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
- Director, Regulatory CMC - Cell Therapy Overview Responsible for overseeing management of multiple development and life-cycle management... ...strategic direction based on global regulatory guidelines and... ...analytical topics Understanding of scientific content and drug development...ScientificShift work
$199.95k - $242.3k
...Job Summary The GRS‑CMC Director oversees multiple... ...and lifecycle management projects, represents the... ...as a spokesperson in regulatory engagements. Responsibilities... ...direction based on global regulatory guidelines... ...Deep understanding of scientific content and drug development...ScientificFull timeShift work$199.95k - $242.3k
## Director, Regulatory CMC - Cell TherapyMadison - Giralda - NJ - USFind... ...responsible for overseeing management of multiple development and... ...strategic direction based on global regulatory guidelines and... ...analytical* Understanding of scientific content and complexities and...ScientificHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- ...in Morristown, NJ is seeking a GRA CMC Lead to manage regulatory strategies for the R&D team. This role... ...candidate will have a BS/BA in a scientific field, with a preference for advanced... ...bring life-changing medicines to patients globally. #J-18808-Ljbffr Eacademy SanofiScientific
- ...Myers Squibb EU Policy is seeking a Director for Regulatory CMC in Cell Therapy. In this role, you will oversee management of multiple development projects, represent... ...and possess strong leadership, negotiation, and scientific communication skills. Join us in making...Scientific
- In this position, the Regulatory Affairs CMC Director will lead the international... ...the development of sound global CMC regulatory registration... ...and Quality. Direct and manage regulatory CMC activities and... ...BS degree in a scientific discipline (e.g., Pharmaceutical...Scientific
- EmergencyMD is seeking a regulatory CMC specialist to provide global regulatory support throughout the product lifecycle in Morristown, New Jersey. The role involves managing high-quality CMC regulatory submissions and ensuring timely execution of corporate goals. The ideal...
- HUTCHMED seeks a Regulatory Affairs CMC Director to lead the regulatory team and develop global CMC strategies to support biologics and chemical drug approvals in the US... ...communication skills. Responsibilities include managing CMC activities, addressing regulatory...
$130k - $200k
Director, Regulatory Affairs - Infectious Disease About Tonix... .... This role oversees global regulatory strategy,... ...strategies across nonclinical, CMC, and clinical... ...lead discussions, and manage responses to queries.... ...and Abilities Strong scientific foundation in immunology...ScientificTemporary workWork at officeLocal areaRemote workFlexible 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
$199.95k - $242.3k
Bristol Myers Squibb is seeking a Director, Regulatory CMC to oversee multiple development projects and represent the organization... .... This role is essential in ensuring compliance with global regulatory guidelines and managing the growth of direct reports. The ideal candidate...$190.8k - $300.3k
...Description Principal Scientist / Director, GLOBAL REGULATORY CMC Biologics (R5) Under general... ...according to defined timelines. Manage execution of CMC documentation including... ...of submissions to ensure compliance, scientific excellence, accuracy and completeness...ScientificFull timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work$129k - $203.1k
...Job Description The Associate Director in Global Clinical Supply (GCS) Compliance is a... ...training, audits/inspections, analytics, risk management, and EHS. Associate Directors are... ...Education & Experience: Bachelor’s degree in a Scientific, Engineering, or related field with 8+...ScientificFor contractorsLocal area- Bristol-Myers Squibb is seeking a Director, Regulatory CMC for Cell Therapy in Madison, NJ. In... ...multiple development and lifecycle management projects, ensuring regulatory compliance... ...strategic direction in alignment with global guidelines. The ideal candidate will have...
$166k - $203k
...The Associate Director, Regulatory Affairs (Advertising and Promotion... ..., Medical Affairs, Legal, Global Regulatory Affairs, Labeling... ...materials in BioNTech’s content management applications and systems... ...Education ~ Minimum BS in scientific discipline...ScientificWork at officeLocal areaWorldwide- Global Regulatory Strategist Job title: Global Regulatory Strategist Location... ...with nonclinical, clinical, CMC, commercial, and other... ...documents focused on strategy and scientific content and leading team... ...knowledge of electronic document management systems (e.g. Veeva Vault...ScientificLocal area
- The Associate Director in Global Clinical Supply (GCS) Compliance is a subject matter expert... ..., audits/inspections, analytics, risk management, and EHS. Partners closely with GCS... .... Requirements Bachelor’s degree in a Scientific, Engineering, or related field with 8+ years...ScientificLocal area
- Job Title: Scientific Fellow, AI-Enabled CMC Reports to: Global Head of Computational & AI Strategy, R&D Location: Cambridge, MA / Morristown, NJ About the... ...person will advise senior leaders and corporate management on emerging scientific and technological advances,...Scientific
- ...NJ. This role focuses on executing the global medical strategy for zola-cel in rheumatology... ...ideal candidate will have an advanced scientific or medical degree and at least 3 years... ...leading medical education initiatives and managing scientific partnerships. #J-18808-...Scientific
- ...Communications Lead. This leadership role involves overseeing external scientific communications for the Cell Therapy portfolio and ensuring... ...communication and strong leadership capabilities in a global environment, contributing significantly to patient-centered solutions...ScientificWorldwide
- ...Communications. This senior role involves strategic oversight of scientific communications, ensuring compliance and quality in... ...scientific communications, particularly in cell therapy, and will lead global teams while maintaining standards and best practices in Med Communications...ScientificWorldwide
- ...Specialist in Summit, NJ, to support regulatory strategy for Cell Therapy clinical portfolios... ...across technical functions and management of CMC documentation for submissions. Successful... ...including co-authoring scientific content, ensuring document clarity, and...Scientific
- Jobsbl in Parsippany, NJ is seeking a Manager of Scientific Affairs to oversee clinical studies and ensure compliance with regulatory standards. This hybrid role requires strong leadership skills and a deep understanding of clinical practices. The ideal candidate will have...Scientific
$255.8k - $402.7k
...for Biologics (Biologics-CMC) is accountable for managing a team of CMC professionals... ...and ensuring rigor in CMC regulatory strategy as well as delivery... ...As a Senior member of the Global Regulatory Affairs and... ...in place to maintain the scientific, technical and regulatory...ScientificFor contractorsWork at officeRemote workRelocationVisa sponsorshipFlexible hoursShift work3 days per week- Sanofi is seeking a Global Medical Director for Stakeholder Engagement in Morristown, NJ. This role will lead the strategic engagement... ...and thought leaders. The ideal candidate will have an advanced scientific degree and a strong background in immunology, with over 6 years...Scientific
- ...search for a Senior Director, Global Regulatory Clinical Strategy at a... ...focused on non-opioid pain management and regenerative health solutions... ...Clinical Development, Nonclinical, CMC, Commercial, and Executive... ...Authority interactions Scientific fluency across drug development...Scientific
- .... 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...ScientificFull timeLocal areaWorldwide
- ...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... ...in the department. Coordinate with global and local affiliates. Education and...Local area
- ...ManpowerGroup Global, Inc. is seeking a Medical Writer II to join their team remotely. In this role, you will develop and edit vital scientific documents, manage content libraries, and translate complex scientific data into clear written materials. Candidates should possess...ScientificRemote workFlexible hours
- Sanofi in the United States seeks a Scientific Fellow, AI-Enabled CMC, a senior scientist who will shape strategy at the intersection of AI, computational science and Chemistry, Manufacturing and Controls. You will influence development, scale-up, tech transfer and manufacturing...Scientific
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