Quality Control Associate 1 - Promega Corporation : Job Details

Job Description OUR TEAM: Our Quality Control team plays a vital role in supporting Promega's Manufacturing and New Product Development teams at the San Luis Obispo, CA facility. Using a variety of advanced analytical techniques, we ensure the quality and reliability of our diverse product portfolio. We value integrity, clear communication, and a collaborative spirit in our team members. By fostering a culture of continuous improvement and innovation, we strive to enhance our processes and create a dynamic, supportive,and engaging workplace where every team member can thrive. YOUR ROLE: As a QC Associate 1 on Promega's Quality Control team, you will play an essential role in ensuring the quality of our manufactured products. Collaborating with team members, you will conduct product testing using established protocols and report your findings with reliability and clarity. Your responsibilities will include attending daily morning meetings to help prioritize testing and tasks, ensuring alignment with team goals. A successful candidate will perform tests with precision and accuracy while maintaining clear and effective communication with team members-a crucial aspect of this role. Join us to contribute to Promega's commitment to delivering high-quality products that make a difference! JOB OBJECTIVE: Conducts routine and non-routine analyses of samples submitted to the QC Lab, including but not limited to chemical and biochemical analysis of raw materials, in-process, finished product and stability testing according to established operating procedures. Reviews and interprets data for adherence to specifications and reports anomalies. Participate in lab investigations, data compilation and report preparation. Maintains analytical instruments and troubleshoots as needed. Ability to work independently in the QC Lab according to established priorities and demonstrates good judgement as to when further guidance is needed. The expected salary range is $53,000 - $56,000, depending on experience. The full salary range for this position is $51,825 - $77,738. CORE DUTIES: 1. Analyzes routine and non-routine raw material, intermediate and finished good samples submitted to QC, following written test methods and inspection plans, according to inventory deadlines. 2. Analyzes routine and non-routine in-process samples under the guidance of an experienced analyst. 3. Evaluates and interprets results from analytical instruments commonly used in the QC lab for product testing such as HPLC, LC/MS, NMR and Spectrophotometer, performing calculations as required. Reviews sample data obtained for adherence to specifications or targets, and reports abnormalities or potential non-conformance to Supervisor. Demonstrates good judgement to determine appropriate action. Participate in lab investigations and troubleshooting as needed. 4. Enters data evaluated for compliance to specification into Quality database with accompanying documentation of test data, according to QC lab policies and procedures. 5. Analyzes routine stability samples, as assigned by Supervisor. Reports abnormalities or inconsistencies observed. 6. Performs routine instrument maintenance and troubleshooting as needed, under the guidance of an experienced analyst. Reports on anomalies in instrument performance to Supervisor. 7. Learns and effectively uses instrument software, Microsoft Office applications, ERP system such as SAP, and any other software applications needed to support data processing and QC documentation. 8. Supports day-to-day function of QC lab with manufacture of buffers, reagents and mobile phases, and recommendation for replenishment of supplies and standards. As assigned, performs testing to support processes such as plant water quality, environmental monitoring or cleaning operations. 9. Creates and revises written test methods and QC Lab procedures as assigned by Supervisor, describing tasks and processes clearly and concisely. 10. Participates in preparation of summaries and reports, as assigned by Supervisor. Tracks and trends current QC data and compiles historical data. Presents data in Quality group or project team meeting. 11. May occasionally work on QC Lab projects, or perform any other job-related duty, as assigned by Supervisor. 12. May travel on occasion. 13. Understands and complies with all applicable elements of PBI's quality management system. 14. Understands and complies with all applicable elements of PBI's EHS processes. Participates in weekly lab safety checks. 15. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others. 16. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 17. Understands and complies with ethical, legal and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. BS in Chemistry, Biochemistry, or other related lab science, plus 0-2 years' experience in an analytical lab. 2. Must possess fundamental skills in use of standard laboratory equipment, for example various pipettes, volumetric flasks, analytical balance. 3. Working knowledge of common analytical instruments used in a Quality Control laboratory, for example GC, IR, Spectrophotometer, HPLC. 4. Ability to quickly learn operation and maintenance of analytical instruments and associated software for routine QC testing of small molecules, for example HPLC, Mass Spec, NMR, Karl Fischer, Spectrophotometer and Luminometer. 5. Must possess a very high level of attention to detail and utilize scientific thought and critical thinking in a Quality Control Laboratory setting. Must possess problem solving skills. 6. Ability to work collaboratively in a team environment. PREFERRED QUALIFICATIONS: 1. Experience using analytical instruments for routine QC testing of small molecules, for example HPLC, Mass Spec, NMR, Karl Fischer, Spectrophotometer, Luminometer. 2. Ability to use analytical instrument software, Microsoft Office, and other data processing tools. PHYSICAL DEMANDS: 1. Must be able to move about the facility and labs while performing the tasks described above. 2. Must be able to remain stationary for several hours at a time. 3. Must be able to effectively operate all aspects of analytical instrumentation and prepare samples using associated lab equipment such as pipettes and balances. 4. Must be able to identify and distinguish colors. 5. Must be able to work with chemical reagents required for analytical testing. 6. Must be able to wear appropriate personal protective equipment such as lab coat, mask, gloves, hair covering and safety glasses and work in a laminar flow hood. 7. Must be able to move and transport objects averaging 10 pounds. 8. Must be able to position oneself in a low position. 9. Must be able to position oneself in a high position to access instrumentation and reagent bottles. 10. Must be able to use a computer for several hours at a time throughout the day. At Promega, we value diversity and strive to create an inclusive workplace. We are proud to be an Equal Opportunity Employer, making employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.