Inteldot

Packaging Technical Specialist


PayCompetitive
LocationNew Albany/Ohio
Employment typeFull-Time
  • Job Description

      Req#: ef6f6e575a63

      Inteldot has over 14 years in the life sciences industry with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in the USA.

      Employment Type: Contract / Full-Time

      Shift: Administrative (8:00AM - 5:00PM) unless the project demands.

      Job Description

      We are looking for a highly skilled Technical Packaging Specialist to play a pivotal role in ensuring the efficient, safe, and compliant packaging of biotechnology and pharmaceutical products at New Albany, Ohio. In this position, you will provide technical expertise and support to optimize packaging processes, equipment, and systems, ensuring alignment with regulatory standards and operational objectives. As part of a cross-functional team, you will collaborate closely with engineering, quality assurance, and production to uphold product quality and continuously improve packaging operations.

      Functions

      • Responsible for executing packaging design, validation, and implementation activities in alignment with client engineering standards, project scope, and regulatory requirements.
      • Hands-on technical expertise in packaging systems ensuring that all packaging-related deliverables meet quality, safety, and compliance expectations throughout the project lifecycle.
      • Coordination experience, and the ability to interface effectively with engineering, quality, and operations teams.

      Requirements

      • Bachelor's degree in engineering, Computer Science, Life Sciences, or related field
      • Experience: 5+ years of experience in packaging design, validation, or equipment integration, preferably within pharmaceutical, biotechnology, or life sciences industries.
      • Proven experience with packaging systems, machinery, and process optimization in a manufacturing setting.
      • Familiarity with cGMP, validation protocols (DQ, IQ, OQ, PQ), and FDA regulations.
      • Experience with AutoCAD, SolidWorks, or equivalent CAD software, Office 365
      • Proficiency in e-Builder, MS Project, or other project management tools preferred.
      • Strong project management and communication skills
      • Bilingual (English/Spanish)

      Important Note

      This is an onsite role based in Ohio.
      No travel, relocation, visa sponsorship, or work permit support will be provided by the client.

  • About the company

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