Said quite simply, the culture is amazing!Documentation SpecialistJob Summary:Prepares loan documentation using Laser Pro for certain non-complex commercial purpose loans, to include loans made under the Small Business Association (SBA) programs. Responsibilities:• Analyzes loan request and prepares...
We are seeking a detail-oriented and organized .The successful candidate will assist project teams with the preparation of regulatory documents and provide project management support.As a project team member, you will support prescribed activities for client and internal projects, adhering to strict...
Documentation Specialist for a Contractassignment with one of our premier Pharmaceutical Services clients in Madison, NJ. Responsibilities:Review document folders in boxes and sort documents, log/track files, scanning, copying, filingSort and prepare documentation (i. ...
Responsibilities for the Quality Assurance Specialist. Qualifications for the Quality Assurance Specialist. Compensation for the Quality Assurance Specialist. Quality Assurance Specialist, QA, Pharmaceutical, Branchburg, NJ, New Jersey, FDA, GMP, Batch Record, Manufacturing, GDP, cGMP, Clinical Manu...
QA, quality assurance, biotech, biotechnology, cell therapy, cell therapies, QMS, quality management system, document management, training, trainer, training system, batch record, batch records, document review, lifecycle documents, deliverables, quality management, Phase I, Phase One, Phase 1, Phas...
Innova Solutions has a client that is immediately hiring for a .Position type: Full-time, Contract....
The Lead Technical Writer will work closely with experienced writers and other internal employees to interpret contractual specifications, engineering drawings, reports, and other data to ensure production of technical documentation that complies with customer requirements. The Lead Technical Writer...
One of our large pharmaceutical clients is looking to hire a Quality Person In Plant to join the growing External Quality team within Advanced Therapeutics. Solid quality-centric experience and mindset (QA/QC) -Strong interpersonal skills both written and verbal. This individual will be providing Qu...
GLOBAL GMP QUALITY ASSURANCE & COMPLIANCE. Support GMP quality program and implement quality programs for all commercial and clinical manufacturing operations to achieve corporate compliance goals. Solid understanding of quality management including global cGMP requirements, ISO 13485, ICH Q8, Q...
Proven experience as a Technical Writer, preferably in a regulated environment (e. Known for a commitment to being a better model of problem solving, Process Alliance provides tailored solutions that address unique client challenges in areas such as process improvement, technical compliance, and ope...
Environmental Compliance Specialist. Environmental Compliance Specialist. These screenings will be conducted by Dewberry's background vendor of choice and will be conducted in compliance with all applicable federal, state, and local law. ...
Environmental Compliance Specialist. These screenings will be conducted by Dewberry’s background vendor of choice and will be conducted in compliance with all applicable federal, state, and local law. ...
The Document Retrieval Specialist is responsible for contacting healthcare providers to request and obtain billing documents and processes document request cancellations. Meets or exceeds the Document Retrieval Performance Standards established by the Document Retrieval department. Assisting the nur...
Responsibilities for the Quality Assurance Specialist. Qualifications for the Quality Assurance Specialist. Compensation for the Quality Assurance Specialist. ...
As a Quality & Regulatory Affairs Specialist (m/w/d), you will be in charge of providing support to Capital Equipment servicing as well as to EMEA Quality and Regulatory Organisation to ensure quality and regulatory compliance. Ability to prepare high quality, clear communication materials to the ap...
Technical Writer – Pharma (Onsite, Warren, NJ). We are looking for a Technical Writer for our client, a Global Biopharmaceutical Company. Technical Writer – Pharma (Onsite, Warren, NJ). ...
As the Senior Technical Writer, you will be responsible for writing and publishing technical documents and associated content for products and solutions. Do you dream of working in a company that is driven by a meaningful purpose? One that continuously creates an inclusive environment where you are ...
Experience with Quality and Food Safety Programs such as HACCP, GMP, FSSC22000, Foreign Bodies and Allergens Controls, Documentation, Batch records, thermal process. ...
Experienced Administrative professional providing high level administrative and strategic support to the Head of North America Medical. The Executive Assistant is expected to develop a complete understanding of department functions and areas of responsibility and must have a strong commitment to pro...
Supervises all non-clinical administrative functions such as van repairs, office supplies, building/house maintenance, various quality assurance controls. ...
Primary responsibility for processing Accounts Payable and providing administrative assistance in support of projects on the Finance Team as a task specialist by utilizing processes and resources in a manner that is efficient, effective, and contributes to the overall success of the Finance Team wit...
IQVIA is hiring a team of Hospital Clinical Specialists – Diagnostic in partnership with our client DiaSorin. The primary objective of the Hospital Clinical Specialist – Diagnostic is to encourage the use of DiaSorin’s LIAISON® MeMed BV® test in the hospital setting – with emergency medicine and inf...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. The ideal candidate must be agile and have well-developed orga...