QC Associate III Job Details | Wacker Chemie AG We use cookies to offer you the best possible website experience. Your cookie preferences will be stored in your browser’s local storage. This includes cookies necessary for the website's operation. Additionally, you can freely decide and change any time whether you accept cookies or choose to opt out of cookies to improve website's performance, as well as cookies used to display content tailored to your interests. Your experience of the site and the services we are able to offer may be impacted if you do not accept all cookies. 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Country/Region All City All Functional Area All Career Level All Employment type All Clear Select how often (in days) to receive an alert: Create Alert × Select how often (in days) to receive an alert: Apply now » Apply now + Start apply with LinkedIn + Apply Now Start + Please wait... Date: Nov 15, 2024 Location: San Diego Company: Wacker BioTech US Inc. Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future. To strengthen our team inSan Diego, we are looking for you as a(n)QC Associate III. The QC Associate III (Analytical) position performs routine and non-routine analytical testing to support Operations, and Process Development at Wacker Biotech US with minimal supervision. This position may perform method transfers, method development, and method qualification with minimal supervision. This position will perform quality investigations (OOT, deviation, etc). As part of the QC team, this position will be responsible for maintaining the QC laboratory, including cleaning the area, performing routine preventative maintenance, and ordering supplies. This position requires hands-on laboratory work and close collaboration with the QC control team, Process Development Team, and the Operations team. This position is expected to rigorously adhere to relevant cGMP guidelines, test methods, and SOP’s. Essential Functions of this Position: + Perform routine and non-routine complex analytical testing with minimal supervision. + Develop, qualify, and validate complex analytical testing following international guidance’s, and client requirements with some supervision. + Perform routine laboratory maintenance including, monthly routine cleaning procedures to ensure safety of laboratory personnel as well as monitor disposable equipment and reagent supplies to make certain materials are available for use. + Prioritize daily tasks, related to operations, technology transfers, analytical testing and validation including equipment and procedures. + Document and investigate any out of specification results, deviations, or investigations with minimal assistance. Assist in resolving any out of specification and out of trending results as well as performing and developing any corrective and preventative measures. + Develop and revise SOPs under data integrity guidelines as well as perform periodic revisions to ensure the procedures are up to date to current standards. + Trains new analysts and ensures personnel understand various analytical assays and standard operation procedures as well as conform to any departmental procedures . + Assist Quality Assurance in ensuring compliance with applicable quality standards and regulatory requirements. + Capable of leading projects and adhering to timelines with supervision. Position Qualifications: + Bachelor or Masters of Science Degree in the Biological Sciences, Bioengineering or Chemistry with a combination of education and experience performing biochemistry, molecular biology, microbiology, and chemistry. + Minimum of 5+ years relevant experience with a Bachelor’s Degree or minimum of 3+ years relevant expereince with a Master’s Degree. + The QC Associate III must be accountable for the work performed, productive within the company, provide open communication, and exemplify effective teamwork skills. + The QC Associate must be capable of reading, understanding, and adhering to relevant test methods, SOP’s, and industry guidance’s. + The QC Associate must be knowledgeable in basic chemistry and analytical principles. They should understand basic statistical analysis. + The position is responsible for performing and demonstrating the highest form of quality in the pharmaceutical industry, understanding the cGMP regulations, and implementing these practices on the work being performed. + Knowledgeable using Microsoft Office as well as developing any documentation and creating tables for laboratory inventory and data entry. + Highly organized, detail oriented, with excellent record keeping skills. + Sound scientific judgement with good communication skills and the ability to work effectively with others. + Experience working in a GMP facility is highly desirable. + Experience analyzing plasmid DNA is highly desirable. What do we offer? WACKER is an equal opportunity employer committed to diversity, equity, inclusion, and sustainability. We are innovators, researchers, and pioneers and we believe that our individual differences are our collective strength. We foster an inclusive environment that promotes individuality, celebrates diversity, and builds cohesive teams. Together, we create exceptional value for our employees, our customers, and our communities by creating a culture of inclusion and equity that enables, empowers, and values our diverse contributions. WACKER strives to reward its employees in a fair and equitable manner. Our Total Rewards Package considers employee wellbeing and is comprised of compensation, benefits, work-life balance, performance & recognition, and career development. + Compensation and Incentive plans + Medical, Dental, and Vision Insurance effective day 1 + Paid Time Off in addition to personal days and holidays + Paid parental leave + Wellbeing fund + Flexible hybrid work arrangements + 401(k) with company match + Education Assistance Program + Career development and advancement opportunities + Support for Community Involvement We are looking forward to your online application at www.wacker.com. Reference Code: 28220 #LI-CE1 The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. A minimum requirement for this US-based position is the ability to work legally in the United States on a permanent unrestricted basis. Visa sponsorship is not available for this position, including for any type of US permanent residency (e.g., for a green card). WACKER is proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.