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Job description
Manufacturing Associate 3 (Drug Substance Manufacturing)Build life-changing medicines with a team that trusts you to lead on the manufacturing floor. As a Manufacturing Associate 3 (Drug Substance Manufacturing), you'll take ownership of critical processing steps, help bring new capacity online, and keep a 24/7 operation running safely, compliantly, and on time. If you thrive in hands-on, fast-paced environments and enjoy guiding others, this is your next step.About UsWe are a 24/7 biopharmaceutical manufacturing facility focused on bulk drug substance (Drug Substance Manufacturing, DSM).Our teams partner across functions to ensure safe, reliable, and compliant production in accordance with current Good Manufacturing Practices (cGMP).We value curiosity, teamwork, and continuous improvement, and we welcome people from all backgrounds to grow their careers with us.Responsibilities Project phase (operational readiness)Contribute to readiness for bulk drug substance manufacturing (systems, equipment, and documentation).Support projects such as: Reviewing and creating procedures.Developing or transferring manufacturing business processes.Supporting equipment and system testing and commissioning.Travel up to 0–25% (domestic or international) may be required during the project phase.In operationsLead, execute, and document manufacturing processing steps and/or manufacturing support activities, including process monitoring and control.Perform in?process testing (for example: pH, conductivity, visual inspection).Execute validation protocols in alignment with cGMP Standard Operating Procedures (SOPs).Maintain all required training to perform assigned manufacturing activities.Assist with and/or lead cycle counts; manage materials for the assigned manufacturing area.Work shifts that include weekends and may include nights, in support of a 24/7 operation.Perform other duties as assigned.Minimum qualificationsEducation and experience (one of the following): High school diploma or GED and 4 years of related experience in a manufacturing environment; orAssociate's degree; orBachelor's degree (BA/BS), preferably in Life Sciences or Engineering; orAssociate's degree plus 2 years of related experience in a cGMP manufacturing environment; orEquivalent military training or experience.Qualified experience in at least one unit operation: DPFG Filler; orCell Culture – Seed Train.Knowledge, skills, and abilities: Ability to assist in troubleshooting.Strong verbal and written communication skills.Knowledge of production equipment operation relevant to assigned unit operations.Basic understanding of manufacturing run cadence and the order of shift activities.Knowledge of cGMP, safety, and operational procedures.Ability to work effectively in a team environment.Exercises considerable judgment and initiative; determines methods and procedures on new assignments; may act as an informal team leader.Preferred qualificationsBioWorks or BTEC Capstone cGMP coursework.Physical requirements and working environmentMay require respiratory protection.May work in mechanical/production spaces requiring hearing protection and participation in a hearing conservation program.May operate a motor vehicle or Powered Industrial Truck (PIT).Ability to discern audible cues.Ability to inspect/perform tasks with 20/20 corrected vision, including color distinction.Ability to ascend/descend ladders, scaffolding, ramps, etc.Ability to stand and sit for prolonged periods.Ability to perform repetitive motions (wrists, hands, and/or fingers).Ability to operate machinery and/or power tools.Ability to move objects up to 33 lbs.Ability to bend, push/pull, and reach to retrieve materials from 18" to 60" in height, using twisting motions.Environmental conditions: Not routinely exposed to warm/cold extremes, outdoor elements, or small/enclosed spaces.May work at heights greater than 4 feet.BenefitsCompetitive compensation with shift differentials for eligible schedules.Comprehensive health and wellness coverage for you and your family.Retirement savings plan with company support.Paid time off, holidays, and paid leave programs.Training, certification support, and continuous learning (including cGMP skill development).Career growth in a 24/7 advanced manufacturing environment.Inclusive culture, employee resource groups, and a strong focus on safety.All required personal protective equipment (PPE) provided.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.EEO InformationFujifilm 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.ADA InformationIf 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 ( ).
Worksite address
holly springs, NC, 27540, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.