Novartis Gene Therapies Manufacturing Quality Associate // Shop Floor Quality (Night Shift) in Libertyville, Illinois
Ready to join a team committed to developing and commercializing gene therapies for patients and families devastated by rare neurological genetic diseases? Since 2013, Novartis Gene Therapies (formerly AveXis) has had one focus: bringing change to those devastated by genetic diseases.
The Novartis Gene Therapies culture embraces this mission. As a compassionate and dedicated team, we are enthusiastic about the science behind our work and finding answers to difficult questions. We are dedicated to communities affected by rare diseases, and these patients and families are the motivation for everything we do.
We have built a team with exceptional depth of experience, unified by a common vision; to develop gene therapies with the potential to positively impact the lives of the patients and families devastated by rare and life-threatening neurological genetic diseases. Though we are proud of what we have achieved to date, we remain relentlessly focused on making that vision a reality.
The successful candidate will be responsible for the Quality oversight of manufacturing operations on the floor and working in collaboration with Novartis Gene Therapies staff. Responsiblities include but are not limited to the following: review and approve written procedures, on the floor batch record documentation review, monitor and control the manufacturing environment, plant hygiene, process validation, people/process/waste flow patterns, aseptic certification, nonconformance review/disposition, and monitoring compliance with all requirements of good manufacturing practice. The Manufacturing Quality Associate is responsible for supporting the design and implementation of robust Quality Systems for a new viral gene manufacturing site and quality on the manufacturing floor.
The Manufacturing Quality Associate will be responsible for quality related business systems such as non-conformance/CAPA, by contributing and reviewing for approval and assisting with the implementation and supporting on-going continuous improvements. The Manufacturing Associate will use risk based decision to address any issues on the Manufacturing floor and will serve as the quality point of contact for the operations. Will provide critical quality expertise to transition a novel gene therapy into a commercially approved product. This individual must have a good knowledge of and application of the CFR’s and cGMP’s .
Complete on the floor quality audits and sampling during the manufacturing processes; knowledge of AQLs and visual inspection preferred
Good understanding of batch record execution, GMP and GDP. Knowledge of upstream and downstream processing necessary.
Work effectively with operators on the floor and make on the spot, risk based decisions; escalate issues to management as necessary
Assist in developing and delivering robust overall quality systems resulting ina fully compliant facility with respect to procedures and processes Contribute to the key plant metrics for the Quality Management Review meeting (QMR) to ensure a state of control and drive action where appropriate along with reporting on a specific set of quality and compliance metrics; reporting to management all necessary information from plant floor
Provide support on quality input on the translation of commercial product requirements into a technical product profile that includes defining critical quality attributes (CQA’s) and critical processing parameters (CPP’s)
Support and review of SOPs/Document Management: documentation management and SOPs all instruction sets, specifications, batch records etc. and other Quality procedures directly related to operations and other cGMP activities o On the floor Batch record review.
Ability to review controlled documentation during processing for GMP and GDP
Non-conformance/CAPA Management support and initial review of Non-conformances and CAPAs
Ensure all Non-conformances from established procedures are appropriately documented and investigated to determine and fix root cause; provide input on the creation and effectiveness of Corrective and Preventive Action plans and assist in determining a root cause o In process sampling/ AQL sampling
Ensure all required assessment and testing is carried out to support Quality approval or rejection, as appropriate, for starting materials, packaging materials, intermediates, bulk and finished product
Minimum B.S. degree in preferably microbiology, chemistry or biochemistry or 5 years applicable industry experience
A minimum of 3 years of experience in biopharmaceutical based GMP manufacturing operations including direct experience in cell culture, purification and aseptic fill/finish
Experience with viral gene therapies and/or orphan disease indications is a plus
Knowledge of FDA regulations and experience in US and international regulatory agency inspections
Direct experience reviewing standard operating procedures and partnering with operations on product related investigations and Non-conformances
Excellent oral and written communication skills with strong technical writing experience required
Experience with internal audits responsibilities and activities may change at any time with or without notice.
Willing to work off-shift hours as directed.
This position will be located out of our Chicago area office. Limited travel.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job.
Novartis Gene Therapies is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, national origin, genetics, disability, age, sexual orientation or veteran status.
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Job Locations US-IL-Libertyville
Posted Date 6 days ago (10/15/2020 3:36 PM)
Job ID 2020-5390
# of Openings 1
Novartis Gene Therapies
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