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Quality Control Associate

Devens, MA

Posted: 03/07/2023 Job Number: 23290383

Job Description

QUALITY CONTROL ASSOCIATE
DEVENS, MA
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

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Jennifer Hernandez

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