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Make an impact. Build a career. At Pace, we're committed to continuously moving science forward; to innovate and advance sustainable practices that improve the health and safety of our communities and lives. Ask any of us, and you'll hear the same thing repeated again and again we work here because what we do positively impacts the world. If you're curious, driven and ins
Posted 16 days ago
Lead and manage multiple commissioning / qualification / validation activities performed at facility with minimal supervision. Equipment Qualification / Re Qualification (IQ, OQ, PQ) for process equipment, QC equipment, packaging equipment, clean utilities. Cleaning Verification / Validation studies for transferred products. Media Fills / process simulations protocols. En
Posted 18 days ago
Participates on project teams to advance discovery portfolio projects. Presents/defends scientific findings in multi functional project teams/initiatives Independently designs, analyzes, and interprets experimental results and technical reports, etc. Support Molecular Biology experiments for designing expression vectors. Protein expression experience in Mammalian and E.co
Posted 21 days ago
Mallinckrodt Pharmaceuticals
- Long Branch, NJ / New Brunswick, NJ / Jersey City, NJ / 5 more...
The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough
Posted 22 days ago
WIRB - Copernicus Group
- Princeton, NJ / Research Triangle Park, NC
The CTMS Business Analyst is responsible for providing high quality calendar builds and accurate financial entry services (service deliverables) for site clients who utilize a Clinical Trial Management System for clinical research financial oversight and patient enrollment management. WCG SSU services are culminated by the CTMS service deliverables, triggering the start d
Posted 22 days ago
The Clinical Trial Documentation Specialist position is based within our Clinical Operations group, and works with departmental management and the Principal Investigator in the implementation of project clinical trial protocols. Job Type Full Time Base Hours 9 00AM 6 00PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be a
Posted 23 days ago
Under general supervision, assist in the performance of laboratory research and procedures by performing a variety of routine experimental techniques such as electrophoresis, centrifugation, chromatography, and the like. Collect, verify, record, and compile data and information in support of research. Essential Duties and Responsibilities (Specific duties will depend on n
Posted 24 days ago
Merit Medical Systems, Inc.
- South Jordan, UT / Pittsburgh, PA / Dallas, TX / 4 more...
DETAILS This position develops, documents and executes pre market and post market clinical evidence strategies for medical devices across product platforms. Works with cross functional teams and key stakeholders to execute on clinical evidence strategies for specific products/product families. For established products in the EU market, writes post market clinical follow up
Posted 8 days ago
Design, execute, oversee, and interpret experiments in partnership with other team members. Independently draft, review, and finalize both technical protocols and scientific reports while interacting in a cross specialty environment. Help determine process parameters range for cell culture and downstream processing to optimize PSC starting material yield and quality in a
Posted 15 days ago
Mallinckrodt Pharmaceuticals
- Long Branch, NJ / New Brunswick, NJ / Philadelphia, PA / 5 more...
The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough
Posted 22 days ago
You are an expert facilitator you open doors, foster communication, and bridge the gap. In this role, you will operate as the subject matter expert on reimbursement, access, and coverage issues affecting the clients product. Educate HCPs and their staff on matters related to reimbursement, access and coverage to facilitate appropriate patient access. You will Analyze acce
Posted 6 days ago
BrightSpring Health Services
- Bethlehem, PA / Horsham, PA / Harrisburg, PA
PHARMACIST CONSULTANT Job Locations US PA BETHLEHEM | US PA HORSHAM | US PA HARRISBURG ID 2024 142022 Line of Business PharMerica Position Type Full Time Pay Min USD $56.00/Hr. Pay Max USD $60.00/Hr. Our Company PharMerica Overview Our Pharmacy group focuses on providing exceptional customer service and meeting the pharmacy needs for hospitals, rehabilitation hospitals, l
Posted 9 days ago
Mallinckrodt Pharmaceuticals
- Long Branch, NJ / New Brunswick, NJ / Jersey City, NJ / 6 more...
The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough
Posted 22 days ago
Manage Regulatory Affairs, Advertising & Promotion and Compliance Group Manage the US RA Ad Promo, submission operations, labeling and compliance group staff, including objective setting and career development activities and motivate line reports to achieve shared and individual goals. Regulatory Leadership of Advertising and Promotional Materials Serve as subject matter
Posted 22 days ago
R esponsibilities for the Software Quality , Lead position include Identify and manage cross functional process improvement projects across the Quality Assurance organization ; Manage CAPA and deviation identification, tracking, follow up, and closure; E valuate and approve proposed changes of GxP and non GxP systems prior to implementation ; R eview and a pprove system r
Posted 22 days ago
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