of and ensure compliance with cGMP, regulatory, and internal quality requirements applicable to global pharmaceutical packaging operations.
  • Provide all packaging-related support to enable new product launches.
  • Support regulatory submissions, inspections, and responses related to packaging and labeling and serialization activities, as needed.
  • Ensure all supplies are controlled and distributed in accordance with GMP, GCP, and GDP.
  • Develop, maintain and enforce department's business processes and/or SOPs.
  • Identify and implement process improvements to increase efficiency, reduce costs, and minimize waste.

Required Experience, Skills, and Education:
  • B.S. or M.S. in, Mechanical or Packaging Engineering, or related field with 8+ years of experience in pharmaceutical logistics and inventory management.
  • Strong knowledge of cGMPs, pharmaceutical manufacturing principles, and global packaging standards.
  • Technical proficiency, independent thinking, teamwork and collaboration, including driving continuous improvement.
  • Demonstrated experience with primary, secondary and tertiary packaging for solid dose products
  • Experience supporting new product introductions, technology transfers, and commercial launches in major global markets.
  • Proven experience working with and managing external contract packaging organizations.
  • Experience managing complex, cross functional projects across multiple regions and time zones.
  • Knowledge of distribution and cold chain shipping requirements for pharmaceutical products; experience with shipping qualifications and transportation studies is a plus.
  • Financial acumen related to budgeting, forecasting, and cost optimization.
  • Working knowledge of statistical methods and software to support packaging process optimization and troubleshooting.
  • Working knowledge of pharmaceutical commercial manufacturing, regulatory, and quality assurance.
  • Solid project management, facilitation, and problem-solving skills.
  • Solid organizational and time management skills.
  • Strong communicator and connector between Commercial, Finance, Quality, Regulatory and Supply Chain teams.
  • Effective, open, and transparent communication skills (verbal and written).
  • Capable of working on multiple projects/tasks and able to meet timelines.
  • Self-starter with a high level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results.
  • A team-oriented, progressive thinker who enjoys participating in an innovative and creative work environment.

Preferred Skills, Experience and Education:
  • Familiarity with pharmaceutical serialization requirements, including DSCSA and EU Falsified Medicines Directive (FMD).

#LI-CT1 #LIHybrid
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$164,000-$205,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

Apply