Mindlace
This range is provided by Mindlace. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $28.00/hr - $32.00/hr
Direct message the job poster from Mindlace
Job Title Quality Control Technician II
Location Worcester, MA
Duration 6+ months with possible extension
Shift Monday to Friday Second shift 12-8:30PM
Sunday to Thursday morning shift 9-5:30PM
Responsibilities
Perform micro test methods as written to support product/material release. Effectively perform a multitude of laboratory techniques with minimal error for which they will be trained on.
Understand, implement, and maintain GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements.
Accept responsibility to complete assigned tasks as committed.
Support investigation writers and approvers to gather data.
Write or revise procedures with guidance.
Work under the guidance of a supervisor but manage own time to ensure timely completion of assigned duties.
Trend data to support trend reports.
Willing to work on weekends and holidays.
Top Skills
QC Micro experience – hands‑on experience with lab testing and/or EM.
Hands‑on working experience in Biosafety hoods preferable.
Attention to detail while running assays/tasks in the lab and while performing EM is required.
Good organizational skills, ability to prioritize workload, and extremely thorough with excellent attention to detail.
Will perform tasks with supervision guidance, taking responsibility for complying with GMP requirements.
Must be flexible working weekends and holidays.
Strong interpersonal / communication skills. Maintaining good working relationships within and outside the department.
Adjusting quickly to new situations. Reprioritizing to meet schedule demands in continually changing work environment.
Knowledge with the LIMS system, specifically entering results is preferred.
Nice to have
Knowledge of applicable regulations and standards affecting Pharmaceutical Products (e.g. USP, EP, JP pharmacopoeias, ICH guidelines, cGMP).
GMP and/or Clean‑Room experience.
Clean‑Room Gowning.
Required Experience and Education Experience Level: 3-5 Years
BS in Biology or other life science required.
Experience with cGMP documentation and record maintenance is required.
Must be comfortable standing for most of their shift. Shuttling between AbbVie buildings is required. Also, must be flexible to work some weekends and holidays (pre‑scheduled).
Seniority level Associate
Employment type Contract
Job function Research and Manufacturing
Industries Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
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Base pay range $28.00/hr - $32.00/hr
Direct message the job poster from Mindlace
Job Title Quality Control Technician II
Location Worcester, MA
Duration 6+ months with possible extension
Shift Monday to Friday Second shift 12-8:30PM
Sunday to Thursday morning shift 9-5:30PM
Responsibilities
Perform micro test methods as written to support product/material release. Effectively perform a multitude of laboratory techniques with minimal error for which they will be trained on.
Understand, implement, and maintain GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements.
Accept responsibility to complete assigned tasks as committed.
Support investigation writers and approvers to gather data.
Write or revise procedures with guidance.
Work under the guidance of a supervisor but manage own time to ensure timely completion of assigned duties.
Trend data to support trend reports.
Willing to work on weekends and holidays.
Top Skills
QC Micro experience – hands‑on experience with lab testing and/or EM.
Hands‑on working experience in Biosafety hoods preferable.
Attention to detail while running assays/tasks in the lab and while performing EM is required.
Good organizational skills, ability to prioritize workload, and extremely thorough with excellent attention to detail.
Will perform tasks with supervision guidance, taking responsibility for complying with GMP requirements.
Must be flexible working weekends and holidays.
Strong interpersonal / communication skills. Maintaining good working relationships within and outside the department.
Adjusting quickly to new situations. Reprioritizing to meet schedule demands in continually changing work environment.
Knowledge with the LIMS system, specifically entering results is preferred.
Nice to have
Knowledge of applicable regulations and standards affecting Pharmaceutical Products (e.g. USP, EP, JP pharmacopoeias, ICH guidelines, cGMP).
GMP and/or Clean‑Room experience.
Clean‑Room Gowning.
Required Experience and Education Experience Level: 3-5 Years
BS in Biology or other life science required.
Experience with cGMP documentation and record maintenance is required.
Must be comfortable standing for most of their shift. Shuttling between AbbVie buildings is required. Also, must be flexible to work some weekends and holidays (pre‑scheduled).
Seniority level Associate
Employment type Contract
Job function Research and Manufacturing
Industries Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
#J-18808-Ljbffr