associate scientist.

• morristown , new jersey

• posted 7 days ago

job details

summary

• $21.88 - $25.74 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference49442

job details

job summary:

As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: Morristown, New Jersey

job type: Contract

salary: $21.88 - 25.74 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

Job Summary

The Associate Scientist Analytical Development performs extensive laboratory work to support specialized software-based stability studies. The Associate Scientist, with minimum supervision, ensures all tests are completed on time, results are accurate, and all activities are documented. The Associate Scientist effectively presents the results in the AD meetings.

Job Responsibilities

• Performs extensive laboratory work to support the specialized software-based stability studies for the determination of shelf-life of the drug product

• Write SOPs/guidelines/OI/reports related to the stability studies, specialized stability software and any other as needed.

• Must be able to perform the Assay method, Impurities method and dissolution method for the drug products

• 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.

• Interacts with analysts on the data review to recommend appropriate corrections / modifications / improvements needed to build consistency with respect to documentation practice guideline.

• Perform other duties as assigned.

qualifications:

Education & Qualifications

• Bachelor's degree in science with 2+ years of proven Pharmaceutical Analytical Laboratory experience.

• A Master's degree or higher in Science, with 1+ years of proven Pharmaceutical Analytical Laboratory experience.

• Must have a minimum of 1 year experience in the QC or R&D in pharmaceutical industry

• Must have Hands-on experience with Waters & Agilent HPLC / UPLC and dissolution apparatus (USP Type 1 and 2)

• Hands-on experience in using Waters Empower3 software. Understands fundamental analytical chemistry and chromatography.

• Able to quickly learn specialized-stability studies software.

• Able to troubleshoot testing and/or analytical method related issues.

• Understands and follows GMP / SOP requirements - Familiar with analytical laboratory documentation practices

• 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.

Preferences

• Goes the extra mile to get things done at high quality

• Ownership of the work

skills: HPLC, Chemistry, Chromatography, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.