PM Operator-3

Siegfried•Grafton, WI

About The Position

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: At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. We are seeking Your role: • Demonstrates full competency in the operation of all production equipment and understanding of chemical processes. • Ability to operate and troubleshoot equipment but not limited to, fixed reactors, filters, pumps, dryers, glassware, chillers and mills. • Ensures good document practices in the recording, maintenance, and organizing of batch records, forms, documents and logbooks for responsible areas. • Must be able to obtain and interpret information shown by instruments, such as temperature, pressure, vacuum, or flow indicators, recorders or controllers and make corrective adjustments as required on equipment, based upon information obtained. • Must keep accurate Batch Log Record Sheets showing materials used, produced and pertinent operating information such as pressure, temperature, and vacuum. Accurately labels containers i.e. drums, bottles. • Immediately informs the Supervisor of deviations in the process and completes deviation forms as required. • Carries out all work as instructed by the Supervisor, assists when investigations have to be conducted, and takes immediate action in case of emergencies. • Properly collects and submits various samples for quality analysis. • Disposes of wastes in a correct manner and is responsible for good housekeeping and cleanliness at workstation. • Aims at the highest possible productivity considering all relevant safety, environmental and quality (cGMP) regulations and guidelines. • Knows and follows all relevant Standard Operating Procedures. • All other duties as assigned. Your Profile: Your Profile • HS Diploma or equivalent is required. • Must be able to read and write legibly in English and perform mathematical calculations such as yield and scale-down batch ratios. • Prior pharmaceutical manufacturing experience or batch chemical experience required. Or candidate must have 2-3 years prior experience in light industrial setting, prior pharmaceutical manufacturing experience or batch chemical experience would be preferred. • Must be able to work accurately and according to written and verbal instructions. • Must be able to work in a chemical manufacturing plant environment. • Must be able to lift minimum of 50 lbs. • Must be able to obtain respirator clearance. • Must be clean shaven to wear a tight-fitting respirator • Must be able to learn and operate computer-controlled equipment. • Having additional computer skills is a plus • Ability to stand for long periods of time. • Must be able to work overtime as needed Your Benefits: Paid Time Off, Health Insurance, Retirement Planning 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. Application Submission & Screening: Share your qualifications and enthusiasm through our application process. We review each submission to identify candidates whose skills best match the role. Initial Interview: We’ll explore your background, aspirations, and how you could contribute to our mission and culture. On-Site Interview: If possible, we invite you to meet us in person, connect with future colleagues, and get a feel for our workspace. Offer Stage: Congrats! If selected, you'll receive a detailed offer including compensation, benefits, and the exciting opportunities ahead. Onboarding: After you accept, we’ll guide you through a smooth, tailored onboarding experience to help you settle into your new role. Feedback & Improvement: Your feedback helps us continuously improve and enhance the candidate experience for others. Create an account by clicking ‘Sign In’ at the top of the page to set up personalized email alerts when new roles that match your aspirations become available.

Requirements

HS Diploma or equivalent is required.
Must be able to read and write legibly in English and perform mathematical calculations such as yield and scale-down batch ratios.
Prior pharmaceutical manufacturing experience or batch chemical experience required. Or candidate must have 2-3 years prior experience in light industrial setting, prior pharmaceutical manufacturing experience or batch chemical experience would be preferred.
Must be able to work accurately and according to written and verbal instructions.
Must be able to work in a chemical manufacturing plant environment.
Must be able to lift minimum of 50 lbs.
Must be able to obtain respirator clearance.
Must be clean shaven to wear a tight-fitting respirator
Must be able to learn and operate computer-controlled equipment.
Ability to stand for long periods of time.
Must be able to work overtime as needed

Nice To Haves

Having additional computer skills is a plus
prior pharmaceutical manufacturing experience or batch chemical experience would be preferred.

Responsibilities

Demonstrates full competency in the operation of all production equipment and understanding of chemical processes.
Ability to operate and troubleshoot equipment but not limited to, fixed reactors, filters, pumps, dryers, glassware, chillers and mills.
Ensures good document practices in the recording, maintenance, and organizing of batch records, forms, documents and logbooks for responsible areas.
Must be able to obtain and interpret information shown by instruments, such as temperature, pressure, vacuum, or flow indicators, recorders or controllers and make corrective adjustments as required on equipment, based upon information obtained.
Must keep accurate Batch Log Record Sheets showing materials used, produced and pertinent operating information such as pressure, temperature, and vacuum. Accurately labels containers i.e. drums, bottles.
Immediately informs the Supervisor of deviations in the process and completes deviation forms as required.
Carries out all work as instructed by the Supervisor, assists when investigations have to be conducted, and takes immediate action in case of emergencies.
Properly collects and submits various samples for quality analysis.
Disposes of wastes in a correct manner and is responsible for good housekeeping and cleanliness at workstation.
Aims at the highest possible productivity considering all relevant safety, environmental and quality (cGMP) regulations and guidelines.
Knows and follows all relevant Standard Operating Procedures.
All other duties as assigned.