GxP Compliance Specialist II, R&D Quality & Regulatory
BioSpace
BioSpace is looking for a qualified individual to ensure GxP compliance with AbbVie policies and global regulatory requirements. The role involves proactive evaluation of compliance needs and managing process improvements to enhance efficiency. Candidates should possess a Bachelor's degree in a scientific field and have experience in an R&D environment. This position requires strong interpersonal skills and the ability to communicate effectively. A comprehensive benefits package including paid time off and medical insurance is offered to eligible employees. #J-18808-Ljbffr BioSpace
- 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...Regulatory
$102.85k - $133.1k
...This role is part of Alcon's Quality & Regulatory Affairs function, a critical... .... The Sr. Associate II, Regulatory Affairs Strategy... ...responsible for supporting regulatory compliance activities for Alcon's... ...regulations. Adhere to Good Practice (GxP) regulations by following...QualityRegulatoryHourly payLocal areaWorldwideVisa sponsorshipRelocation packageFlexible hours- ...pharmaceutical company in North Chicago is seeking a Quality Assurance Specialist to monitor Supplier Change Notifications and ensure compliance with quality systems. The ideal candidate... ...field. Familiarity with SAP and Regulatory Pharma is essential. This role provides...QualityRegulatory
- ...candidate is responsible for providing quality assurance support for some or all parts... ...and affiliates. The person will ensure compliance to the quality system as it pertains to... ...Soltraqs/Trackwise experience. Experience in a Regulatory Pharmaceutical Industry. #LI-KH1 #J-18...QualityRegulatory
- ...Development (Analytical R&D) is a global analytical scientific... ...: For the Scientist II position, we are seeking... ...Development (DPD), and Quality Assurance (QA) and CMC-Regulatory. Responsibilities:... ...compounds, and GxP compliance, where applicable. Qualifications...QualityRegulatoryFull timeTemporary workLocal area
- ...Development (Analytical R&D) is a global analytical scientific... ...: For the Scientist II position, we are seeking... ...Development (DPD), and Quality Assurance (QA) and CMC-Regulatory. Responsibilities:... ...compounds, and GxP compliance, where applicable. Qualifications...QualityRegulatoryFull timeTemporary workLocal area
- ...core job responsibilities by providing quality consultation, training, auditing and coordination... ...internal system audits and external GxP supplier audits. Maintain approved... ...satisfactory resolution of quality and regulatory compliance issues. Provide guidance and...QualityRegulatoryWorldwide
$84.5k - $162k
...Job Title Ensure GxP compliance to AbbVie policies/processes/procedures, global regulatory requirements, and industry guidelines.... ...provide input to develop/shape quality system and corporate policy.... ...experience. Experience working in a R&D environment preferred....QualityRegulatoryContract workTemporary workWork at officeImmediate startRemote workMonday to Friday- ...Director II, Clinical Field Excellence AbbVie's mission is... ...strategy and delivery. Compliance and Quality : Maintain a comprehensive understanding of regulatory, quality, and compliance standards... ...with affiliate One R&D model collaboration and AbbVie...QualityRegulatory
$182k
...across its multi-billion-dollar annual R&D investment. The Director II, Portfolio Insights will lead a team... ...evaluations, and delivers high-quality outputs that support enterprise decision... ...&D functions: Clinical Development, Regulatory, Statistics, R&D Strategic...QualityRegulatoryTemporary workLocal area- ...Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible... ...and ensuring regulatory compliance in the design,... ...devices (including Class I and II devices, software as a medical... ...approvals, supporting quality management system (QMS) objectives...QualityRegulatory
- Alcon MX is seeking a Sr. Associate II in Regulatory Affairs Strategy to ensure compliance and quality in our Surgical portfolio. This role, based in Lake Forest, Illinois, will involve coordinating product submissions and developing regulatory strategies for medical devices...QualityRegulatory
- ...Development Sciences within AbbVie’s R&D, is a global organization that... ...position of Senior Scientist II / Principal Scientist I,... ...-on experience with authoring regulatory filings for biologics and sterile... ...products Experience with quality risk management and control...QualityRegulatoryTemporary workLocal area
- ...seeks a qualified individual to manage compliance with restricted substances regulations.... ...data management and the implementation of regulatory requirements such as EU REACH and US Prop... ...with experience in manufacturing or quality assurance. #J-18808-Ljbffr Planet Pharma...QualityRegulatory
- ...Development Sciences, R&D. The tLNP CMC team focuses... ...parameters on critical quality attributes. First‑... ...Technical Document (CTD) for regulatory submissions. Building... ...of materials, and GMP compliance. Direct mentorship of... ...experience. Scientist II: BS with 7+ years, MS with...QualityRegulatoryTemporary work
