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Associate Asq Cqa Jobs (NOW HIRING)

Astrix Inc

Document Control Specialist II

Vista, CA · On-site

$39 - $52/hr

Associate's degree in a science or related field with a minimum of 5 years in a GMP/manufacturing ... ASQ Certified Quality Process Analyst, or * Certified Quality Auditor (CQA), or * Certified Quality ...

Sub-Zero & Wolf Appliance

Senior Quality Engineer

Madison, WI · On-site

$89K - $120K/yr

Bachelor's degree in a STEM field, or a bachelor's or associate degree with equivalent quality ... ASQ certification such as Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or a ...

RED CAT HOLDINGS

Quality Specialist

Salt Lake City, UT · On-site

ASQ certifications such as Certified Quality Auditor (CQA), Certified Quality Technician (CQT), or Certified Quality Improvement Associate (CQIA). * Experience supporting customer, regulatory, and ...

Advanced Energy

Sr Quality Technician

Vancouver, WA · On-site

Associate degree (AAS) in a technical field or equivalent experience * ASQ certification (CQT, CQI, CQIA, CQA, CCT) or equivalent experience COMPENSATION: As required by multiple state pay ...

Bachem AG

Quality Assurance Specialist II

Vista, CA

$77K - $96K/yr

Associate's Degree in Science or related field and a minimum of 5 years' experience in the GMP ... Certified Quality Process Analyst - ASQ Preferred or * CQA Preferred or * CQE certification desired ...

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As of Jul 13, 2026, the average hourly pay for associate asq cqa in the United States is $29.47, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $35.58 per hour, depending on experience, location, and employer.
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Document Control Specialist II

Document Control Specialist II

Astrix Inc

Vista, CA • On-site

$39 - $52/hr

Full-time

Re-posted 9 days ago

Job description

Pay Rate Low: 39 | Pay Rate High: 52
Document Control Specialist II
Position Summary
A growing manufacturer of drug substances is seeking a Document Control Specialist II to join its QA team.
In this role you will help ensure that drug substances are produced in compliance with FDA and international regulatory requirements across research, pre-clinical, clinical, and commercial stages. The position centers on the review and processing of GMP documentation, day-to-day quality oversight, guidance to other functions on cGMP matters, and support for customer and regulatory audits. You will also help maintain GMP records and the supporting electronic quality systems.
Location: Onsite in Vista, CA | Hours: M-F 8-5 | Type: 1-year contract | Compensation: $39-$52/hour
What You Will Do
Core Responsibilities
  • Carry out clearance verifications for production rooms, the dispensary, and shipments as needed
  • Revise standard operating procedures (SOPs) and other GMP documents such as stability protocols, raw material specifications, and environmental monitoring trend reports
  • Administer GMP documentation and the associated workflows for the department
  • Review and verify QC data output from chromatographic systems (HPLC, UPLC, or GC), confirming the accuracy of scanned batch records, chromatograms, and associated analytical records, and ensuring documents are correctly labeled and packaged for archival
  • Provide support during regulatory, customer, and internal audits
  • Help implement and maintain the Quality Management System
  • Scan, verify, and archive internal and external GMP records
  • Represent QA on cross-functional and cross-site projects, including system and process harmonization and the rollout of new systems

Qualifications
Education & Experience
  • Bachelor's degree in organic chemistry or a related field required; master's degree in organic chemistry or a related field preferred, or
  • Bachelor's degree in a science or related field with a minimum of 3 years in a GMP/manufacturing setting, or
  • Associate's degree in a science or related field with a minimum of 5 years in a GMP/manufacturing setting
  • 3-5 years in Quality Assurance and/or Quality Control
  • 3-5 years in internal auditing and in working with regulatory agencies
  • 3-5 years in an ISO 7 and ISO 8 controlled environment, with experience supporting real-time batch record review
  • Demonstrated experience reviewing QC chromatographic data output from HPLC, UPLC, or GC systems in a GMP environment

Knowledge & Skills
  • Working knowledge of cGMP and FDA regulations and guidance
  • Familiarity with Quality Management Systems and GxP
  • Ability to review scanned batch records and QC chromatographic data output (HPLC, UPLC, or GC) with a high degree of accuracy
  • Detail-oriented, with sound problem-solving and troubleshooting ability
  • Able to work independently, manage your own time, and contribute effectively within a team

Certifications
  • ASQ Certified Quality Process Analyst, or
  • Certified Quality Auditor (CQA), or
  • Certified Quality Engineer (CQE)
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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