Quality Systems Specialist: Document Control & Compliance

QuVa - Advancing Healthcare Possibilities

Sugar Land (TX)

On-site

USD 55,000 - 75,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Comprehensive health and wellness
401k with company match
17 paid days off + 8 holidays
Overtime opportunities with advance通知
Career advancement opportunities

Job summary

QuVa - Advancing Healthcare Possibilities in Sugar Land, TX is seeking a Quality Systems Specialist to manage documents, change control, and quality systems. You will process changes to batch records, ensure current procedures, and support audits to maintain cGMP compliance.

The role is full-time, on-site, M-F, 7:00 AM to 4:00 PM, with limited overtime and a focus on precision and safety in pharmaceutical operations.

Qualifications

  • High school diploma or GED required.
  • 1/2 year to 1 year experience at Quva Pharma.
  • Understanding of archival process and document controls preferred.
  • Authorized to work in the United States on a full-time basis; no visa sponsorship.

Responsibilities

  • Review and write document change requests.
  • Coordinate updates to procedures, forms and batch records.
  • Maintain quality management systems.
  • Generate workflows for procedures, forms and batch records.
  • Ensure documents have current version at all times.
  • Assist audits with document retrieval.
  • Administer controlled documents for Quality functions.

Skills

Attention to detail
Verbal communication
Written communication

Education

High school diploma or GED
Bachelor’s degree in life science

Tools

Microsoft Office
Adobe
Word
Excel

Job description

QuVa - Advancing Healthcare Possibilities in Sugar Land, TX is seeking a Quality Systems Specialist to manage documents, change control, and quality systems. You will process changes to batch records, ensure current procedures, and support audits to maintain cGMP compliance.

The role is full-time, on-site, M-F, 7:00 AM to 4:00 PM, with limited overtime and a focus on precision and safety in pharmaceutical operations.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Quality Systems Specialist — cGMP Documentation & Change Control
Quality Systems Specialist — cGMP Documentation & Change Control

QuVa Pharma, Inc. • Sugar Land (TX)

On-site
USD 60,000 - 85,000
Quality Systems Specialist 1st Shift
Quality Systems Specialist 1st Shift

QuVa Pharma, Inc. • Sugar Land (TX)

On-site
USD 60,000 - 85,000
Quality Systems Specialist 1st Shift
Quality Systems Specialist 1st Shift

QuVa - Advancing Healthcare Possibilities • Sugar Land (TX)

On-site
USD 55,000 - 75,000
Comprehensive health and wellness
401k with company match
17 paid days off + 8 holidays
+2
Quality Assurance Specialist - Document Control
Quality Assurance Specialist - Document Control

Xseerpharma • Los Angeles (CA)

On-site
USD 75,000 - 110,000
Regulatory QA Document Control Specialist
Regulatory QA Document Control Specialist

Swiss American CDMO, LLC. • Carrollton (TX)

On-site
USD 60,000 - 85,000
Quality Documentation Specialist: QMS, Audits & Compliance
Quality Documentation Specialist: QMS, Audits & Compliance

Allied Medical LLC • Earth City (MO)

On-site
USD 42,000 - 62,000
2nd-Shift Pharma QA Technician
2nd-Shift Pharma QA Technician

Quva • Sugar Land (TX)

On-site
USD 52,000 - 65,000
Comprehensive health and wellness (med
401k retirement with company match
17 paid days off + 8 paid holidays
+2
Quality Systems SOP & Change Control Specialist
Quality Systems SOP & Change Control Specialist

Hims & Hers • Mesa (AZ)

On-site
USD 85,000 - 110,000
Comprehensive health benefits
401k with employer matching
Document Control Specialist
Document Control Specialist

Swiss American CDMO, LLC. • Carrollton (TX)

On-site
USD 55,000 - 85,000
Quality Systems Specialist
Quality Systems Specialist

Planet Pharma • Waltham (MA)

On-site
USD 55,104 - 68,880