Scientific - Global Regulatory CMC Manager
TechDigital Group
Must Have List: 5+ years of experience with the following: Library Science MS Office including Word, Adobe, Visio. Document Scanning experience FDA Documentation & Compliance like 21 CFR Part 11/CGMP Ability to manage competing priorities Accuracy and Attention to Detail Schedule: This person may be required to work weekends. End date for this contract is 31 DEC 2024. PURPOSE AND SCOPE OF POSITION: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for Client Jump site records management. Responsibilities include but are not limited to receiving and reconciliation of GMP records, management of scanning, archival and retention of GMP records. REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: Education: Bachelor's degree or equivalent. Library Science a plus. Experience Basic Qualifications: Minimum of 5 - 8 years of relevant document control records management experience in a cGMP/FDA regulated environment Strong communication and customer service skills. Experience with Part 11 adherence regarding scanning of records and electronic archiving. Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System) Must demonstrate the following behaviors consistently: Innovative, proactive, and resourceful; committed to quality and continuous improvement Able to prioritize, manage time well, multi-task, and troubleshoot effectively Ability to work effectively and collaboratively at a fast pace with cross functional departments to finalize time-sensitive deliverables Possess project management skills. Strong knowledge of cGMPs and domestic regulatory requirements Must complete tasks independently, notify manager of decisions outside of established processes and the ability to build an internal network DUTIES AND RESPONSIBILITIES: Responsible for the organization of cGXP controlled document files within the Document Center and ensure that records are readily retrievable and sent off to final archive facility as needed. Assist with managing the Document Center Archive room Thorough Knowledge of Records Management, Scanning and organization functions Follow Policies, SOPs, and work instructions to support the document approval process, assign effective dates and training workflows, and archive documents and document change requests #J-18808-Ljbffr TechDigital Group
- Job-ID29499131Reference26-29348Scientific - Global Regulatory CMC Manager EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”Scientific
- ...Summary: The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages... ...Members of the organization develop global regulatory CMC strategies and... ...regarding drug products. The GRS-CMC Manager is responsible for content development...SuggestedFull time
- US Tech Solutions in Madison, NJ seeks a CMC Regulatory Manager to provide strategic regulatory expertise across development through post-approval for biotech products. You will interface with Global Regulatory Sciences and related teams, guide change management, and ensure...SuggestedContract work
$90 - $100 per hour
...Job Title: Global Regulatory CMC Manager Location: 50% Onsite – Giralda Farms, NJ Duration: 6 Months (Contract) Pay Range: $90–$100/hr... ...Required Qualifications ~ Bachelor's degree in a relevant scientific or technical discipline. ~6+ years of Regulatory CMC...ScientificFull timeContract workMonday to Friday- ...Associate Director in the Regulatory Affairs CMC Department. The successful... ...regional requirements and scientific and company policies and... ...to project teams and senior management in a timely manner. Initiates... ...to local and / or global process improvements, which...ScientificContract workLocal area
- Associate Director - CMC - European Union Location... ...to join a global pharmaceutical services... ...across technical, quality, regulatory and commercial functions... ...clients and internal scientific and operational teams,... ...at a strategic level, managing expectations, priorities...Scientific
$249.1k - $327k
...to hear from you.The Senior Director, Global Regulatory Affairs, Neurology will identify and implement... ...authorities (e.g., meeting requests/scientific advice requests, and other complex... ...risks and maximize success. Direct, and manage financial planning/forecasting and budget...ScientificFull timeTemporary workRemote work3 days per week$201.8k - $264.8k
...and negotiates evidence with regulatory agencies. Interacts and negotiates... ...(e.g., meeting requests/scientific advice requests, iPSPs/PSPs,... ...requests). As a Regional or Global Regulatory Lead, initiate and... ...probability of success. Manage regulatory strategy team(s) including...ScientificWork at officeRemote work3 days per week$182k - $346k
.... Job Description The Director Regulatory Affairs Global Regulatory Lead (GRL II), Global Regulatory... ...with global regulatory requirements. Manages compounds through all phases of... ...initiatives. Based on experience and scientific strengths, expands knowledge of TA and...ScientificWorldwide- CMC Project Manager - European Union Location: European Union About The Role Our client is a global contract development and manufacturing partner supporting... ...Operations, Quality, Regulatory, and Supply Chain.... ...between clients and internal scientific, manufacturing, and...ScientificContract workWork experience placementRemote work
$200k - $275k
Senior Director, Regulatory Affairs - Infectious Disease... .... The role will shape global development and... ...clinical, nonclinical, and CMC disciplines. The ideal... ...commercialization, and lifecycle management. Lead preparation,... ...field; an advanced scientific degree is strongly...ScientificTemporary workLocal areaFlexible hours$133.2k - $172.37k
