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$23.5 - $52.5 per hour
...submissions of our products Support the acquisition and management of files to meet applicable regulations Attend project team meetings with RA lead to assist in strategic discussions to hone team collaboration skillset Learn regulatory affairs competencies to ensure product...SuggestedHourly payFull timeSummer workInternshipSummer internshipH1bWork at officeLocal areaRemote work$125k - $155k
...healthcare through innovative technology to support our quality assurance and regulatory compliance efforts. Reporting to the Director of QA/RA within the Quality Assurance and Regulatory Affairs department, and working closely with Product and Engineering stakeholders, the...SuggestedRemote workWork from homeFlexible hours$120.3k - $222.6k
...submission strategies and package review in collaboration with Regulatory Affairs and other operational team members (e.g., CTA, EC/RA submissions, responses, and approvals). Proactively identifies potential operational challenges and in collaboration with senior...SuggestedInterim roleLocal areaRemote workFlexible hours- ...testing . The Regulatory Advisor plays a key role in developing and driving regulatory strategy on behalf of the regulatory affairs (RA) team, specifically focusing on FDA Pharma and IVDR initiatives. At Natera, we remember there is a person behind every sample . This...SuggestedWorldwide
- ...Commercialization Manager this role is the day-to-day project owner for Topicals Innovation, partnering across Marketing, R&D, Creative, RA/QA, Clinical, Supply Chain, Operations, Finance, Sales, and external manufacturing partners to bring structure, pace, and clarity to...SuggestedFull time
- ...benchmarking and optimization of computational methods including error modeling and longitudinal tracking Partner with molecular biology, QA/RA, clinical, and software engineering teams on assay alignment Requirements Extensive experience with NGS-based oncology assays...Suggested
- ...regarding ICSR Management Unit - Reviewing and updating PrimeVigilance operating procedures and guidelines, as applicable - Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified...SuggestedFull timeWork experience placementLocal area
- ...regulations, guidelines, and policy statements. Skills: Regulatory Submissions, including IND and CTAs Reviewing and Editing RA documents Education/Experience: ~ Combination of the following can be considered: PhD or PharmD with 2+ years of pharmaceutical...SuggestedRemote job
$166k - $216k
...making through architecture reviews and hands-on embedded systems support Partner cross-functionally with electrical, software, QA/RA teams on requirements and delivery alignment Improve team effectiveness by identifying workflow bottlenecks, tooling gaps, and...Suggested$173k - $299k
...you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-****@*****.***) or contact AskGS to be directed to your accommodation resource. The Company maintains highly competitive...SuggestedFull timeTemporary workWork experience placementLocal areaRemote work- ...zoning, or structural permits • Experience managing reviewers, creating SOPs, or supporting permitting process improvement • PE, RA, CASp, or similar professional credentials • Experience supporting product, software, data labeling, AI evaluation, or workflow...SuggestedRemote jobFull timeLocal area
- ...updates, providing line of sight to key issues and accomplishments. Secondary Responsibilities Collaborate with Operations, QA, RA and other members of the CMC team to plan, sequence and track technology transfer, comparability, process scale-up and validation...SuggestedTemporary workVisa sponsorshipWork visa
- ...health authority requirements. The role will act as the key regulatory interface between the manufacturing site and the Central RA team , ensuring that site information, documents, changes and regulatory commitments are accurately captured, maintained and provided...SuggestedFull time
$32.69 - $38.46 per hour
...as work orders, service appointments, start times, parts inventory, consumption and returns, assigned computer-based training, and QA/RA work. Keep up to date on administrative responsibilities such as maintaining customer service orders and internal service records...SuggestedHourly payOdd jobFull timePart timeLocal areaRemote workHome officeFlexible hoursNight shift- ...UC/CD), Cardiovascular, Liver, Nephrology, Immunology, Rare Disease, Diabetes, Obesity, Dyslipidemia, Women's Health, Rheumatology, (RA, SLE, Gout), Cell & Gene Therapy and CAR-T in Autoimmune. Desired location- West or Central region, preferably. The Clinical...SuggestedRemote jobFull timeContract workWork at officeLocal area
