Project Manager

Payrate: $44.00 - $46.00/hr.Summary:Seeking an experienced Senior Project Manager to support global Quality Control technology implementation initiatives in a regulated biotech/pharma environment. This role will manage high-level, complex, cross-functional projects within defined scope, quality, timeline, and cost expectations to deliver agreed business and operational requirements. The Project Manager will coordinate global and site-level workstreams, maintain integrated project plans, manage risks, issues, dependencies, decisions, and action items, and ensure project objectives and requirements are clearly documented.Responsibilities:

• Manage the integrated project plan for QC technology implementation activities across global and site-level workstreams.
• Coordinate with site project managers to track milestones, dependencies, risks, issues, decisions, and action items.
• Facilitate routine project meetings, governance forums, and cross-functional working sessions.
• Partner with QC SMEs, Quality, IT, Validation, Regulatory, and site teams to drive alignment on implementation activities.
• Track progress against key deliverables, including procedural updates, change controls, qualification readiness, training, regulatory readiness, and operational handoff activities.
• Maintain project tools and documentation, including schedules, dashboards, risk registers, decision logs, action logs, and status reports.
• Identify risks or blockers early, drive mitigation plans, and escalate issues requiring leadership support.
• Prepare concise project updates, executive summaries, and decision options for sponsors and stakeholders.
• Support coordination of hypercare and post-implementation activities to ensure smooth transition to business ownership.

Requirements:

• The ideal candidate has demonstrated experience running medium to large-scale projects, strong knowledge of project management processes and best practices, excellent analytical and communication skills, and the ability to work effectively across cross-functional teams and management levels.
• Experience with business process development, change management, collaboration tools, and project documentation tools such as MS Project, Excel, PowerPoint, Word, Smartsheet, or equivalent is strongly preferred.
• Familiarity with GMP Quality Control operations, laboratory systems, data integrity, SOPs, change controls, and qualification/validation activities is highly desirable.

Top 3 Must Have Skill Sets:

• Global project/program management for complex technology implementations: Ability to manage integrated project plans, milestones, dependencies, risks, decisions, and governance across multiple workstreams and sites.
• Quality Control / GMP operational knowledge in biotech or pharma: Working understanding of QC laboratory operations, regulated implementation activities, SOP updates, change controls, qualification, regulatory readiness, and data integrity expectations.
• Cross-functional stakeholder leadership and executive communication: Ability to align site teams, QC SMEs, Quality, IT, Validation, Regulatory, and business stakeholders; facilitate decisions; escalate risks; and produce clear status updates for leadership.

Pay Transparency: The typical base pay for this role across the U.S. is: $44.00 - $46.00 /hr. Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match,  life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law.  Consent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary. You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts. You also acknowledge and agree to Aditi Consulting LLC’s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions. Calls may be recorded. Consent is not a condition of purchasing any property, goods, or services. You may revoke your consent at any time by replying “STOP” to :messages or by contacting

privacy@aditiconsulting.com

. For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy#AditiConsulting#26-03105