Quality Assurance

Integrated Resources INC

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Andover, MA, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

· The scope of work for this role is to provide QA Validation support to validation activities associated with Quality Control (QC) Laboratory instruments. The main responsibility is review and approval of validation documentation including specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the site’s data integrity initiative

· Successful candidate requires a strong working knowledge of global GMPs with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures.

· Candidate requires strong interpersonal, oral and written communication skills as there is a high degree of collaboration required between members of QA Validation, Instrument Validation and QC personnel.

· Candidate must be detail oriented as the main job responsibility is review and approval of validation documentation.

· Candidate must have at a minimum a BS in biology, engineering or related sciences with at least 3 years of pharmaceutical or biopharmaceutical experience in a quality assurance and/or validation role.

· Past experience working with QC instrumentation, Labware, Trackwise, and/or Documentum in the pharma/biopharmaceutical field is preferred but not required.

· Minimum BS in biology, engineering or related sciences with at least 3 years of pharma/biopharma experience in a QA or validation role

· Strong working knowledge of global GMPs with emphasis on validation, including computer validation

· Strong interpersonal, oral and written skills

We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

Thanks & Regards,

Jasmine Jogewar

Sr. Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

(Direct) 732-844-8720| (F) 732-549-5549

www.irionline.com , www.linkedin.com/in/Jasmine-Jogewar

Gold Seal JCAHO Certified ™ for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

About this role

Summary

Provide QA validation support for pharmaceutical validation activities and documentation review.

Job title

Quality Assurance

Experience level

3+ years

Industry

healthcare

Location requirements

Onsite in Andover, MA, no remote work allowed.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

GMPvalidationcomputer validationdocumentation reviewpharmaceutical

Preferred skills

QC instrumentationLabwareTrackwiseDocumentum

Specializations

validationGMPcomputer system validation21 CFR Parts 210 and 211Part 11
Locations

Structured locations inferred from the posting.

Andover, MA, USA

On-site City
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