Senior Scientist jobs in United States
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AstraZeneca · 17 hours ago

Senior Scientist

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. The Senior Scientist role is responsible for supporting the development of pressurized metered dose inhalers and oral solid dosage forms, requiring expertise in drug development and strong collaboration skills.

BiopharmaBiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Collaborate with both internal and external partners (e.g. analytical, cRO/cMOs, academic institutions, manufacturing, formulation, device, quality assurance, statistics, and regulatory affairs) to effectively deliver on project and team objectives
Effectively plan, complete and communicate technical development activities within AZ project teams
Lead/Author complex technical protocols for the development of drug products using both internal and external resources
Lead/participate in technical development teams with focus on product development, characterization, root cause analysis and risk mitigation
Lead/participate in drug product project technical investigations and provide analysis/recommendations to team
Prioritize and interpret large data sets and communicate data impact or value to senior R&D leadership
Contribute to/and or lead continuous improvement projects and other GPD initiatives
Maintain lab notebooks following SOP requirements and keep clear and complete records. Ensure GMP/GLS compliance
Maintain lab equipment and lab environments following SOP requirements and keep clear and complete records. Ensure GMP/GLS compliance
Complete procurement activities for lab/project (Requestioning, PO generation, invoicing)
Ability to work in a laboratory environment for up to 50% of time, conducting characterization testing, formulation development, spray drying development activities
Ability to work in office environment and familiarity with PCs (MS office proficiency required)

Qualification

Drug development experienceAnalytical characterization techniquesTechnical protocol authoringRegulatory document authoringLean/Six Sigma familiarityJMP statistical softwareCommunication skillsCollaboration skillsProblem-solving skills

Required

Bachelor's Degree
Minimum 3+ years of experience
Excellent written and verbal communication skills
Collaborate with both internal and external partners (e.g. analytical, cRO/cMOs, academic institutions, manufacturing, formulation, device, quality assurance, statistics, and regulatory affairs) to effectively deliver on project and team objectives
Effectively plan, complete and communicate technical development activities within AZ project teams
Working knowledge of key analytical characterization techniques (e.g. Karl Fischer moisture analysis, HPLC, pH, solid state particle analysis)
Lead/Author complex technical protocols for the development of drug products using both internal and external resources
Lead/participate in technical development teams with focus on product development, characterization, root cause analysis and risk mitigation
Lead/participate in drug product project technical investigations and provide analysis/recommendations to team
Prioritize and interpret large data sets and communicate data impact or value to senior R&D leadership
Contribute to/and or lead continuous improvement projects and other GPD initiatives
Maintain lab notebooks following SOP requirements and keep clear and complete records. Ensure GMP/GLS compliance
Maintain lab equipment and lab environments following SOP requirements and keep clear and complete records. Ensure GMP/GLS compliance
Complete procurement activities for lab/project (Requestioning, PO generation, invoicing)
Ability to work in a laboratory environment for up to 50% of time, conducting characterization testing, formulation development, spray drying development activities
Ability to work in office environment and familiarity with PCs (MS office proficiency required)

Preferred

Experience authoring US and international regulatory documents is desired
Author sections of regulatory documents (e.g., DMFs, INDs, NDAs, etc.)
Participate/lead the interactions with Health Authorities for regulatory meetings
Familiarity with Lean and or Six Sigma
Familiarity with JMP statistical software

Company

AstraZeneca

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AstraZeneca is a pharmaceutical company that discovers, develops, manufactures, and markets prescription medicines. It is a sub-organization of Investor.

H1B Sponsorship

AstraZeneca has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2021 (2)
2020 (11)

Funding

Current Stage
Public Company
Total Funding
$5.26B
2024-07-30Post Ipo Debt· $1.51B
2023-02-28Post Ipo Debt· $2.25B
2023-02-24Post Ipo Debt· $1.5B

Leadership Team

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Pascal Soriot
Executive Director and Chief Executive Officer
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Aradhana Sarin
Group CFO and Executive Director
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Company data provided by crunchbase