Quality Control Associate

100% onsite - Mon-Fri (normal business hours).

Required Skills:

• Knowledge of science generally attained through studies resulting in a BS in the physical or life sciences, a related discipline, or the equivalent in related experience, degree preferred.
• Knowledge of basic laboratory techniques such as pH, volumetric measurement, pipetting, analytical weighing, and basic laboratory safety practices preferred.
• Experience with cGLP or cGMP.
• Attention to detail and demonstrated organizational skills.
• Demonstrated manual dexterity.
• Knowledge of basic electronic systems (email, MS Office, etc.).
• Demonstrated ability to work independently as well as part of a team, to complete assignments within defined time constraints.
• Demonstrates problem solving skills.
• Overtime work may be required on weekdays, weekends, holidays, and during adverse weather conditions in support of manufacturing facility.
• Flexibility to work irregular hours and short notice overtime.

Project Description:

• Performs routine testing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment.
• Executes routine procedures based on methodologies/responsibilities of the specific QC sub-team.
• Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).
• Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within QC, in order to exchange information regarding testing completed, in process and planned.
• Daily contact with her/his supervisory staff for work assignments.
• Routine contact with supervisor for coaching and general performance management discussions.
• Occasional contact with other line management staff relating to specific project responsibilities may be expected.
• Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials.

This 12+ month position starts ASAP.

Please E-MAIL your resume (attachment to email) with rate and availability to Jennifer: jennifer@alphaconsulting.com

ALPHA'S REQUIREMENT #23-00496
MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE