Project Controls Lead

16 ore fa


parma, Italia GlaxoSmithKline A tempo pieno

Site Name: Italy - Parma, Italy - RosiaPosted Date: Jan 8 2026Job DescriptionWe create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK.Locations: Parma (Italy), Rosia (Italy)Reports To: Project Controls Director EU&UKDepartment: Project Controls, Global Capital Projects (GCP)ScopeAs Project Controls Lead within Global Capital Projects (GCP), you will be responsible for overseeing project control functions across capital investment projects in Europe. You will ensure robust planning, cost control, risk management, and performance reporting to support timely and compliant project delivery in a regulated environment – with a team of Planners, Cost managers, Contracts managers, Risk managers etc. You will be working alongside Project Managers to deliver one or more projects within cost, schedule, scope.This role will directly report to the Project Controls Director EU&UK and will be part of Project Controls function.In this role you willPlanning & SchedulingDevelop and manage integrated project schedules for pharmaceutical capital projects using tools like Primavera P6 or MS Project.Coordinate with engineering, validation, and quality teams to align timelines with regulatory milestones.Monitor progress and proactively identify schedule risks, delays, and mitigation strategies.Cost ManagementEstablish and maintain cost control systems tailored to pharma project structures.Track budgets, forecasts, commitments, and actuals across multiple workstreams.Support financial reporting and capital expenditure tracking in collaboration with Finance.Risk & Change ManagementFacilitate risk identification and mitigation planning, especially around regulatory, quality, and supply chain impacts.Manage change control processes and assess impact on cost, schedule, and compliance.Reporting & GovernanceGenerate and present project performance dashboards and reports to senior stakeholders.Ensure compliance with internal governance, GMP requirements, and external audit standards.Support stage-gate reviews and portfolio-level reporting.Stakeholder EngagementCollaborate with cross-functional teams including Engineering, Quality Assurance, Regulatory Affairs, Procurement, and Manufacturing.Act as a key interface between project teams and senior leadership.Team LeadershipLead and mentor project controls professionals across multiple projects or sites.Promote continuous improvement in project controls practices and tools.Why you?Qualifications & SkillsWe are looking for professionals with these required skills to achieve our goals:Bachelor’s degree in Engineering, Project Management, Finance, or related field.10+ years of experience in project controls, with at least 3 years in a leadership role within the pharmaceutical or life sciences industry.Hands on experience working as Project Planner/ Scheduler or Cost manager within Capital project environment.Good knowledge and experience of Planning, Cost Management, Commercial management, Contract management, Risk management and Project management.Strong senior stakeholder management and project reporting capabilities.Fluent in English and Italian, both written and spoken.Preferred Qualifications & SkillsMSc or other Chartered / Professional Qualification in a relevant discipline.Good pharma background or working experience from capital projects.Familiar with the GCP Project Management Framework (PMF), relevant engineering standards and compliance requirement as well as Quality Management Systems.PMP (Project Management Professional) or CCP (Certified Cost Professional) or PMI-SP (Scheduling Professional) or Lean Six Sigma or similar process improvement credentials.What We OfferPermanent contract in a very Inclusive environmentFlexible BenefitsCompany Healthcare PlanIntegrative pension fundEmployee Assistance ProgrammeSustainable Mobility ProgrammeCompany canteenPerformance RewardClosing Date for Applications – 22 of JanuaryPlease note that relocation support cannot be provided; therefore, only candidates who are already based in the indicated country can be considered.Please take a copy of the Job Description, as this will not be available post closure of the advert.When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.Why GSK?Uniting science, technology and talent to get ahead of disease together.GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.Please note, if you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at



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