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Grifols

Supervisor, Manufacturing – IGIV Bulk

Grifols

. Oversee the manufacturing process and department personnel on a designated shift .

Posted 9/18/2026full-timeLos Angeles • California • United StatesJuniorMid-Level💰 $90,000 - $98,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in overseeing pharmaceutical manufacturing processes while ensuring compliance with cGMP and FDA regulations. Capable of training and developing personnel, managing production methods, and maintaining high standards of product quality and safety.

Highest-signal resume keywords
Pharmaceutical Manufacturing OperationsCGMP ComplianceAseptic ProcessingLeadership and Personnel DevelopmentProject Management

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
Protein PurificationRegulatory ComplianceBatch Documentation ReviewProcess TroubleshootingWritten Investigation ReportsComputer LiteracyMS Office Proficiency
Soft Skills
Organizational SkillsAnalytical SkillsProblem-Solving SkillsInterpersonal SkillsCommunication Skills
Industry Keywords
FDA RegulationsPharmaceutical IndustryGMP EnvironmentAseptic OperationsInternal InspectionsEmployee Health and Safety

About the role

Key responsibilities & impact
  • Oversee the manufacturing process and department personnel on a designated shift
  • Ensure processes meet cGMP and company standards for aseptic operations
  • Train and develop department technicians
  • Supervise employees, assign tasks, check work, and maintain schedules
  • Review department batch documentation for completeness and accuracy
  • Initiate facility work orders when equipment requires repair
  • Participate in process and product troubleshooting to maintain aseptic processing, product yields, and facility environmental control
  • Recommend and implement improvements to production methods, equipment performance, facility layout, and product quality
  • Ensure compliance with regulatory requirements and maintain knowledge of regulatory and industry standards
  • Generate written investigation reports for out-of-specification results and out-of-procedure events
  • Participate in regulatory and internal inspections/audits and provide written responses
  • Provide hands-on guidance and training to direct reports
  • Appraise and monitor department personnel performance
  • Coach, counsel, address complaints, and resolve employee issues with Human Resources
  • Lead employee health and safety efforts
  • Participate in interviewing and selection for hiring or promotion of department personnel
  • Frequently drive to site locations, with occasional travel within the United States

Requirements

What you’ll need
  • Associate’s degree required; emphasis in Biology, Chemistry, Chemical Engineering or closely related scientific / technical discipline preferred
  • In lieu of an Associate's degree, a High school diploma or GED and a minimum of 4 years of related experience in a pharmaceutical, GMP, or FDA regulated environment
  • Minimum of 2 years of related experience in a pharmaceutical, GMP, or FDA regulated environment
  • In-depth understanding of pharmaceutical manufacturing operations, including protein purification and aseptic processing
  • Comprehensive knowledge and understanding of cGMPs, FDA regulations, and industry guidelines
  • Prior supervisory or leadership experience highly preferred
  • Leadership, coaching, training, and personnel development skills
  • Demonstrated project management skills
  • Strong organizational, analytical, and problem-solving skills
  • Proactive, results-oriented, detail-oriented, and able to exercise good judgment
  • Ability to prioritize and manage multiple tasks to meet deadlines
  • Strong interpersonal skills and ability to work in a team environment
  • Excellent verbal and written communication skills in English
  • Computer literacy and proficiency in MS Office (Outlook, Word, Excel, PowerPoint)
  • Flexibility with working hours/shifts for 24-hour, 7-day plant operation
  • Ability to work with personal protective equipment and in environments involving biological fluids, infectious organisms, chemicals, moving machinery, cold, and high noise
  • Ability to lift and carry up to 35 lbs
  • Ability to work independently, communicate complex information, and obtain consensus with diverse groups

Benefits

Comp & perks
  • Up to 8% of the company bonus pool
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life insurance
  • PTO
  • Paid holidays
  • Up to 5% 401(k) match
  • Tuition reimbursement
  • Opportunities for professional growth and career progression
  • Family-like culture