QA Associate Director - Global Complaints & Regulatory Lead
Merck
Merck is seeking an Associate Director to guide the Manufacturing division's product quality complaint management, ensuring compliance with worldwide MDCP regulatory expectations. The role serves as a subject matter expert for receipt, handling, trending, and health authority reporting of PQCs. You will collaborate with Global Safety, site operations, and external partners to address investigations, lead cross-functional teams, and drive continuous improvements in processes, including the use of #J-18808-Ljbffr Merck
- ...cost.Job Description• Flex position in Global Labeling, for a Global Labeling Product... ..., alignment of labeling text with data, regulatory requirements, consistency (where appropriate... ...United States Package Insert (USPI) and associated patient labeling, EU Product Information...RegulatoryWork at officeImmediate startFlexible hours
- ...Co., Inc. in West Point, PA is seeking an Associate Director of HVAC Engineering to lead design and execution of HVAC systems for global capital projects in manufacturing,... ...You will develop basis of design, ensure regulatory compliance, mentor engineers, and drive standardization...Regulatory
- Scorpion Therapeutics is seeking an Associate Director, Regulatory Affairs - Power Platform Solutions Specialist to lead the configuration and optimization of the Microsoft Power Platform within Global Regulatory Affairs and Clinical Safety. The role emphasizes data migration...Regulatory
- Merck is seeking an Associate Director to lead end-to-end project management of major supply chain changes, coordinating cross-divisional... ...project governance, and strong collaboration across Regulatory, Quality and Global Supply Chain functions. The ideal candidate will...Regulatory
$142.4k - $224.1k
...Job Description The Associate Director, New Products plays a key role within our company Global Vaccines and Infectious Disease (GVID) organization, with responsibility... .... This individual will serve as the Commercial Lead for our global Ebola vaccine, leading global commercial...SuggestedContract workTemporary workFor contractorsLocal areaRelocationVisa sponsorshipRelocation packageFlexible hoursShift work$142.4k - $224.1k
Job Description The Associate Director is responsible for providing... ...product quality complaint management processes... ...combination product (MDCP) regulatory expectations.... ...trending and reporting of global product quality... ...our Company processes. Leads/participates on cross...RegulatoryComplaintsFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work$142.4k - $224.1k
Your role as Associate Director, Media Capabilities and Agency Lead, carries the vital responsibility of advancing our... ...Ensure compliance with legal and regulatory requirements, processes, guidelines... ...end date. Our company is a global health care leader with a diversified...RegulatoryFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- ...The Opportunity Lead the strategic operations of a sustainable, world-class knowledge... ..., and personnel management of the Global Knowledge Management (GKM) team. This role... ...access, share, and apply relevant scientific, regulatory, and industry information that supports organizational...RegulatoryContract workShift work
$156.9k - $247k
...have an exciting opportunity to join our global oncology marketing team focusing on an... ...settings. We are recruiting for an Associate Director of Global Oncology Marketing focusing on... ...to work through ambiguity, experience leading strategy development and implementation...Full timeFor contractorsLocal areaFlexible hours- Scorpion Therapeutics is seeking a Senior Scientist, Global Labeling Lead to develop and maintain compliant labeling content for development... ...teams, provide strategic labeling guidance, and act as the regulatory labeling contact for global submissions, shaping labeling...Regulatory
$142.4k - $224.1k
...oriented marketer to serve as Brand Strategy Lead for key brands. This individual will be... ...Research, Finance, Operations, and Global teams. The successful candidate will leverage... ...vaccines Understanding of US commercial and regulatory requirements Required Skills Adaptability...RegulatoryFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- Role: Senior Scientist, Global Labeling Lead, responsible for developing and maintaining compliant labeling content for development and marketed... ..., US, and EU Labeling. Objectives: ensure high-quality, regulatory-compliant labeling documents to support safe product use...Regulatory
$242k - $270k
...Director, Senior Global Regulatory Lead (Sr. GRL) Global Regulatory Strategy (GRS) Location: King of Prussia, PA | Waltham, MA | Maidenhead, UK | Zurich, Switzerland Work Arrangement: Hybrid – 3 days onsite per week About CSL CSL’s R&D organization is accelerating...Regulatory3 days per week- CSL, headquartered in King of Prussia, seeks a Senior Manager Global Regulatory Affairs CMC to drive regulatory strategy for biological and non-biological products. You will partner with R&D, Manufacturing, Quality, and Regulatory Affairs to meet evolving CMC requirements...Regulatory
