Job description

must-have,QSR,staff’sthemanager’sthehe,problem-solvingday-to-dayguidesandonadvancedacolleaguesa,must-haveThree must-have skill sets (all not one or two out of three) are lateral flow, immune assay, and product development (verification, validation, tech transfer, etc). Please verify that any submitted candidates for review have these 3 skillsets.

Able to go a little over pay rate but not much too many low-end candidates PhD. in Chemistry or Chemistry Background no masters candidates Temp to permanent after contract length Open to relocation candidates if stellar Lateral Flow Assays Typical Sandwich 5 plus years experience or Competitive Format preferred They will be working with products to detect drug screen results for Fentinol, PCP, THC, and so on

RESPONSIBILITIES: · Executes and conducts research; may develop or recommend new procedures related to R&D processes. · Uses advanced professional concepts to contribute to the development of company concepts and principles and to achieve objectives in creative and effective ways. · Investigates, and may create and develop new methods and technologies for project advancement with guidance from more experienced colleagues. · Possesses and applies knowledge of principles, practices, and procedures of a particular field of specialization to the completion of moderately complex assignments. · Works on problems of moderate and diverse scope in which analysis of data requires evaluation of identifiable factors. Proposes potential solutions to more advanced problems. · Conducts experiments on more complex projects, and seeks advice when needed from more experienced colleagues for more complicated technical and design challenges. able to handle multiple projects independently. · Determine methods and procedures on new assignments and guides junior personnel. · May direct less experienced RAs in their day-to-day work and assist in problem-solving. · Provides sound and original suggestions for new problems. · Perform analytical test methods on the finished products based on CLSI and other FDA guidelines · Participate as an integral member of the scientific staff in research strategy and methodology to resolve issues · Provide recommendations and observations to scientific staff and management on results of projects/tasks. Play a key role in the research strategies and tactics for new or existing R&D projects. · May Conduct interviewing, training employees, planning, assigning, directing work, and resolving technical problems. · Maintain records of laboratory activities and notebooks in a professional, accurate manner. May provide support to regulatory and intellectual property activities. · Transfer developed processes to the Manufacturing Team. Write and revise process document reports and transfer protocols. · Ability to create, review, and work with SOPs, MPs, and Batch Records · Operate complex laboratory equipment and perform routine maintenance and repair. Interface with contracted repair technicians as required. Understand the theoretical basis for analytical instrumentation. · Functionally direct junior research staff, as required. · Initiate literature review and searches to support ongoing research activities. Summarize findings in final form to management and recommend follow-up actions. · Generate oral and written reports and summarize laboratory activities and projects per the R&D manager’s request. Initiate communication with the R&D manager and functions as necessary to coordinate other staff’s activities effectively. · Monitor and maintain necessary laboratory supplies, with approval by senior department staff or R&D manager · Write verification and validation protocols and reports with minimal guidance. order materials needed to complete procedures. · Work involving urine, blood, or other potentially infectious materials may be required · Knowledgeable of federal and other regulations, e.g. QSR, ISO, ISO 13485, CMDR · Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification, and validation, manufacturing and testing activities. · Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships · Carries out duties in compliance with established business policies · Other duties as assigned, according to the changing needs of the business

Job Type: Full-time

Pay: $40.00 per hour

Benefits:

• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 5x8
• 8 hour shift
• Day shift
• Monday to Friday

Ability to commute/relocate:

• San Diego, CA: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Doctorate (Required)

Experience:

• Molecular biology: 1 year (Preferred)

Work Location: One location

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