- Aldevron (Miami, FL)
- …and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketing, to develop labeling strategies that align ... with regulatory requirements and company branding.In this role, you will...creation, issuance, and reconciliation. Implement control mechanisms, such as document control, change management, and review cycles, to maintain… more
- System One (Pittsburgh, PA)
- Job Title: QA Document Specialist Location: Onsite/Pittsburgh, PA 15219 Type: Direct-Hire Start date: End of May Overview: Join an innovative biotech team at the ... Cell and Gene Therapy! We are seeking a QA Document Specialist to manage critical documentation and...records, and other forms according to company standards and regulatory requirements. + Electronic Document Management System… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …losses in the process and build improved efficiency + Under guidance of the Senior QA Specialist Document Control, the QA Specialist - Document Control ... Quality Assurance Specialist , Document Control Department: QA Manufacturing...Support all cross functional teams within the site for document control related needs + Support regulatory … more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Document Control Specialist - Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization ... North America. Catalent Pharma Solutions is hiring a QA Document Control Specialist who is responsible for...Management Systems (LMS: ComplianeWire) preferred; + Familiar with applicable regulatory requirements (eg, 21 CFR Parts 11, 210, 211,… more
- F & S Fresh Foods (Vineland, NJ)
- Technical Document Specialist Vineland, NJ (http://maps.google.com/maps?q=500+W+Elmer+Road+Vineland+NJ+USA+08360) Description Join the Fresh Revolution with F&S ... and nourishing a fresh, healthy future for everyone! Grow Your Career as aTechnical Document Specialist ; Join our Team and Harvest Success! Join Our Team as… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Regulatory Affairs Specialist Senior (Department of Ophthalmology) Job Profile Title ... Regulatory Affairs Specialist Senior Job Description Summary Ophthalmology seeks ...document tools, as well as, to provide direct regulatory /compliance guidance and oversight of investigator-initiated trials and investigator-initiated… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile Title Clinical ... Research Regulatory Specialist B Job Description Summary The...WebEx, BlueJeans etc. Knowledge and/or experience working with web-based e- regulatory document management systems such as eFlorence,… more
- AdventHealth (Orlando, FL)
- ** Regulatory Specialist II: AdventHealth Orlando** **All the benefits and perks you need for you and your family:** - Benefits from Day One - Paid Days Off from ... outpatients each year **The role you'll contribute:** The Research Regulatory Specialist II, provides regulatory ...exemption (IDE) or biologics applications. + Provides data and document collection and compilation for regulatory filing… more
- Catalent Pharma Solutions (Manassas, VA)
- ** Document Control Specialist ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... complex formulations to help create engaging new products consumers will love. The ** Document Control Specialist ** is responsible for creation and maintenance of… more
- Astrix Technology (Indianapolis, IN)
- ** Document Control Specialist ** Quality Assurance Indianapolis, IN, US Pay Rate Low: 26.42 | Pay Rate High: 31.25 + Added - 21/03/2025 Apply for Job _Our client ... is seeking a Document Control Specialist to join their growing...Ensure that all documents comply with company policies and regulatory requirements. + Maintain and update the document… more
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