Global Clinical QA Program Lead
Johnson & Johnson Innovative Medicine
Johnson & Johnson Innovative Medicine seeks a Manager, Clinical QA Program Lead to oversee audit strategies for clinical programs, systems, and suppliers, with locations in Raritan, NJ, or Titusville, NJ, and other global sites worldwide. You will lead audits, develop tactical plans, ensure regulatory compliance, and drive quality improvements across therapeutic areas in a dynamic, cross-functional team environment. #J-18808-Ljbffr Johnson & Johnson Innovative Medicine
$68.05k - $109.87k
Legend Biotech is a global biotechnology company dedicated to... ...Legend Biotech is seeking QA Investigations Lead I as part of the Quality team... ...manufacturing compliance, clinical quality, or cell therapy.... ...and peer‑to‑peer recognition programs; demonstrating our ongoing...SuggestedPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaWorldwideFlexible hours- ...ensuring quality oversight of internal sites and CDMOs, and leading an independent QA function to maintain compliance with industry regulations.... ...over 10 years of experience in Quality Assurance within a global pharmaceutical organization, strong leadership capabilities...Suggested
- ...Site Reliability Engineering) Systems-level QA Success Criteria The contractor will be... ...in one or more general purpose programming languages. Good understanding of agile methodologies... ...Experience and desire to work in a Global delivery environment Desired Skills: Working...SuggestedContract workFor contractorsLocal areaShift work
- Tris Pharma, Inc. is seeking an experienced Senior/Executive Director of R&D Quality Assurance to lead global QA/Compliance programs across R&D, Clinical, and Pharmacovigilance. The role demands strategic leadership, regulatory liaison with FDA/EMA, and building a robust...Suggested
- ...Quality Assurance leader to oversee a small QA/R&D unit. The role provides strategic guidance on GxP compliance for clinical and nonclinical programs, pharmacovigilance and medical affairs,... ...D and Regulatory groups. The incumbent leads QA governance, inspection readiness and...Suggested
- Legend Biotech seeks a QA Investigations Lead I to oversee quality investigations in Raritan, NJ. This role involves ensuring robust investigations... ...of relevant experience, preferably in quality assurance or clinical quality within aseptic manufacturing. Benefits include...
- ...Director of Research and Development Quality Assurance to lead our R&D QA programs in a hybrid NJ setting. This senior role partners with R&D,... ...integrity, patient safety, and regulatory readiness across global development stages. You will drive risk-based quality governance...
$122k - $212.75k
...Responsibilities: Represents Global Quality on the... ...oversees the necessary QA resource for global and... ...her assigned products.Leads a comprehensive Quality... ...assures Quality throughout clinical, DS, DP, FF & device: development... ...’s long-term incentive program.Subject to the terms of...Full timeLocal areaImmediate start$124k
...person who joins in. As a global biopharmaceutical... ..., you'll independently lead and oversee all QC activities... ..., Regulatory Affairs, QA, and Supply Chain to... ...successful execution of testing programs and resolution of... ...documents for clinical and commercial programs...Full timeContract workWork at officeLocal areaFlexible hours$184.24k - $276.36k
Initial Therapeutics, Inc. is seeking a Director, PV QA DSI to lead the Quality Assurance strategy within Clinical Safety and Pharmacovigilance (CSPV). This role will oversee PV QA activities, ensuring compliance with regulatory requirements while leading a high-performing...$149.16k - $223.74k
...Quality CMO - RDDirect Reports: 2 reports in EuropeAreas Managed: QA operations oversighting Manufacturing External Supply... ...perimeter, for implementing the Annual Product Quality Reviews (APQR) program in connection with the external manufacturers, for each product...Temporary workWork at officeLocal areaNight shiftWeekend work3 days per week- Johnson & Johnson Innovative Medicine seeks a Pharmacovigilance QA Auditor Specialist to join our team in the Raritan, NJ area or Titusville, NJ or Horsham, PA locations. The role focuses on planning, conducting, and reporting PV audits to ensure compliance with regulatory...
