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Grifols

Lead Technician – Manufacturing

Grifols

. Oversee coordination and operations of the production schedule, shift, and personnel .

Posted 9/18/2026full-timeLos Angeles • California • United StatesSenior💰 $34 - $35 per hourWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in overseeing production operations in a biologics processing environment, ensuring compliance with FDA regulations and cGMP standards. Capable of training personnel and performing complex process analyses while maintaining a strong focus on safety and quality.

Highest-signal resume keywords
Biologics Processing OperationsFDA Regulations ComplianceCGMP KnowledgeLeadership and TrainingProcess Analysis

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
Process AnalysisPH MeasurementRefractive Index MeasurementTurbidity MeasurementConductivity MeasurementUltrafiltration OperationChromatography OperationCIP System OperationSIP System OperationCentrifuge Operation
Soft Skills
Leadership SkillsAttention to DetailInterpersonal SkillsProactive AttitudeStrong Work Ethic
Tools & Technologies
Operator Interface TerminalsMS Office
Certifications & Qualifications
High School DiplomaGED
Industry Keywords
Pharmaceutical IndustryGMP EnvironmentFDA Regulated EnvironmentSafety PoliciesTeam Environment

About the role

Key responsibilities & impact
  • Oversee coordination and operations of the production schedule, shift, and personnel
  • Set up and operate equipment in a biologics processing environment for plasma-derived pharmaceuticals
  • Follow procedures and practices according to FDA regulations
  • Complete documentation according to FDA regulations
  • Adhere to departmental and corporate safety policies
  • Clean facilities and equipment
  • Perform basic process analyses, including pH, refractive index, turbidity, and conductivity measurements
  • Operate ultrafiltration units, chromatography columns, CIP systems, SIP systems, and centrifuges
  • Utilize touch-screen Operator Interface Terminals
  • Train entry-level personnel
  • Perform complex and advanced job tasks
  • Assist management with coordinating and scheduling day-to-day departmental operations
  • Serve in a leadership role when direct supervision is absent
  • Perform other assigned duties

Requirements

What you’ll need
  • High school diploma or GED required
  • Minimum of 3 years of related experience in a pharmaceutical, GMP, or FDA regulated environment
  • Demonstrated leadership skills with ability to motivate, guide, train, coach and develop department personnel
  • Comprehensive knowledge of cGMPs, FDA regulations, and industry guidelines
  • Ability to work independently with minimum supervision
  • Proactive, results-oriented, and strong attention to detail
  • Strong work ethic and good judgment
  • Ability to prioritize and manage multiple tasks to meet deadlines
  • Strong interpersonal skills and ability to interact with personnel at all levels in a team environment
  • Must be able to read, write, and speak English
  • Computer literacy and proficiency in MS Office (Outlook, Word, Excel, PowerPoint)
  • Flexibility to work varying hours/shifts for 24-hour, 7-day plant operation
  • Ability to perform the stated occupational demands, including standing, walking, lifting, operating equipment, and wearing required personal protective equipment

Benefits

Comp & perks
  • Up to 5% company bonus pool
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life insurance
  • PTO
  • Paid holidays
  • Up to 5% 401(K) match
  • Tuition reimbursement
  • Professional growth and career progression opportunities