Analytical Scientist II

Aveva Drug Delivery Systems Inc; Florida; On-site; USD 65,000 - 90,000; Full time

Job summary

A laboratory position at Aveva Drug Delivery Systems Inc supports development and validation of analytical methods for pharmaceutical components and drug products. You will perform HPLC/GC/UV-VIS tests, dissolution studies, and stabilitywork in a cGMP environment under supervision.

The role requires strong data interpretation, method transfer, and documentation; collaboration with project teams, and adherence to SOPs, STPs, and safety regulations.

Qualifications

• Bachelor’s degree in chemistry or related field; MS preferred.
• 2–5 years of pharmaceutical lab experience for BS holders; MS candidates may have 0–3 years.
• Knowledge of analytical methods, validation, and cGMP requirements.
• Ability to write and review SOPs, STPs, and reports.

Responsibilities

• Develop and validate analytical methods for drug products and components.
• Perform HPLC, GC, UV-VIS, dissolution, pH, and titration testing.
• Conduct stability testing and method transfer under supervision.
• Document experiments and communicate results to supervisors.

Skills

Statistics

Analytical chemistry

HPLC

Data analysis

GMP

Education

Bachelor's degree in Chemistry

Master's degree

Tools

HPLC

GC

UV-Vis

Dissolution Instruments

Job description

Job Summary:Laboratory position which involves development and validation of analytical methodology in support of the research projects involving testing of pharmaceutical components and/or drug products. Under general supervision, the position may require proficiency in support formulation, development method improvement and validation, testing per compendial pharmacopeia, etc.Job ResponsibilitiesProficiency in multiple instrumentation techniques such as HPLC, GC, UV-VIS, dissolution equipment, pH measurement, titration, etc.General knowledge of cGMP and FDA requirements.Perform stability testing for GMP and R&D finished productsConduct analytical testing of API, excipients and components following compedial and validated methodsPerform analytical method validation and method transfer with a minimum supervision.Follow company’s SOPs, STPS and comply with safety regulations.Maintain detailed record of experiments in the laboratory notebook.Timely communicate to supervisor(s) the obtained data and any issues aroused during testingAbility to analyze and interpret the analytical data under minimum supervision.Interpret specifications, standard operating procedures, and standard testing procedures.Writes/reviews protocols, reports, SOPs and STPs applicable to analytical laboratory under the supervision.Works as a member of a team to achieve all outcomesOperates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements.Performs all work in support of our Values: Collaboration, Courage, Perseverance, and PassionAll other relevant duties as assignedJob RequirementsEducationBachelor’s degree (B.S.) in chemistry or related fieldMaster’s degree (M.S.)Knowledge, Skills and AbilitiesGeneral statistical applications such as normal ant T-test distribution, regression analysis, determination of test reliability and validity, analysis of variance, correlation techniquesAnalytical chemistry and common instrumentationGeneral understanding of HPLC, GC, Drug Release, UV, IR, Titration.Using common computer software and analytical applications programs.Writing and interaction in EnglishExperienceAt least two (2) to five (5) years experience in pharmaceutical laboratory (B.S)At least zero (0) to three (3) years experience (M.S.)