Job Description Summary

#LI-Onsite

This role is located on-site in Indianapolis, IN. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for experienced Manufacturing professionals to help us reach our ambitious goals.

The Process Expert provides direct front line support to production activities using technical understanding and knowledge of cGMPS, SOPs, and process steps. This individual is accountable to support process issues, protocol generation, general documentation support, deviation investigations, and continuous improvement of the process.

Job Description

Major accountabilities:

Responsibilities include but not are limited to:
Support a culture of safety, quality, diversity, and inclusion.
Provide front line support to manufacturing shifts to ensure safe, quality, and timely completion of product batches.
Manage and maintain manufacturing documentation including Master Batch Record, applicable SOPs, risk assessments, protocols, and other documentation as needed.
Track and trend critical process parameters and in process checks as part of ongoing process verification (OPV) and identify CAPAs to address any trends.
Identify, assess, and own technical changes through GMP change control processes.
Investigate deviations and determine root causes and identify CAPA.
Act as Subject Matter Expert (SME) for process flow and support data gathering for Annual Product Review.
Ensure processes are inspection ready at all times.
Support continuous improvement through identification of opportunities, technologies, and owning changes to implement improvements.
Support on going self learning and ensuring training is up to date.
Provide support to production team through training and knowledge sharing.

Minimum Requirements:

Bachelor's degree in Engineering, Pharmacy, Pharmaceutical Technology, Chemistry or other science related fields or equivalent experience.
1+ years of experience in a manufacturing environment, preferably in pharmaceutical manufacturing
Direct experience in a GMP or aseptic/sterile environment is highly desired.
Radio pharma experience is a plus
Word, Excel, Powerpoint, and Teams Experience
Ability to work in a cross functional team
Technical writing experience preferred
Excellent communication skills
English fluently, verbally and in writing

Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range

$84,000.00 - $126,000.00

Skills Desired

Change Control, Chemical Engineering, Continual Improvement Process, Efficiency, Employment Discrimination, Flexibility, General Hse Knowledge, Good Documentation Practice, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Physics, Process Control, Production Line, Productivity, Risk Management, Root Cause Analysis (RCA), Scheduler, Technology Transfer, Well-Being