Quality Control Analyst

Quality Control Analyst Employer Siegfried Location Grafton, WI Start date May 9, 2026 View more categories View less categories Discipline Quality , Quality Control Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details "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:

The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples.

Your Profile:

Schedule:

Saturday - Tuesday (nights 4x10 hour shifts) Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc. Perform chromatography (Liquid/GC) after extensive qualification and training Perform wet chemistry assays Regularly perform water sample collection Back up for QC analytical instrument maintenance and calibration Performance of QC general laboratory equipment maintenance, laboratory housekeeping and preparation of the laboratory for audits Assist in the review of QC data and provide summaries to management as needed Assist QC Management, as needed, in the completion of OOS, deviations and CAPAs investigations for QC Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure.

Your Benefits:

Education, experience, certification and licensures Required

• Bachelor's degree in chemistry or related field
• Minimum 0-3 years' pharmaceutical experience or equivalent combination of education and experience Preferred
• Experience in a cGMP or GLP pharmaceutical industry environment Knowledge, skills and abilities 1.

Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public 2. Ability to meet deadlines and work under pressure with limited supervision 3. Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently 4. Ability to read, analyze, and interpret, professional journals, technical procedures, or governmental regulations 5. Ability to write reports, business correspondence, and procedure manuals 6. Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations 7. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis 8. Ability to define problems, collect data, establish facts, and draw valid conclusions 9. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables 10. Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems 11. Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; walk; or sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is often required to climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and risk of electrical shock (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee will be responsible for generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials.

Your Benefits:

401(k) Health Insurance Dental/Vision Insurance Paid Time Off 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. Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert