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Investigator
$61k-90k (estimate)
Full Time Just Posted
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myGwork - LGBTQ+ Business Community is Hiring an Investigator Near King of Prussia, PA

This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ business community. Site Name: Upper Merion, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence
Posted Date: May 16 2024
Preferred Site Locations: Upper Merion, Stevenage, Upper Providence. 2-3 days on-site per week is required.
Are you energized by a highly collaborative scientific role in analytical chemistry platforms that allows you to accelerate scientific and R&D delivery? If so, this role could be an ideal opportunity to explore.
The Digital Analytical Platforms team within Analytical Development is responsible for innovations to assess and when warranted implement platforms that enhance analytical chemistry through digitization and efficiency gains. The primary purpose of this collaborative role is to supervise, improve, and leverage the fleet of open-access non-GMP chromatography platforms to accelerate discovery and development across a diverse and global user group. These open-access instruments are integral to our license to operate, and support most of our potential medicines.
As an Investigator in Digital Analytical Platforms, you will design and deliver near term tactical solutions and long term strategic solutions. You will use quantitative and/or qualitative data and analysis using chromatography instruments and methods, and systems engineering to develop platform technologies. In addition, you will enable a high standard of data integrity and technical efficiency applied towards scientific methodology.
ResponsibilitiesThis role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
  • Independently select the design and execution of root cause analysis and experiments based on interpretation of results
  • Implement and maintain a scientifically current to state-of-the-art chromatography systems
  • Provide attention to data quality, integrity and archiving for own work and of others
  • Initiate new research directions and innovative strategies to achieve project, platform, and department goals
  • Perform complex data management and data interpretation tasks/analyses
  • Identify new scientific and or engineering opportunities, which may include analytical data pipeline and visualization projects that support the discovery and development of candidate medicines.
  • Identify bottlenecks, and systematically evaluate and assess root causes of errors in the laboratory, differentiating with rigor between inefficiencies arising from human, software, hardware, firmware, and/or chemical sources.
  • Deliver automated and/or digital solutions to reduce or eliminate common failure modes
  • Seek peer challenge and review of scientific ideas and experimental design
  • Influence project and team's direction by interpreting results outside area of expertise
  • Maintain and grow our support network with partner departments
  • Sustain a collaboration with Agilent to deliver improvements as required
  • Develop networking skills with external key opinion leaders and experts in specific scientific disciplines
  • Ensure that design and interpretation of complex experiments and data management activities impact Research and Development decision making
  • Make effective decisions to achieve desired outcomes of project team through technical or scientific interpretation of results
  • Take a leadership role for safety, regulatory and compliance within the department
  • Cooperate as a technical resource by acting as mentor and training new users
  • Peer-review of others' work
  • Prepare detailed oral or written reports of results in the context of strategic fit, feasibility and rationale for projects
  • Author, review, and approve key documentation to support deployment and maintenance of the chromatography operating software
  • As situationally warranted, independently author scientific papers
  • Present at internal Research and Development forums and external meetings subject to budget availability
  • Independently prepares and communicate conclusions and recommendations for next steps
  • Demonstrate networking skills through interactions across departments and divisions
  • Lead small projects/project sub teams to achieve technical or business outcomes
  • Active and influential scientific participant in at least one project/program
  • Update supervisor and matrix leaders to inform progress and activities
  • Anticipate problems and proactively seek input from other teams/divisions within Research and Development
  • Use scientific and or engineering technical expertise to solve project related problems of colleagues and of other projects
Why you? Basic QualificationsWe are looking for professionals with these required skills to achieve our goals:
Ph.D. or comparable industrial experience in one or more of the following areas:
Preferred: chemistry (analytical, organic, biochemistry), engineering (chemistry, systems, data, computer, software, industrial, materials), data science or engineering, computer science
Considered: chemistry (inorganic, forensic, physical, environmental), engineering (mechanical, biomedical, environmental)
  • Proven track record of solving complex problems
  • Experience analyzing data
  • Clear concise communication
  • Learning agility
  • Non-GMP systems
Preferred QualificationsIf you have the following characteristics, it would be a plus:
  • Knowledge of regulatory requirements and drug development process
  • Scientific expertise
  • Chromatography expertise (HPLC, GC, LC/MS)
  • Data visualization expertise (Spotfire or other)
  • Project management and matrix leadership experience
  • Ability to influence others
  • Coding (Python, C#, R, VBA or demonstrated learning agility to develop these skills, and/or experience working in GitHub)
  • GMP systems
  • Software development and testing, and familiarity with Kanban and Agile frameworks
  • Risk assessment and or management
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or 1 801 567 5155 (outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.

Job Summary

JOB TYPE

Full Time

SALARY

$61k-90k (estimate)

POST DATE

05/24/2024

EXPIRATION DATE

06/15/2024

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