Aseptic Manufacturing Supervisor — Lead & Develop Team

Grifols; Los Angeles (CA); On-site; USD 90,000 - 98,000; Full time

Benefits offered by this job

Medical, Dental, Vision

PTO

401(K) match

Tuition reimbursement

Job summary

Grifols is seeking a Supervisory, Manufacturing to oversee the manufacturing process and the department personnel on the designated shift, ensuring cGMP compliance and aseptic operation while training technicians.

The role focuses on regulatory knowledge, leadership, and continuous improvement; you will generate written reports, support inspections, and guide team development. California-based position with strong growth in a global healthcare company.

Qualifications

• Associate’s degree required; Bachelor’s degree preferred in Biology, Chemistry, Chemical Engineering or closely related scientific / technical discipline.
• Minimum of 2 years of related experience in a pharmaceutical, GMP, or FDA regulated environment is 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 is highly preferred.
• Demonstrated ability to inspire high performance in others and align team members around shared goals.
• Demonstrated leadership skills with the ability to motivate, guide, train, coach and develop department personnel.
• Demonstrated project management skills.
• Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.
• Must be proactive, results oriented, and have strong attention to detail.
• Self-starter with strong work ethic and the ability to exercise good judgment.
• Ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.
• Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.
• Excellent verbal and written communication skills in the English language.
• Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint).
• Must be flexible with working hours / shifts in order to accommodate the 24-hour, 7-day plant operation.

Responsibilities

• Supervise a unit, assign tasks, and manage schedules.
• Review batch documentation for completeness and accuracy.
• Initiate facility work orders for equipment repair.
• Troubleshoot processes to maintain aseptic processing.
• Improve production methods and layout for quality.
• Ensure compliance with regulatory requirements.
• Lead training and development of department staff.
• Provide guidance and performance appraisals.
• Participate in inspections and provide written responses.
• Maintain safety and health standards.
• Interview/hiring duties for department positions.

Skills

Supervisory experience

Leadership

Regulatory knowledge

cGMP/FDA knowledge

Process improvement

Documentation accuracy

English communication

Project management

Team development

Education

Associate degree

Bachelor’s degree preferred

High school diploma/GED with 4 years related experience

Tools

MS Office

Job description

Grifols is seeking a Supervisory, Manufacturing to oversee the manufacturing process and the department personnel on the designated shift, ensuring cGMP compliance and aseptic operation while training technicians.

The role focuses on regulatory knowledge, leadership, and continuous improvement; you will generate written reports, support inspections, and guide team development. California-based position with strong growth in a global healthcare company.