Regulatory Compliance Specialist
Mindlance
Job-ID29095910Reference26-23457Remote50% Remote Experience • 3–5 years of experience in regulatory compliance, information security, and/or data privacy • Demonstrated experience working within cross-functional teams including Legal, IT, Security Operations, and Governance Core Responsibilities • Coordinate Information Security and Privacy Regulatory Requirements implementation into Policy and Control Frameworks • Coordinate and monitor across Information Security and Privacy audits (e.g, NIS2, CCPA, SWIFT and PCI) • Coordinate and/or assist with readiness reviews across Information Security and Privacy audits (e.g, NIS2, CCPA, SWIFT and PCI) • Monitor adherence to applicable regulations and internal policies; flag and escalate gaps • Support internal and external audits, compliance reviews, and security/privacy documentation reviews • Collaborate with IT teams to identify and mitigate system-level security threats and risks • Administer and maintain compliance, security, and governance program documentation Soft Skills & Competencies • Excellent written and verbal communication skills, with the ability to present compliance issues to both technical and non-technical stakeholders • Strong analytical and critical thinking skills • Ability to manage multiple priorities and deadlines in a fast-paced environment • High attention to detail with a strong ethical compass • Collaborative team player who can work independently when needed EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”
$30 - $35 per hour
...Regulatory Affairs Associate/Specialist/Data Analyst I Client Industry: Pharmaceutical/Medical Device/Biotechnology; Job Title: Regulatory Affairs... ...Regulatory Submission Coordinator Regulatory Compliance Analyst Quality Compliance Specialist with health authority...SuggestedHourly payContract workTemporary workRemote workRelocation- ICU Medical seeks a Regulatory Operations Specialist to provide regulatory support for global and US electronic publishing and submissions of medical... ..., tracking deliverables, and ensuring full regulatory compliance. You will collaborate with Global Regulatory Leaders and...Suggested
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- ...Regulatory Affairs AssociateLocation: Lake Forest, ILDuration: 12 MonthsPay Rate: $33-$35 on W2 per hour.Position SummaryProvides regulatory... ...of global registration dossiers. Assures full regulatory compliance of all documentation for submissions and change management.Essential...SuggestedHourly pay
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...SUMMARY: The Compliance Officer is responsible for administering and improving all aspects of the credit union's compliance management... ...FUNCTIONS: Ensures compliance with all state and federal regulatory requirements including, but not limited to, Anti-Money...Local area$67.5k - $96.75k
Position Summary Provides regulatory support and expertise associated with global and US electronic publishing and submission of medical... ...of global registration dossiers. Assures full regulatory compliance of all documentation for submissions and change management. Essential...- ...and support functions at the manufacturing facility operate in compliance with all applicable regulations and standards.... ...operations within the facility. Provides support with company and regulatory agency (i.e. DEA, FDA) inspections. Follow up on audits to assure...Temporary workWork experience placement
$68k - $136k
...instruments, providing lab results for millions of people. The Regulatory Affairs Specialist II is responsible for implementing and maintaining the... ..., implements, and maintains the quality policy. Ensures compliance and is able to demonstrate knowledge of site and division...Work experience placementWorldwide- Abbott in Lake Forest, IL is seeking a Regulatory Affairs Specialist II to implement and maintain the quality system and support change control in manufacturing/operations. You will prepare U.S. regulatory submissions and coordinate with international affiliates to secure...
$61.3k - $122.7k
...female executives, and scientists. The Opportunity The Regulatory Affairs Specialist II (Medical Events) position supports the Infectious Disease... ...’s products. You will be accountable for ensuring compliance with Medical Device Reporting regulations (including 21 CFR...Worldwide$97.5k - $139.75k
Position Summary Provides regulatory support and expertise associated with global and US registration of medical device products, including... ...of global registration dossiers. Assures full regulatory compliance of all documentation for submissions and change management. Essential...Work at officeLocal area- Planet Pharma is seeking a Regulatory Information Management support professional in Illinois. The role focuses on regional regulatory submissions, system-based data stewardship, and ensuring alignment with central data standards. Fresh graduates with relevant life sciences...
- ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations for medical devices. The role involves... ...planning registration packages, liaising with agencies, and ensuring compliance across changes and submissions. Candidates should have strong...
- ICU Medical is seeking a regulatory professional to support global and US electronic publishing and submission of medical devices. You will help structure submissions, organize packages, and track deliverables under supervision, ensuring compliant documentation and change...
$30 - $35 per hour
...Search Jobs # Job Description Quality Assurance Compliance Specialist Contract: North chicago, Illinois, US Salary Range:... .... This role is responsible for ensuring compliance with regulatory requirements, quality standards, and internal procedures across...Hourly payContract workTemporary work- Spectraforce Technologies in North Chicago, IL is seeking a Regulatory Information Management Contractor to monitor COSMOS activity, ensure data completeness, and maintain regulatory records for assigned products. You will follow data standards for RIM objects, create...For contractors
- Abbott, a global healthcare leader, seeks a Regulatory Affairs Specialist II (Medical Events) in Lake Forest, IL on site. You will review and submit... ...Device Reports (MDRs) and vigilance reports, ensuring compliance with 21 CFR 803 and related regulations. You will work...
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- ...Regulatory Affairs Specialist Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Authoring and submitting PMA supplements (30-day Notice, Real-Time...
$42 - $44 per hour
Randstad is seeking a Compliance Specialist for our global biopharmaceutical in Mettawa, IL. Location: Mettawa, IL 60045 Pay Rate... ...improvement projects that balance business agility with strict regulatory controls. Provide expert advisory: Serve as the main...Hourly payPermanent employmentContract workTemporary workWork experience placementLocal areaHome officeShift work- ...Compliance Specialist Randstad is seeking a Compliance Specialist for our global biopharmaceutical in Mettawa, IL. Location: Mettawa, IL 60045 Pay Rate: $42.00 – $44.00 per hour Contract Duration: 1 Year, possible extension Qualifications Must-haves: Education & Experience...Hourly payContract work
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- ...Position Title: Compliance Analyst Length of Contract: 1 year (Potential Extension) Location/Site: North Chicago, IL (Hybrid module) Minimal... ...to compliance. Prior pharma experience a plus PURPOSE: The Specialist, Commercial Compliance will meaningfully contribute to the US...Contract workWork experience placementRemote workHome office
$66 - $72 per hour
Job Title: Regulatory Affairs Associate I Job Description The Regulatory Affairs Associate I plays a key role in driving process excellence... ...issue records to Exception Reports when warranted by risk, compliance impact, or process significance. Project manage Exception...Contract workTemporary workWork at officeRemote work$65 - $70 per hour
...Pharmacology, or a related field. 5+ years of experience within Regulatory Affairs, pharmaceutical, biotechnology, medical device,... ...deviations, investigations, exception reporting, or comparable compliance workflows . Experience performing or supporting root cause analysis...
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