Production Coordinator (Manufacturing Supervisor) - 2nd Shift

BioSpace; Irvine (CA); On-site; USD 100,000 - 120,000; Full time

Benefits offered by this job

Generous Time Off

Medical, Dental, Vision

Flexible Spending & HSA Options

Life Insurance

Short & Long Term Disability

Pet Insurance

401K

Job summary

Siegfried in Irvine, CA is hiring a Production Supervisor for the 2nd shift to lead our pharmaceutical manufacturing team. This hands-on role requires GMP-regulated, sterile or aseptic experience and a readiness to drive accuracy and efficiency in a fast-paced setting.

You'll supervise 2nd shift operations, ensure compliance with GMP, FDA, ISO, and safety standards, review batch records, and coach staff to achieve quality and continuous improvement.

Qualifications

• 5–7+ years of pharma manufacturing or packaging experience.
• Experience in sterile/aseptic processing required.
• Proven team leadership skills.
• Strong knowledge of GMP operations and documentation.
• Bachelor’s degree in Chemistry, Engineering, or related field preferred.

Responsibilities

• Lead and supervise 2nd Shift production operations
• Ensure compliance with GMP, FDA, ISO, and safety standards
• Execute production schedules and drive efficiency
• Review batch records, SOPs, and production documentation
• Investigate deviations and support continuous improvement
• Coach, train, and develop manufacturing staff

Skills

Pharma manufacturing

Team leadership

Sterile/aseptic processing

GMP knowledge

Education

Bachelor's degree in Chemistry/Engineering or related field

Job description

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.

Your Role

We’re hiring a Production Supervisor to lead our 2nd shift pharmaceutical manufacturing team. This role is ideal for a hands-on leader with experience in GMP-regulated, sterile or aseptic environments who thrives in fast-paced production settings.

2nd Shift Hours: 2 PM - 10:30 PM

Your Profile

What You’ll Do

• Lead and supervise 2nd Shift production operations
• Ensure compliance with GMP, FDA, ISO, and safety standards
• Execute production schedules and drive efficiency
• Review batch records, SOPs, and production documentation
• Investigate deviations and support continuous improvement
• Coach, train, and develop manufacturing staff

What You Bring

• 5–7+ years of pharma manufacturing or packaging experience
• Experience in sterile/aseptic processing required
• Proven team leadership skills
• Strong knowledge of GMP operations and documentation
• Bachelor’s degree in Chemistry, Engineering, or related field preferred

Why This Role

• Lead a dedicated 2nd shift team of Compounders, Aseptic Filling Operators and Component Prep technicians
• High-impact role in a regulated pharmaceutical environment
• Opportunity to drive quality, safety, and operational excellence

Target Salary Range: $100,000 - 120,000

Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.

Your Benefits

• Generous Time Off between PTO, Sick Time & Holidays
• Medical, Dental, Vision
• Flexible Spending & HSA Options
• Life Insurance, Short & Long Term Disability
• Pet Insurance
• 401K

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.