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Director of Product Security — Medical Devices (Remote) (Houston)

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🛡️ Verified Career Listing Directly reviewed and cross-referenced with hiring sources.

LivaNova PLC

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🎓 Pharma
📍 Glenshire, Houston
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LivaNova PLC in Houston, TX is seeking a Director of Product Security to drive the strategic vision for the company's product security program. This key leader will manage a dedicated team to ensure the cybersecurity posture of medical devices throughout their lifecycle, from design to post-market surveillance. The ideal candidate has over 15 years of experience in the medical device sector, with significant expertise in cybersecurity. This role offers a competitive salary of $185,000 – $225,00...

Job Overview

Particulars Details
Position Director of Product Security — Medical Devices (Remote) (Houston)
Company LivaNova PLC
Location Glenshire, Houston
Job Type
Category / Department Pharma
Application Mode Online

🏢 About LivaNova PLC

A leading organization in its sector, LivaNova PLC is dedicated to providing innovative solutions and delivering exceptional value. We foster an inclusive, collaborative culture that empowers our employees to learn, grow, and make a significant impact.
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Office Location
Corporate Headquarters, Glenshire, Houston

💡 Editor's Note / Preparation Tip

For the Director of Product Security — Medical Devices (Remote) (Houston) role, candidates should review core concepts of Software Development. Be prepared to discuss past projects where you successfully demonstrated these skills and overcame technical or procedural hurdles.

📝 Job Description

We are seeking a qualified and motivated Director of Product Security — Medical Devices (Remote) (Houston) to join our team at LivaNova PLC. This position is located in Glenshire, Houston.


Job Overview


LivaNova PLC in Houston, TX is seeking a Director of Product Security to drive the strategic vision for the company's product security program. This key leader will manage a dedicated team to ensure the cybersecurity posture of medical devices throughout their lifecycle, from design to post-market surveillance. The ideal candidate has over 15 years of experience in the medical device sector, with significant expertise in cybersecurity. This role offers a competitive salary of $185,000 – $225,00...


Key Responsibilities



  • Design, write, and maintain clean and scalable code
  • Debug and resolve application issues
  • Participate in code reviews and team meetings
  • Collaborate with designers and product managers.


Required Skills & Qualifications



  • Software Development
  • Programming (C# / Java / JS)
  • Database Management
  • Problem Solving
  • Version Control (Git)


About the Company


A leading organization in its sector, LivaNova PLC is dedicated to providing innovative solutions and delivering exceptional value. We foster an inclusive, collaborative culture that empowers our employees to learn, grow, and make a significant impact.


To learn more or apply, click on the official application link.

🎯 Key Responsibilities

  • Design, write, and maintain clean and scalable code; Debug and resolve application issues; Participate in code reviews and team meetings; Collaborate with designers and product managers.

💡 Required Qualifications & Skills

Software Development, Programming (C# / Java / JS), Database Management, Problem Solving, Version Control (Git)
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🚀 Career Guidance & Interview Insights

To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.

This Director of Product Security — Medical Devices (Remote) (Houston) role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.

Expected Career Progression Roadmap:

Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.

Expected Technical & Behavioral Questions:

  • Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
    Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles.
  • Q2: What steps do you take when a quality deviation is detected in a product batch?
    Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action).
  • Q3: How do you manage safety protocols while handling toxic chemicals?
    Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
💡 Pro-Tip: Before your interview, research the company's recent news, product launches, and Glassdoor work reviews. Prepare 2-3 thoughtful questions for the interviewer regarding team dynamics and success metrics for this role.

To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:

  • Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
  • Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
  • Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated Market Compensation in India:

Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.

Suggested Professional Certifications:

Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.

Frequently Asked Questions

Q: What is the primary work setting?
A: The position is based in Glenshire, Houston. Please check the job link to confirm remote or hybrid possibilities.

Q: What are the key skills required?
A: Important skills for this position are: Software Development, Programming (C# / Java / JS), Database Management, Problem Solving, Version Control (Git).

Q: How can I apply for this position?
A: Use the provided Job Link to submit your application directly to the employer or recruiter platform.

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