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.
As a part of Novo Nordisk, Catalent, Indiana LLC. in Bloomington, Indiana, 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.
Primary - Drug Product Primary Manufacturing produces sterile pharmaceuticals. The department includes equipment preparation, product formulation, material staging, and aseptic filling. Product in this area is filled into vials, syringes, or cartridges inside sterile isolator barriers. The sterile barrier isolator provides a physical barrier between the manufacturing equipment and the personnel controlling the machine. The Drug Product Primary Manufacturing area is a cleanroom environment. Personnel working in this area are required to wear scrubs and/or coveralls, gloves, hairnet, safety glasses, and steel toed shoes.
Secondary - The Secondary Manufacturing department is responsible for the execution of clinical and commercial manufacturing in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include manual, semi-automated and automated inspection, complex and bulk packaging. Further, manufacturing operations is tasked to utilize continuous improvement methodologies to realize process optimization, efficiency gains, and waste reduction to maximize capacity outputs.
Drug Substance - The Drug Substance - Operations department is responsible for the execution of clinical and commercial manufacturing in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include solution preparation, master/working cell bank production, upstream cell culture, downstream protein purification, mRNA and molecular therapeutics production. Further, manufacturing operations is tasked to utilize continuous improvement methodologies to realize process optimization, efficiency gains, and waste reduction to maximize capacity outputs.
The Position
In general, this position provides direct technical support to operations area as it relates to documentation, equipment procurement, testing, operational excellence, and training. This role works collaboratively with multiple company functions to ensure production systems operate in a safe, and quality-oriented manner.
Essential Functions
• Provide support for all Client and Regulatory Agency Audits
• Management of process and procedural improvements
• Ownership of Corrective Actions, Change Management, Audit Support as SME, GMP and document revision, review and approval
• Lead and participate in continuous improvement process changes
• Has advanced and specialized expertise in an analytical/scientific method or operational process, typically developed through a combination of job-related training and considerable on-the-job experience
• Completes assignments and facilitates the work activities of others; may coordinate work beyond own area
• Proposes improvements to processes and methods
• Direct interaction with Client and Regulatory Auditors
• Lead and guide all tours related to client and regulatory audits
• Acts as a lead, coordinating the work of others
• Works autonomously within established procedures and practices
• Competent at-risk mitigation for function
• Write and revise SOP's and WI's
• Support or own work orders, deviations, and audit observations for equipment activities
• Actively participates, suggests solutions to problems, and drives to timelines
• Ensure documentation is accurate and effectively assessing and mitigating risk associated with manufacturing activities
• Create and assist in implementation of Corrective and Preventative Actions (CAPAs) Primary -
• Possesses expertise in a range of processes or procedures through job-related training and considerable on-the-job experience
• Completes a variety of atypical assignments, as needed
• Completes work autonomously
• Subject matter expert for processes and procedures within primary manufacturing
• Proposes, develops and owns process improvements related to equipment and processes
• Collaborates with Production Supervisors, Room Leads, and QA floor support to solve issues real time
• Technical expert for machine setup, troubleshooting, and maintaining overall efficiency
• Develops training strategies for Primary Operations
• Proficient in coaching and training floor operations in all aspects of primary manufacturing
• Technical representative of Primary Manufacturing in audit activities
• Review and approve documents in EDMS
• Own, revise, and route documents through EDMS
• Executes other duties as assigned In general, this position's primary duty is to support an assigned production area regarding process control, including data collection and metric reporting.
• Collect and/or enter departmental data regarding the performance of people, processes, and equipment
• Organize and/or create visual representations (spreadsheets, reports, slide shows, etc.) of data for multiple audiences
• Complete projects and special assignments by establishing objectives, determining priorities, managing time, gaining cooperation of others, monitoring progress, problem solving and adjusting plans
• Improve quality results by studying, evaluating, and redesigning processes
• Implement changes and manage visual communications
• Has developed expertise in a variety of work processes or activities typically developed through a combination of job-related training and considerable on-the-job experience
• Leads a team, coordinating the work of others
• Manages limited and assigned Supervisory duties in absence of Department Supervisor
• Works autonomously within established procedures and practices
• Routinely suggests new, innovative solutions to routine and complex problems
• Skilled at-risk mitigation and prediction 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:
• High School/GED required
• 5+ years' pharmaceutical and/or manufacturing experience required
• 5+ years GMP experience
• Technical Requirements:
• Proficient in Excel, Word, and other office systems
• Prior work experience with quality, operations and/or scientific management software such as TrackWise , ComplianceWire , JD Edwards , DeltaV , Chromatography (i.e. Unicorn ), etc.
• Ability to understand and independently apply CGMPs as it relates to clinical and commercial operations
• Demonstrates understanding of the work tasks assigned
• Executes complex with high quality
• Knowledge of cGMP, ICH, FDA, EMA regulations or guidelines
• Intermediate understanding of pharmaceutical laboratory and/or production operations
• Capable of learning unfamiliar principles or techniques with training
• Prior experience leading deviation investigations using root cause analysis tools
• Champion change control and corrective / preventative actions
• Ability to interpret data and analyze trends and provide insight into potential issues and suggest solutions
• Authors and/or approves Standard Operating Procedures (SOPs), Batch Production Records (BPRs) and reports
• Ability to lead technical calls and discussions regarding investigations, audits, or other issues
• Seeks best practices for daily work activities
• Ability to support Risk Assessments, especially Hazard Analysis, Fault Tree Analysis, FMEA, etc.
• Behavioural 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 . click apply for full job details
Date Posted: 28 March 2025
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