Newark, DE · On-site
$171 - $304/hr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
New
Newark, DE · On-site
$171 - $304/hr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
New
NY · On-site
$170.70 - $303.60/hr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
NY · On-site
$170.70 - $303.60/hr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
Menlo Park, CA · Hybrid
$84K - $109K/yr
Primary responsibilities include facilitating and supporting Complaint Handling/Post Market Surveillance. This individual contributes to a positive environment of accountability and performance ...
Menlo Park, CA · Hybrid
$84K - $109K/yr
Primary responsibilities include facilitating and supporting Complaint Handling/Post Market Surveillance. This individual contributes to a positive environment of accountability and performance ...
Plymouth, MN · On-site
$30 - $32/hr
The Product Surveillance Analyst supports post-market surveillance activities through the inspection, testing, and evaluation of returned medical devices. This position assists in product complaint ...
Plymouth, MN · On-site
$30 - $32/hr
The Product Surveillance Analyst supports post-market surveillance activities through the inspection, testing, and evaluation of returned medical devices. This position assists in product complaint ...
MN · On-site
$30 - $32/hr
The Product Surveillance Analyst supports post-market surveillance activities through the inspection, testing, and evaluation of returned medical devices. This position assists in product complaint ...
New
Marlborough, MA · On-site
$170K - $303K/yr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
Marlborough, MA · On-site
$170K - $303K/yr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
Marlborough, MA · On-site
$170K - $303K/yr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
Marlborough, MA · On-site
$170K - $303K/yr
This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...
$92K - $144K/yr
The Specialist owns and leads the Post Market Surveillance Review Boards (PMS RBs), presenting product performance metrics, trend summaries, and identified signals requiring follow up. Working in ...
$92K - $144K/yr
The Specialist owns and leads the Post Market Surveillance Review Boards (PMS RBs), presenting product performance metrics, trend summaries, and identified signals requiring follow up. Working in ...
Burlingame, CA · On-site
$35 - $40/hr
This role will focus on post-market surveillance (PMS), complaint investigations, and customer quality activities supporting regulated products. The ideal candidate will have experience handling ...
Burlingame, CA · On-site
$35 - $40/hr
This role will focus on post-market surveillance (PMS), complaint investigations, and customer quality activities supporting regulated products. The ideal candidate will have experience handling ...
Newark, DE · On-site
$92K - $144K/yr
The Specialist owns and leads the Post Market Surveillance Review Boards (PMS RBs), presenting product performance metrics, trend summaries, and identified signals requiring follow up. Working in ...
Newark, DE · On-site
$92K - $144K/yr
The Specialist owns and leads the Post Market Surveillance Review Boards (PMS RBs), presenting product performance metrics, trend summaries, and identified signals requiring follow up. Working in ...
... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs other duties and tasks, as needed. ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS • Lifting -- Not to ...
... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs other duties and tasks, as needed. ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS • Lifting -- Not to ...
Actively participate in FDA inspections and lead internal/corporate audits, notified body audits and applicable external certification audits including any post-audit responses. * Provide support for ...
Actively participate in FDA inspections and lead internal/corporate audits, notified body audits and applicable external certification audits including any post-audit responses. * Provide support for ...
... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs other duties and tasks, as needed. ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS Lifting -- Not to exceed 50 ...
... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs other duties and tasks, as needed. ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS Lifting -- Not to exceed 50 ...
Trumbull, CT · On-site +1
$160K/yr
The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical Device performance and Post Market Surveillance activities within the PMS team as well as the broader QA ...
Trumbull, CT · On-site +1
$160K/yr
The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical Device performance and Post Market Surveillance activities within the PMS team as well as the broader QA ...
... any post-audit responses. * Provide support for assessment of published regulatory guidance ... Standard TRAVEL: Yes, 15 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES:
... any post-audit responses. * Provide support for assessment of published regulatory guidance ... Standard TRAVEL: Yes, 15 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES:
... any post-audit responses. * Provide support for assessment of published regulatory guidance ... Standard TRAVEL: Yes, 15 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES:
... any post-audit responses. * Provide support for assessment of published regulatory guidance ... Standard TRAVEL: Yes, 15 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES:
... any post-audit responses. * Provide support for assessment of published regulatory guidance ... Standard TRAVEL: Yes, 15 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES:
... any post-audit responses. * Provide support for assessment of published regulatory guidance ... Standard TRAVEL: Yes, 15 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES:
A Day in the Life The Senior Principal Clinical Research Specialist - Post Market Surveillance and Evidence provides enterprise leadership in the strategic application of real world data (RWD) to ...
A Day in the Life The Senior Principal Clinical Research Specialist - Post Market Surveillance and Evidence provides enterprise leadership in the strategic application of real world data (RWD) to ...
A Day in the Life The Senior Principal Clinical Research Specialist - Post Market Surveillance and Evidence provides enterprise leadership in the strategic application of real world data (RWD) to ...