...to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized... ...office based/hybrid position. The Manager, Regulatory Affairs CMC is located in Philadelphia PA, El... ..., ensuring alignment with global regulatory requirements for cell therapy...ScientificFull timeContract workFor contractorsWork at officeLocal areaRemote workRelocationFlexible hours- ...based in New Jersey is seeking a professional in Global Medical Affairs. This role requires... ...position involves engaging with external medical and scientific leaders to develop sound medical rationale and support regulatory submissions. Join us to make a significant impact...Scientific
$142.4k - $224.1k
...DescriptionAssociate Principal Scientist, Regulatory CMC, Synthetic Moities of ADCs &... ...robust, phase-appropriate global Regulatory CMC strategies... ..., and regulatory milestones.Manage preparation and execution of... ...to ensure compliance, scientific excellence, accuracy and...ScientificFull timeFor contractorsLocal area$170k
...Summary The Principal Scientist, Regulatory CMC will report to the Director,... ...in the development of global Chemistry, Manufacturing and... ...investigational and marketed products and manage the preparation of dossiers... ...involves the close study of scientific and regulatory documents....ScientificTemporary workMonday to FridayFlexible hours- ...DescriptionResponsible for implementing regulatory strategy and managing operational activities for assigned regions.Provides input into global regulatory strategy, including... ...InformationRichha SainiSenior Clinical/Scientific Recruiter360 Mt. Kemble Avenue, Suite...ScientificWork at officeImmediate startWorldwide
- ...financial flexibility by offering contingent labor as a variable cost.Job Description• Assist and support regulatory CMC managers in the following activities:• Defining global CMC regulatory strategy and decisions for development projects or marketed products to achieve...Immediate start
- Merck in Rahway, NJ seeks an experienced Regulatory Affairs professional to develop and... ...pharmaceutical products. The role focuses on CMC dossiers, global submissions, and coordination with... ...for regulatory submissions, and manage risk assessment and milestone delivery...
- ...applications. Lead, guide, and train the CMC team to ensure highly qualified... ...activities, prior to new product launch Manage regulatory correspondence mainly to CDER, FDA, User... ...individuals in the department. Coordinate with global and local affiliates. Education and Experience...Local area
- EPM Scientific is recruiting a Senior Regulatory Affairs Specialist in Summit, New Jersey. The candidate will lead regulatory strategy, interact with FDA/other health authorities, and manage global submissions for both development and marketed products. The role partners...Scientific
$168.1k - $268.7k
...As an Associate Director in Regulatory Affairs, Advertising and Promotion... ...therapies that improve global health. You’ll lead... ...materials using BioNTech’s content management systems to ensure compliance... ...A Bachelor’s degree in a scientific discipline (minimum requirement...ScientificHourly payWork at office- Scorpion Therapeutics is seeking a Senior Scientist (R3) in Regulatory CMC Biologics to lead global regulatory strategies across development and post-... ...will develop and execute robust CMC regulatory plans, manage INDs, BLAs, and post-approval variations, and ensure compliance...
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$140k - $170k
Senior Manager, Regulatory Program Support (RPS) (Finance) Overview The Regulatory... ...partners with the global regulatory lead and cross-functional... ...Affairs (i.e., Development, CMC, Labeling, Advertising and... ...requirements. Substantive scientific or strategic content approval...ScientificFull timeWork at officeLocal areaShift work- ...Senior Manager of Global Patient Safety (GPS) At Regeneron, we use science and innovation to develop life-changing medicines for people... ...Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical...ScientificWorldwide
$142.4k - $224.1k
...Manufacturing and Control regulatory strategies for... ...products in accordance with global regulations, guidances... ...execution of change management and conduct all activities... ...in reviewing scientific information to assess... ...Management Regulatory CMC Regulatory Strategy DevelopmentRegulatory...ScientificContract workFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$173.2k - $272.6k
...integrated stage-appropriate CMC development and... ...technical, operational & regulatory success or timelines.... ...with our company's Global and regulatory requirements... ...through demonstrated scientific excellence in at least... ...with all levels of management.Must have strong understanding...ScientificFull timeFor contractorsLocal areaFlexible hours- Shionogi Inc. in Florham Park, NJ, seeks a Senior Manager, Regulatory Affairs CMC to lead strategy and coordination of CMC regulatory activities under the Senior Director, CMC. You will partner with R&D, QA, manufacturing, and regulatory authorities to ensure compliant...
$210.4k - $331.1k
Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) position... ...driving execution of the Global Medical and Scientific Affairs (GMSA) portion for their... ...Scientific Affairs (EDSA) review process.Manages programs (patient support, educational or...ScientificFull timeFor contractorsLocal areaFlexible hours- ...operations, the company caters to its globally positioned clients by... ...controller architecture and content management system. Our services also... ...science summaries in support of Regulatory Submissions. Engage with external medical and scientific leaders in support of medical...Scientific
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