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Job Description The Senior Research Scientist I, Purification Process Development (Pivotal and Commercial) will be responsible for leading all aspects of purification development including process development and process characterization at internal or external facilities for Gilead biologics entities during pivotal and commercial development phases.
$209,330 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Title: Sr Thought Leader LiaisonLocation: Remote with heavy travelThe Manager, Thought Leader Liaison for Alastin Business Unit, U.S. is a field-based position responsible for working closely with Key Thought Leaders (KTLs) and Key External Experts (KEEs) to ensure cross-functional scientific and commercial engagement.
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Health and Wellness - In collaboration with External Relations establish and develop relationships with health care providers and community based organizations to provide onsite health education classes focusing on prevention and wellness management.
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Be the LMS administrator for the organization, facilitating both internal and external learners. Location: Carlsbad, CA (Hybrid Schedule 2 days remote, 3 days in office)Primary Responsibilities: Play a key role in defining the learning content strategy for internal and external audiences, ensuring alignment with business objectives through the design, development, and evaluation of training content.
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As such, each Pharmaceutical Sales Rep will represent the assigned brand products and their approved indications; helping external customers such as physicians, nurses, etc. As a Pharmaceutical Sales Rep field professional, you have consistently met or exceeded sales and other critical business goals and metrics in a highly complex and competitive market.
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Work EnvironmentThe Landscape Gardener works on-site at an apartment community and interfaces with external/internal customers, residents, and vendors on a regular basis. Regularly provides information to the Landscape Supervisor/Maintenance Supervisor or Property Manager regarding safety concerns and the general appearance of the community to ensure, high quality, safe living environment for the residents and marketability of the community.
$16 - $17 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Progress towards external designations such as CFA, CVA, CPA/ABV, or ASA a plus. The Valuation Senior Associate can be based out of any of our U.S. office locations (New York, NY; Philadelphia, PA; Boston, MA; Braintree, MA; Woburn, MA; Princeton, NJ; Whippany, NJ; East Brunswick NJ; Red Bank, NJ; Saddle Brook, NJ; Providence, RI; Baltimore, MD; Bethesda, MD; Nashville, TN; Boca Raton, FL; Orlando, FL; San Diego, CA; Los Angeles, CA; Orange County, CA; San Francisco, CA; San Ramon, CA; Portland, OR; Seattle, WA.
$100,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Ownership of the site EHS program, including Process Safety Management (PSM) to deliver 100% compliance, plus, leadership of the site EHS team including prioritization and assignment of tasks for the internal team and external consultants as appropriate.
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Initiates new manufacturing processes with external vendors. MiniTab or JMP. Experience with 3D CAD software, preferably SolidWorks. Education and Experience Undergraduate degree in mechanical or biomedical engineering 3-5 years of product and process development experience, preferably in medical devices.
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Regulatory Affairs Specialist III – Global SubmissionsThe Role:As a Regulatory Affairs Specialist III at Thermo Fisher Scientific Inc., you will have the exceptional opportunity to play a crucial role in the planning, managing, and tracking of regulatory submissions and documentation for the production of biological medicines.
$125,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our headquarters, in Vista, CA is home to sales, marketing & consumer engagement, research & development, insights & innovation, quality control, regulatory affairs, and distribution. ASQ or Six Sigma Green/Black Belt certification is preferred.
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Our Quality Specialist collaborates with key internal stakeholders to enhance the performance of the overall Quality Management System (QMS). Working knowledge of Quality Systems and quality related tools, such as FMEA, SPC, Cpk, AQP, DOE.
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Oversee, host and/or lead regulatory, sponsor, external vendor and/or partner lab inspections/audits, and perform related internal GMP, GCLP and CLIA Regulatory Compliance Audits. Responsibilities include the management of personnel and compliance for assay validation, clinical study development and testing, IVD manufacturing, and overall Quality Systems (change control, CAPA, equipment, computerized systems, etc.
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2nd shift 2:20 - 10:50pm $18- $20 hour plus shift differential Job Summary: Responsible for assisting the Machinists in carrying out machining functions to meet the standards of excellence required by internal and external customers in compliance with domestic and international regulatory requirements in order to deliver the highest quality products.
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As Loss Prevention Supervisor you will improve company profitability by executing company programs around external theft deterrence, internal investigations and operational shortage. Identify external and internal theft trends within assigned location(s.
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external affairs jobs Company: Columbia University in Carlsbad, CA
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