Product Executive
1 month ago
Job Responsibilities
Design, develop, and manage pack inserts, labels, and product packaging artwork, ensuring alignment with regulatory guidelines (e.g., IVDR, ISO standards).
Collaborate with the regulatory and quality teams to ensure all packaging and labeling meet compliance requirements.
Coordinate with external vendors, printers, and designers to produce high-quality, compliant materials.
Coordinate the execution of clinical validation activities across departments, acting as the point of contact for R&D, Quality, and production teams.
Track progress through each stage of validation, from planning to execution, ensuring adherence to timelines and high standards.
Facilitate communication and information flow between departments, identifying and mitigating potential roadblocks.
Develop and maintain project timelines for packaging and validation, ensuring deadlines are met.
Implement tracking tools and reports to provide visibility into the progress of clinical validation projects.
Provide logistical and administrative support (in terms of coordination only) to the R&D team for validation studies.
Qualifications:
Education : Master’s or PhD degree in Life Sciences, Project Management, or a related field.
Experience : 3+ years of experience in product labeling, artwork management (technical aspects), and/or project coordination in a healthcare, pharmaceutical, or medical device setting.
Skills :
Strong organizational and project management skills.
Familiarity with regulatory requirements related to packaging and labeling in the medical industry.
Excellent communication and interpersonal skills for cross-departmental collaboration.
Detail-oriented with a proactive approach to managing multiple projects simultaneously.
Additional Requirements :
Ability to work effectively under tight deadlines.
Experience coordinating clinical or scientific projects is preferred.
Willingness to adapt to fast-paced environments and navigate challenges in cross-functional collaboration.
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