Aseptic Manufacturing Supervisor – 8% Bonus Eligible

Grifols Shared Services North America, Inc; Los Angeles (CA); On-site; USD 90,000 - 100,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

PTO

401(k) match

Tuition reimbursement

Life insurance

Job summary

Grifols Shared Services North America, Inc seeks a Supervisor, Manufacturing to oversee the production process and department personnel on designated shift, ensuring cGMP compliance and aseptic operation. You will train and develop technicians and maintain production schedules.

The role requires strong supervisory experience, knowledge of regulatory requirements, and ability to improve processes and tooling while ensuring safe, compliant operations.

Qualifications

• Associate’s degree required; Bachelor's degree preferred in Biology, Chemistry, Chemical Engineering, or related field.
• Minimum of 2 years of related experience in pharmaceutical, GMP, or FDA-regulated environment is required.
• Equivalency: 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 is highly preferred.

Responsibilities

• 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 in order to correct/maintain aseptic processing and desirable product yields, as well as environmental control of facility.
• 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.
• Maintain current knowledge of regulatory and industry standards.
• Generate thorough written reports, when required, that summarize investigations performed for out-of-specification results or out-of-procedure events.
• Participate in regulatory and internal inspections/audits including providing written responses as applicable for area of responsibility.
• 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 with the collaboration of Human Resources.
• Provide a leadership role ensuring employee health and safety.
• Involved in interviewing/selection process of hiring or promoting department personnel.

Skills

Supervisory experience

cGMP knowledge

Regulatory compliance

Training & development

Process improvement

Data analysis

Education

Associate’s degree required; Bachelor's preferred (Biology/Chemistry/Chemical Eng or related)

High school diploma or GED with 4 years related experience

Tools

MS Office

Job description

Grifols Shared Services North America, Inc seeks a Supervisor, Manufacturing to oversee the production process and department personnel on designated shift, ensuring cGMP compliance and aseptic operation. You will train and develop technicians and maintain production schedules.

The role requires strong supervisory experience, knowledge of regulatory requirements, and ability to improve processes and tooling while ensuring safe, compliant operations.