Associate Scientist I

Sakura Finetek USA, Inc.•Torrance, CA

1d•Onsite

About The Position

As a member of the product development team, among the Associate Scientist I’s main responsibilities are the execution of experimental protocols and collection of data. The Associate Scientist I is expected to actively participate in protocol development and design, as well as data interpretation. Areas of research and development may include any of Sakura’s anatomic pathology product lines. As such, the successful candidate is expected to learn the function and operation of all Sakura instrument systems, tissue fixation, processing, embedding, sectioning and staining. The candidate must be able to collate data and write up results in a clear and concise manner. The technical experience required for this position includes some of the following areas: microtomy, immunohistochemistry, immunofluorescence, in situ hybridization, immunoassays, formulation of reagents, spectrophotometric analysis, experimental design with proper selection and implementation of controls, replicates, and acceptance criteria, and general laboratory testing or quality evaluation activities.

Requirements

BS.degree in cell biology, immunology, biochemistry, or other relevant scientific/engineering discipline, or equivalent combination of education and experience.
1-2 years of experience in research, product development or manufacturing setting.
Requires clear and concise verbal and written communication skills; good technical writing skills; good computer skills (Microsoft Word, Excel, etc.).
Excellent analytical, organizational, and problem-solving skills.
This position requires the employee to work in a laboratory environment.
It involves frequent walking, standing, and sitting.
In addition, the employee is required to use hands and fingers and reach with hands and arms.
Must be able to occasionally lift and/or move up to 50 pounds.
Ability to successfully respond to multiple work pressures.
Requires reading, math, analyzing and drawing conclusions from data; developing and implementing methodologies/plans/processes for accomplishing a goal.

Nice To Haves

Experience in the medical device, pharmaceutical, or FDA regulated laboratory environment.
Experience in pathology, immunohistochemistry/immunofluorescence, histology, biotechnology, reagent optimization, or reagent packaging is a plus.
Preference given to candidates with product development/design control/IVD experience.

Responsibilities

Executes experimental protocols.
Collects and collates data.
Provides clearly written documentation of experimental results.
Prepares reagents and tissues.
Operates and maintains laboratory equipment.
Facilitates technology development processes.
Works in a multi-disciplined scientific environment.
Engages in design, testing and troubleshooting software, consumables, reagents and instrumentation.
Is in compliance with all applicable environmental, health, and safety regulations.
Contributes to company’s patent applications or development of proprietary technology.
Works with all functions within the Sakura group to launch new products.
Participates on product development teams, task forces, audits, and business or technical meetings.
Maintain laboratory organization and cleanliness.
Assist with chemical inventory management and consumable tracking.
Assist with waste removal and laboratory maintenance activities.
Performs other duties and projects assigned.
Adheres to GxP requirements, including Good Laboratory Practice (GLP), Good Documentation Practices (GDP), and Good Manufacturing Practices (GMP).
Ensures compliance with all applicable environmental, health, and safety regulations.
Provides clear and concise technical information in experimental notebooks.
Keeps management informed by creating meaningful summaries of developmental results.
Interacts with managers and team members in a professional and proactive manner.