Job summary
Job post source
This job is directly from Quva
Job overview
The Senior Scientist, Analytical R&D at Quva is responsible for managing cGMP analytical method development, validation, and transfer, ensuring medication quality and safety to impact healthcare positively.
Responsibilities and impact
The role involves developing and transferring analytical methods, improving QC methods, impurity analysis, stability testing, adhering to regulatory standards, writing SOPs, supervising junior staff, and collaborating with vendors.
Compensation and benefits
The position offers a full-time schedule, comprehensive health benefits including medical, dental, and vision, a 401k with company match, 17 paid days off plus 8 holidays, and occasional overtime opportunities.
Experience and skills
Candidates must have a Ph.D. in analytical chemistry or a Master's with extensive experience, at least 5 years in a cGMP pharmaceutical lab, expertise in analytical methods, knowledge of regulatory guidelines, and proficiency with HPLC and UPLC systems.
Career development
Quva is a high-growth company offering future career advancement opportunities within its progressive and integrated platform.
Work environment and culture
Quva promotes a culture of innovation, collaboration, continuous improvement, and equal opportunity, fostering a discrimination-free work environment.
Company information
Quva provides health-system pharmacy services including sterile injectable outsourcing and AI-based data solutions, supporting pharmacy management and patient care across multiple facilities.
Unique job features
The role includes working with advanced analytical technologies and contributing to critical medication quality assurance in a mission-driven company.
Company overview
Quva is a technology company specializing in data analytics and artificial intelligence solutions designed to help businesses optimize operations and make data-driven decisions. The company generates revenue by offering cloud-based software platforms and customized AI tools to enterprise clients across sectors such as retail, finance, and manufacturing. Founded by a team of data scientists and engineers, Quva has built a reputation for delivering scalable, secure, and user-friendly products that integrate seamlessly with existing business systems. Notably, Quva has formed strategic partnerships with leading cloud providers to enhance its service offerings and accelerate client adoption. Candidates should be aware of Quva’s commitment to innovation, customer-centric approach, and its rapid growth trajectory in the competitive AI technology landscape.
How to land this job
Tailor your resume to highlight your expertise in cGMP analytical method development, validation, and transfer, emphasizing your experience with HPLC and UPLC systems as these are critical for the Senior Scientist, Analytical R&D role at Quva.
Focus on showcasing your knowledge of FDA, ICH, USP guidelines, and your ability to write and improve SOPs and regulated documents, which are essential qualifications mentioned in the job description.
Apply through multiple channels including Quva’s corporate careers page and LinkedIn to maximize your visibility and chances of being noticed for this specialized role.
Connect with current employees in Quva’s Analytical R&D or Quality Control divisions on LinkedIn; use ice breakers like commenting on recent company innovations in sterile injectable outsourcing or AI-driven pharmacy solutions to start meaningful conversations.
Optimize your resume for ATS by incorporating keywords such as 'cGMP', 'analytical method validation', 'HPLC', 'UPLC', 'FDA guidelines', 'SOP writing', and 'impurity identification' to ensure it passes initial automated screenings.
Consider using Jennie Johnson’s Power Apply feature to automate resume tailoring, multi-channel application submission, and LinkedIn networking, allowing you to focus your energy on preparing for interviews and strategic job search activities.
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