EDUCATION:

• Bachelor’s degree in Life Sciences. HLA, Molecular and/or Antibody experience a plus
• An MS or MBA is a plus

EXPERIENCE:

• A minimum of 3 years’ experience in the medical device manufacturing industry, with a strong grasp of Quality and Regulatory standards
• A minimum of 3 years’ project management experience
• Experience developing RUO and IVD assays and reagents, including clinical study performance is preferred
• Experience managing programs with clinical components is preferred
• PMP certification highly desirable
• Six Sigma certification highly desirable

KNOWLEDGE, SKILLS & ABILITIES:

• Demonstrated excellence of project management skills, consistently achieving timeline adherence, deliverable tracking, and proactive risk management.
• Proficiency in handling complex issues and adapting to a changing, cross-functional environment to support business needs.
• Exceptional communication, presentation, and interpersonal abilities.
• Strong attention to detail, commitment to quality, and a track record of contributing to a healthy workplace culture through practical examples.
• Skilled in collaboration and conflict resolution.

Please refer the Job description for details