Senior Scientist, Analytical Chemistry

Phlow Corporation; Richmond (VA); Vor Ort; USD 90.000 - 115.000; Vollzeit

Benefits dieser Stelle

Bonus program

Stock options

Comprehensive benefits

Paid time off

Retirement plan

Education benefits

Zusammenfassung

Phlow Corporation is seeking an analytical chemist to provide analytical chemistry support, develop and validate methods, and support FDA-regulated API development and CDMO projects. The role reports to Senior Director, Analytical Chemistry and emphasizes safety, integrity, and collaboration.

The candidate will manage analytical tasks with minimal supervision, coordinate external labs, and generate technical reports and regulatory documents while meeting cGXP requirements.

Qualifikationen

• Advanced degree in chemistry, pharmaceutics, or related field.
• 1–3 years’ experience in analytical method development, validation, and FDA-regulated API/drug product development.
• Working knowledge of MS Office, MS Project, Excel, Visio, and SharePoint.
• Ability to work independently and in a team.
• Broad range of analytical chemistry, compound purification, spectral analysis/interpretation.
• Experience with HPLC, LC/MS, GC, GC/MS, KF, LOD, DSC, TGA, NMR, UV, LC-MS.
• Excellent written and verbal communication skills.
• Strong interpersonal skills.

Aufgaben

• Conduct analytical method development, validation, and project support.
• Identify technical challenges and perform troubleshooting.
• Manage CMO/CRO analytical project resources as needed.
• Provide data production, review, analysis, and interpretation with scientific rigor.
• Author and review technical reports, regulatory submissions, SOPs, validation protocols.
• Ensure activities comply with cGXP and regulatory requirements.
• Oversee day-to-day laboratory activities for analytical equipment.
• Plan studies in accordance with standards to facilitate product development.
• Coordinate equipment maintenance and vendor relations.

Kenntnisse

Analytical method development

Data analysis

Communication skills

Team collaboration

Analytical chemistry

Spectral analysis/interpretation

Problem solving

Regulatory submissions

Ausbildung

Advanced degree in chemistry

PhD with ≥2 years experience

MS with ≥5 years experience

BS with ≥10 years experience

Tools

MS Office

MS Project

Excel

Visio

SharePoint

Jobbeschreibung

Description

The purpose of this role is to provide analytical chemistry support to Phlow. This is an exciting opportunity for graduates or individuals with analytical chemistry experience to develop and perform analytical experiments under the direction of the Senior Director, Analytical Chemistry, or other team members. The candidate will support Phlow’s contract development and manufacturing services to ensure business objectives are met for execution of the internal Phlow API development as well as commercial projects. The candidate will personify Phlow’s shared values and culture, both internally and externally. The candidate will work with the highest standards of safety, integrity, transparency, and ethics to create win-win scenarios for patients, customers, partners, and colleagues.

Requirements

• Independently conduct analytical method development, validation, and project support
• Identify technical challenges during analytical method development and perform analytical method troubleshooting.
• Manage CMO/CRO analytical project resources as required such as contractors and contract laboratories, as needed.
• Manage technical direction of analytical projects; identify key deliverables and next steps and communicate to the team.
• Responsible for data production, review, analysis, and interpretation from a variety of sources. Provide accurate summaries and make recommendations to stakeholders with scientific rigor.
• Author and review technical reports, regulatory submissions, SOPs, validation protocols, and other cGMP documents.
• Performs the assigned analytical tasks with minimum supervision in support of product development and clinical trial material.
• Performs activities within the assigned timelines and in compliance with cGXP's, regulatory requirements, and company practices and procedures.
• Responsible for the design and conduct of studies in accordance with company and regulatory standards to facilitate new product development.
• Manage day-to-day laboratory activities for analytical equipment, including sourcing consumables, troubleshooting, maintaining equipment and calibrations with various vendors.

The salary range for this position is $90,000 to $115,000, with the final offer determined based on factors such as the candidate's experience, qualifications, skills, and education. In addition to a competitive base salary, this position is eligible to participate in Phlow's bonus and stock option programs. Phlow also offers a comprehensive benefits package that includes medical, life, and disability insurance; retirement savings plans; paid time off and company holidays; and education-related benefits. Many of these programs are fully funded or significantly subsidized by the company, reflecting our commitment to supporting the health, well-being, and professional development of our employees.

Experience & Qualifications

• Advanced degree in chemistry, pharmaceutics, or related field.
• 1-3 years experience in analytical method development, validation, and API and/or drug product development activities regulated by FDA.
• Working knowledge of standard Office tools (MS Office, MS Project, Excel, Visio, SharePoint).
• Ability to work well both independently and with a team.
• Broad range of functional expertise in analytical chemistry, compound purification, spectral analysis/interpretation.
• Experience with common analytical techniques such as: HPLC, LC/MS, GC, GC/MS, KF, LOD, DSC, TGA, NMR, UV, LC-MS
• Excellent written and verbal communication skills
• Strong interpersonal skills

Preferred Qualifications

• Ph.D. with a minimum 2 years of experience, M.S with a minimum 5 years of experience, or B.S. degree with a minimum 10 years of experience in Analytical Chemistry, Pharmaceutical Sciences, or a related scientific field
• Knowledge of ICH and cGMP requirements
• Experience working for a contract organization (CROs/CMOs/CDMOs) is a plus.
• Experience with technical and operational risk assessments (e.g., process robustness, mutagenic impurities, nitrosamines, etc.) is a plus.
• Experience with the development and implementation of Process Analytical Technology (PAT) is a plus.
• Experience with Design of Experiments (DOE) is a plus.

Physical Requirements

• Constantly required to see to utilize computer screens and monitors to perform job duties including reading & writing, as well as when presenting information and communicating with others.
• Frequently required to talk or hear to communicate with employees, candidates, vendors, and others, including presenting information in front of groups.
• Frequently required to reach with arms and hands performing repetitive motions and using finger dexterity to work primarily at a computer keyboard and with a mouse.
• Frequently required to sit, and occasionally required to stand or walk to move around primarily in an office environment.
• Occasionally lift and/or move up to 10 pounds.
• This position may require up to 5% travel with occasional increase in travel demands based on business needs.