Analytical Development Associate
- Job Title
- Analytical Development Associate
- Job ID
- 27767854
- Location
- Oklahoma City, OK, 73102
- Other Location
- Description
-
Job Description: Analytical Development Associate
Position Overview: Wheeler Bio is seeking a motivated analytical mind with a passion for problem solving and fast-paced environments to join the analytical team. The Analytical Development Associate will participate in the development of robust analytical techniques designed for seamless transition to a quality control environment in a manner to emphasize “right first time” and prolonged success. The position will require scientific knowledge of bioanalytical techniques that are used to assess and characterize proteins with a focus on monoclonal antibodies.
Key Responsibilities:
1. Analytical testing and data analysis:
· Possesses basic knowledge of protein biochemistry and analytical techniques.
· Understands and performs analytical testing according to pre-defined plans and protocols
· Participates in method development, transfer, and qualification with supervision.
· Applies complex instrumentation, computer systems and software for data acquisition and analysis.
· Ensures lab is maintained (organized, clean, properly supplied).
2. Communication:
· Accurately documents tasks and maintains a laboratory notebook according to company guidelines.
· Participates in writing analytical plans, protocols, SOPs, and reports.
· Able to logically assemble and present analytical results
· Collaborates with team members to troubleshoot and solve complex problems to meet project needs.
3. Continuous improvement:
· Integrates ongoing quality and operational improvement strategies into workflows.
· Actively expands technical expertise to encompass multiple analytical modalities.
4. Other duties as assigned.
Qualifications:
Preferred Master’s or Bachelors degree (in biochemistry, chemistry, microbiology, or other life-science discipline) with previous experience.
Preferred knowledge of and experience with various analytical techniques (e.g., HPLC, ELISA, enzyme activity, BLI/SPR, mass spectrometry, bioassays) demonstrated through industry or academic performance.
Preferred experience in assay development
Ability to work independently with supervision and professionally as part of a team.
Ability to generate technical reports and presentations to clearly communicate scientific information.
Ability to write and perform detailed analytical procedures.
Basic knowledge of FDA, ICH, EMA, JP, and other regulatory guidance on CGMP manufacturing.
Experience with statistical analysis techniques and specialty software.
