Associate Representative QA 324407

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 lifechanging careers and the opportunity to help improve the quality of life for millions of people around the world.

As a part of Novo Nordisk Catalent Indiana LLC. in Bloomington Indiana is a stateoftheart 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:

1. Leading pay and annual performance bonus for all positions
2. All employees enjoy generous paid time off including14 paid holidays
3. Health Insurance Dental Insurance Vision Insurance effective day one
4. Guaranteed 8 401K contribution plus individual company match option
5. Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
6. Free access to Novo Nordiskmarketed pharmaceutical products
7. Tuition Assistance
8. Life & Disability Insurance
9. 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.

The Quality Assurance department is responsible for all aspects of the quality assurance functions. The departments primary function is to ensure compliance with FDA and other regulatory agency requirements as well as internal quality systems requirements. This includes systems implementation and maintenance documentation management sitewide systems training internal and external auditing project review for accuracy and compliance and material disposition. Quality Assurance safeguards all systems processes and actions to ensure regulatory compliance which is essential in providing high quality drug products for our clients and their patients.

Quality Assurance Systems group has ownership over the quality systems including deviations and CAPAs change controls document control supplier quality management raw material testing and disposition and training as well as oversight of the equipment calibration and preventive maintenance program and validation activities.

Quality Assurance Operations group has oversight of the manufacturing areas including process technology transfer master batch record review and approval onthefloor support product disposition and shipping.

Quality & Compliance group has oversight of internal and client audits as well as regulatory agency inspections compliance and regulatory support initiatives and process validation activities.

The Position

MW 6PM6:30AM one week and MThursday 6PM6:30 other week

Relationships

Reports to: Manager QA

Essential Functions

Essential Functions

• Operational Excellence
  • Accountable for of the QA on the Floor program
  • Partner with Manufacturing and other support teams
  • Performs on the floor activities supporting client projects including room release observing critical processes reviewing batch documentation in real time cleaning documentation logbooks and resolving issues that occur during manufacturing
  • Review batch documents
  • Assist with revision of GMP documentation such as Standard Operating Procedures Master Batch Record review and SMPs
  • Initiate deviations as required when observed on the floor
  • Provides dedicated quality floor oversight of GMP operations for the manufacture of master/working cell banks bulk drug substance and/or final drug product 70 of day is spent on the floor
  • Perform audits of manufacturing and support areas including inprocess batch record review for adherence to internal procedures and Good Documentation Practices
  • Make solid quality decisions with limited oversight
  • Identify continuous improvement initiatives
  • Participate in site and corporate quality and process improvement initiatives
  • Represent perspective as necessary
  • Guides personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance internal procedures regulatory requirements and industry best practices
  • Notifies Management of potential quality or regulatory issues that may affect product quality or regulatory compliance
  • Other duties as assigned

• Product Quality
  • Supports of QA on the Floor program
  • Supports issuance of controlled documents for production including Batch Production Records Product Labels and forms
  • Notifies Management of potential quality or regulatory issues that may affect product quality or regulatory compliance
  • Other duties as assigned

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.

Qualifications

• Education/Experience:
  • Bachelors degree and 02 years of experience OR
  • Associates Degree and 2 years of experience
  • Must be able to read and understand Englishwritten job instructions and safety requirements
• 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 Catalents 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 were 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. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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 were 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. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.