Senior Representative, Quality Assurance ( M-F Day Shift )

Location: Bloomington
Posted on: June 23, 2025

Job Description:

About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility where talented teams work with innovators to help develop, manufacture and supply products to patients around the world. What we offer you: Leading pay and annual performance bonus for all positions All employees enjoy generous paid time off including 14 paid holidays Health Insurance, Dental Insurance, Vision Insurance – effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave Free access to Novo Nordisk-marketed pharmaceutical products Tuition Assistance Life & Disability Insurance Employee Referral Awards At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters. About The Position Relationships Reports to Manager Essential Functions Collaborates with Quality Control, Materials Management, Supply Chain and Manufacturing to ensure that materials are available for use Provides support for the introduction of new material and service suppliers Assists in the customer and supplier auditing process providing administrative support including information gathering and organization Provide quality support to Quality Control, Materials Management Center, and Supply Chain Review / Approve all incoming Material Specification Sheets Review / Release all inspected incoming materials Act as subject matter expert to internal and external customers regarding supplier qualification, material receipt / inspection / release and storage requirements Review and approve supply quality related records (e.g. deviations change controls, etc.) to ensure compliance to regulatory and procedural requirements is maintained Process supplier complaint investigation records and drive CAPA and disposition decisions Gather and report area metrics Perform supplier risk assessments Support maintenance of the approved supplier list Compile supplier pre audit data packages Support supplier performance monitoring program Assess damaged materials / product within warehouse spaces Perform routine Gemba walks of warehouse spaces Perform system, cold storage equipment, and material holds as appropriate Follow all safety and environmental requirements in the performance of duties Other duties as assigned Product Quality Accountable for review and approval of project related documents such as Master Batch Production Records, technical transfer, and process characterization reports Responsible for representing Quality Assurance as the primary contact for assigned projects, which includes cross functional internal and external collaboration, supporting integration of the client programs into the Catalent Quality Management System and ensuring effective management of client expectations Responsible for interfacing with the clients and managing internal communication to sustain and enhance the Client quality relationships Accountable for ensuring that Finished Products are manufactured and tested in a manner consistent with the applicable regulatory or client requirements Maintains a sufficient understanding of the quality systems and operations to provide consultation and guidance for Manufacturing personnel regarding execution of the Quality Management Systems Supports execution of QA on the Floor program Supports issuance of controlled documents for production, including Batch Production Records, Product Labels, and forms Reviews executed batch records Ensures all in-process specifications are met Ensures all corrections found are made to batch records Interacts with clients in a professional manner to ensure timely resolution of post-disposition corrections Physical Requirements Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed. Walking and/or standing for up to 8 to 12 hours depending on assigned area. Successful completion of gowning certification to enter and support the aseptic manufacturing areas. Qualifications STEM Bachelor’s degree, highly preferred 5 - 8 years of relevant experience with Bachelor’s degree, required 5 years of experience or demonstrated excellence in role with justification, required 5 years GxP experience or other regulated industry, required Excellent written and verbal communication skills with the ability to share vision, direction, and data with colleagues across all levels and in a wide range of different work groups including senior leadership and regulatory agencies Strong analytical and problem-solving abilities. Capable of making decisions using experience along with site process and procedures Robust interpersonal skills, organizational skills, and project management skills, with the ability to balance multiple priorities and projects Must be able to read and understand English-written job instructions and safety requirements Prior experience working in and/or supporting aseptic operations in a cGMP environment as it relates to cleaning and sanitization, regulatory (worldwide), deviation investigation, product and process validation, environmental testing, and investigations, preferred A strong working knowledge of quality systems and processes, preferred Technical Requirements Ability to use Excel, Word, and other office systems Ability to learn and use quality management software such as TrackWise® or ComplianceWire® Ability to understand and independently apply CGMPs to everyday work Demonstrates understanding of the work tasks assigned Executes procedures of moderate complexity with high quality Intermediate understanding of pharmaceutical laboratory and/or production operations Capable of learning unfamiliar principles or techniques with training Ability to contribute to investigations, deviations, and change controls with initial consultation from supervisor Ability to problem solve and execute and monitor corrective actions Ability to interpret data and analyze trends and provide insight into potential issues and suggest solutions Edits Standard Operating Procedures (SOPs) and reports with guidance from supervisor Seeks best practices for daily work activities Behavioral Requirements Ability to see and hear and read and write clear English Ability to communicate effectively and follow/retain detailed written and verbal instruction in an accurate, timely, safe, and professional manner with supervisor, group members, and other departments as necessary, in a professional and accurate manner Ability to manage time effectively to complete assignments in expected time frame and independently seek out additional work when tasks are completed ahead of time Ability to cooperate with coworkers within an organized team environment or work alone Detail oriented and well organized with ability to work effectively under high pressure with multiple deadlines Ability to put aside personal opinions and focus on business needs, department needs or group needs Ability to transfer knowledge to others via training or mentoring Demonstrated ability to guide others thorough communication and learning Ability to make decisions which have moderate impact on immediate work unit Leadership Requirements Lead by example according to the Company's values and culture Builds on contacts and relationships with peers Take initiative for personal and professional development Takes initiative when necessary to address changes in scope and procedural errors Builds trust and respect for self and department We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

Keywords: , Bloomington , Senior Representative, Quality Assurance ( M-F Day Shift ), Science, Research & Development , Bloomington, Indiana