A Day in the Life The Senior Principal Clinical Research Specialist - Post Market Surveillance and Evidence provides enterprise leadership in the strategic application of real world data (RWD) to ...
A Day in the Life The Senior Principal Clinical Research Specialist - Post Market Surveillance and Evidence provides enterprise leadership in the strategic application of real world data (RWD) to ...
A Day in the Life The Senior Principal Clinical Research Specialist - Post Market Surveillance and Evidence provides enterprise leadership in the strategic application of real world data (RWD) to ...
$82K - $84.3K
8% of jobs
$84.3K - $86.6K
8% of jobs
$88.9K is the 25th percentile. Wages below this are outliers.
$86.6K - $89K
10% of jobs
$89K - $91.3K
10% of jobs
$91.3K - $93.6K
10% of jobs
The median wage is $95.1K / yr.
$93.6K - $95.9K
8% of jobs
$95.9K - $98.2K
10% of jobs
$98.2K - $100.5K
10% of jobs
$101.1K is the 75th percentile. Wages above this are outliers.
$100.5K - $102.9K
10% of jobs
$102.9K - $105.2K
8% of jobs
$105.2K - $107.5K
10% of jobs
$82K
$96K
$107.5K
A Post Market Surveillance (PMS) job involves monitoring the safety, performance, and compliance of medical devices or pharmaceuticals after they have been released to the market. PMS professionals collect and analyze data from customer feedback, adverse event reports, clinical studies, and regulatory sources to ensure product safety. They work closely with regulatory authorities to report findings and take corrective actions if needed. This role helps companies meet compliance requirements and improve product quality over time.
In a Post Market Surveillance role, you can expect to review and analyze data from product complaints, adverse events, and customer feedback to identify potential product issues or trends. Your daily tasks often include preparing regulatory reports, coordinating with cross-functional teams like Quality Assurance, Regulatory Affairs, and R&D, and ensuring timely communication of possible risks or recalls. The job involves a mix of hands-on data analysis, documentation, and collaboration to constantly monitor the safety and performance of products in the market. These responsibilities play a critical part in continuous product improvement and maintaining regulatory compliance.
To excel in Post Market Surveillance, you need a strong understanding of regulatory requirements, data analysis, and medical device or pharmaceutical product knowledge, often supported by a degree in science or engineering. Familiarity with quality management systems (QMS), complaint handling databases, and regulatory submission tools is typically required, alongside certifications like ISO 13485 or Six Sigma being advantageous. Excellent analytical thinking, attention to detail, and effective communication skills help professionals collaborate across departments and accurately report findings. These capabilities ensure timely identification and mitigation of product issues, safeguarding both patient safety and company compliance.
Cities with the most Post Market Surveillance job openings:
The most popular types of Post Market Surveillance jobs are:
States with the most job openings for Post Market Surveillance jobs include:
The top searched job categories for Post Market Surveillance jobs are:
$171 - $304/hr
Other
This job post has expired today. Applications are no longer accepted.
8.0
Based on 25 frontline employees who took The Breakroom Quiz
178th of 490 rated machine equipment manufacturers
Director Post Market Compliance
Marlborough, MA, United States
Newark, DE, United States
Hologic is a global leader in medical devices and diagnostics dedicated to improving lives through innovative healthcare solutions. The Director of Post Market Compliance, Corporate plays a critical role in ensuring that the company’s systems for managing product and customer concerns are effective, compliant, and continuously improving. This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain regulatory compliance and enhance product quality.
KnowledgeDeep understanding of medical device regulatory requirements and compliance standards across domestic and international markets.
Knowledge of complaint handling, post market surveillance, medical device reporting, vigilance, and field action processes.
Familiarity with FDA-regulated cGMP environments and audit requirements.
Understanding of quality management systems and electronic complaint/quality record systems.
Awareness of emerging regulatory changes and their impact on post market processes.
Strong leadership and stakeholder management skills with the ability to influence cross-functional and international teams.
Strategic and analytical thinking to translate corporate goals into actionable plans.
Project and program management capabilities to drive process improvements.
Data analysis skills using quality data management tools to identify trends and improvement opportunities.
Effective communication and reporting skills for presenting performance metrics and quality insights to senior leadership.
Demonstrating strong accountability for regulatory compliance and product quality.
Collaborative and proactive in working with multiple departments including service, IS, and international teams.
Results-driven mindset focused on continuous improvement and operational efficiency.
Strong problem-solving approach when identifying compliance gaps and implementing corrective actions.
Commitment to fostering a culture of quality and transparency across the organization.
Bachelor’s Degree in business, engineering, science, or a related discipline, or equivalent experience.
Minimum of 10 years of progressive experience in quality assurance within the medical device industry.
Proven experience managing post market processes such as complaints, vigilance, and field actions.
Demonstrated success in managing audits in FDA-regulated cGMP facilities.
Experience leading teams, managing projects, and building a strong culture of quality.
We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
The annualized base salary range for this role is $170,700 - $303,600 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
Sourced by ZipRecruiter
5,001 - 10,000 Employees
Marlborough, MA, US
1985
