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External Innovation Pharmaceutical Jobs in Utah (NOW HIRING)

Flowserve Corporation

Maintenance Mechanic

Springville, UT · On-site

$23 - $29.50/hr

If a culture of excellence, innovation and ownership is what you're searching for, consider putting ... external stakeholders as needed * Read and utilize schematics (mechanical/electrical/pneumatic ...

Flowserve Corporation

Maintenance Mechanic

Springville, UT · On-site

$23 - $29.50/hr

If a culture of excellence, innovation and ownership is what you're searching for, consider putting ... external stakeholders as needed * Read and utilize schematics (mechanical/electrical/pneumatic ...

University of Utah

Biomedical Engineers

Salt Lake City, UT · On-site

$48K - $55K/yr

... Molecular Pharmaceutics Location Campus City Salt Lake City, UT Type of Recruitment External ... innovation and quality in healthcare technologies. Contribute to project development with an ...

New

Reckitt

Technical Analytical Assistant

Salt Lake City, UT · On-site

$36K - $42K/yr

... innovation to develop and enhance our existing portfolio, never compromising on quality or ... Bachelor's degree in Chemistry, Biochemistry, Biology, Food Science, Pharmaceutical Sciences, or a ...

Reckitt

Technical Analytical Assistant

Salt Lake City, UT · On-site

$36K - $42K/yr

... innovation to develop and enhance our existing portfolio, never compromising on quality or ... Bachelor's degree in Chemistry, Biochemistry, Biology, Food Science, Pharmaceutical Sciences, or a ...

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Showing results 21-40

All JobsExternal Innovation Pharmaceutical JobsExternal Innovation Pharmaceutical Jobs in Utah

External Innovation Pharmaceutical information

What is external innovation in the pharmaceutical industry?

External innovation in the pharmaceutical industry refers to the process by which companies seek new ideas, technologies, or products from outside their own organization. This often involves collaborating with academic institutions, biotech startups, or other pharmaceutical companies through partnerships, licensing agreements, or acquisitions. The goal of external innovation is to accelerate drug discovery and development, reduce costs, and bring innovative medicines to market more efficiently. It complements internal research and development efforts by leveraging external expertise and resources.

How does the external innovation role in pharmaceuticals typically collaborate with internal R&D and external partners?

In an External Innovation Pharmaceutical role, professionals act as a bridge between internal research teams and external partners such as biotech firms, academic institutions, and startups. Collaboration involves identifying promising technologies or assets outside the company, facilitating due diligence, and aligning external opportunities with internal R&D objectives. Regular cross-functional meetings and joint project teams are common, ensuring transparent communication and alignment of goals. This collaborative approach accelerates innovation while managing potential risks and intellectual property concerns.

What are the key skills and qualifications needed to thrive as an external innovation specialist in the pharmaceutical industry, and why are they important?

To excel as an External Innovation Specialist in pharmaceuticals, you need a strong scientific background, expertise in drug development, and knowledge of partnership or licensing processes, typically backed by an advanced degree in life sciences or related fields. Familiarity with databases for scouting technologies, intellectual property management systems, and project management tools is highly valued. Outstanding networking, negotiation, and analytical thinking skills set professionals apart in this collaborative and strategic role. These capabilities are crucial for identifying and securing external opportunities that drive innovation and long-term growth in a competitive industry.

What is the difference between External Innovation Pharmaceutical vs External Innovation Pharmaceutical?

AspectExternal Innovation Pharmaceutical

Since the comparison is with the same job title, there is no difference between External Innovation Pharmaceutical and External Innovation Pharmaceutical. Both roles focus on identifying and collaborating with external partners to drive pharmaceutical innovation, requiring similar credentials, work environment, and industry usage. This role typically involves liaising with biotech firms, academic institutions, and other external entities to source new drug candidates or technologies, making it a key position in pharmaceutical R&D collaborations.

What are popular job titles related to External Innovation Pharmaceutical jobs in Utah?

For External Innovation Pharmaceutical jobs in Utah, the most frequently searched job titles are:

What cities in Utah are hiring for External Innovation Pharmaceutical jobs?

Cities in Utah with the most External Innovation Pharmaceutical job openings:

External Innovation Pharmaceutical jobs near you

Executive Director & Site Quality Lead

Denali Therapeutics

Salt Lake City, UT

Full-time

Medical, Retirement

Posted 12 days ago

Key responsibilities

  • Oversee GMP/GLP quality operations, including quality control laboratories/testing, batch record reviews and release, environmental monitoring, and external testing laboratories.

  • Ensure the site is in an inspection-ready state and maintain overall compliance for health authority inspections.

  • Build, supervise, develop, and train the GxP QC and QA teams, and represent Quality on the Utah Site Leadership Team and Denali Quality Leadership Team.

Job description

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.

Reporting to the Vice President of Quality, the Executive Director & Site Quality Lead will be a member of the site leadership team, and a successful hands-on contributor to the continued build and evolution of Denali's Clinical and Commercial manufacturing site in Utah. This individual will be accountable for building and leading the QA and QC teams in Utah and ensuring the site is in an inspection-ready state for anticipated commercial product launch. This leader will foster an environment that encourages Denali's Core Values, innovation, and continuous improvement.

Key Accountabilities/Core Job Responsibilities:

  • Oversee GMP/GLP Quality operations in Utah including quality control laboratories/testing, batch record reviews and release, environmental monitoring, and external testing laboratories.

  • Accountable for the overall compliance and inspection readiness of the site in preparation for key health authority inspections (PLI, general GMPs, etc.)

  • Key strategic partner to the Utah site head in developing and maintaining site culture, long term strategy and inspection readiness

  • Responsible for building, supervising, developing, promoting, hiring and training for the GxP QC and QA team.

  • Represent Quality on the Utah Site Leadership Team and Denali Quality Leadership Team.

  • Establish and monitor site quality metrics and KPIs for site performance monitoring and Quality System Management Reviews.

  • Implement, maintain and optimize quality systems including document control, change management, deviations, CAPAs, audits and compliance initiatives.

  • Support GMP site qualification including review and approval of SOPs, work instructions, specifications, stability studies, method validations, test methods, and utility and equipment/room qualifications.

  • Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.

Qualifications/Skills:

  • Typically requires a BS in a scientific discipline (with an MS and professional certification in quality, compliance and/or regulatory preferred) and 15+ years of GMP experience in the Pharmaceutical industry, to include 12+ years of people leadership experience.

  • Experience with in house manufacturing, QC testing, and CMC development

  • Large molecule or commercialization experience is a plus.

  • Experience with inspection management, mock inspections and Health Authority interactions

  • Current and strong working knowledge of 21 CFR 210-211, Part 11, 610 & 820 cGMP/GLPs; EU cGMP/GLPs; and ICH quality and development guidelines.

  • Familiarity with eQMS systems.

  • Able to travel domestically and internationally.

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more athttps://www.denalitherapeutics.com/careers

Thiscompensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.

Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

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