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Remote Quality Assurance Operations Manager Jobs Near Me

Versova

Quality Assurance Lead

Johnstown, OH · On-site

This position works directly with the Compliance Team, Operations Managers and Supervisors, Quality Assurance personnel, Safety Team, and People Operations to support the production and delivery of ...

Abercrombie

Manager, Quality Assurance

Columbus, OH · Remote

The Manager, Quality Assurance is responsible for leading Home Office-based quality strategy, cross ... accountability, operational consistency, and cross-functional ways of working. Leadership ...

Trident Care

Quality Assurance Analyst RCM

Columbus, OH

$45K/yr

Operations Management * Assists with management of the functionality and efficient operation of the ... This is a remote position but candidate shoudl reside within 50 miles of one of these locations for ...

PACS

Quality Assurance Nurse (QA)

Lancaster, OH · On-site

... Provides remote or on-site support as needed for clinical and operational needs Primary ... Resident Management Review all falls for root cause and intervention accuracy Ensure timely ...

gaylor

Quality Assurance Manager

Jeffersonville, OH · On-site

The Quality Assurance Manager must be independent self-motivated, innovative, resourceful, and possess strong organizational and communication skills. The Quality Assurance Manager is pivotal in ...

gaylor

Quality Assurance Manager

Jeffersonville, OH · On-site

The Quality Assurance Manager must be independent self-motivated, innovative, resourceful, and possess strong organizational and communication skills. The Quality Assurance Manager is pivotal in ...

Computech Corporation

Quality Assurance

Columbus, OH · On-site

Work closely with and follow direction from QA Manager * Contribute to the establishment of and meet quality goals and objectives for the project. * Contribute to all aspects of quality assurance for ...

Actalent

Qa/qc Manager

Westerville, OH · On-site

$40 - $50/hr

Job Title: QA/QC Manager The QA/QC Manager supports operations by implementing and maintaining quality assurance and quality control programs across heavy civil and industrial construction projects.

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How much do remote quality assurance operations manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for remote quality assurance operations manager in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.
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A map of the United States highlighting the number of Remote Quality Assurance Operations Manager job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Remote Quality Assurance Operations Manager job openings in each state, with California having the most at 2 and Alaska the least at 0.

Quality Assurance Technician

STAQ Pharma Inc

Columbus, OH • On-site

$24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

Position Summary:

The Quality Assurance Technician I supports Quality Assurance operations within a 503B pharmaceutical manufacturing environment by helping ensure products, processes, documentation, materials, and labeling activities meet cGMP, company procedure, and quality system expectations. This role provides day-to-day QA support across Production, Warehouse, Receiving, and Quality while helping protect patient safety through accurate inspection, documentation, escalation, and follow-up.

This position is a strong fit for someone who is detail-oriented, organized, comfortable working in a regulated manufacturing environment, and motivated to grow within pharmaceutical Quality Assurance. The QA Technician I may support a mix of floor-based quality checks and documentation-based activities, including finished goods and inspection, labeling coordination, GMP document review, training/document control support, and follow-up on quality events or process concerns.

What This Role Does Day-to-Day:

In this role, the QA Technician I helps verify that work performed in manufacturing and support areas is completed accurately, consistently, and in accordance with approved procedures. Daily activities may include inspecting in-process and finished products, verifying label or component information, reviewing room and equipment logs, entering quality data, label inventory audits.

The QA Technician I may also support investigations, CAPAs, effectiveness checks, receiving inspection support. The role requires the ability to recognize when something does not match the procedure, documentation, label, material, product, or expected process, and to escalate the concern before moving forward.

Because this position supports multiple departments, the ideal candidate must be comfortable communicating with Production, Warehouse, Receiving, Quality Control, Quality Assurance, and leadership. Success in this role requires strong attention to detail, sound judgment, professionalism, follow-through, and the ability to balance urgency with compliance in a fast-paced manufacturing environment.

