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JOB-10034470
Anticipated Start Date
October 17, 2022

Location
Morristown, NJ

Type of Employment
Contract Hire – 1 Year

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
The Sr. Scientist Analytical Development performs extensive laboratory work to support pre-formulation development, formulation development, technology transfer activities, clinical trials, and evaluation of product performance and stability. The Sr. Scientist, with minimum supervision, manages projects to ensure all tests are completed in time, results are accurate, and all activities are documented. The Sr. Scientist effectively communicates to all stakeholders the analytical activities and findings.

Job Description
• Performs extensive laboratory work to support pre-formulation development, formulation development, technology transfer activities, clinical trials, and evaluation of product performance and stability.
• Conduct analytical method development, method validation and transfer
• Perform analytical laboratory work to support product development
• Accurately and timely document the experiments and results into the notebooks, ELN and LIMS (if required)
• With minimum supervision, manages projects to ensure all tests are completed in time, results are accurate, and all activities are documented.
• Effectively communicates to all stakeholders the analytical activities and findings.
• Follow SOPs/OIs and analytical laboratory practices to ensure the work quality and compliance
• Write the analytical methods, specifications, method validation reports, experimental reports, and SOPs/OIs
• Perform GMP comprehensive review of analytical activities such as but not limited to method development, method validations, method transfer, testing of analytical product development batches, process optimization batches, stability submission batches and Instrument technical records
• Interact with analyst on the data review to recommend appropriate corrections / modifications / improvements needed to build consistency with respect to documentation practice guideline
• Other related duties as assigned
• Perform other duties as assigned

Skills Required
• Must have QC or R&D experience in pharmaceutical industry
• Specific Hand-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 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.
• Go extra miles to get things done at a high quality
• Ownership of the work

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
• Worker Shift Start Time: AM - 08:00 AM
• IMPORTANT NOTE for POTENTIAL US CANDIDATES: Our client expects its colleagues to be fully vaccinated against COVID-19. Colleagues are also expected to disclose their vaccination status and if fully vaccinated, provide proof of vaccination status to Occupational Medicine. Our client defines fully vaccinated in alignment with CDC which is two weeks after completing the two-dose vaccine regimen or two weeks after completing the one-dose regimen. Additionally, colleagues are also required to comply with state, local and customer requirements.
• ONSITE POSITION

Pay Rate/Salary
• Up to $50.00 per hour depending on experience

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, age, citizenship, color, religion, sex, marital status, national origin, disability status, gender identity or expression, protected veteran status, or any other characteristic protected by law.


Reference : Expert Level Chemist jobs

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Published at 08-10-2022
Viewed: 114 times