What are the responsibilities and job description for the Technical Writer II / Method Validation documents / Remote work position at Pioneer Data?
Position Details:
Our client, a world-leading Pharmaceutical Company is currently looking for an Technical Writer II to join their expanding team.
Job Title: Technical Writer II / Method Validation documents / Remote work
Duration: 12 months contract, extendable up to 48 months
Location: Remote Worker
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Our client, a world-leading Pharmaceutical Company is currently looking for an Technical Writer II to join their expanding team.
Job Title: Technical Writer II / Method Validation documents / Remote work
Duration: 12 months contract, extendable up to 48 months
Location: Remote Worker
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Technical Writing, Author method validation documents.
This role will provide non-testing support to the QC Product Technical Support department.
This scope includes coordination of generating validation documents to support product validation at the client Andover site.
The technical skills within scope will require understanding of the scientific principles of test methods, data analysis and cGMP requirement.
The candidate will be responsible for facilitating lifecycle management through collaboration with laboratory subject matter experts (SMEs) and analysts.
The key responsibilities of the candidate are as follows:
Authoring method validation documents using client document workflow, through collaboration with SMEs Use of the Laboratory Management System (LIMS) Supporting assay improvement activities and generating supporting documents.
Participating in across site meetings and tracking the project timeline Successful candidate requires: Knowledge of QC microbial support and technical writing Strong interpersonal and written communication skills
A detail-oriented approach to deliverables as the main job responsibility is data review and generation of GMP documentation A degree in science, preferably in microbiology or related technical discipline Past experience supporting GMP writing in the biopharmaceutical field
Authoring method validation documents using client document workflow, through collaboration with SMEs Use of the Laboratory Management System (LIMS) Supporting assay improvement activities and generating supporting documents.
Participating in across site meetings and tracking the project timeline Successful candidate requires: Knowledge of QC microbial support and technical writing Strong interpersonal and written communication skills
A detail-oriented approach to deliverables as the main job responsibility is data review and generation of GMP documentation A degree in science, preferably in microbiology or related technical discipline Past experience supporting GMP writing in the biopharmaceutical field