GxP Compliance Specialist I - R&D & Regulatory Impact
BioSpace, Inc.
BioSpace in North Chicago is looking for a candidate to ensure GxP compliance with AbbVie policies and global regulations. The role requires managing compliance initiatives and working effectively within team environments. A Bachelor’s degree in a scientific field is required, along with significant related industry experience. The candidate should excel in interpersonal and problem-solving skills and be capable of meeting compliance needs efficiently. #J-18808-Ljbffr BioSpace, Inc.
- ...and affiliates. The person will ensure compliance to the quality system as it pertains to... ...Evaluate Change Notifications to determine impacted materials and manufacturing sites using... .../Trackwise experience. Experience in a Regulatory Pharmaceutical Industry. #LI-KH1 #J-1...Regulatory
- ...leading medical device company in Vernon Hills is seeking a Sr. R&D Engineer to lead the development of innovative medical... ...responsible for designing and testing new products while ensuring compliance with regulatory standards. The ideal candidate has at least 6 years of...Regulatory
- ...A leading distributor of shipping materials is seeking an International Trade Compliance Specialist in Waukegan, IL. This role involves tackling regulatory hurdles and managing trade compliance programs while supporting the global economy. Candidates should hold a Bachelor...Regulatory
- ...Responsibilities The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product... ...registrations and ensuring regulatory compliance in the design, manufacturing, and... ...business understands relevant impacts Lead corrective and preventive action...Regulatory
$29 - $32.29 per hour
job summary: Ready to elevate your regulatory career? This opportunity allows you to take... ...variations, directly influencing global compliance and product lifecycles. Based out of a... ...experience specifically in Regulatory Affairs, R&D, or Manufacturing (focused on CTD Module...RegulatoryHourly payContract workTemporary workWork experience placementRemote work$80.9k - $127.05k
...What Regulatory Affairs contributes to Cardinal Health Regulatory... ...Principal Regulatory Affairs Specialist will support the Medical Solutions... ...Review product labeling for compliance with global labeling... ...medical devices and advise on impact of such regulations to the business...RegulatoryTemporary workWork experience placementWork at officeLocal areaFlexible hours- ...Senior International Trade Compliance Specialist Corporate Headquarters 12575 Uline Drive, Pleasant Prairie, WI 53158 Interested in... ...Senior International Trade Compliance Specialist, you’ll tackle regulatory hurdles, find tariff savings and bring Uline’s high quality...Regulatory
$97.5k - $139.75k
...Regulatory Affairs Specialist Provides regulatory support and expertise associated with global and US... ...registration dossiers. Assures full regulatory compliance of all documentation for submissions... ...and labeling changes for regulatory impact. Accurately describes these changes...RegulatoryFull timeWork at officeLocal area- ...challenges of tomorrow. It impacts people’s lives across... ...quality management, compliance with corporate policies... ...quality interface across R&D, influencing quality... ...GCP quality assurance, regulatory affairs, clinical development... ...among other RDQA GXP functions and business...RegulatoryLocal area
- ...PPE services 48 states. Job Description Job Summary: The Compliance Assurance Specialist will be responsible for the obtaining and maintaining of... ...Correcting any non-compliance notices cited by the regulatory agencies (5-10% of position) Researching codes and requirements...Regulatory
- ...North Chicago is seeking a Quality Assurance Specialist to monitor Supplier Change Notifications and ensure compliance with quality systems. The ideal candidate should... ...Engineering field. Familiarity with SAP and Regulatory Pharma is essential. This role provides an opportunity...Regulatory
- ...and have a remarkable impact on people’s lives. As a... ...research & development, R&D Quality Assurance (RDQA... ..., industry innovation, regulatory landscape, and AbbVie’s... ...integrity, fosters regulatory compliance, and contributes to the... ...management, other GxP functions, and external...RegulatoryTemporary workLocal areaWorldwide
- ...About the job R&D Assistant At TA Resources we have re-imagined traditional staffing and HR consulting with Small to mid... ...opportunities for growth reporting directly to the Director of Regulatory. Job Responsibilities: Work closely with R&D,...RegulatoryFull timeContract workWork at office
- ...Regulatory Affairs Associate I Are you a recent life sciences graduate looking to launch your career with a Top-Tier Global Pharma Leader? This hybrid Regulatory Affairs Associate I role in North Chicago, IL, offers an incredible opportunity to gain hands-on experience...RegulatoryContract work
