Develop a Cell & Gene Therapy and Biologics go-to-market strategiesbased on market intel and competitive landscape analysis with oversightfrom senior management. OTHER EXPERIENCE AND QUALIFICATIONS: Mustpossess at least 7 years of experience as a Researcher or related rolewith drug discovery and the product development process withpharmaceutical or biotech companies.

In this position, you would contribute to the manufacturing and testing of bioassay cell lines and other reagents. We are a dedicated group, passionate about cell culture and the role that reliable in-vitro models play in furthering medicine and disease treatment.

Responsibilities:The cGMP Biomanufacturing group is responsible for current Good Manufacturing Practices (cGMP) production activities, including master/working cell bank production, upstream cell culture, downstream protein purification, and mRNA therapeutics production.

In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology.

We are looking to add a Study Director - ADME to our Drug Metabolism team in Madison, WI. We provide a comprehensive range of ADME services to support drug discovery and development programs.

The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI, and our market leading biologics analytical services as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA. Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent.

The DSA will work with multiple sites (including PM and Commercial Operations) across the Catalent Cell and Gene Therapy (CGT) network to oversee customer communication and program strategy.

The individual will use their knowledge of molecular biology or protein biochemistry to work within the Antigen Sciences group which works cross-functionally to build custom target molecules to support antibody discovery, optimize and characterize lead drug molecules, and implement new practices to improve Invenra’s drug discovery platform.

4 years of consulting experience or senior-level HCM operations experienceExperience leading and executing HCM Business Process Discovery and AssessmentsExperience leading large, full life cycle ERP implementation(s) Workday PreferredSuperior communication skills, both written and verbalExperience building and managing high performance teamsPassionate interest in continuous learning and professional growth, particularly in payroll systems.

Assist in routine filing of Quality records Other duties as assignedEDUCATION AND PROFESSIONAL EXPERIENCE High school diploma with 8+ years of relevant GMP experience; Bachelor's degree in a science or related discipline with 2-5 years of relevant experienceSKILLS Experience executing GMP quality systems in a pharmaceutical/biotech/medical device environment preferred Experience supporting the manufacturing and conducting training is preferred.

Arrowhead is seeking a highly motivated associate analytical scientist/scientist to join our growing Discovery Analytical Chemistry team. The successful candidate will be tasked with chemical/biological sample preparation and running HPLC/LC-MS to support ongoing discovery activities.

Perform all duties and responsibilities in compliance with standard operating procedures, Safety Quality Identity Potency Purity (SQUIPP), regulations outlined in the Code of Federal Regulations (CFR), Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), and other applicable Federal, state and local regulations.

Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

The Regulatory Affairs Director will be responsible for leading the overall Regulatory Affairs strategy and direction for Promega. We are Promega: an international bio-tech company made up of scientists and non-scientists, with over 4000 high quality products that have been sparking inspiration and discovery in science for over 40 years.

Director, Regulatory AffairsWe challenge you to change the world. This is an onsite position located in Madison, WI.To apply, view a complete job description, and learn more about our company, please visit: is important at Promega.