- CSL Behring in King of Prussia, PA seeks a Senior Manager Global Regulatory Affairs CMC—Biological & Non-Biol. Products to lead regulatory strategy and submissions for a dynamic product portfolio. You will partner with R&D, Manufacturing, Quality, and Regulatory Affairs...Regulatory
- CSL is seeking a Senior Manager Global Regulatory Affairs CMC for Biological & Non-Biological products in the United States. You will define... ...strategies, interact with regulators as an authorized official, and lead cross-functional teams across R&D, Manufacturing, Quality,...Regulatory
- Scorpion Therapeutics seeks an Executive Director of Regulatory Affairs Liaison in General Medicine to lead global regulatory strategy for ophthalmology programs, with oversight of retinal disease indications and external representation. The role requires extensive drug...Regulatory
- A global pharmaceutical organization is seeking a Contractor Quality & Regulatory Lead to oversee product quality and compliance for external manufacturers. This role demands over 10 years of experience in GXP settings and requires expertise in regulatory affairs and quality...RegulatoryFor contractorsRemote work
$142.4k - $224.1k
Job Description Associate Director, US Marketing Ophthalmology... ...and Affordability Lead Job Description: Our... ...state laws, AE/product complaint reporting), and partner... ...of US commercial and regulatory requirements.... ...026 Our company is a global health care leader with...RegulatoryComplaintsFor contractorsLocal area- MSD is seeking an Associate Director to lead end-to-end project management for major supply chain changes within the Manufacturing Network Strategy... ...meet timelines, define business requirements, and ensure regulatory readiness across complex programs. The role emphasizes...Regulatory
$129k - $203.1k
Job DescriptionThe Associate Director, Clinical Supplies Quality, Global Development Quality provides quality oversight,... ...use, and compliant with applicable regulatory requirements. Key areas of... ...incumbent is expected to independently lead and execute the following...RegulatoryFull timeFor contractorsLocal areaFlexible hours- ...GSK is seeking an Associate Director of Global Epidemiology and Real-World Evidence in the United States. You will lead epidemiology programs, design observational studies using real... ...with clinical development, safety, regulatory, outcomes, and commercial teams to inform...Regulatory
- Johnson & Johnson is seeking a senior leader to drive enterprise regulatory compliance across its External Manufacturing network within... ...strengthening programs, and increasing visibility of risks across a global matrixed organization. The position requires 15+ years in GMP...Regulatory
- Integrated Resources Inc. is seeking a Regulatory Compliance Manager to oversee change management and ensure quality assurance across contract... ...in a GXP setting. This position involves managing customer complaints and collaborating with various teams as the regulatory expert....RegulatoryComplaintsContract work
- The Global Trade Compliance Manager at Dorman Products oversees the company’s global trade... ...supporting business operations. You will lead broker management, CTPAT program... ...teams and external providers to monitor regulatory changes, implement process improvements,...Regulatory
- Merck & Co. in the USA seeks the Head, Site Budgets to lead the global site budgeting capability and the Trial Initiation Specialist organization... ...strategy, drive performance, and ensure governance and regulatory alignment across regions and countries. You will partner...Regulatory
- Merck & Co. in West Point, Pennsylvania, is seeking an Associate Director - Project Manager to lead end-to-end manufacturing network changes. You will... ...cases, managing project portfolios, and maintaining regulatory compliance while coordinating strategic inventory transitions...Regulatory
$359.23k - $431.27k
...metabolic dysfunction-associated steatohepatitis (MASH)... ...by our shared purpose: leading the fight against MASH... ...in the right way. Global Medical Lead, MASH... ...Leading a team of Medical Directors supporting MASH, the Global... ..., HTA bodies, payers, regulatory agencies, and patient...RegulatoryMinimum wageFull timeLocal areaWorldwideFlexible hours- ICON is seeking a Senior Director, Regulatory Affairs to lead global regulatory strategy for the organization’s therapeutic area teams and manage a large regulatory staff. You will drive submissions, provide regulatory guidance, and collaborate with cross-functional colleagues...Regulatory
- ...Role Overview The Associate Director is responsible for the review and... ...serving as the promotional regulatory expert with legal, medical and... ...participate in labeling and global regulatory team meetings to... ...APLB) or experience developing/leading the regulatory strategy for...RegulatoryFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work3 days per week
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