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Serialization Manager Jobs in Missouri (NOW HIRING)

Jobgether

This position is listed on behalf of a partner company, who manages all applications and next steps ... Knowledge of Protobuf or comparable schema definition and data serialization technologies.

CMMG

Suppressor Production / Warehouse Associate

Boonville, MO · On-site

$13 - $15.25/hr

Follow serialization and component traceability procedures. Packaging Operations * Package finished ... Good organizational and time management skills. Required Qualifications * Ability to read, write ...

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Serialization Manager information

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 to products to ensure traceability and prevent counterfeiting. This role involves implementing serialization systems, managing compliance with regulations, and coordinating with manufacturing and quality teams. Knowledge of serialization software, industry standards, and regulatory requirements is essential.

What is the highest paid job in logistics?

In logistics, executive roles such as Supply Chain Director or Logistics Vice President tend to be the highest paid, often earning six-figure salaries. These positions require extensive experience, strategic planning skills, and often involve overseeing large teams and complex operations.

What is the highest paid job in pharmacy?

In pharmacy, the highest paid roles are often pharmacy directors or chief pharmacy officers, who oversee pharmacy operations and strategy in healthcare organizations. These positions typically require advanced degrees, extensive experience, and leadership skills, and they can earn salaries exceeding $150,000 annually depending on the organization and location.

What jobs pay 2000 a day?

High-paying roles such as Serialization Managers, specialized consultants, or senior executives can earn around $2,000 per day, especially in industries like manufacturing, technology, or finance. These positions often require extensive experience, advanced skills, and sometimes certifications, and may involve project management or leadership responsibilities.

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 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.
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What cities in Missouri are hiring for Serialization Manager jobs? Cities in Missouri with the most Serialization Manager job openings:
Serialization Manager jobs near you

Manager, Packaging Operations

kindeva

Saint Louis, MO

Other

Posted 21 hours ago

Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Operations Packaging Manager is directly responsible for the safe, compliant, and efficient execution of packaging operations for parenteral drug products and combination products within a contract development and manufacturing organization (CDMO) environment at Kindeva’s Maryland Heights location. This role provides leadership and oversight for packaging operations supporting auto-injector assembly, labeling, cartoning, and final packaging, as well as packaging operations for vials, cartridges, and prefilled syringe products intended for commercial and clinical distribution.

The Packaging Manager is responsible for leading a unionized manufacturing workforce and front-line supervisors to ensure all packaging activities are executed in compliance with current Good Manufacturing Practices (cGMP), internal quality systems, customer requirements, and domestic and international regulatory requirements. The role is accountable for delivering production plans safely, efficiently, and on schedule while meeting quality, labor, and material utilization targets.

Responsibilities

  • Lead and own all packaging operations for sterile injectable and combination products, serving as Subject Matter Expert during audits and regulatory inspections.
  • Ensure all packaging operations are executed in compliance with cGMP requirements, data integrity standards, internal procedures, and customer and regulatory requirements.
  • Partner with Quality and Regulatory teams to support audits, inspections, investigations, deviations, CAPAs, and change control activities.
  • Build and lead a high-performance team by coaching and developing supervisors and unionized personnel, establishing clear expectations, and driving accountability for safety, quality, compliance, productivity, and operational objectives.
  • Ensure packaging operations are appropriately staffed and scheduled to meet production demands while partnering with Inspection and upstream operations to maintain coordinated product flow and minimize disruptions.
  • Drive continuous improvement using operational excellence and structured problem-solving to enhance reliability, efficiency, and throughput.
  • Partner cross-functionally with Engineering, Validation, Maintenance, and Technical Services to support implementation, qualification, optimization, and performance of packaging systems.
  • Support new customer onboarding, technology transfers, and implementation of new packaging capabilities required to support future business growth and evolving customer requirements.
  • Ensure packaging areas maintain inspection readiness and meet safety, housekeeping, and environmental requirements.
  • Ensure all employees are appropriately trained and qualified for assigned responsibilities and that training documentation is maintained in accordance with organizational and regulatory requirements.
  • Maintain effective working relationships with union representatives and ensure compliance with collective bargaining agreements and company policies.
  • Communicate effectively with internal stakeholders, site leadership, customers, and regulatory agencies as required.

Qualifications

  • Bachelor’s degree in a relevant technical field or scientific field
  • 7+ years of manufacturing experience in pharmaceutical, biotech, medical device, or combination product manufacturing environments.
  • Demonstrated knowledge of current Good Manufacturing Practices (cGMP), data integrity requirements, and applicable domestic and international regulatory requirements governing pharmaceutical and combination product manufacturing.
  • Proven leadership experience in manufacturing environments, including development of supervisors and frontline personnel; union manufacturing experience preferred.
  • Experience supporting automated packaging systems, labeling, cartoning, serialization, packaging line integration, equipment implementation, qualification, startup, and technology transfer activities preferred.
  • Proven ability to drive operational excellence, continuous improvement, and cross-functional collaboration in a fast-paced Contract Development and Manufacturing Organization (CDMO) environment.
  • Strong leadership, communication, organizational, and problem-solving skills with the ability to manage multiple priorities, drive accountability, and effectively interact with customers, regulators, and all levels of the organization. 
  • Demonstrated ability to analyze production data and operational metrics to drive performance, troubleshoot issues, and support continuous improvement initiatives.

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