What are the responsibilities and job description for the Analytical Research and Development Chemist position at Aequor?
Title: Analytical Chemist
Location: Somerset, NJ
Duration: 12 Months
Job Description:
The Analytical Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
Essential Duties And Responsibilities
This position may require lifting up to 10 pounds occasionally.
Generally work is performed in a laboratory environment with chemicals and solvents.
Generally work is performed in a laboratory environment.
Must Have
HPLC/GC
Wet chemistry
Method Development
Method Validation
Analytical research and Development chemist
Location: Somerset, NJ
Duration: 12 Months
Job Description:
The Analytical Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
Essential Duties And Responsibilities
- Perform Method Development/Method validation development, including report writing, for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids and Powder for oral suspensions with minimum supervision
- Support the Product Development team in developing new products
- Identification and characterization of the unknown impurities in the drug products and drug substances
- Support or independently perform Method Development/Method validation development for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids and Powder for oral suspensions
- Trouble shoot analytical issues to accomplish desired results
- Bachelor's Degree in Chemistry, Biology, or related field, Master's Degree a plus
- 3-10 years of experience working as an R&D Chemist for a pharmaceutical company
- Operational and technical expertise in developing testing such as HPLC, GC, Dissolution, etc.
- Experience in pharmaceutical Method Development and Method Validation
- Capable of writing reports suitable for regulatory submission with minimum supervision
This position may require lifting up to 10 pounds occasionally.
Generally work is performed in a laboratory environment with chemicals and solvents.
Generally work is performed in a laboratory environment.
Must Have
HPLC/GC
Wet chemistry
Method Development
Method Validation
Analytical research and Development chemist
