About this opportunity
ForDoz Pharma Corp lists this Analytical Scientist III opportunity in east windsor, middlesex county, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
ForDoz Pharma Corp., based in East Windsor, New Jersey, is a fully integrated pharmaceutical company specializing in the development and manufacturing of advanced sterile injectable drug products. Rooted in a commitment to quality excellence, ForDoz continues to expand the expertise and production capacity for both conventional and complex sterile drug formulations in the U.S. Role Description
The Analytical Scientist II is responsible for developing, validating, transferring, and troubleshooting analytical methods that support the development, manufacture, release, and stability of small molecule sterile injectable drug products. This position supports products throughout the development lifecycle, from early-stage R&D through clinical and commercial manufacturing. The ideal candidate has hands-on experience in a cGMP pharmaceutical laboratory, analytical method development and validation, and analytical testing of sterile injectable products.
Key Responsibilities
Develop, optimize, validate, and transfer analytical methods in accordance with ICH, USP, and FDA guidelines.
Perform analytical testing using HPLC/UPLC and other laboratory instrumentation for raw materials, in-process samples, and finished products.
Support stability studies, release testing, and product characterization.
Investigate analytical deviations, OOS/OOT results, and method-related issues.
Author and review analytical methods, validation protocols, reports, SOPs, and laboratory investigations.
Collaborate with Formulation, Manufacturing, Quality, and Regulatory teams to support product development and commercial manufacturing.
Ensure compliance with cGMP, data integrity, and laboratory safety requirements.
Qualifications
EducationM.S. in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or a related discipline.
B.S. with significant relevant pharmaceutical experience may be considered.
Experience 3-5 years of pharmaceutical analytical laboratory experience.
Minimum 2 years supporting sterile injectable drug products.
Experience with small-molecule pharmaceuticals is required.
Experience with complex injectables (liposomes, suspensions, microspheres, emulsions, or long-acting injectables) is preferred.
Experience supporting IND, ANDA, or 505(b)(2) programs is a plus.
Experience in a cGMP pharmaceutical environment is required.
Skills Required:
HPLC/UPLC (Empower preferred)
Analytical method development and validation
Stability testing
Method transfer
OOS/OOT investigations
ICH Q2 and USP analytical guidance
Strong analytical thinking and problem-solving skills
Excellent documentation and scientific writing ability
Effective communication across functions and with external clients
Ability to manage multiple projects and timelines independently
High attention to detail and commitment to quality
Preferred:
LC-MS
Particle size analysis (DLS or laser diffraction)
Dissolution and release testing
LIMS or other electronic laboratory systems
Pay$80,000 - $120,000 per year
Benefits
401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance
ForDoz Pharma Corp. is a specialty pharmaceutical company focusing on development, manufacturing, and commercialization of complex generic products (e.g. oncology and antifungal products) and improved existing products 505(b)(2). ForDoz Pharma Corp. is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristics
Why Join Us
Work on advanced injectable and drug delivery technologies
Hands-on involvement across development, manufacturing, and commercialization
Exposure to regulatory filings and FDA interactions
Collaborative environment with opportunities for growth and leadership
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.