Staff Program Manager at Thermo Fisher Scientific
Fishers, IN 46037, USA -
Full Time


Start Date

Immediate

Expiry Date

25 Aug, 25

Salary

0.0

Posted On

20 Aug, 25

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Biotechnology, Life Sciences, Accountability, Communication Skills

Industry

Pharmaceuticals

Description

POSITION SUMMARY

The Staff Program Manager will be a pivotal contributor in advancing our strategic initiatives within the services business segment. This role involves leading programs that support our laboratory services, facilitating the development of diagnostic assays, overseeing the build of laboratory data infrastructure, and leading strategic partnership activities. To be successful, this high-visibility position demands effective leadership over multiple tasks and teams, requiring a candidate with a collaborative attitude, focus on deliverables, and excellent interpersonal skills. Moreover, this role requires a blend of proficiency in medical diagnostics, program management acumen, and the ability to cultivate strong industry relationships.

EDUCATION AND EXPERIENCE

  • Bachelor’s degree in the life sciences, biotechnology, or related clinical diagnostics field with minimum 4 years work experience. Advanced degree in scientific/technical field preferred.
  • Minimum 4 years demonstrated experience in project management.
  • PMP certification a plus.

KNOWLEDGE, SKILLS AND ABILITIES

  • Proven ability to influence and drive accountability across a matrixed organization.
  • Strong interpersonal and influencing skills.
  • Outstanding written and verbal communication skills: assertively and effectively articulates sophisticated concepts and ideas to broad audiences.
  • Excellent problem-solving skills.
  • Self-managing and self-motivating, capable of prioritizing tasks optimally to meet deadlines and expectations. Is curious, innovative, and never satisfied with the status quo. Possesses a proactive, helpful, ‘can-do’ attitude.

How To Apply:

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Responsibilities
  • Lead core teams and conduct regular project meetings (including capturing meeting minutes and assigning action owners), supervise assigned deliverables, develop timelines, and provide project updates and reports to senior leadership.
  • Guide the development, validation, translation, and implementation of assays, aligning them with market needs, regulatory guidelines, and customer requirements.
  • Work closely with the clinical laboratory, R&D, sales, marketing, regulatory affairs, and external partners to define project deliverables. Identify potential risks and issues, along with developing effective mitigation strategies. Proactively address challenges to maintain compliance, product quality, and project execution.
  • Maintain clear communication lines with all team members, providing regular updates on project status and achievements, and resolving barriers to execution to ensure projects are completed on time according to quality standards and within the applicable scope and budget.
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