$134.2k - $201.3k
...upsell across the CGT value chain. Lead executive account strategy: Build multi-year account plans and QBRs with R&D, CMC, MSAT, QA/RA, Procurement, and Legal stakeholders; establish executive sponsorship and governance. Translate science to value: Position...Full timeWork from home$134.2k - $201.3k
...vector, cell therapy, and enabling platforms. Lead complex, consultative sales cycles: Map stakeholders from R&D through CMC, MSAT, QA/RA, Procurement, and Legal; manage evaluations, RFPs, and governance processes. Translate science to value: Position capabilities...Full timeWork from home- ...programs. Senior Manager, Safety, Medical & Regulatory Quality contributes to the management of a RDQA global Safety, Regulatory Affairs (RA) or Medical Affairs (MA) QA team which provides independent quality oversight of safety activities executed by AbbVie’s R&D and non-R...Full time
- ...Maintain regulatory records and submission archives. Leadership & Cross-Functional Partnership Mentor and help develop junior QA/RA personnel. Provide quality and regulatory leadership across Operations, Supply Chain, Customer Service, Product Development, and...Remote jobFull timeTemporary work
- ...campus-scale from site selection through construction, including the site, civil, and utility scope, not only the building PE or RA licensure, or the ability to obtain licensure in target states Time at an owner or developer rather than only at an AE firm or contractor...Permanent employmentFull timeContract workTemporary workFor contractorsLocal areaRemote workNight shift
$195.9k - $244.9k
...manage regional (United States and/or European) regulatory activities as part of a Global Regulatory Team (GRT) Competently represents RA on project team meetings Leads and coordinates project team members in developing regulatory strategy for applicable documents/...Full timeWork at officeLocal areaRemote workFlexible hours$228k - $422.05k
...you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center ( ra-****@*****.*** ) or contact AskGS to be directed to your accommodation resource. Required Skills: Preferred...Full timeLocal areaImmediate startRemote workWorldwide$50k - $70k
...laboratory technology) ~2 years' work experience in clinical research, including a strong working knowledge of the ICH guidelines and RA, IRB/IEC regulations. ~ Fortrea may consider relevant and equivalent experience in lieu of educational requirements. ~ In lieu of...Full timeContract workWork experience placementWork at officeLocal areaRemote work- ...~ Familiarity with Agile/Scrum practices; Scrum Master or related certification a plus. Equal Employment Opportunity RA Outdoors, LLC dba Aspira is an Equal Opportunity Employer. Aspira does not discriminate against any applicant or employee on the basis...Full timeLocal areaWork visa
$116.35k - $210.33k
...CERCLA and RCRA investigations, feasibility studies/corrective measures studies, decision documents, remedial design/remedial action (RD/RA), long-term monitoring and operations, and environmental compliance activities. The successful candidate will provide technical...Permanent employmentFull timeContract workWork at officeLocal areaRemote work$180k - $210k
...healthcare organizations safely and successfully launch and scale radiopharmaceutical programs including Lutetium-177 (¹⁷⁷Lu), Radium-223 (²²³Ra), and Fluorine-18 (¹⁸F) based agents. We are seeking a Theranostics Clinical Program Manager with a Nuclear Medicine Technologist or...Full timeWork at officeRemote workWork from homeHome officeNight shift$71k
...Manager (or designee) during start-up on allocated projects. Prepares and submits Central EC/IRB Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required. Assists with EC/IRB or CA issue...Full timeContract workLocal area- ...Nova pertaining to the analysis of release notes, reporting metrics, validation, and resolution prior to implementation of designated RA and /or SU provided by Epic. Level 3 Analyst/Tech Lead In addition to Level 1 and 2 competencies, Level 3 will, at a minimum:...Full timeImmediate startRemote workNight shift
$65.7k - $85k
...compliance • FDA/CBP regulatory requirements • Regulatory authority and Notified Body coordination Role Boundaries The RA Coordinator serves as the operational SME for established FDA ACE and import-compliance processes and coordinates routine regulatory...Full timeTemporary workFlexible hours- ...VTS RA – Granger Lab The VTS Research Assistant will provide temporary research support across several ongoing studies. Responsibilities will include reviewing, revising, and formatting study materials; assisting with the development and refinement of research protocols...Temporary work