Production Quality Assurance Coordinator

PhytogenX, Inc.

Morgantown (PA)

On-site

USD 65,000 - 90,000

Full time

3 days ago
Be an early applicant
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Job summary

PhytogenX, Inc. is seeking a Production Quality Assurance Coordinator to ensure all products meet quality standards by overseeing QA activities, monitoring manufacturing operations, and supporting continuous improvement initiatives.

You will partner with production, customer service, and quality teams to ensure GMP, GDP, and internal procedures compliance, maintain records, and drive CAPA and change controls.

Qualifications

  • High School Diploma or GED required.
  • Associate's or Bachelor's degree in Quality Management, Manufacturing, Life Sciences, or a related field preferred.
  • Minimum of 2 years of experience in quality assurance, quality control, manufacturing, or a regulated production environment.
  • Experience within FDA-regulated, GMP, or ISO-compliant environments preferred.
  • Proficiency in Microsoft Office applications (Word, Excel, Outlook).
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication skills.
  • Experience with quality management software is a plus.
  • Knowledge of GMP, GDP, CAPA, deviation management, change control processes, and quality systems preferred.

Responsibilities

  • Review and approve fill specification sheets and ensure alignment with customer fill and assembly specifications.
  • Photograph new production jobs to establish quality standards and production references.
  • Organize, maintain, and update production quality standards utilized by Production QA personnel.
  • Partner with Production QA leadership and production management to coordinate customer visits and ensure customer expectations are understood and met.
  • Serve as a liaison between customer service and production teams regarding customer specifications, concerns, and quality-related issues.
  • Report product quality concerns and compliance issues to Quality Management.
  • Write, revise, and implement SOPs related to production quality activities.
  • Verify production balances are functional, calibrated, and maintained in accordance with approved procedures.

Skills

Attention to detail
Written & verbal communication
MS Office
Quality systems
CAPA
GMP/GDP
Problem solving
Multi-project management

Education

Quality/Manufacturing/Life Sciences degree

Tools

MS Office

Job description

The Production Quality Assurance Coordinator is primarily responsible for ensuring that all products meet PhytogenX quality standards by overseeing production quality activities, monitoring manufacturing operations, implementing quality assurance measures, and supporting continuous improvement initiatives. This position serves as the primary quality resource for production operations and works closely with production, customer service, and quality teams to ensure compliance with customer requirements, GMP standards, and internal procedures.