- ...Senior Pharmaceutical Recruiter – Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device... ...Support execution of global regulatory strategies and ensure compliance for submissions and change management. Identify...RegulatoryContract work
- ...strive to have a remarkable impact on people's lives across several... ...The Senior Associate, Regulatory Affairs Submission Management... ...of published output to ensure compliance with Regulatory Standards and... ...preferred but may consider QA, R&D/support, Scientific affairs,...RegulatoryTemporary workLocal area
- ...Responsibilities Support regional Regulatory Information Management (RIM) activities using systems such as COSMOS, HUBBLE, and CIU. Create... ...and approval activities to maintain data integrity and compliance. Support audit and inspection requests related to regulatory submissions...Regulatory
- ...Responsibilities May Include: Uses knowledge of planned submissions and approvals in a region to: Supports regulatory information management activities in the region focusing on key systems and processes, including COSMOS, HUBBLE and CIU Connect with central data management...RegulatoryLocal area
- ...System Validation (CSV) expectations, and global regulatory standards (e.g., 21 CFR Part 11, GAMP5). The role balances compliance, delivery enablement, and risk-based decision... ...→ test → evidence). Oversee deviations, impact assessments, and CAPA. Confirm release readiness...Regulatory
- ...Description Uses knowledge of planned submissions and approvals in a region to: Supports regulatory information management activities in the region focusing on key systems and processes, including COSMOS, HUBBLE and CIU Connect with central data management team and following...RegulatoryFull timeLocal area
- ...will ensure that all software changes and releases comply with regulatory standards, managing SLC documentation and quality assurance... ...the quality gate before deployments, overseeing validation and compliance, and identifying compliance risks early. This role is critical...Regulatory
$33 - $36 per hour
...analytical data, and ensures strict compliance with GMP/GLP and safety... ...and contribute to impactful scientific projects. Responsibilities... ...and results in compliance with GxP, GMP, and GLP requirements. Interpret... ...safety procedures, regulatory standards, and quality system...RegulatoryContract workTemporary work$55.64k - $92.73k
...SUMMARY: The Compliance Officer is responsible for administering and improving all aspects of the credit union's compliance management... ...ESSENTIAL FUNCTIONS: Ensures compliance with all state and federal regulatory requirements including, but not limited to, Anti-Money...RegulatoryLocal area$27 - $30 per hour
...Regulatory Affairs Associate I Onsite - Lake County - Hybrid (Tues, Wed, Thurs onsite) Length of assignment: 1 year Hourly Pay Rate: $27-30/hr (individual medical benefits available at a cost) Orion Group has partnered with a global pharmaceutical leader, seeking to hire...RegulatoryHourly payWork at officeLocal areaWorldwide- ...strive to have a remarkable impact on people's lives across several... ...process understanding, and regulatory submission content. Major... ...and communicate to Analytical R&D functions and CMC business partners... ...code of conduct, safety, and GXP compliance. Qualifications...RegulatoryWork experience placementLocal area
- ...strive to have a remarkable impact on people's lives across several... ...& Development (Analytical R&D) is a global analytical scientific... ...Assurance (QA) and CMC-Regulatory. Responsibilities: Performs... ...radioactive compounds, and GxP compliance, where applicable....RegulatoryFull timeTemporary workLocal area
- ...technologies across the organization. Scope & Impact Enterprise scope supporting high-... ...functions , including commercial, R&D, and enterprise productivity tools... ...property and licensing considerations Regulatory and compliance implications Draft, review, and negotiate...RegulatoryContract work
$124.5k
...strive to have a remarkable impact on people's lives... ...management, and ensure compliance with corporate policies... ...cross-functionally in R&D for the product, this individual... ...quality assurance or regulatory affairs or clinical... ...among other RDQA GXP functions and with business...RegulatoryLocal area- Responsibilities Principal Regulatory Affairs is responsible for regulatory... ...global commercialization and compliance, driving innovation and... ...international regulations. Assess the impacts of relevant drug and... ...globally with Clinical Affairs, R&D, QA, and Business Development...RegulatoryImmediate startRemote work
- Katalyst CRO is seeking a professional for a Regulatory Affairs position located in North Chicago. Responsibilities include supporting... ...Management activities, maintaining regulatory records, and ensuring compliance across markets. The ideal candidate will have a Bachelor's...Regulatory
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