- ...cylinders, PPE provides services such as quality storage cabinets, safety protection,... .... Job Description Job Summary: The Compliance Assurance Specialist will be responsible for the... ...non-compliance notices cited by the regulatory agencies (5-10% of position) Researching...QualityRegulatory
- International Trade Compliance Specialist job at Uline. Waukegan, IL. Corporate Headquarters 12575 Uline Drive... ...International Trade Compliance Specialist, tackle regulatory hurdles, find tariff savings and bring Uline’s high quality products to international destinations....QualityRegulatory
$84.5k - $162k
...Senior Associate, Regulatory Affairs Submission Management AbbVie... ...the timely delivery of high quality dossiers that meet technical... ...of published output to ensure compliance with Regulatory Standards and... ...preferred but may consider QA, R&D/support, Scientific affairs,...QualityRegulatoryTemporary workWork at officeImmediate startRemote workMonday to Friday- ...Research & Development (Biologics Analytical R&D) is a global analytical sciences... ...experience. Qualification for Senior Scientist II: Ph.D. with 4+ years of experience is... ...writer and communication of research or other regulatory materials. Experience with analytical Multivariate...RegulatoryTemporary workLocal area
- ...Job Description: The SQA is the quality authority for regulated software initiatives, ensuring... ...Validation (CSV) expectations, and global regulatory standards (e.g., 21 CFR Part 11, GAMP5). The role balances compliance, delivery enablement, and risk-based...QualityRegulatory
- ...Solutions Services, LLC is seeking a Software Quality Assurance (SQA) professional in Waukegan... ...changes and releases comply with regulatory standards, managing SLC documentation and... ...deployments, overseeing validation and compliance, and identifying compliance risks early....QualityRegulatory
- ...Cardiac Sonographer II-Concierge Medicine Part Time Days... ...Code of Ethics and Corporate Compliance Program, and complies with all... ...procedures, guidelines and all other regulatory and accreditation standards.... ...obtaining optimal quality study per ICAEL standards....QualityRegulatoryPart time
$70k - $90k
...our team as a Credit Analyst II. In this role, you'll have the... ...collateral, verify covenant compliance, calculate borrowing bases, review... ...risk-rating methodology, and regulatory requirements; provide... ...Deliver accurate, timely, high-quality reporting. Working knowledge...QualityRegulatoryFull timeWork at officeLocal area$90k - $125k
...Senior Design Assurance Quality Engineer I-II Location: Libertyville, IL... ...representing Global Quality and Regulatory Affairs (GQRA) on new... ...application of design controls in compliance with global regulatory... ...or New Product Development/R&D Working Knowledge with Statistics...QualityRegulatoryWork at officeWorldwideVisa sponsorship- ...** The Cardiac Sonographer II reflects the mission, vision... ...Code of Ethics and Corporate Compliance Program, and complies with... ...procedures, guidelines and all other regulatory and accreditation standards.... ...obtaining optimal quality study per ICAEL standards....QualityRegulatoryPart timeLocal areaRelocation package
- ...candidates only. Responsible for managing the quality oversight of assigned small molecule... ...delivery of products while assuring compliance with the client policies and standards,... ...decisions on product quality and compliance and regulatory conformance issues for pharmaceutical...QualityRegulatoryLocal area
- ...Title: Engineer Process Support II Duration: 12 Months... ...as increase in process yield, quality improvements, cycle time/throughput... ...and assure they are in compliance with applicable procedures and... ...and technical support during regulatory audits and agency inspections...QualityRegulatoryRemote workMonday to Friday
- ...The Sterile Processing Tech II reflects the mission, vision... ...Code of Ethics and Corporate Compliance Program, and complies with all... ..., guidelines and all other regulatory and accreditation standards.... ...sterilization container. Performs quality assurance and biological...QualityRegulatoryCasual workLocal areaRelocation packageShift work
- ...Marketing Manager I/II – DTC Patient Marketing The Marketing Manager I/II – DTC Patient... ...testimonial programs, from brief through regulatory approval and launch. Champion patient-... ..., digital) ensuring delivery of high-quality work on time and within budget....QualityRegulatoryWork at officeRemote workMonday to Friday
- ...transfer of new and existing products from R&D to global manufacturing sites and third-... ...Apply first-principles engineering and Quality by Design (QbD) methodologies to establish... ...and reports, tech transfer packages, and regulatory submissions (e.g., CMC sections of INDs/NDAs...QualityRegulatoryContract workTemporary work
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