QC Associate II - 3rd Shift

"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:  

QC Associate II, 3rd Shift (10 PM - 6:30 AM Sunday night - Friday morning)

The Quality Control Associate II will execute critical functions to support the manufacturing of sterile drug products. Supports the Raw Materials team by aseptically sampling incoming goods for chemical and microbiological testing. Performs environmental monitoring and evaluates results in an aseptic manufacturing facility to support the production of sterile drug products. Performs physical testing using instrumentation and dimensional analysis of components used in the manufacture of sterile drug products. The QC Associate will also learn Chemistry and Microbiology analyses to support timely release of In-Process Control test results and timely completion of batch release.

Your Profile:

Responsibilities

• Perform sampling of raw materials for chemistry and microbiology testing in clean room classified areas, minimizing contamination using aseptic technique.
• Execute Environmental Monitoring program, including viable and nonviable sampling and data analysis.
• Perform sampling and inspection in compliance with cGMP. All activities performed in GMP/GDP environment.
• Support media fills through personnel monitoring, scribing aseptic behavior and reading cultures after incubation.
• Document raw data contemporaneously and report results promptly. Utilize assigned NB's and LIMS system.
• Execute support functions (i.e. washing glassware, preparing media, running autoclave, changing charts).
• Maintain the working areas in a clean and organized state. Assist in Quality oversight of warehouse operations.

Required Knowledge, Skills and Abilities

• Able to gown aseptically and maintain certification to internal requirements.

• Ability to sample aseptically, perform fine measurements using tools and learn new instrumentation.

• Competency with routine software programs (i.e. MS Word, MS Excel).

• Aptitude for learning new programs (i.e. Labware LIMS, SAP).

• Capable of using good reason and judgment to make and defend recommendations.

• Positive team player in a fast-paced environment.

Required Education and Experience

• B.A or B.S. in Microbiology (preferred), Chemistry or other Pharmaceutical-relevant degree will be considered

• 3+ years of Experience in QC or QA (preferred)

• 3+ years of Experience in FDA Regulated industry (preferred)

Target Pay Range: $30-32/hour + 15% Shift Differential for working on 3rd Shift (10:00 PM - 6:30 AM Sunday night - Friday morning)

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

Your Benefits: 

• Medical, Dental, Vision, Life
• Voluntary Accident, Hospital, Pet
• 401K
• Generous Time Off Structure

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.