QA Specialist III

Integrated Resources INC

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Foster City, CA, 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 led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

• Lead/participate in project team to streamline Clinical QA processes and SOPs by reviewing existing workflows and identifying areas for improvement.

• Perform SOPs periodic review, write/revise SOPs and design process flowcharts

• Responsible for ensuring CAPA/ audit observations responses are appropriately implemented and closed in a timely manner

• Coordinate inspection and audit support for Clinical QA during internal / regulatory inspections and audits

• Manage Clinical QA training requirements and curricula, OJT qualification programs, and New Employee Onboarding programs to drive improved employee qualification and training compliance

• Maintain systems for organizing, tracking, trending and reporting Deviation, CAPA, batch disposition and review metrics

• Review existing quality workflows and assist in identifying areas for improvement. Write, revise and may review standard operating procedures.

• Other responsibilities as assigned

• In depth knowledge of Quality Systems and international cGMP standards

• In depth knowledge and experience with Operational Excellence Principles

• An accountable team player who is detail and quality oriented with an in-depth understanding of quality assurance principles, systems and procedures

• Excellent attitude with good verbal and interpersonal communication skills, excellent judgment, and multitasking skills who can work well in a dynamic environment

• Strong leadership and negotiation skills

• An accountable leader who is detail and quality oriented with a solid understanding of quality principles, methods, and procedures

• Critical and strategic thinking skills

• Working knowledge of GMPs and regulatory requirements (US, Canada, and EU)

• Experience generating key metrics

• Technical writing skills

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.


Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (732)-844-8715

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

Lead clinical QA processes, review SOPs, support audits, and ensure compliance with cGMP standards

Job title

QA Specialist III

Experience level

not specified

Industry

healthcare

Location requirements

Foster City, CA, US; remote work not specified

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

quality assurancecGMPSOP writingregulatory complianceaudit support

Preferred skills

operational excellencetechnical writingleadershipnegotiationmetrics generation

Specializations

clinical QASOPsCAPAregulatory inspectionsquality systems
Locations

Structured locations inferred from the posting.

Foster City, CA, USA

On-site City
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