Key Responsibilities:

  • Perform inspection of in-process and finished pharmaceutical products according to approved procedures, specifications, and quality expectations.
  • Support and facilitate finished product labeling activities, including label coordination, verification, reconciliation support, documentation, and escalation of labeling discrepancies as assigned.
  • Review GMP documentation, including,room logs, equipment logs, inspection records, forms, checklists, and other quality-related documents for accuracy, completeness, and compliance.
  • Support manufacturing and receiving activities by verifying materials, components, documentation, or inspection requirements as assigned.
  • Assist with investigations related to deviations, documentation discrepancies, process concerns, product issues, label discrepancies, complaints, or other quality events.
  • Identify and escalate documentation errors, missing information, product defects, material concerns, label mismatches, or process issues to the appropriate Quality or operational leader.
  • Work cross-functionally with Production, Warehouse, Receiving, QC, QA, and leadership to support compliant operations, timely issue resolution, and product quality.
  • Maintain accurate, timely, legible, complete, and attributable documentation in accordance with GDP expectations.
  • Follow all applicable cGMP, GDP, FDA, OSHA, DEA, company procedure, safety, PPE, and quality system requirements.
  • Support continuous improvement by identifying recurring issues, communicating improvement opportunities.
  • Perform other duties as assigned based on business and quality needs.

What Success Looks Like:

  • Understands that QA support directly impacts patient safety, product quality, product release, and regulatory compliance.
  • Reviews documentation carefully and catches missing, inconsistent, incomplete, or inaccurate information before it creates a larger issue.
  • Identifies product, material, label, documentation, or process concerns and escalates appropriately instead of making assumptions or unsupported decisions.
  • Communicates clearly with Production, Warehouse, Receiving, QC, QA, and leadership, especially when priorities shift or concerns need follow-up.
  • Stays organized while managing multiple tasks, open items, deadlines, and documentation requirements.
  • Follows SOPs and work instructions exactly and understands the importance of cGMP, GDP, and data integrity.
  • Demonstrates accountability, curiosity, and willingness to learn pharmaceutical manufacturing processes.
  • Shows motivation to grow within Quality Assurance and take on additional documentation and/or floor support responsibilities over time.

Physical Requirements:

  • Ability to sit, stand, walk, bend, reach, or perform computer-based work for extended periods as required by business needs.
  • Ability to lift up to 50-75 pounds at times.
  • Ability to work in office, manufacturing, warehouse, receiving, controlled, or quality support areas as needed.
  • Ability to wear required PPE and follow safety, cleanliness, gowning, and facility requirements.
  • Ability to review documentation, labels, product information, and computer-based records for extended periods

Work Environment:

This role supports Quality Assurance activities in a 503B pharmaceutical manufacturing environment. Work may take place in office, production, warehouse, receiving, controlled, or other quality support areas. Employees are expected to follow cGMP, GDP, PPE, safety, documentation, cleanliness, and conduct expectations at all times. The role may involve working near production materials, finished products, labels, packaging components, equipment, or manufacturing documentation that must be handled according to approved procedures.

This is a quality-focused role where accuracy, consistency, escalation, and documentation matter. The QA Technician I helps ensure that issues are identified early, records are complete and accurate, and operational teams have the QA support needed to maintain compliant manufacturing and product quality.

Benefits:

We offer a comprehensive and competitive benefits package designed to support the health, well-being, and financial security of our employees and their families.

At STAQ Pharma, all full time employees have access to:

  • Medical, dental, and vision insurance options
  • Employer-paid life insurance and disability coverage
  • Employee Assistance Program
  • 401(k) retirement plan with employer match
  • Paid time off (PTO), sick leave
  • 7 paid holidays
  • Opportunities for professional growth in a regulated pharmaceutical manufacturing environment
  • Employee-focused culture emphasizing safety, quality, and teamwork

The application window for this position is anticipated to be open at least 25 days