QC Metrologist

"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: Oversees all metrology activities, including equipment calibration, maintenance, troubleshooting, and documentation to ensure compliance with cGMP, regulatory, and industry standards. Manages reference standards through receipt, qualification, inventory tracking, and disposal while supporting analytical development, regulatory submissions, and continuous improvement of laboratory operations. Your Profile: Essential Duties, Responsibilities and Accountabilities: Installs and calibrates measurement instruments and systems. Perform routine maintenance and troubleshooting of measurement equipment. Analyze measurement data to ensure accuracy and consistency Develop measurement procedures and protocols Ensure compliance with industry standards and regulatory requirements Provide technical support and training to other departments Document and report measurement and calibration results Conduct research to improve measurement techniques and technologies Collaborate with engineers and scientists to resolve measurement challenges Certify equipment and processes according to national and international standards. Maintains all QC Laboratory equipment and stability chambers. Maintains all AR&D equipment. Maintains Environmental equipment. Maintains Production lab balance. Assists Chemical Development with equipment acquisition and maintenance. Troubleshoots all equipment issues in a timely fashion. Aids in Lab Investigations that are equipment related. Aids in IQ/OQ/PQ documents where a service contract is not applicable. Aids in CSV tasks for new instrumentation and routine reviews. Acts as the main contact for services reps associated with instrumentation. Negotiates service contracts on essential equipment. Trains new analysts on maintenance of instruments. Writes and/or revises SOP’s associated with reference calibration of instruments. Writes capital appropriation requests for new equipment purchases. Compiles all routine calibration data for equipment files. Maintain calibration records and instrument tagging. Assists IT with Empower administration. Purchases consumables, reference standards, equipment, etc. when needed. Creates purchase requisitions and works with purchasing department. Administrator for USP subscription. Provides 24-hour support as needed on call. Reference Standards Receive, process, store, and track the inventory of reference standards and related materials (like chromatographic columns). Perform reconciliation and coordinate the disposal of expired or used standards. Monitor and support the integrated inventory management process. Works with AR&D on the development of new standards for new methods. Submits all standards for testing to applicable in-house or external labs. Writes and/or revises SOPs associated with reference standards. Ensures USP standards are current to the most recently issued USP Catalog. Compiles standard qualification data for reference standard files. Maintains reference standard files. Provides reference standard CoA’s to regulatory for submission in current DMF. Supports sales with customer standard requests. Repackages standards from bulk containers. Tracks standard inventory. Arranges for disposition of expired/out of spec material. Adheres to all applicable cGMP and SHE regulations. Performs any other laboratory task deemed necessary by the Director of Quality Control. Adheres to personal moral, ethical, legal, and behavioral conduct that is in compliance with the Siegfried Code of Conduct. Supervisory responsibilities This position has no direct reports. Education, experience, certification and licensures A B.S. or advanced degree in science with at least 5 years of Metrology experience in a pharmaceutical environment is required as well as maintenance training on Agilent HPLC and GC. Knowledge, skills and abilities Ability to recognize what needs to be done, act, and accomplish results. Strong oral and written communication skills, including effective listening. Demonstrated ability to effectively utilize team resources. Expert in cGMP, USP, EP and FDA regulations. Technical competence including the understanding of theory and interpretation of all techniques. Proficient use of computer software, including Microsoft Office Suite (excel, word) and other required software. Must have a thorough understanding of computer hardware and software and how it interfaces with analytical equipment. Strong organizational skills with the ability to multi-task Prior experience and knowledge in FDA GMPs (21 CFR) Your Benefits: Additional Benefits Competitive performance-based bonus Employee Share Matching Plan 401(k) Match Medical, Dental, and Vision Offerings Life, Sickness and Accident insurance, and Long-term disability Increased Voluntary Life Insurance (employee and family) (optional) The salary for this role is anticipated to be between $82,000 and $105,000 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. 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.