At BASF, we create chemistry through the power of connected minds. By balancing economic success with environmental protection and social responsibility, we are building a more sustainable future through chemistry. As the world?s leading chemical company, we help our customers in nearly every industry meet the current and future needs of society through science and innovation. We provide a challenging and rewarding work environment with strong emphasis process safety, as well as safety of our employees and the communities we operate in, and are always working to form the best team?especially from within, through an emphasis on lifelong learning and development. Where the Chemistry Happens? Quality Assurance Assistant (1901744) – Bishop, TX As a valued member of Bishop Quality Assurance team, you will be responsible for maintaining all controlled documentation in compliance with current Good Manufacturing Practices (cGMP). This function includes maintenance of all controlled documentation for management of change and FDA Compliance. You will be reporting to the Bishop QA/QC Manager.Create Your Own Chemistry: What We Offer You? Adding value to our customers begins with adding value to you. You @BASF is the suite of benefits, perks, programs and unique opportunities we offer to support you?the whole you?in all stages of your life and career. With you@BASF, you create your own chemistry. The total rewards that you receive as a BASF employee go way beyond a paycheck. From competitive health and insurance plans, to robust retirement benefits that include company-matching contributions, to making sure you never stop learning, we believe in you is investing in our success. Working for a large, global organization, you?ll have a chance to grow professionally and personally, expand your network and build a rewarding and dynamic career. Principal responsibilities include, but are not limited to: ? Leveraging your professional experience in a Quality Assurance role, you will maintain database(s) of batch review data for review and analysis by Quality Assurance and to track revision status of controlled documents.? You will maintain original copies of controlled documents, including ?obsolete? documents and records of revisions for management of change purposes.? Create Purchase Requisitions in SAP? Issuance of Packaging or Batch records; Product Labels and Laboratory Protocols? Maintain Records of Non-CBT and Management of change (MOC) ? Your commitment to workplace safety will be critical as you will be required to comply with safety procedures such as Safe Work, management of change, good housekeeping and incident reporting/investigation.? Train new employees on document control requirements and compliance.Basic qualifications: ? High School Diploma or GED? Minimum of 2 years? experience in an FDA or ISO regulated environment? Minimum of 3 years? of SAP experience? Minimum of 2 years' experience with MS Office suite (Word, Excel, PowerPoint, Access)Preferred qualifications: ? Two years of college/university coursework in a Science-related discipline? Highly organized and detail oriented? Good working knowledge of ISO, GMP and FDA guidelines ? Team player and good problem-solving skills We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law. BASF recognizes institutions of higher education accredited by the Council for Higher Education Accreditation or equivalent.Apply for this job.