Senior QA Manager

Job description

Essential Duties and Responsibilities Plan and deliver • Build and maintain the detailed workstream plan, including milestones, dependencies, owners and critical path. • Track progress against the plan and raise schedule risks early, with options. • Maintain the deliverables register and a readiness view for the workstream. Manage risks, decisions and actions • Own the workstream risk, assumption, issue and dependency log. Drive mitigation and escalate to the Program Manager when needed. • Maintain the action register, decision log and responsibility matrix for major activities and deliverables. Run governance • Lead the weekly workstream review and prepare escalations for the Core Team. • Produce status reports, dashboards and steering committee material. • Provide inputs for program-level reporting. Bridge technical and program leadership • Understand the scientific content well enough to judge whether risk assessments, testing and technical reports are on track and realistic. • Raise concerns early and communicate trade-offs clearly to scientific and leadership audiences. Coordinate across functions • Work with MSAT, Quality, Regulatory, laboratories and manufacturing sites to keep work aligned and moving. • Direct any project support or technical writing resources assigned to the workstream. Sustain the work • In the later phase of the term, prepare handoff and closeout so that ownership, process changes and run-state responsibilities are clear.Purpose of the Role The Technical Workstream Project Manager partners with the Technical Workstream Lead to deliver the technical workstream of the Nitrosamine Control Program over a two-year term. The role connects MSAT's technical teams with the Program Manager, so that technical work stays on plan, risks surface early, and decisions are well informed. It requires a strong scientific foundation and proven project management discipline. Key Responsibilities Minimum Qualifications • Degree in chemistry, pharmacy, pharmaceutical sciences or a related scientific discipline. • 8+ years in pharmaceuticals or another regulated industry, including 5+ years managing technical projects. • Project management certification is required: PMP or PRINCE2 Practitioner. • Working knowledge of quality and compliance expectations in a regulated environment. • Proven ability to drive accountability across functions without direct authority. • Excellent written and spoken English, and strong Excel and MS Office reporting skills. • Ability to work EU business hours with regular US overlap. Skill Requirements Other Requirements Apply now Information at a Glance Why HCLTech? At HCLTech, you'll supercharge your potential. You'll find your career. And you'll find your spark. All at a place that knows that helping its customers stay on top starts by putting its people first. HCLTech is a global technology company, home to more than 230,000 people across 60 countries, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG, and Public Services. Consolidated revenues as of 12 months ending September 2026 totaled $14.8 billion. • Disclaimer • Privacy Statement • Terms of use • Sitemap • Raise a Grievance • We use cookies on our site. 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