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US-MA-Andover
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Role: Sr Scientist

Location: 200 Bulfinch Drive Suite 100 Andover MA 01810

Duration: 12 months on W2

JOB DESCRIPTION:

As a member of the Pharmaceutical Technology team, the employee will support the development of new products for the Diabetes Care business by focusing on driving drug-device compatibility.

This includes contributing to material selection and drug-device compatibility using applicable techniques, at device subsystem and system levels.

The scientist will develop new test methods, plan studies, execute testing, analyze data and report findings to the extended team, including contextualized summaries and recommendations for next steps.

Perform assigned product development activities.

Set priorities for self and contribute to team planning. Develop an assessment of competitive products, processes, or new trends. Develop an overview of relevant technologies and products.

Ensure compliance with embecta quality policies, procedures, and practices; through appropriate communication, training and education of sound quality assurance principles.

RESPONSIBILITIES:

Support design and development activities for products within the current portfolio offerings as well as new product development. These activities include, test method & measurement system development and validation, fixture design, testing optimization, and testing in support of design verification and design validation.

Develop novel test methods and/or adapt, when available, test methods from standards, compendia and literature using best practices for physical and chemical characterization of materials and drugs

Document test methods, protocols and reports, including qualification and validation activities as needed in collaboration with quality assurance

Design and execute testing, analyze samples and data and, reports findings to the extended team

Troubleshoot technical issues of moderate complexity and contribute to failure analysis efforts

Propose and implement improvements to methodologies, processes, products, and systems related to the project as needed

Experience Requires-

Developing technical, interpersonal, and influencing skills. Sound technical judgment and good communication skills. Developing skills in project planning and leadership. regulatory and quality requirements. Strong motivational fit. Strong fit with embecta values.

Works independently with general guidance

Knowledge of analytical chemistry techniques, including HPLC/UPLC and Micro Flow Imaging (MFI) technology

Ability to work in a cross-functional team

Knowledge of chemistry principles

Knowledge of plate based technology, UV-Vis spectroscopy, and/or viscometry is a plus

Knowledge of DFSS and statistical analysis tools is a plus and optional training in these areas can be provided

Collaborate with other team members to distribute responsibilities and resources effectively to meet project milestones.

Design and execute studies with scientists and engineers from other embecta sites, external consulting groups, and contract research laboratories

Education:

B.S., M.S., or Ph.D. in Pharmacy, Biochemistry, Pharmaceutical Sciences or other similar field with a Ph.D. (Title and Compensation dependent on experience.) Medical Industry experience required - please indicate which employer is specific to that industry in your recruiter notes when submitting candidates.

Thanks & Regards,

Kalyan K | Technical Recruiter

Email: Kalyan@intellectt.com

Direct: +1 (732) 769-3893

Desk Number: 732-412-6999 Ext: 274

(link removed)

517 Route 1 South, Suite 1115 Iselin, NJ 08830

Intellectt INC

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