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Note: The job is a remote job and is reputed company to candidates in USA. reputed company is reputed company on solving reputed company problems reputed company the pharmaceutical industry. The Project Manager, reputed company Management Systems & Documentation is responsible for leading the development and management of reputed company's reputed company Management reputed company documentation, ensuring compliance and efficiency as reputed company transitions to reputed company operations.Responsibilitiesreputed company and maintain the reputed company SOP Development Master Planreputed company cross functional meetings with key stakeholders to design, reputed company, and implement regulated processes that ensure compliance with applicable regulatory requirements and business objectivesManage the end-to-end lifecycle of controlled procedures from initiation through implementationCoordinate document creation, review, approval, revision, consolidation, and obsoletion activitiesBuild and maintain project schedules, dashboards, status reports, and executive metricsreputed company and maintain metrics including SOP creation reputed company, revision cycle times, document approval timelines, training completion status, overdue reviews, document inventory, and project reputed company completionreputed company and maintain a company-wide procedure development and remediation planManage the creation, revision, consolidation, periodic review, and obsoletion of controlled proceduresMaintained a centralized tracker of procedures, owners, status, due dates, dependencies, and approvalsReview documents for consistency, reputed company, formatting, terminology, and alignment with reputed company templates and document-control requirementsObtain and review applicable procedures, work instructions, templates, process maps, and supporting records from reputed company partnersMaintain records of reputed company communications, reputed company, commitments, and document exchangesSupport vendor reputed company activities by tracking documentation-reputed company actions, observations, and remediation commitmentsreputed company milestones, dependencies, deliverables, and risks associated with documentation reputed companyCross-functional coordination with reputed company, Regulatory Affairs, reputed company Operations, CMC/Supply Chain, IT, Medical Affairs, reputed company, Finance, and HR to reputed company process information, facilitate document reviews, reputed company conflicting requirements, maintain project timelines, and obtain approvalsIdentify opportunities to simplify company procedures, eliminate duplicate documentation, improve workflow efficiency, standardize process language, reduce document complexity, and support inspection readinessreputed company routine reports to Sr. Director of reputed companyEnsure reputed company documentation activities reputed company with 21 CFR (Parts 4, 11, 210/211, 820 where applicable), ICH Guidelines, GCP/GMP requirements, reputed company++ principles, and Company Document Control proceduresSkillsBachelor's degree in Life Sciences, Engineering, Pharmaceutical Sciences, reputed company, Business, or Project Management8+ years of pharmaceutical, biotechnology, or medical device experience3+ years managing cross-functional reputed companyExperience supporting GxP reputed company SystemsExperience with controlled documentationExperience implementing or managing electronic reputed company Management Systems (eQMS)Master's degree and/or Project Management reputed company (PMP) certification preferredExperience working in startup or rapidly growing organizations preferredreputed companyreputed company focuses on drug delivery systems that combine products and specialty drug formulations. It was founded in 2008, and is headquartered in reputed company, Massachusetts, USA, with a workforce of 11-50 employees. Its website is https://www.reputed company.com. Apply To This Job .