More jobs:
Quality Process Manager
Job in
West Chester, Chester County, Pennsylvania, 19383, USA
Listed on 2026-07-01
Listing for:
Katalyst Healthcares & Life Sciences
Full Time
position Listed on 2026-07-01
Job specializations:
-
IT/Tech
Technical Writer
Job Description & How to Apply Below
Business / Quality Process Manager
We are seeking a Business / Quality Process Manager to join our Process and Data Management (PDM) team within IM Quality Systems. In this role, you will act as a critical bridge between R&D business partners and procedural document deployment, ensuring highly technical and regulatory information is accurately translated into clear, compliant documentation. You will own the end-to-end process mapping, writing, and quality checking of procedural and training documents, ensuring adherence to GCP (Good Clinical Practice) standards within clinical R&D and device business frameworks.
Roles & Responsibilities:
- Process Mapping & Documentation:
Collaborate directly with R&D business partners to extract operational information, translate it into clear procedural documents, and perform rigorous process mapping and quality checks. - GCP Compliance:
Ensure all process documents and procedural content strictly align with Good Clinical Practice (GCP) guidelines and broader Quality Management System (QMS) frameworks. - Training & Curriculum Deployment:
Assist in setting up training curricula, drafting communication materials for training rollouts, and deploying training modules via the Learning Management System (LMS). - Project & Meeting Management:
Define project schedules, support procedural document approvals via the Electronic Document Management System (EDMS), and set up/facilitate alignment meetings with internal and external stakeholders. - Cross-Functional Collaboration:
Maintain continuous communication with business owners, resolve procedural issues, and ensure compliant documents are fully installed for dedicated processes.
Qualifications & Requirements:
- Education:
Bachelor's degree required. - Experience:
5+ years of relevant professional experience in a medium to large corporate organization (Pharma, Biotech, or Clinical R&D preferred). - Domain Expertise:
Deep understanding of GCP (Good Clinical Practice) content and regulatory requirements applicable to procedural documents. - Core
Skills:
Exceptional technical writing, process mapping, and verbal communication skills. Ability to interview business partners, extract complex details, and synthesize them into clear processes. - System Knowledge:
Familiarity with automated systems, specifically Electronic Document Management Systems (EDMS) and Learning Management Systems (LMS). - Logistics:
Must be comfortable working in the EST time zone (if remote) or commuting hybrid (3 days onsite in West Chester, PA).
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×