Manufacturing Supervisor

Grifols

Supervisor overseeing manufacturing processes in a global healthcare company. Ensuring compliance with regulations and training department personnel to enhance production quality.

Posted 7/17/2026full-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 pharmaceutical manufacturing operations, including protein purification and aseptic processing, while ensuring compliance with cGMPs and FDA regulations. Proven ability to lead and develop teams, manage projects, and enhance production methods for improved quality and efficiency.

Highest-signal resume keywords

Pharmaceutical Manufacturing OperationsCGMP ComplianceProtein PurificationAseptic ProcessingProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Pharmaceutical ManufacturingRegulatory ComplianceBatch Documentation ReviewProcess TroubleshootingQuality Control

Soft Skills

LeadershipCoachingProblem-SolvingCommunicationOrganizational Skills

Tools & Technologies

MS OfficeExcelWordPowerPointOutlook

Industry Keywords

GMPFDA RegulationsBiologyChemistryChemical Engineering

About the role

Key responsibilities & impact

Oversees the manufacturing process and the department personnel on designated shift
Trains and develops department technicians
Provides immediate supervision to a unit or group of employees, assigning tasks, checking work at frequent intervals, and maintaining schedules
Oversee production review of all department batch documentation for completeness and accuracy
Initiate Facility Work Orders when equipment requires repair
Participate in process/product troubleshooting
Recommend and implement measures to improve production methods, equipment performance, facility layout, and quality of product
Maintain a quality presence to ensure compliance with all regulatory requirements
Generate thorough written reports
Participate in regulatory and internal inspections/audits
Provide guidance and hands-on training to direct reports
Appraise and monitor performance of department personnel
Coach, counsel, address complaints and resolve employee related issues
Provide a leadership role ensuring employee health and safety

Requirements

What you’ll need

Associate’s degree required
Bachelor's degree preferred
Emphasis in Biology, Chemistry, Chemical Engineering or closely related scientific / technical discipline preferred
Minimum of 2 years of related experience in a pharmaceutical, GMP, or FDA regulated environment required
Equivalency: In lieu of an Associate's degree, candidate must have a High school diploma or GED, and a minimum of 4 years of related experience in a pharmaceutical, GMP, or FDA regulated environment
Requires an 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
Demonstrated project management skills
Strong organizational, analytical, and problem-solving skills
Excellent verbal and written communication skills in English
Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint)

Benefits

Comp & perks

Medical
Dental
Vision
life insurance
PTO
paid holidays
up to 5% 401(K) match
tuition reimbursement