Location
Edge, TX | United States
Job description
Expert Level Scientist
JOB-10040691
Anticipated Start Date
03/18/2024
Location
Morristown, NJ
Type of Employment
Contract
Employer Info
As a global leader in agriculture enterprise, our client is recognized for their multiple brands and renowned reputation. Their research and development teams combine knowledge and ingenuity to create the most innovative ideas. With their cutting-edge products, they have a common goal: improved quality of life for all.
Job Summary
If you're interested in an Expert Level Scientist job, then this is the best role for you. This role performs extensive laboratory work to support pre-formulation, formulation development, technology transfer activities, clinical trials, and evaluation of product performance and stability.
Job Description
- Performs extensive laboratory work to support pre-formulation, formulation development, technology transfer activities, clinical trials, and evaluation of product performance and stability.
- Conducts analytical method development, method validation and transfer.
- Performs analytical laboratory work to support product development.
- Accurately and timely documents the experiments and results into the notebooks, ELN and LIMS (if required).
- With minimum supervision, manages projects to ensure all tests are completed on time, results are accurate, and all activities are documented.
- Effectively communicates to all stakeholders the analytical activities and findings.
- Follows SOPs/OIs and analytical laboratory practices to ensure the work quality and compliance
- Writes the analytical methods, specifications, method validation reports, experimental reports, and SOPs/OIs
- Performs GMP comprehensive review of analytical activities such as but not limited to method development, method validation, method transfer, testing of analytical product development batches, process optimization batches, stability submission batches and instrument technical records.
- Interacts with analysts on the data review to recommend appropriate corrections, modifications and/or improvements needed to build consistency with respect to documentation practice guideline.
- Perform other duties as assigned.
Skills Required
- Must have QC or R&D experience in pharmaceutical industry.
- Specific Hands-on experience with Waters & Agilent HPLC / UPLC and dissolution apparatus (USP Type 1 and 2).
- Understands fundamental analytical chemistry and chromatography.
- Able to troubleshoot testing and/or analytical method related issues.
- Understands and follows GMP / SOP requirements.
- Familiar with analytical laboratory documentation practices.
- Expertise in Waters Empower3 CDS.
- Expertise in MS Office, such as Word, Excel, and PowerPoint.
- Good communication and interpersonal skills
- This individual must be highly motivated, have a positive “can-do” attitude and the ability to work in a fast-paced environment as a collaborative team player.
- Practical knowledge and experience with application of analytical method development and method validation activities.
Education/Training/Certifications
- A bachelor’s degree in science, or international equivalent, with a 7+ years of proven Pharmaceutical Analytical Laboratory experience.
- A master’s degree or higher in science, or international equivalent, with a 5+ years of proven Pharmaceutical Analytical Laboratory experience.
Additional Requirements
- Must be able to pass drug screen & criminal background check.
- Shift: AM - 08:00 AM
Pay Rate/Salary
- Estimated Salary: $42.00 to $50.00 per hour based on qualifications.
"We are an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state, or local laws."
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