- Salary
- $20 – $22
- Location
- Irvine, United States of America
- Type
- Full-time
- Education
- High School
- Source
- Workday
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:
As part of our Contract Development and Manufacturing Organization (CDMO) operations, the Packaging Operator plays a critical role in the final stages of pharmaceutical product manufacturing. This position is responsible for packaging finished products, operating packaging equipment, performing visual inspections, and ensuring products conform to established quality and regulatory specifications. The ideal candidate is detail-oriented, safety-conscious, and committed to maintaining compliance within a GMP-regulated environment.Your Profile:
Essential Responsibilities
- Complete required training on gowning procedures and entry/exit protocols for designated production areas.
- Perform packaging operations on packaging lines, including equipment setup, assembly, disassembly, preparation, and adjustments of labeling and packaging machinery.
- Visually inspect labels, packaging components, and finished goods to ensure conformance to specifications and quality standards.
- Manually label and package finished products according to specifications when automated machinery is unavailable.
- Maintain accurate and complete batch records, forms, logbooks, and related documentation in accordance with Good Documentation Practices (GDP).
- Ensure proper labeling, handling, and disposal of hazardous waste generated from packaging operations.
- Assist team members in manufacturing areas as needed to support production goals.
- Maintain an organized, clean, and safe work environment, including packaging equipment, tools, and workstations.
- Adhere to all applicable SOPs, Good Manufacturing Practices (GMPs), ISO requirements, and company policies.
- Perform other related duties as assigned by the immediate supervisor.
Required Knowledge, Skills, and Abilities
- Strong verbal and written communication skills.
- Ability to work effectively in a team environment.
- Strong problem-solving skills and attention to detail.
- Demonstrated initiative and manual dexterity.
- Ability to stand continuously for two or more hours.
- Ability to safely operate material handling equipment and follow all safety procedures.
- Basic math skills.
- Ability to work overtime as required to meet production demands.
Required Education and Experience
- High school diploma or equivalent required.
- No prior experience required; training will be provided.
- Previous experience in the pharmaceutical, biotechnology, medical device, or manufacturing industry is preferred.
Why Join Us?
Join a growing CDMO organization dedicated to helping bring life-changing therapies and products to market. We offer a collaborative environment, comprehensive training, opportunities for advancement, and a commitment to quality, safety, and employee success.
Target Pay Range: $20-22/hour + 10% Differential when working on 2nd Shift (2 PM - 10:30 PM
Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications, and other job-related reasons.
Apply today to start your career in pharmaceutical manufacturing and packaging on our 2nd Shift team.
Your Benefits:
- Medical, Dental, Vision, Life
- Voluntary Accident, Hospital, Pet
- 401K
- Generous Time Off Structure including PTO, Holidays, Sick & Personal
Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 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.
