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Job Runner

 
  • Category: Science
  • Employment Length: part-time
  • Pay / Salary: $15 Hourly
  • Source: Business
  • Ad #: 7281
 
Via: kellyjobsmnetwork Apply / More Info
 
Full Details

 

QA Validation Intern, Madison, WI

 

Kelly Services is currently seeking a QA Validation Intern to support Analytical Development for one of our top clients in Madison, WI.

 

Candidate should be a current 3rd or 4th year undergraduate student (i.e. you will graduate May 2018 or 2019 with a BACHELORS) in technical discipline (e.g. biology, biotechnology, engineering) or related life science program.

 

 

Projected Duration: 12/26/17 - 06/25/18

Type: Contract

Pay Rate: $15

Hours: Part Time, 16-24 hours a week, can work around school schedule.

 

Responsibilities:

  • Applies existing validation programs for the commissioning and qualification of new equipment, instruments, including major capital projects and computer systems.
  • Maintains validation programs for existing equipment, utility commissioning and qualification, and computer systems.
  • Drafts, reviews, and executes protocols and reports related to equipment, facility, and computer validation. This includes deviation reporting during execution.
  • Provides statistical support for Quality Systems monitoring and review.
  • Assists in customer/regulatory audits and responding to audit observations and corrective actions.
  • Collaborates significantly with cross functional groups, including Quality, Manufacturing, Process Development, Facilities, and Regulatory Affairs.
  • Files and maintains controlled documents.
  • Other duties as assigned.            

 

Minimum Qualifications: 

  • Current 3rd or 4th year undergraduate student (i.e. you will graduate May 2018 or 2019 with a BACHELORS) in technical discipline (e.g. biology, biotechnology, engineering) or related life science program.
  • Ability to understand and independently apply GMPs to everyday work with regard to documentation and review.
  • Ability to apply applicable regulatory authority and guidelines with training.
  • Demonstrates theoretical understanding of the work tasks assigned.
  • Ability to operate within a clean room environment as needed.
  • Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs. Ability to learn and use quality management software (e.g. TrackWise®, ComplianceWire®).
  • Ability to learn and retain technical information.
  • Executes routine procedures and process with high quality.
  • Ability to operate assigned office equipment.
  • Ability to complete investigation, deviation, and change control forms with initial consultation from supervisor as needed
  • Capable of learning of unfamiliar principles or techniques with training.
  • Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form.
  • Edits Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and reports independently and accurately

 

 

If you are interested in the position, please apply to this posting with an updated resume. Thank you for your time and I look forward to working with you.

 

Lauren Rogers, Kelly Services Scientific Recruiter

 

 

 

 
Map: Madison WI
 
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