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    "requisitionDescription": "<p><strong><span style=\"font-family: arial, sans-serif; font-size: 16px;\">About the Role</span></strong></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\">Woodstock Sterile Solutions is seeking a skilled and driven <strong>Project Manager&nbsp;</strong>to lead technical projects supporting new product development within our facility. This role is critical in managing drug development projects from feasibility through pre-commercialization, as well as overseeing technical transfers and customer product qualifications. &nbsp;You will serve as the primary point of contact for clients while coordinating cross-functional teams to deliver high-quality results on time and within scope.</span></p><hr><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><br></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 16px;\"><strong>Key Responsibilities</strong></span></p><ul><li data-pasted=\"true\" style=\"font-family: arial, sans-serif; font-size: 14px;\">Develop, manage, and maintain detailed project timelines using MS Project, including task planning, resource allocation, and deliverables tracking</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Lead projects through the full lifecycle, ensuring milestones and client commitments are met</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Coordinate internal teams and client stakeholders to drive project execution and communication</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Identify risks, anticipate delays, and implement mitigation strategies</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Maintain accurate project documentation, plans, and status reports</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Track deliverables, project health, and customer satisfaction metrics</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Facilitate internal and external project meetings, including agendas and follow-ups</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Manage project-related contracts and requests</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Serve as the primary liaison for customers, ensuring strong communication and relationship management</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Support revenue tracking and billing through business systems (e.g., JDE)</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Ensure compliance with quality systems, cGMP standards, and safety requirements</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Host customer visits and provide project updates to leadership</li></ul><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><br></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 16px;\"><strong>Qualifications</strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>Education:</strong></span></p><ul><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Bachelor&#39;s degree in Chemistry, Pharmacy, Engineering, or related field (required)</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">PMP certification (preferred)</li></ul><p><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong>Experience:</strong></span></p><ul><li style=\"font-family: arial, sans-serif; font-size: 14px;\">5+ years of relevant experience in pharmaceutical development and project management</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Experience managing client-facing projects strongly preferred</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Have worked in CDMO/CMO industry</li><li style=\"font-family: arial, sans-serif; font-size: 14px;\">Deep understanding of cGMP standards and FDA/ICH regulatory guidelines</li></ul><p><strong>Skills &amp; Competencies</strong></p><ul><li data-pasted=\"true\">Strong project management and organizational skills</li><li>Excellent written and verbal communication abilities</li><li>Proven ability to manage multiple projects and priorities simultaneously</li><li>Strong analytical thinking and problem-solving skills</li><li>High attention to detail and documentation accuracy</li><li>Ability to work independently and in cross-functional teams</li><li>Proficiency with business software tools (MS Office, project management systems, etc.)</li><li>Knowledge of cGMP and pharmaceutical development processes</li><li>Ability to perform risk assessments and drive proactive solutions</li></ul><p><strong>Physical Requirements</strong></p><ul><li>Regular sitting, standing, walking, and computer use</li><li>Occasional lifting (up to 30 lbs.) and physical movement as needed</li></ul><p><strong>Work Environment</strong></p><ul><li data-pasted=\"true\">Fast-paced, performance-driven setting</li><li>Collaborative and team-oriented culture</li><li>Strong focus on customer satisfaction and quality</li></ul><p><br></p><p><em>Notice to Agency and Search Firm Representatives: Woodstock Sterile Solutions is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Woodstock Sterile Solutions employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Woodstock Sterile Solutions. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.</em></p>\n",
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