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Grifols

Fractionation Technician – Nights

Grifols

. Manufacture products derived from human blood plasma .

Posted 10/23/2026full-timeClayton • North Carolina • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Good Manufacturing Practices (cGMP) and adherence to safety guidelines and Standard Operating Procedures (SOPs) while effectively operating manufacturing process control systems and equipment. Capable of performing in-process analytical analysis and maintaining accurate production records.

Highest-signal resume keywords
Good Manufacturing Practices (cGMP)Batch Production Records (BPRs)Clean In Place (CIP) Equipment OperationSAP and/or ACSIS TransactionsBioworks Certificate

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Manufacturing Process Control SystemsIn-Process Analytical AnalysisData EntryBuffer and Process Solutions PreparationMechanical Aptitude
Soft Skills
Detail-Oriented ApproachTeam CollaborationGood JudgmentEffective CommunicationAdaptability
Tools & Technologies
SAPACSISManufacturing Equipment
Certifications & Qualifications
Bioworks Certificate
Industry Keywords
Standard Operating Procedures (SOPs)Safety GuidelinesHealth, Environment and Safety RegulationsPlasma ManufacturingCommissioning and Validation Activities

About the role

Key responsibilities & impact
  • Manufacture products derived from human blood plasma
  • Follow company safety guidelines, programs, and Standard Operating Procedures (SOPs)
  • Complete Batch Production Records (BPRs) and maintain records according to current Good Manufacturing Practices
  • Operate manufacturing process control systems and equipment
  • Operate Clean In Place (CIP) equipment
  • Perform in-process analytical analysis
  • Monitor manufacturing processes
  • Assist with sampling operations and harvesting intermediate products
  • Prepare, set up, and transfer buffer and process solutions
  • Transfer intermediate product, raw materials, and waste
  • Stage plasma, intermediate paste, and raw materials
  • Clean and sanitize designated manufacturing areas
  • Use SAP and/or ACSIS transactions
  • Support production supply-chain requirements
  • Assist team members and supervisors with additional tasks
  • Execute commissioning and validation activities for a new building
  • Communicate with operators, technicians, and supervisors
  • Work ethically and compliantly to manufacture safe drug products

Requirements

What you’ll need
  • Basic math skills
  • Basic computer skills
  • Mechanical aptitude
  • Detail-oriented approach
  • Ability to work in a team environment and exercise good judgment
  • High school diploma or equivalent
  • Ability to work a 24/7 rotating shift schedule
  • Knowledge of company safety guidelines and SOPs
  • Strong knowledge of current Good Manufacturing Practices (cGMP)
  • Knowledge of State and Federal Health, Environment and Safety regulations
  • Excellent oral and written communication skills
  • Comfortable using different computer systems for data entry
  • Willingness to work with and learn from other manufacturing team members
  • Ability to perform frequent repetitive hand movements
  • Ability to lift and carry up to 50 lbs.
  • Ability to work at heights on platforms and/or ladders
  • Ability to adapt to a fluid schedule during commissioning and validation
  • Bioworks Certificate preferred

Benefits

Comp & perks
  • Regular full-time employment
  • 12-hour night shifts
  • Equal employment opportunities
  • Personal protective equipment provided/required for job duties