Site Name: USA - Pennsylvania - Marietta
Posted Date: Jun 12 2025
As a Senior Project Manager/Project Engineering Manager at GlaxoSmithKline (GSK), you will be responsible for leading and managing the project engineering, construction, and commissioning/ qualification activities of pharmaceutical manufacturing facility projects from concept through completion. You will oversee the design, planning, execution, and delivery of projects, ensuring they meet safety, quality, scope, schedule, and cost requirements. Your role will involve coordination of large cross-functional teams, managing tasks on schedule, supervising resources, and ensuring compliance with regulatory and safety standards. In this role, you will leverage your strong technical expertise and leadership skills to drive the successful execution of complex construction/engineering projects of pharmaceutical facilities designed for drug substance and drug product manufacturing. You will work closely with stakeholders, including internal teams, contractors, suppliers, and local authorities to ensure project objectives are achieved. Your ability to concurrently manage multiple tasks or projects, solve technical and operational challenges, communicate effectively, and work efficiently in a fast-paced environment will be key to your success. Your key responsibilities include:
- The management of construction/engineering projects of pharmaceutical facilities that are designed to produce drug substance and drug products, from concept, through detailed engineering, procurement, construction, to qualification. You will successfully lead the development, execution and delivery of these projects to meet or exceed safety, quality, scope, schedule, and cost objectives.
- Project Engineering: Lead and/or contribute to the scoping, concept, basic, and detailed design/engineering of pharmaceutical R&D and manufacturing facilities including, facility systems, clean utilities, process equipment, process automation, building automation systems, clean rooms, cold chains, and effluent handling systems.
- Project Delivery: Lead all aspects of the delivery of the project including bidding process, vendor selection, contractor onboarding, construction phasing, construction safety, facility fit out, equipment installation, utility connection, prestart up activities, SAT, commissioning, IQ and OQ, and transfer of assets to manufacturing for process qualification.
- Project Management: Lead key aspects of the project management and be accountable for delivering projects on scope, schedule and cost. Should be skilled in relevant areas including resource loaded schedule development, critical path analysis, schedule derisking, schedule management, cost basis assessment, cost control, quantity estimate, quality control, and change management.
- Project Control: Experience developing relevant leading and lagging project KPIs such as SV, BV, EV, CPI, SPI, OTCI, CSAT, and NOCR and use them to proactively assess and control the progress of the project.
- Construction Management and Safety: Experience developing and executing construction plan for large capex projects, mobilization of trades/equipment/materials, securing appropriate permits, implementing rigorous construction safety processes and metrics, and complying with
- local (OSHA) and global construction safety processes to complete the construction in the most efficient manner with zero safety incidents or lost time.
- Project Commissioning: Experience generating Turnover packages (TOP) of facility, utility, process, equipment, and automation systems to successfully complete the commissioning of pharma R&D and manufacturing facilities. Experience leading checkout, dry run, wet run, punch list, SAT, commissioning, Installation Qualification, Operational Qualification, change control strategy, validation strategy, and the development and execution of related protocols and reports.
- Project Communication: Experience developing and delivering communication plan for the project, including tier meetings, steering meetings, safety reviews, gate reviews, and town halls. Maintain effective dialogue with stakeholders, leadership, site personnel, contractor base, and key departments including engineering, facilities, quality, finance, and validation.
Why you?
Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:
- Bachelor's degree in Engineering or Project Management or Business
- 10+ years of prior project and/or engineering experience
- Prior project experience in the design, construction, start-up and operation of large bulk biopharmaceutical drug substance AND drug product fill / finish facilities.
- Experience in Risk Management
- Experience in a regulated environment focused on design, qualification, and troubleshooting of processes and equipment.
- Position may require employees to work shifts, holidays, and weekends
Preferred Qualifications: If you have the following characteristics, it would be a plus:
- Master's Degree or higher; PMP Certification
- Detailed understanding of Design, Installation, and Commissioning / Qualification / Validation of new pharmaceutical equipment and/or utilities.
- Knowledge of biological/vaccines manufacturing and its management, including relevant regulations governing the manufacture and supply of pharmaceutical products, is a plus.
- Proficiency with ERP (ex/SAP) and Power Apps
- Must be able to interact well with peers, subordinates, and senior personnel in scientific, engineering, and operational disciplines.
- Demonstrated ability to participate as a leader or member on cross-functional and self-directed work teams.
- Must be comfortable and thrive in ambiguity and think strategically to solve complex problems.
- Strong interpersonal, written and oral communication skills
- Strong organizational and leadership skills; ability to lead a team and make critical decisions
- Project Management Professional (PMP) or other relevant certification is a plus.
- Strong knowledge of project scheduling principles, methodologies, and best practices.
- Advanced organizational and time management skills.
- Ability to work collaboratively with cross-functional teams and stakeholders.
- Strong analytical and problem-solving abilities.
- Proven experience in project scheduling, preferably within the pharmaceutical, healthcare, or construction industries.
- Strong knowledge of project scheduling principles, methodologies, and best practices.
- Proven expertise in project scheduling software and tools (e.g., Microsoft Project, Primavera P6).
- Ability to work collaboratively with cross-functional teams and stakeholders.
- Strong technical writing skills
- Influence, persuasion, and or change management
- GPS, Six Sigma, OE, or similar continuous improvement methodologies
- Ability to work in a digital engineering environment
- Proficiency in project scheduling software and tools (e.g., MS Project, Primavera 6 (P6), MS Timeline, l).
- ICT skills (software, operating systems, hardware, etc.)
- Digitization and electronic work environment experience, including experience with MES, CAD, large language models for improving efficiency, and application of digital tools to improving performance.
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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/ Agencies GSK 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 https://openpaymentsdata.cms.gov/
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