183202 - Scientist
Industry
ENG
Region
CA-S.Cali-Los Angeles/Orange Counties
City
West Hills
State
CA
Rate
Up to $25.00 DOE
Duration
3 Months
Description
Chipton-Ross is seeking a Scientist for an opening in West Hills, CA.

RESPONSIBILITIES:
The Scientist I, Manufacturing Sciences is responsible to manage and prioritize assigned projects related to development and improvement of DNA-based diagnostic reagents with supervision.
Simultaneously manage and prioritize multiple projects and products across multiple functional groups while meeting target due dates with guidance of supervisor/lead.

Design, create experimental task, run tests and be able to look at data and complete analysis using Fusion, Orchid, or equivalent software. Can provide experimental task(s) to designated Scientist with Supervisor approval.

Be able to identify improvements, initiate and implement the solutions with the guidance of the supervisor.

Adapt, implement and train current and new Scientist I lab functions/procedure to other Scientists and provide guidance and support throughout projects and product builds (SAP, Operate UV spectrophotometer, and thermal cycler, agarose gel electrophoresis, UV image analyzer, Luminex 200, FlexMAP3D, high speed centrifuge and other hardware. Reconstitution, quantification, QC test, organization and maintenance of all raw materials such as oligonucleotides, ancillary reagents, and genomic DNAs, etc.).

Coordinate, plan and manage the day-to-day tasks to maintain the project(s)/product(s) workflow with guidance from Scientist II/III/Supervisor.

Manage, plan, and design experimental methods under supervision as needed to achieve technical objectives as well as identify and solve problems with minimum complexity.

Prepare accurate and timely reports to Scientist II-III/Management.

Conduct maintenance and organization of reagents and equipment.

Maintain and perform all aspects of receiving and quality control testing of raw materials.

Update and maintain raw material and semi inventories. Be able to do Cycle count.

Prepare and QC buffer solutions.

Maintain and update all required SOP’s and quality records of equipment maintenance, tests, analyses and other relevant data with the guidance of Scientist II/III/Supervisor.

Implement and execute Practical knowledge of PPI Business System/LEAN concepts including continuous improvement with supervision

Be able to identify goals, review and update Supervisor throughout the year and complete the PMD

REQUIRED EXPERIENCE:
Knows basic principles, methods and practices of HLA and scientific/technical field or software, typically via formal study and/or work in the field
General knowledge of procedures and activities within own work area
Understands industry practices and standards and is able to relate day-to-day work to business problems
Recognizes and understands the technologies within organization and understands the value to the organization
Knowledge and hands-on experience of molecular biology and recombinant DNA techniques
Able to complete assigned tasks in a timely manner
Strong organizational and time management skills, as well as ability to work in a detail-oriented manner
Ability to exercise decision making with the guidance of Management/Scientist II-III
Collects and organizes data in an appropriate manner, including documenting all experiments in a laboratory notebook or appropriate documentation
Ability to use PCs for data input and/or analysis
Excellent computer MSOffice skills
Plan and organize oneself in a consistent manner and maintain work schedules. Be a self-starter with the ability to positively motivate others in a cooperative fashion
Follow oral and written directions
Read, understand and implement written laboratory procedures
Communicate clearly and concisely, orally and in writing
Builds productive cross-functional relationships with colleagues in other functions, including but not limited to the following: Marketing, Sales, R&D, Operations, Regulatory/Quality, Supply Chain, and Product Management
Ability to collaborate effectively with all functions of the business
Encourages/challenges others and self for continuous improvement
During situations that have high impact to the business, quickly escalate them by bringing solutions and consulting with Supervisor
Be able to efficiently handle multiple tasks and projects simultaneously
Develop skills to perform other duties as assigned
All laboratory personnel are expected to notify their immediate supervisor of any unsafe conditions and/or practices and to take appropriate corrective action. This position will have daily contact with other laboratory personnel
Maintain confidentiality of sensitive laboratory and business data
Ensure that safe laboratory procedures and protocols are followed at all times, especially in the application of universal precautions in handling of all blood and blood products
Ensure all processes and teams are in adherence of cGMP and GDP
Ensure compliance with corporate, site, and regulatory policies, practices, and guidelines
Communicate effectively with members of the group as well as those in other departments
Work as a cooperative member of a Production team

Working Conditions/Physical Requirements:
Frequently work at lab bench, low temperature freezers and PC workstations
Handle blood samples and blood byproducts occasionally
Some lifting of objects including laboratory instrumentation of 35 pounds
Work in office/computer/analysis

EDUCATION:
Accredited Bachelor’s degree in Biological Sciences, Chemistry, Molecular Biology or related field

WORK HOURS:
1st Shift
Full-Time


Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.

Contact
Tyler Harrell
tharrell@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293

Phone: (310) 414-7800 x307 or (800) 927-9318 x307

Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.

Employment will be contingent on candidate clearing pre-employment drug screen and background check.

Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.