Manufacturing Controls Jobs in Indianapolis, IN
Manufacturing Controls Jobs in Indianapolis, IN

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Your Role & ResponsibilitiesLead the effort and collaborate with District management supervision and employees on maintaining a sustainable safety culture within the District in concert with Company goals and objectives.Responsible for ensuring all Safety Regulatory & Quality More...
Title: Senior Director Technical Excellence Location: Washington DC or EGPAF Presence Country AfricaReports To: Vice President Program Management & Technical Excellence Classification: Full-time exemptClosing Date for Applications: Wednesday September 10 2025The Senior More...
Radiation Safety Lead/rso â Isotopes Manufacturing
BandLevel 4Job Description SummaryAt Novartis we are pioneering the future of cancer treatment through Radioligand Therapy (RLT) - a powerful fusion of nuclear medicine and precision oncology. As we expand our global RLT manufacturing footprint we are seeking passionate purpose-driven More...
Radiation Safety Lead/rso â Isotopes Manufacturing
Job Description SummaryAt Novartis we are pioneering the future of cancer treatment through Radioligand Therapy (RLT) - a powerful fusion of nuclear medicine and precision oncology. As we expand our global RLT manufacturing footprint we are seeking passionate purpose-driven individual More...
Details:Stefanini Groupis looking for Senior InTune Specialistfor a globally recognized company!For interested applicants click the apply button or you may reach out to Pragy Sharma at / for faster processing. Thank you!Position Overview:We are looking for a highly skilled and motivat More...
The Associate Director Statistics - Oncology provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials patient safety and global medical affairs (GMA). The Associate More...
This position is responsible for designing planning and executing statistical components of plans for research studies that prove the clinical economic and humanistic value of pharmaceutical assets. Position uses sound statistical methodology to conduct studies develops/or applies sta More...
About The Position The KIPP Foundation is seeking a Director of Transformation to drive strategic change and innovation across its operations. The Senior Director will be responsible for leading strategic transformation efforts across KIPP Foundation teams (i.e. Finance Schools T More...
Travel: 10% TravelThe Associate Director of Virtual Health will play a key leadership role in the development implementation and oversight of virtual care services across the organization. This individual will be responsible for supporting operational excellence driving clinical quali More...
As a Senior Reimbursement Specialist you play a crucial role in driving the financial success of our organization. Collaborating with our billing tool provider and internal teams you will optimize billing operations in alignment with Guardant Healths mission and values.In this role yo More...
Under the general direction of the Vice President manages the day-to-day operations and staff responsible for both external and internal engagement on all California state regulatory matters. For external engagement manages the ISOs participation in processes at the Califo More...
Further develop your expertise and join our team as Director CMC Product Development. Must have Medical Device experience. The Product Development Director (PDD) will be a member of the Operations Strategy & Pipeline Leadership (OSPL) team within the Product Development More...
The Senior Regulatory Affairs Manager - Screening will provide direct regulatory support for IVD cancer screening products (Shield CRC and future blood-based cancer screening tests) in all stages of the product lifecycle. This role will actively lead and support development and implem More...
Senior Regulatory Affairs Manager OncologyPosition SummaryThe Senior Regulatory Affairs Manager - Oncology will provide direct regulatory support for Oncology IVD/CDx products (Guardant360 CDx and future products such as Tissue IVD/CDx) in all stages of the product lifecycle. Th More...
Senior Regulatory Affairs Manager OncologyPosition SummaryThe Senior Regulatory Affairs Manager will provide direct regulatory support for Oncology IVD/CDx products (Guardant360 CDx and future products such as Tissue IVD/CDx) in all stages of the product lifecycle. This role will act More...
*Remote or Hybrid in AbbVie Location. Position title and grade level will be based on qualifications listed below and location hired.PurposeRole is responsible for leading evidence modelling teams to design and execute evidence-synthesis health economic models. Position applies method More...
Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. Th More...
Job TItle: Global Medical Affairs Liver Diseases / Virology Job Duration: 6 months Job Location: Foster City California Job Description Reporting to the Sr. Director of Viral Hepatitis Global Medical Affairs this role is a key position within the Global Liver Inflammation Virol More...
Eurofins Medical Device Consulting is seeking an experienced and influential Regulatory Affairs Thought Leader to serve as a strategic partner to our marketing and sales teams and a visible representative of our brand in the marketplace. This individual will elevate our presence at tr More...
Manufacturing Operator needs GMP environment and 5 years experience Manufacturing Operator requires: Ability to work overtime weekends and off shifts. Shifts structure 24/7 schedule (3 work shifts 2 off shifts 2 work shifts 3 off shifts). 12hours shifts. 6.00pm/6.00am. Shift structur More...
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