Document Management Specialist

The US Pharma Lab is seeking a skilled Documentation Specialist to join our team. As a key member of the Quality Assurance department, you will be responsible for creating, distributing, collecting, storing, and maintaining accurate and compliant documentation.The ideal candidate will have a strong understanding of quality assurance principles and experience...

The US Pharma Lab is hiring a QA Documentation Specialist to support our Quality Assurance team. In this role, you will be responsible for creating, reviewing, and maintaining various documentation types, including product specifications and compliance documents.You will work closely with cross-functional teams to ensure that all documentation is accurate,...

About the RoleAs a Quality Assurance Documentation Associate, you will play a vital role in ensuring the accuracy and completeness of our company's documentation. Your attention to detail and organizational skills will enable you to excel in this position.Main Responsibilities:Daily tracking of raw materials, shipping, results, and status.Review and issue...

Job DescriptionDate 06/2018 Location 1300 Airport Road, North Brunswick NJ Title Associate, Quality Assurance Documentation Department Quality Assurance Reports to Manager, Quality Assurance FLSA (Exempt or Non-Exempt Exempt Role Overview Level 1 The Associate, QA Documentation 1, will be responsible for the writing, distribution, collection, storage, and...

Date 08/2021 Location 1300 Airport Road, North Brunswick NJ Title Associate, Quality Assurance Documentation 2 Department Quality Assurance Reports to Director, Quality Assurance FLSA (Exempt or Non-Exempt Exempt Role Overview An Associate, QA Documentation 2 will be responsible for the writing, distribution, collection, storage, and maintenance of our...

Job DescriptionKey Responsibilities:Manage document preparation of CMC regulatory submission documents to company standards and ensure final document compliance to ensure submission content meets formatting requirements.Manage the logistical process in the authoring system for CMC regulatory submissions.Facilitate data verification to ensure accuracy of...

Key ResponsibilitiesThe Human Resources Manager will oversee and coordinate the administrative and operational functions of the HR department. This includes supervising key HR team members such as recruiters, payroll specialists, and other assigned staff.

About the RoleWe are seeking a highly organized and detail-oriented individual to join our team as a Document Controller.About UsISEE Careers is a dynamic company that specializes in the development, manufacture, and marketing of in-vitro diagnostics (IVD) tests.Key ResponsibilitiesDevelop and implement production processes related to document control and...

Job Summary:We are seeking a detail-oriented and organized Logistics Operations Specialist to join our team. As a key member of our logistics operations, you will be responsible for inspecting, inventorying, and documenting incoming and outgoing shipments of property.Responsibilities:Inspect transporters' shipping documents (bills of lading, Customs Forms)...

We are seeking a skilled Facilities Engineering Specialist to join our Architecture/Engineering Process Practice. In this role, you will support clients in the advanced technology, pharmaceutical, food & beverage, bulk chemical, and bulk gas industries. You will work closely with project teams, clients, and vendors to deliver high-quality solutions. Our...

81728TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.Our client, a leading pharmaceutical company is hiring a Documentation Analyst.Must possess working knowledge of regulatory CMC submissions. Experience in Cell Therapy is a plus.MUST have a clear understanding of CMC submission structure with respect to the...

About the job Document Controller Company Overview The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests. Responsibilities Develop and implement production processes related to document control and management Collect and register all technical document, such as drawings and blueprints in the Companys system Review and update...

About the Role:At Zobility, we are seeking a skilled AS9100 Documentation Specialist to join our team. This individual will play a critical role in ensuring the accuracy and efficiency of our First Article Inspection (FAI) documentation process.Key Responsibilities:Transferring inspection information from blueprints to formal AS9100 FAI documentsBallooning...

GFL Environmental is seeking a highly skilled Waste Management Specialist to join our team. As a Waste Management Specialist, you will be responsible for operating a container delivery truck and ancillary equipment on an assigned route to service customers by delivering and removing solid waste dumpster containers in a safe and efficient manner.Key...

At Alliance Health System, we are seeking a highly skilled Clinical Support Specialist to join our team. In this role, you will play a vital part in ensuring efficient and effective patient care delivery within the orthopedic department.The Clinical Support Specialist is responsible for providing administrative and clinical support to patients, healthcare...

Salary & BenefitsThe Treatment Coordinator role at MAX Surgical Specialty Management offers a competitive salary and benefits package. As a member of our team, you can expect a comprehensive compensation plan that reflects your skills and experience.Our benefits package includes a range of perks and advantages designed to support your well-being and career...

Gotham Enterprises Ltd is seeking a dedicated Medical Rehabilitation Specialist to join our orthopedic outpatient practice in East Brunswick, New Jersey.This role involves helping patients regain mobility and improve their quality of life. Our state-of-the-art facility provides a supportive team environment.Responsibilities:Assess and develop individualized...

About the RoleWe are seeking a detail-oriented and organized individual to join our team as a Document Controller.About Our CompanyISEE Careers is a leader in the field of in-vitro diagnostics (IVD) tests.Key ResponsibilitiesDevelop and implement production processes related to document control and management.Collect and register all technical documents,...

About the PositionWe are seeking a qualified Document Controller to join our team at ISEE Careers.About Our CompanyISEE Careers is a reputable company in the field of in-vitro diagnostics (IVD) tests.Job SummaryDevelop and implement production processes related to document control and management.Collect and register all technical documents, such as drawings...

Job DescriptionJob DescriptionJob Title: Documentation AnalystLocation: RemoteDuration: 6+ MonthsWork Schedule: Mon - Fri, Business HoursSummary:This role will be responsible for managing the documentation activities for marketing applications and/or post-approval regulatory submissions for cell therapy brands.This role may also require the preparation of...