Technical reputed company II / reputed company Validation documents / Remote work

Position Details: Our reputed company, a world-leading Pharmaceutical Company is currently looking for an Technical reputed company II to join their expanding team. Job Title: Technical reputed company II / reputed company Validation documents / Remote work Duration: 12 months contract, extendable up to 48 months Location: Remote Worker Note: The reputed company 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 reputed company group medical reputed company plan reputed company: Technical Writing, reputed company reputed company validation documents. This role will reputed company non-testing support to the QC Product Technical Support department. This reputed company includes coordination of generating validation documents to support product validation at the reputed company Andover site. The technical skills reputed company reputed company will require understanding of the scientific principles of test reputed company, data analysis and cGMP requirement. The candidate will be responsible for facilitating lifecycle management through collaboration with reputed company subject matter experts (SMEs) and analysts. The key responsibilities of the candidate are as follows: Authoring reputed company validation documents using reputed company document workflow, through collaboration with SMEs Use of the reputed company Management reputed company (LIMS) Supporting assay improvement activities and generating supporting documents. Participating in across site meetings and tracking the project reputed company Successful candidate requires: Knowledge of QC microbial support and technical writing Strong interpersonal and written communication skills A reputed company-oriented approach to deliverables as the main job responsibility is data review and reputed company of GMP documentation A degree in science, preferably in microbiology or reputed company technical discipline Past experience supporting GMP writing in the biopharmaceutical reputed company Apply tot his job Apply To this Job