Sr. Manager, Program Management at Thermo Fisher Scientific

Hyderabad, Telangana, India

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Medical Devices, Life Sciences, HealthcareIndustries

Requirements

Bachelor’s degree or equivalent experience in Life Sciences, Pharmacology, Engineering, or a related field; advanced degree preferred
15+ years of experience in lab, industrial, medical device and/or IVD environments
Solid understanding of medical device regulatory and compliance requirements
Demonstrated success leading complex, multi-region regulatory programs
Proven leadership experience in program or portfolio management
Excellent written, verbal, and presentation skills
Strong interpersonal skills along with effective planning, prioritization, and follow-through capabilities
Program/project management certification (e.g., PMP, PgMP, or equivalent) and/or regulatory certification such as RAC preferred
High adaptability, resilience, and facilitation skills; able to lead cross-functional teams, drive alignment, resolve conflicts, and deliver results under time pressure

Responsibilities

Establish and own the program roadmap, including scope, achievements, important metrics, risks, and dependencies across pre-launch and post-market activities
Direct program planning, prioritization, and resource coordination for Quality & Regulatory teams
Coordinate and track preparation, review, and delivery of regulatory dossiers to ensure timely, high-quality submissions
Govern post-market surveillance programs, ensuring robust tracking and reporting
Own program dashboards for regulatory data management, ensuring transparency, data integrity, and timely renewals
Coordinate program governance for document control and records management
Coordinate environmental and chemical compliance initiatives
Lead automation and digitalization projects within Regulatory & Quality
Establish and run regular program reviews (steerco, governance forums), providing clear status, risk/issue customer concern, and data-driven recommendations to senior leadership
Mentor and guide project managers and team leads within the program, building strong execution rigor, ownership of important metrics, and a culture of continuous improvement

Skills

Key technologies and capabilities for this role

Program ManagementRegulatory AffairsMedical DeviceQuality ManagementRisk ManagementPost-Market SurveillanceDocument ControlData ManagementAutomationDigitalizationSteering CommitteeGovernanceRoadmap PlanningResource CoordinationMetrics Tracking

Questions & Answers

Common questions about this position

What qualifications and experience are required for the Senior Program Manager role?

A Bachelor’s degree or equivalent in Life Sciences, Pharmacology, Engineering, or related field is required, with an advanced degree preferred; 15+ years of experience in lab, industrial, medical device and/or IVD environments; solid understanding of medical device regulatory requirements; demonstrated success leading complex multi-region programs; proven leadership in program/portfolio management; and program/project management certification like PMP or regulatory certification like RAC preferred.

What is the work arrangement or location for this position?

This is a full-time standard Monday-Friday office-based role in an office environmental condition.

What is the salary or compensation for this role?

This information is not specified in the job description.

What leadership and soft skills are needed for this position?

Excellent written, verbal, and presentation skills; strong interpersonal skills; effective planning, prioritization, and follow-through; high adaptability, resilience, and facilitation skills to lead cross-functional teams, drive alignment, resolve conflicts, and deliver under time pressure.

What makes a candidate stand out for this Senior Program Manager position?

Candidates with 15+ years in medical device/IVD environments, proven success leading complex multi-region regulatory programs, program management certifications like PMP, and the ability to mentor teams while driving continuous improvement will stand out.

Thermo Fisher Scientific

Provides life sciences products and services

About Thermo Fisher Scientific

Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.

Waltham, MassachusettsHeadquarters

1956Year Founded

$17MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Increased competition in single-use bioprocessing may impact market share.

Sale of anatomical pathology business could create a temporary product gap.

Investment in miDiagnostics may face regulatory challenges affecting returns.

Differentiation

Thermo Fisher offers a comprehensive range of life sciences products and services.

Their well-known brands include Thermo Scientific, Applied Biosystems, and Invitrogen.

They provide strong customer support and educational resources to optimize client workflows.

Upsides

Expansion of biologics production facility enhances capacity for precision biologics monitoring.

Investment in miDiagnostics aligns with demand for rapid diagnostic solutions in BioPharma.

Collaboration with Mainz Biomed positions them in the growing cancer detection market.

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