Role And Responsibilities
  • Review and approve fill specification sheets and ensure alignment with customer fill and assembly specifications.
  • Photograph new production jobs to establish quality standards and production references.
  • Organize, maintain, and update production quality standards utilized by Production QA personnel.
  • Partner with Production QA leadership and production management to coordinate customer visits and ensure customer expectations are understood and met.
  • Serve as a liaison between customer service and production teams regarding customer specifications, concerns, and qualityrelated issues.
  • Report product quality concerns and compliance issues to Quality Management.
  • Write, revise, and implement Standard Operating Procedures (SOPs) related to production quality activities.
  • Verify production balances are functional, calibrated, and maintained in accordance with approved procedures.
  • Maintain detailed records of inspections, deviations, nonconformances, corrective actions, and rework activities.
  • Monitor production processes to identify quality concerns and opportunities for improvement.
  • Enforce health, safety, environmental, GMP, GDP, and hygiene standards within production operations.
  • Facilitate quality training sessions for production personnel on procedures, expectations, and best practices.
  • Collaborate with operations and quality teams to drive continuous quality improvement initiatives.
Quality Assurance Support
  • Crosstrain in Quality Assurance Associate responsibilities to provide departmental support and ensure continuity of quality operations.
  • Maintain a working knowledge of quality systems, regulatory requirements, FDA expectations, and ISO 22716 standards.
  • Assist in maintaining cGMP compliance and promoting quality awareness throughout the organization.
  • Support and reinforce Good Documentation Practices (GDP).
  • Review and track batch records for completeness and compliance.
  • Generate and review Certificates of Analysis (CoAs).
  • Assist with authoring, reviewing, and maintaining validation documentation.
  • Support Annual Product Reviews (APRs) and other quality system activities.
  • Monitor the timely completion of CAPAs, deviations, nonconformances, investigations, and change controls.
  • Assist with customer complaint investigations and qualityrelated documentation.
  • Support the review, revision, and implementation of SOPs as needed.
  • Conduct training sessions and presentations related to quality programs and procedures.
  • Provide flexible support across Quality functions to meet departmental needs and business objectives.
Experience, Qualifications And Education Requirements
  • High School Diploma or GED required.
  • Associate's or Bachelor's degree in Quality Management, Manufacturing, Life Sciences, or a related field preferred.
  • Minimum of 2 years of experience in quality assurance, quality control, manufacturing, or a regulated production environment.
  • Experience within FDAregulated, GMP, or ISOcompliant environments preferred.
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication skills.
  • Proficiency in Microsoft Office applications (Word, Excel, Outlook).
  • Experience with quality management software is a plus.
  • Strong problemsolving, investigation, and decisionmaking abilities.
  • Ability to manage multiple projects and priorities simultaneously.
  • Selfmotivated with the ability to work independently and collaboratively.
  • Knowledge of GMP, GDP, CAPA, deviation management, change control processes, and quality systems preferred.
  • Reliable, dependable, and committed to maintaining high quality standards.
Physical Demands
  • Ability to stand for extended periods and work within a fastpaced production environment.
  • Exposure to production equipment, noise, dust, and manufacturing activities.
  • Ability to work on a computer for extended periods.
  • Ability to hear and understand spoken information in person and over the phone.
  • Ability to read, analyze, and interpret technical documents, procedures, and quality records.
  • Ability to occasionally lift and/or move objects up to 25 pounds.
  • Ability to walk between office, laboratory, warehouse, and production environments as needed.

PhytogenX is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, national origin, disability, veteran status, or any other protected status. Employment decisions are based on qualifications, merit, and business needs.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Production QA Specialist: Quality & Compliance
Production QA Specialist: Quality & Compliance

PhytogenX, Inc. • Morgantown (PA)

On-site
USD 65,000 - 90,000
Quality Technician
Quality Technician

Adept Life Sciences, Inc • Gilbert (AZ)

On-site
USD 42,000 - 62,000
Quality Operations Primary Packaging Tier I (Shift 1 6:00 am to 6:30 pm)
Quality Operations Primary Packaging Tier I (Shift 1 6:00 am to 6:30 pm)

Nephron Pharmaceuticals • West Columbia (SC)

On-site
USD 40,000 - 60,000
Quality Operations Primary Packaging Tier I (Shift 1 6:00 am to 6:30 pm)
Quality Operations Primary Packaging Tier I (Shift 1 6:00 am to 6:30 pm)

Nephron Pharmaceuticals Corp • Columbia (SC)

On-site
USD 40,000 - 60,000
Quality Operations Primary Packaging Tier I (Nights 6:00pm - 6:30am)
Quality Operations Primary Packaging Tier I (Nights 6:00pm - 6:30am)

Nephron Pharmaceuticals Corporation • West Columbia (SC)

On-site
USD 42,000 - 64,000
Quality Engineer II-III, Quality Assurance
Quality Engineer II-III, Quality Assurance

MedPharm Ltd • Durham (NC)

On-site
USD 90,000 - 120,000
Quality Engineer II-III, Quality Assurance
Quality Engineer II-III, Quality Assurance

MedPharm • Durham (NC)

On-site
USD 85,000 - 120,000
QA Technician – Weigh Room & Production Lines
QA Technician – Weigh Room & Production Lines

NVE Pharmaceuticals • Green Township (NJ)

On-site
USD 42,000 - 62,000
Health insurance
Paid time off
Retirement savings options
QA Technician
QA Technician

Tribute Baking Company • Miami (FL)

On-site
USD 52,000 - 76,000
Quality Assurance Specialist I
Quality Assurance Specialist I

Kindeva • Maryland Heights (MO)

On-site
USD 60,000 - 80,000