49 Manufacturing jobs in Benson

• Architect and deploy robust IO and IoT network solutions for manufacturing environments, including edge-to-cloud integrations.
• Collaborate with cross-functional teams (OT, IT, DevOps, Engineering) to define requirements and deliver scalable network solutions.
• Develop and maintain documentation for network configurations, security policies, and deployment blueprints in line with Gartners IoT Reference Model
• Provide technical leadership in troubleshooting, risk mitigation, and continuous improvement of network operations.
• Support IoT platform rollouts, including wireless sensor architecture and enterprise edge node deployments

• Proficiency in industrial protocols (MQTT, OPC-UA, Modbus, LoRaWAN) and cloud platforms (AWS, Azure).
• Ability to work in cross-functional teams and manage vendor relationships
• Excellent communication and documentation skills.

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models, including remote and hybrid work arrangements, where possible

Responsibilities: * Lead IT projects within the pharmaceutical manufacturing environment, ensuring successful delivery and implementation. * Collaborate with cross-functional teams to define project scope, goals, and deliverables that support business objectives. * Develop full-scale project plans and associated communication documents. * Effectively communicate project expectations to team members and stakeholders in a timely and clear fashion. * Estimate the resources and participants needed to achieve project goals. * Draft and submit budget proposals, recommend subsequent budget changes where necessary. * Plan, schedule, and track project timelines, milestones, and deliverables using appropriate tools. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: . Requirements: * Proven experience as a Project Manager within IT or automation in manufacturing or production environments. o Pharmaceutical highly preferred * A minimum of 2 years of direct work experience in a project management capacity. * Practical knowledge of process automation systems such as DeltaV and Syncade preferred. * Bachelors degree in Engineering or related field * Ability to lead projects from conception to completion within tightly prescribed timelines. * Exceptional written and oral communication skills.

This role will perform manufacturing support activities to ensure compliant and reliable production. This manufacturing facility is 24/7 operational and the role may require to be flexible with working hours. 

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit:

What You’ll Do

• During the project phase, you will lead operational readiness initiatives as well as site commissioning and qualification efforts
• Lead troubleshooting for their respective process area
• Recommend and perform documentation updates
• Coordinate non-batch activities and creation of associated documentation for tech transfer, changeover, preventive maintenance plans (PMs), column packing
• Create change management records, investigations, corrective and preventive actions (CAPAs) and continuous improvement (CI) activities to support manufacturing
• Execute and drive general improvement projects within Drug substance manufacturing
• Work with cross-functional groups to organize equipment startup and transfer into GMP manufacturing
• Support Inspections and audits by providing requested manufacturing documents 
• Other duties as assigned 

Basic Requirements

• High School Diploma or GED and 6 years of related experience OR Associates degree with 4 years of direct experience OR
• BA/BS with 2 years of direct experience
• Equivalent Military training/experience

Preferred Requirements

• Associates or Bachelor’s in life sciences or engineering
• BioWorks or BTEC Capstone cGMP coursework preferred

PHYSICAL REQUIREMENTS

PHYSICAL DEMANDS

• Ability to discern audible cues

WORKING ENVIRONMENT

PHYSICAL DEMANDS   

• Ability to stand for prolonged periods of time.  
• Ability to sit for prolonged periods of time.   
• Ability to conduct activities using repetitive motions that include wrist, hands and/or fingers.
• Ability to conduct work that includes moving objects up to 10 lbs.

ENVIRONMENTAL CONDITIONS

• Will work in heights greater than 4 feet

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ( ).

Position Overview

The Associate Director, Digital Manufacturing leads and drives the Recipe Driven Operation (RDO) design for the global implementation at FUJIFILM Biotechnologies. This role also leads the global technology transfer activities and standards definition as they relate to Automation while defining and supporting the governance for life cycle of RDO and Configuration Environment for Batch Activities (CEBA). This role continues to develop as the organization evolves.

Job Description

What You'll Do

• Develops and implements strategies aligned with the company's goals to optimize processes, improve efficiency, and reduce costs

• Serves as the system owner for Configuration Environment for Batch Activities (CEBA) application

• Drives the technical implementation of RDO and CEBA for all sites, globally

• Defines and supports the governance of RDO and CEBA cross-site and within the Large-Scale Business Unit (LSBU)

• Ensures effective implementation and adoption of RDO and CEBA throughout all sites

• Defines and updates the Automation technology transfer process standards for all sites

• Identifies and implements changes to support production and improve quality, as needed

• Trains and shares information of RDO and CEBA to the Automation teams and required stakeholders

• Leads global colleagues to effectively implement processes, procedures, and work standards

• Manages relationships with external vendors to properly execute Automation tasks, as needed

• Ensures standards, systems, and processes comply with regulatory requirements (e.g., Good Manufacturing Practices (GMP))

• Directs the technical activities related to RDO and CEBA to align with the company's objectives

• Identifies, develops, and revises standard operating procedures (SOPs), as needed

• Identifies opportunities for improvement and collaborates with stakeholders to implement continuous improvement initiatives

• Provides guidance and training to Automation teams globally

• Encourages a culture of continuous learning and development while providing real-time feedback and coaching

• Completes required administrative tasks (e.g., timecard approvals, time off approvals, expense reports etc.)

• Evaluates team performance, addresses gaps, employee questions and concerns, and partners with HR as needed for resolution, as needed

• Performs other duties, as assigned

Knowledge and Skills

• Ability to adapt communication styles to differing audiences and advise on difficult matters

• Knowledge of biopharmaceutical production within Fill Finish, Utility, Pen's/devices, and Automation/IT

• Strong strategic thinking skills

• Ability to coach, lead, and train individual contributors

• Ability to effectively present complex information to others

• Effective communication, both written and oral

Basic Requirement

• Bachelor's degree in Chemical, Electrical, Mechanical Engineering or other relevant field with 11+ years of experience of experience in a regulated industry

• 8+ years of people management/ leadership experience

• Prior experience working in a CGMP facility

• ISA-S88

• ISA-S95

Preferred Requirements

• Master's degree in a technical field of study relevant to Automation, Instrumentation & Controls, or Business Management with 9+ years of related experience in a regulated industry

• Experience with Lean Six Sigma or other continuous improvement methodologies

• ISA-S18.2

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

Ability to stand for prolonged periods of time. No X Yes 30 minutes (If yes, may specify frequency/duration: up to 15, 30, 120, 240 minutes)

Ability to sit for prolonged periods of time. No X Yes 30 minutes (If yes, may specify frequency/duration: up to 15, 30, 120, 240 minutes)Ability to operate machinery and/or power tools. X No Yes

Ability to conduct work that includes moving objects up to X pounds. No X Yes If yes, X 10 lbs. 33 lbs.

Job Locations US-NC-Holly Springs

Posted Date 1 month ago (7/24/2025 6:03 PM)

Requisition ID 2025-35194

Category Management

Company (Portal Searching) FUJIFILM Biotechnologies