Procedure Writer - New Brunswick

Prepares and revises standard operating procedures for GMP laboratories including types related to laboratory operation instruments and microbiology and chemistry testing. · Will need to interview subject matter experts and translate their description of process into actionable i ...

This role involves planning developing organizing writing and editing Job Aids and Standard Operating Procedures. · ...

Job summary · A Technical Procedure Writer is responsible for creating and maintaining clear, concise, and accurate procedural documentation that guides employees and ensures compliance with industry standards. · Bachelor's degree in Technical Writing, English or Communications. ...

A Technical Procedure Writer creates and maintains clear and accurate procedural documentation for retail branch operations. · ...

A Technical Procedure Writer is responsible for creating and maintaining clear, concise, and accurate procedural documentation that guides employees and ensures compliance with industry standards. This role will be primarily focused on our retail branch operations. · Create detai ...

We are seeking a skilled Technical Writer/Procedure Document Specialist to collaborate with colleagues, customers and stakeholders on projects focused on process enhancement and continuous improvement within the CMR Strategic Operations. · ...

We are seeking a Technical Writer/Procedure Document Specialist IV to join our team. The successful candidate will have 7+ years of professional experience in the pharmaceutical industry and strong writing, documentation, and communication skills. · ...

The client is seeking a Technical Writer/Procedure Document Specialist IV with experience in pharmaceutical business processes and change management to manage multiple projects simultaneously. · ...

We are seeking an experienced Technical Writer/Procedure Document Specialist IV to join our team at Xoriant Corporation.This role is responsible for designing and documenting pharmaceutical business processes and change management procedures. · ...

Kelly Science and Clinical FSP is seeking a EUMDR Medical Writer for remote long term engagement with Global Medical Device client. · ...

Dice is the leading career destination for tech experts at every stage of their careers. · ...

Perform investigations and assist manufacturing and packaging operations on investigations, Product quality complaints. Assist in cross functional investigations for out of specification (OOS), out of trend (OOT), Laboratory Events, CAPAs, and change controls. · ...

Kelly Science and Clinical FSP is currently seeking a EUMDR Medical Writer for remote engagement with Global Medical Device client. · ...

Kelly Science and Clinical FSP is seeking a EUMDR Medical Writer for a remote long-term engagement with one of our Global Medical Device clients. · This person will join our Kelly FSP (Functional Service Provider) division. · As a Kelly FSP employee you may be eligible for paid ...

The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). This individual will be responsible for delivering CMC documentation to support the regulatory strategy for ...

This individual will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. · Co-authors/ authors scientific content for CTD ...

This individual will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. · Co-authors/authors scientific content for CTD ...

This individual will be responsible for delivering CMC documentation to support the regulatory strategy for the Cell Therapy clinical portfolio. · Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy. · Plan and facilitate submission ki ...

This individual will be responsible for delivering CMC documentation to support the regulatory strategy for the Cell Therapy clinical portfolio.The role requires effective collaboration across technical functions to deliver on timelines for submissions. · ...

We have a new opening for a SAS Developer in Brunswick, New Jersey for a 1 year contract who can come in-person. · I wanted to reach you out and see if you have any consultants available to work on the east coast. · ...