Associate Scientist

ALLTECH CONSULTING SVC INC; Kansas City (MO); On-site; USD 65,000 - 80,000; Full time

Job summary

A leading consulting service in Kansas City is seeking an Associate Scientist II for testing samples and drafting methods under cGMP regulations for Large Molecules and Biologics product development. The ideal candidate holds a Bachelor’s Degree in Life Sciences or Physical Science. Responsibilities include executing laboratory testing using various techniques and maintaining compliance with documentation. Strong communication skills and attention to detail are crucial for success in this entry-level role.

Qualifications

• Bachelor’s Degree in Life Sciences or Physical Science required, no prior work experience needed.
• Basic knowledge of biology, chemistry, or biochemistry principles.
• Excellent written and verbal communication skills.
• Ability to work effectively under pressure to meet deadlines.
• Attention to detail and exhibit critical thinking.

Responsibilities

• Testing samples and drafting methods under cGMP regulations.
• Executing laboratory testing using various techniques.
• Following Standard Operating procedures with attention to detail.
• Maintaining compliance with cGMP documentation requirements.
• Adheres to policies for operating laboratory equipment safely and compliantly.
• Understands the Company’s culture, programs, and communication processes regarding quality, safety, and ethical practices.
• All other duties as assigned.

Skills

Biology

Chemistry

Biochemistry

Excellent communication skills

Multitasking

Attention to detail

Critical thinking

Attention to detail

Good written/verbal communication

Multitasking

Education

Bachelor’s Degree in Life Sciences or Physical Science

Job description

Position Overview

Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.

Laboratory Testing Techniques

In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required:

• Mammalian cell culture
• Sterile technique
• In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.)
• ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD)
• Molecular biology (e.g., qPCR, PCR, etc.)
• Kinetic binding assessment (e.g., BLI or SPR)
• Flow cytometry
• Other technologies/methodologies as required by management

Essential Functions

• Reads and follows Standard Operating procedures with attention to details
• Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required
• Applies basic scientific and laboratory concepts and theories related to specific testing in the group
• Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports.
• Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner
• Understands the Company’s culture, programs, and communication processes regarding quality, safety, and ethical practices
• All other duties as assigned

Position Requirements

Education and Experience

• Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required

Knowledge/Skills Requirements

• Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry).
• Excellent written and verbal communications skills with internal customers, colleagues, and supervisor
• Well organized with ability to multitask and be flexible with daily work schedule
• Ability to work effectively under pressure to meet deadlines
• Ability to pay attention to detail and exhibit critical thinking