Novartis
BioProcess Engineer I/II/III - Upstream (2-2-3 rotation day shift)
PayCompetitive
LocationDurham/North Carolina
Employment typeFull-Time
This job is now closed
Job Description
- Req#: 388175BR
The BioProcess Engineer I is responsible for assisting with organizing, running, and sustaining the manufacturing operations process at the plant/site. The level of the role will be determined by the years of relevant experience.
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Novartis Gene Therapies is dedicated to developing and commercializing gene therapies for patients and families devastated by rare and life-threatening neurological genetic diseases.
Assists in manufacturing led investigations through partnerships with Quality and other business units at the site.
Produces product, media/buffer preparation, learn to troubleshoot equipment, participate in interviews on deviations, stocking of items in supply/ production / warehouse area, and standardizing equipment and cleaning production area.
Assists in determine root cause, implement a solution and a verification check to ensure the fix was effective.
Assists with creation and on-going maintenance of all pertinent equipment, policies, and procedures.
Produce product, media/buffer preparation, learn to troubleshoot equipment, participate in interviews on deviations, stocking of items in supply/ production / warehouse area, and standardizing equipment and cleaning production area.
Learn aseptic techniques, cell culture, recovery, purification, aseptic fill/finish (upstream and downstream).
Assists in producing clinical and commercial material on an annual basis that meets the site’s strategic objectives and is compliant with cGMPs.
Supports the product requirements to ensure that all products are produced according to plan. Learn cGMP and cGDP and ensure cGMP documentation is being filled out correctly, training is current, and all Quality requirements are being followed.
Maintains quality standards to meet cGMP requirements, CFR’s, and internal company policies directly related to the manufacturing process.
Partners with Quality to ensure a quality and compliant manufacturing environment.About the company
At Novartis, we are reimagining medicine to improve and extend people’s lives. We are working hard to produce breakthroughs and address unmet needs for patients with devastating diseases, including genetic disorders and certain deadly cancers. Learn mo...