$55k
...Summary The Quality Assurance Coordinator is responsible for monitoring the systematic operations of the residential and vocational programs. This person will serve as a liaison between the local office and the national office. This person will be held accountable for...Work experience placementWork at officeLocal areaShift work$226.28k - $377.13k
...0 vision to "be an innovative global healthcare company contributing... ...Organizations (CDMO).The role leads the site's independent Quality... ...for leading an independent QA function, with authority for final... ...to ensure an accurate Clinical Trial Document review process...Contract workLocal area- ...testing strategies, plans, and schedules. Lead all phases of testing, including System... ...& Spiritual Well-being Disaster Relief Programs About Sogeti Part of the Capgemini Group... ...innovation at speed and want a local partner with global scale. With a hands-on culture and close...Full timeLocal areaFlexible hours
$137k - $235.75k
...closely with DSDH teams, Quality, Legal, Global Regulatory Affairs, and Johnson & Johnson... ...or related fields, including experience leading, partnering with, or delivering AI-driven... ...participate in the Company’s long-term incentive program.Subject to the terms of their respective...Full timeLocal areaImmediate start- Delta Community Supports is seeking a Quality Assurance Coordinator in Raritan, NJ to monitor residential and vocational programs and ensure compliance with state rules and agency policies. You will liaison between local and national offices, and help uphold Delta’s standards...Local area
$50 - $55 per hour
...submissions and registration processes- GxP Experience with Veeva Vault RIM (Submissions, Registrations, Publishing) Knowledge of global regulatory requirements Seniority level Mid-Senior level Employment type Full-time Job function Quality Assurance Industries IT...Full time- Initial Therapeutics, Inc. is hiring for a QA management role focusing on ensuring compliance within contract manufacturing operations. The role involves oversight of Quality Management Systems, partnering with quality leaders, and supporting validation efforts for drug...Contract work
$153.6k - $230.4k
Daiichi Sankyo US is seeking a Quality Assurance Lead to oversee Contract Manufacturing compliance in Basking Ridge, New Jersey. The successful candidate will be responsible for ensuring that all contracted organizations comply with FDA regulations and internal quality...Contract work- ...Description Schutz Container System is a Global Packaging Company , We are seeking for a... ...and procedures for quality and safety programs and procedures. Supervising the implementation... ...throughout the plant. Setting QA compliance objectives and ensuring that targets...
$130k - $158k
...company and confidential client compliance programs and participate in continuous improvement... ...team and departmental objectives. Lead by example and model behaviors that are consistent... ...Whenyou join CBRE, you become part of a global leader in commercial real estate...Work at officeVisa sponsorship- Pace® Life Sciences is seeking a Quality Assurance Manager in Lebanon, NJ, to lead the QMS and ensure compliance with FDA, ICH, ISO, and cGMP. You will oversee analytical lab QA activities, documentation, audits, and continuous improvement. The ideal candidate has 7+ years...Full time
- Johnson & Johnson Corporate Headquarters is seeking a Senior Manager, Global Audit & Assurance (GA&A), Compliance Audits & Investigations Group (CA&I) based in New Brunswick, NJ or Bangalore. Lead annual audit plans covering ABAC, GTC and GCC reviews while managing investigations...
- ...reports • Review and complete determination associated Medical Device Report and/or Vigilance Report • Knowledge of and familiarity with global regulations for reporting • Directly interface with service centers, Hospitals, Surgeons, and Internal employees for reporting of...Work experience placement
$120k - $130k
...manage the Quality Assurance (QA), Quality Control (QC), and Laboratory... ...with responsibility to lead the development and... ...and department heads to review program organizational policies, to coordinate... ...Company in North America ~#26 Global Candy Company ~ Makers of...Casual workWork at officeImmediate start$102k - $177.1k
...for developing and supporting programs and providing DEA regulatory guidance... ...and regulatory body audits. Lead and/or support such audits.... .../or support enterprise and/or global standards gap remediations and... ..., ISO 9001 and/or ISO 13485.QA/QC experience in the Pharmaceutical...Full timeWork at officeLocal areaImmediate start- ...Quality Systems and Training within the Global External Manufacturing (ExM) organization... ...Global Process Owners and Global Process Leads for relevant systems • Act as primary ExM... ...in the use of Microsoft Office programs including OneNote and SharePoint platforms...Permanent employmentContract workWork at officeLocal areaFlexible hours
$141.6k - $191.3k
...to develop and implement evidence based programs and services that produce measurable improvements... ...s Specialized Hospital New Brunswick by leading a department, serve as a catalyst and... ..., and research to address both the clinical and social determinants of health....Full timeTemporary workWork experience placementFlexible hoursShift work- ...The Director of Quality & Patient Safety is responsible for leading clinical quality and patient safety efforts for Hunterdon Health System... ...NJDOH, CDC, Leapfrog, etc. Develops and leads system-wide programs to assess departmental and organizational safety culture and...Hourly payShift work
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