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Specialist Quality Control
Spectraforce
Matthews, North Carolina

an hour ago

Job Description

Job Title: Quality Control Specialist
Duration: 10+ months
Location: 27540, Holly Springs, NC
Possible Extension: Yes
 
Job Description
This role is 100% on-site at the Holly Springs, NC facility, working a standard weekday schedule (8am–5pm) with some flexibility (start between 7–9am).
 
Top 3 Must Have Skill Sets:
GMP; Deviation Investigation; Change Control Management
 
The ideal candidate will bring at least
  • 5 year of industry experience within a GMP-regulated biotech or pharmaceutical environment.
  • They must demonstrate strong knowledge of quality systems and QC laboratory operations with a proven ability to write, own, and drive closure of quality records, including deviations, CAPAs, and change controls.
  • This role requires excellent written communication, grammar, and investigative leadership skills. Candidates should be detail-oriented, proactive, and able to navigate shifting priorities in a fast-paced environment with minimal oversight.
  • They will collaborate with multiple cross-functional teams and should be confident leading meetings and pushing investigations independently through to completion.
  • Experience with Veeva Quality Systems is highly desirable.
 
This position will be part of the Quality Control Deviation and Change Control team for start up.
  • Working collaboratively with Quality Control and Quality Assurance teams to author and own change control records and deviations in the DQMS Veeva System.
  • Individual will lead investigation teams and help to collect and report metrics for the systems team.
  • Individual may assist with review of validation documents to support equipment and computerized system onboarding.
  • Individual may author, revise and review documents and reports including but not limited to SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, technical reports.
  • Individual will mentor new deviation owners as required.
  • Support the startup of a GMP QC laboratory.
  • Support routine activities over the weekends and public holidays as required.
 
Basic Qualifications:
Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience
 
Day to Day Responsibilities:
Own deviation records and manage change control tasks and deliverables
 
Red Flags:
no lab experience 
Applicant Notices & Disclaimers
  • For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 42.00/hr.

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