Validation/ Technical Writer - Andover, MA

This is a Technical Writer or Marketing Communications Specialist role that involves creating and maintaining marketing collateral. · ...

+Technical Writer role writes various technical documents such as requirements and user manuals. · +Understands validation concepts in order to produce documentation for validated systems; · +Liaises with clients or developers to gather information; and Organizes literature and w ...

A technology company seeks an electric technical writer with strong technical knowledge. Requirements include computer science or engineering work experience, content management tools like Atlassian Confluence, ASCII Doc, topic-based writing methodology skills and MS Office profi ...

The primary job responsibility will be editing master batch records in Microsoft Word to prepare for upcoming manufacturing campaigns. · Edit documents · Rout documents for review through documentation management system · ...

The Client's Cybersecurity Solutions Team is seeking a versatile Technical Writer or Marketing Communications Specialist to work with Product Management in the creation, publication and maintenance of marketing collateral. · ...

A Technical Writer position is available at an undisclosed company. The role involves authoring technical protocols, reports, and related correspondence. · ...

We are seeking an experienced Technical Writer to join our team in Boston or Andover. As a Technical Writer- Marketing Communication Specialist, you will be responsible for creating and maintaining high-quality marketing collateral materials. · ...

We are hiring Technical Writer for one of our clients. · Location: · Andover MA · ...

The technical writer will assist with verification of data within regulatory documents or reports, support bioprocess R&D teams in tracking document completion, create drafts of new technical or regulatory documents, and prepare documents using Regulatory templates in Microsoft W ...

+This role will provide non-testing support for raw material testing for new and existing products in a cGMP Quality Control Analytical (QCA) department.+ · + Revise and author GMP documents · Create and submit change requests to laboratory information management system (LIMS) bu ...

This position involves supporting regulatory dossier authoring, managing document reviews, ensuring compliance with internal standards and regulatory requirements. · ...

Author technical report summarizing production, laboratory, · validation activities and associated data · ...

This role will provide non-testing support to the QC Analytical department for product life cycle management and technology transfer activities. · The technical skills within scope will require understanding of the scientific principles of test methods, data analysis and cGMP req ...

The Technical Writer position involves creating various technical documents such as requirements specifications test plans and user manuals. · Understands validation concepts to produce documentation for validated systems. · Provides evidence of compliance with legal business and ...

We are looking for a scientist to help with technical report writing rather than an SOP or product documentation writer. · ...

The technical writer provides technical writing, administrative, and logistical support for technology projects. · Authoring of technical protocols, reports, memorandum, records, and related correspondence · Retrieve and compile data from electronic sources / databases and paper ...

The technology technical writer provides technical writing, administrative, and logistical support for technology projects.Write clear accurate reviews of the literature. · ...

The technical services support position provides technical logistical administrative and documentation support for activities pertaining to biologics drug substance production at the Andover location. · Authoring of technical protocols reports memorandum records regulatory submis ...

This Technical Writer II will provide non-testing support to the cGMP QC Analytical department for technology transfer activities. · The scope includes coordination of method transfer activity generating transfer documents to support monoclonal antibody product transfer between C ...

We are hiring Technical Writer II for one of our clients. · This role will provide non-testing support for raw material testing for new and existing products in a cGMP Quality Control Analytical (QCA) department.The candidate will be responsible for documentation support as an in ...

We are hiring Technical Writer III for one of our clients. · ...