BeOne Medicines logo

Associate Director, Small Molecule Plant IT Systems

BeOne Medicines

Pennington, NJJobSeen 3 days agoSeen in employer's feed 3 days ago

Most applications go out cold — see where you stand first. No sign-up to start.

Watch jobs like this.

At a glance

Compensation
No compensation found
Location
Pennington, NJ
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

As a key member of BeOne Medicines’ site IT team at its Hopewell, New Jersey facility, the Associate Director supports the design, construction, and validation of IT infrastructure and systems for a greenfield small-molecule pharmaceutical plant. The role oversees project delivery, collaborates with manufacturing, quality, engineering, and global IT teams, and advances systems and processes in alignment with Pharma 4.0 initiatives.

Skills & qualifications

RequiredNice to have

Skills

GxP ManufacturingGood Manufacturing PracticeGAMP 5Validation DocumentationMESE-LogbooksDCSSCADABMSEMSAsset ManagementNetworkingFirewallsData CentersVirtualized EnvironmentsDistributed InfrastructuresIndustry 4.0ISA 95Allen Bradley PLCsSiemens PLCsAveva PI HistorianWeighing and DispensingGranulationTabletingCoating ProcessesCommunicationExecutive PresentationsInterpersonal SkillsTeamworkDiplomacyProject ManagementBudget ControlLean Six SigmaGreenbelt TrainingWindows Server ADAWSNetwork InfrastructureMS-SQLSmartsheetVeeva

Qualifications

8+ Years IT Management or LeadershipPharmaceutical Manufacturing ExperienceBachelor's in IT, Computer Science, Engineering or Related Field

Full job description

Preferred Experience : Pharmaceutical/Biotech Industry

Location : Hopewell

General Description:

As a key member of the site IT team at BeOne Medicines' Hopewell, NJ facility, this role is centered on supporting the design, construction, and validation of IT infrastructure and systems for a greenfield Small Molecule Pharma plant. Responsibilities encompass overseeing project delivery, supporting project teams, maintaining and strengthening stakeholder relationships, and driving operational excellence. As part of the Global Technology Services (GTS) team, the candidate will be instrumental in advancing systems, processes, and infrastructure in alignment with Pharma 4.0 initiatives to support and drive the company’s growth.

Essential Functions:

IT Infrastructure and Support:

  • Oversee the construction, validation, and support of IT systems specific to Small Molecule Plant operations.

  • Supervise the design, construction, validation, and integrity of IT infrastructure including LAN, networking equipment, and servers.

  • Install, validate, and maintain IT devices and equipment in QC lab and manufacturing plant environments.

Project Management and Collaboration:

  • Work independently to provide technical direction and manage projects with minimal supervision.

  • Act as the primary IT interface to identify and prioritize new site development requests.

  • Work collaboratively with manufacturing and quality teams to ensure the new plant operates reliably and efficiently in a 24/7 commercial manufacturing environment.

Compliance and Security:

  • Partner with project teams and Global IT counterparts to establish a GxP-compliant environment.

  • Collaborate with Engineering and QA teams to assess and enhance system data integrity, security, and system integration.

  • Ensure adherence to corporate IT strategies and standards, recommending changes when necessary.

  • Configure system backups and recovery protocols.

Technology Advancement:

  • Play a key role in delivering technology services that enhance business processes.

  • Implement the IT vision and advance the company's systems, processes, and infrastructure.

  • Introduce new technologies in a dynamic environment, supporting future growth.

Experience and Knowledge:

  • Extensive knowledge of complex, GxP manufacturing facilities and strong understanding of Good Manufacturing Practice (GMP) and GAMP 5.

  • Experienced in authoring and approving validation documents.

  • Familiarity with systems such as MES, E-Logbooks, DCS, SCADA, BMS, EMS, and asset management.

  • Understanding of networks, firewalls, and data centers, with experience in virtualized environments and distributed infrastructures.

  • Experience with Industry 4.0 technologies and proficient understanding of ISA 95 standards.

Technical Skills:

  • Knowledge of Allen Bradley and Siemens PLCs, as well as Aveva PI historian.

  • Understanding of equipment used in weighing and dispensing, granulation, tableting, and coating processes.

Soft Skills:

  • Strong communication and executive presentation abilities.

  • Excellent interpersonal skills for effective teamwork.

  • Diplomacy and capability to rationalize multiple points of view.

Minimum Requirements – Education and Experience:

  • Bachelor’s degree in information technology, Computer Science, engineering or related field

  • 8+ years in IT management or leadership roles, with a preference for experience in pharmaceutical manufacturing, particularly in mid-size plants.

Other Experience:

  • Project Management, Budget Control, Lean Six Sigma, Greenbelt training and experience

Supervisory Responsibilities:

  • Supervise contractors and project resources

Travel:

  • Occasional visits to other BeOne sites, Vendor sites

Computer Skills:

  • Proficiency with Windows Server AD, AWS, Network Infrastructure MS-SQL, Smartsheet, Veeva

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Similar jobs, posted recently

Open roles like this one, listed in the last 30 days.

You've read the whole posting — now see how you match it.