QA Technician II -1st 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:  

Your Profile:

Responsibilities

• Provide Quality support to Manufacturing personnel for compounding and in-process checks.

• Perform line clearance verification, sterilization chart review, scale calibration verification, and QA in-process checks including but not limited to visual inspection, CISIT/PID test, weight check, and torque test.

• Prepare in-process samples for submission to the Quality Control Laboratory.

• Support handling of GMP events and initiation of deviation investigations.

• Read, understand, and follow SOP’s and complies with cGMP.

• Support the issuance of GMP documentation to Manufacturing floor.

• Review executed batch records for completeness, accuracy and compliance with Good Documentation Practices.

• Use computerized system such as SAP, LIMS, and TrackWise for data collection and batch record review.

• Scan and file batch records (physically & electronically).

• Perform other work-related duties as assigned by management.

Required Knowledge, Skills and Abilities

• Good computer skills

• Strong attention to detail

• Good oral and written communication skills

• Ability to work overtime and/or work occasionally on weekend as needed

Required Education and Experience

• General high school degree/GED or equivalent required.

• Some college or technical college preferred.

• Prior experience working in QA function preferred.

• Basic reading, writing, and math skills required.

• 1-2 years' experience working in a Pharmaceutical, Medical Device, or other FDA regulated industries required.

Target Pay Range: $30-33/hourIndividual 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

• 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.