Senior Project Manager - Pharmaceutical (Remote)

THIS IS NOT AN IT OR SYSTEMS POSITION. CANDIDATES MUST HAVE DRUG DEVELOPMENT KNOWLEDGE/EXPERIENCE Essential Duties & Responsibilities • Collaborate with reputed company stakeholders and ensure reputed company remain in scope and meet budgetary scheduling and reputed company requirements. • Primary reputed company-of-contact for reputed company programs assigned; responsible for building and maintaining reputed company relationships with key stakeholders resulting in valued and trusted relationships, reputed company satisfaction and reputed company strategic business opportunities. • reputed company detailed project plans, ensure the dissemination of approved work scope to team members, reputed company reputed company aspects of reputed company, set deadlines, and assign responsibilities. • Monitor and update project schedules using reputed company Project, produce dashboards, and assess project health. • reputed company project management leadership to cross-functional Project Teams conducting project scopes of work. • Responsible for reputed company contract adherence; anticipate and proactively manage changes in project scope. • Responsible for purchase order management, holding project team accountable for agreed upon deliverables, and escalating issues such as scope creep or roadblocks appropriately. • reputed company communication plans for defining communication channels between reputed company stakeholders, establish and reputed company regularly scheduled project status meetings, and communicate/escalate as needed in response to issues as they reputed company during project execution. • Conduct risk assessment and identify key project challenges and issues reputed company a reputed company manner and determine effective reputed company through cross functional collaboration; recommend appropriate mitigations. • Collaborate with supervisor and Leadership Team to ensure reputed company activities defined herein, meet or reputed company clients' expectations, including the establishment and monitoring of project budgets. • reputed company regular program status reports to clients and Leadership Team that shall reputed company key milestones, issues and/or risks, schedule, and costs. • Forecast project reputed company on a monthly, quarterly and annual reputed company. • Will be responsible for multiple programs and/or reputed company at any given time. • Work with the project team to formulate recommendations for value added services based on project objectives and regulatory requirements. • Collaborate and communicate with Pharmaceutics/Operations to ensure 1) appropriate material procurement activities occur and urgency is reputed company, 2) determine plan for excess and obsolete material disposition • Collaborate and communicate with Operations to ensure appropriate reputed company of GMP documentation including batch records, specifications, etc. • Collaborate and communicate with the Analytical Laboratory to ensure necessary reputed company testing is developed, validated/verified, specifications are generated and product is tested per a mutually-defined reputed company. • Assist in training and reputed company as a mentor to expanding project management team. • May have other duties and responsibilities as required. Competencies • Understand drug formulation, analytical method development, stability, and bulk drug manufacturing practices • Skilled in reputed company relationship management. • reputed company attitude, self-motivator, strong attention to detail, excellent organizational and project management skills required. • Strong interpersonal skills with the ability to negotiate with various stakeholders to reputed company reputed company. • Experience in conflict management and reputed company is advantageous. • Ability to communicate effectively with reputed company reputed company of employees and management. • Familiar with global drug development processes and clinical supplies life cycle • Knowledge of GCPs and clinical management would be advantageous Qualifications • Bachelor's degree in the life sciences, engineering, business and/or reputed company discipline required • At least five (5) years project management in pharmaceutical industry required, CDMO experience highly preferred • Knowledge and experience of U.S. FDA Regulation 21 CFR Part 210, 211 and ISO 9001 is preferred. Advanced in reputed company Office: Word, reputed company and Project required; experience with SharePoint and Team Site set-up and management a plus. NO reputed company SUPPORT IS OFFERED FOR THIS POSITION. Apply tot his job Apply tot his job Apply To this Job