Technical Writer
ManpowerGroup Global, Inc., Wind Lake, WI, United States
Our client is seeking a dedicated and detail-oriented Technical Writer to join their team. As a Technical Writer, you will be an integral part of the QC Product Technical Support department, supporting product validation and documentation processes. The ideal candidate will demonstrate strong scientific understanding, excellent communication skills, and a collaborative spirit, aligning seamlessly with the organization’s commitment to quality and innovation.
Job Title:
Technical Writer Location:
Andover, MA Job Overview
Authoring method validation documents using Pfizer document workflow in collaboration with subject matter experts (SMEs). Supporting assay improvement activities and generating supporting documentation. Utilizing Laboratory Management System (LIMS) for data entry and management. Facilitating lifecycle management through cross‑functional collaboration. Participating in site meetings and tracking project timelines to ensure timely completion of deliverables. Qualifications
Knowledge of QC microbial support and technical writing within a GMP environment. Strong interpersonal and written communication skills. Attention to detail with a focus on data review and GMP documentation. A degree in science, preferably in microbiology or a related technical discipline. Previous experience supporting GMP documentation in the biopharmaceutical field is highly desirable. Benefits
Opportunity to contribute to innovative biopharmaceutical projects. Collaborative work environment with a focus on scientific excellence. Engagement in meaningful work supporting product validation and lifecycle management. Potential for professional growth within a global organization. Participation in a company committed to quality and continuous improvement. If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
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Technical Writer Location:
Andover, MA Job Overview
Authoring method validation documents using Pfizer document workflow in collaboration with subject matter experts (SMEs). Supporting assay improvement activities and generating supporting documentation. Utilizing Laboratory Management System (LIMS) for data entry and management. Facilitating lifecycle management through cross‑functional collaboration. Participating in site meetings and tracking project timelines to ensure timely completion of deliverables. Qualifications
Knowledge of QC microbial support and technical writing within a GMP environment. Strong interpersonal and written communication skills. Attention to detail with a focus on data review and GMP documentation. A degree in science, preferably in microbiology or a related technical discipline. Previous experience supporting GMP documentation in the biopharmaceutical field is highly desirable. Benefits
Opportunity to contribute to innovative biopharmaceutical projects. Collaborative work environment with a focus on scientific excellence. Engagement in meaningful work supporting product validation and lifecycle management. Potential for professional growth within a global organization. Participation in a company committed to quality and continuous improvement. If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
#J-18808-Ljbffr