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Quality Operations Manager Jobs in Perth Amboy, NJ

Commercial Catering Company

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Operations Manager

Queens, NY · On-site

$85K - $105K/yr

Partner closely with Quality Assurance to maintain food safety, sanitation, and operational ... Manage and direct the daily activities of supervisors responsible for packing and shipping ...

Oak St. Health

Operations Manager

Manhattan, NY · On-site

$22 - $36/hr

Operations Manager We're building a world of health around every individual shaping a more ... quality in everything we do. Join us and be part of something bigger helping to simplify health ...

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Wylander

Operations Manager

Brooklyn, NY · On-site

$140K/yr

Wylander is recruiting an Operations Manager for a full-service disaster restoration company ... Monitor job progress from start to finish, ensuring quality workmanship, operational efficiency ...

Wylander

Operations Manager

Brooklyn, NY

$140K/yr

Wylander is recruiting an Operations Manager for a full-service disaster restoration company ... Monitor job progress from start to finish, ensuring quality workmanship, operational efficiency ...

Owen Health Care

Operations Manager

Vauxhall, NJ · On-site

Operations Manager Owen Health Care Inc. | Vauxhall, NJ Are you a licensed clinician with ... We provide compassionate, quality, and affordable healthcare services to adults with mental health ...

Wylander

Operations Manager

Brooklyn, NY

$140K/yr

Wylander is recruiting an Operations Manager for a full-service disaster restoration company ... Monitor job progress from start to finish, ensuring quality workmanship, operational efficiency ...

Owen Health Care

Operations Manager

Vauxhall, NJ · On-site

As the Operations Manager for Owen Health Care Inc., you will lead agency-wide operations ... We provide compassionate, quality, and affordable healthcare services to adults with mental health ...

Owen Health Care

Operations Manager

Vauxhall, NJ · On-site

Operations Manager Owen Health Care Inc. | Vauxhall, NJ Are you a licensed clinician with ... We provide compassionate, quality, and affordable healthcare services to adults with mental health ...

CVS Health

Operations Manager

New York, NY · On-site

$22 - $36/hr

... and quality in everything we do. Join us and be part of something bigger - helping to simplify ... Position Summary The Operations Manager is a member of the Store Management team, and as such ...

CVS Health

Operations Manager

New York, NY

$22 - $36/hr

... and quality in everything we do. Join us and be part of something bigger - helping to simplify ... Position Summary The Operations Manager is a member of the Store Management team, and as such ...

CVS Health

Operations Manager

New York, NY

$22 - $36/hr

... and quality in everything we do. Join us and be part of something bigger - helping to simplify ... Position Summary The Operations Manager is a member of the Store Management team, and as such ...

CVS Health

Operations Manager

Bedminster, NJ · On-site

$20.92 - $34.92/hr

... and quality in everything we do. Join us and be part of something bigger - helping to simplify ... Position Summary The Operations Manager is a member of the Store Management team, and as such ...

CVS Health

Operations Manager

Princeton, NJ

$20.92 - $34.92/hr

... and quality in everything we do. Join us and be part of something bigger - helping to simplify ... Position Summary The Operations Manager is a member of the Store Management team, and as such ...

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All JobsQuality Operations JobsQuality Operations Manager JobsQuality Operations Manager Jobs in Perth Amboy, NJ

Quality Operations Manager information

See Perth Amboy, NJ salary details

$39.6K

$93.6K

$142.3K

How much do quality operations manager jobs pay per year?

As of Aug 25, 2026, the average yearly pay for quality operations manager in Perth Amboy, NJ is $93,558.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $113,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality operations manager?

To thrive as a Quality Operations Manager, you need expertise in quality management systems, process improvement, and a background in engineering or a related field, often supported by a bachelor’s degree. Familiarity with ISO standards, Six Sigma or Lean methodologies, and quality management software is typically required. Strong leadership, problem-solving abilities, and effective communication skills help drive quality initiatives and foster a culture of continuous improvement. These competencies are crucial to ensuring product consistency, regulatory compliance, and operational excellence.

How does a quality operations manager typically collaborate with other departments to maintain product standards?

A Quality Operations Manager works closely with departments such as production, supply chain, and R&D to ensure that product quality standards are consistently met. They often participate in cross-functional meetings to address quality concerns, analyze root causes of issues, and implement corrective actions. Effective communication and teamwork are essential, as the manager needs to align quality objectives with overall business goals and foster a culture of continuous improvement across teams.

What is the role of a quality operations manager?

A quality operations manager oversees the implementation and maintenance of quality systems within an organization, ensuring products and services meet safety, quality, and regulatory standards. They analyze processes, lead continuous improvement initiatives, and often use tools like Six Sigma or ISO standards to enhance efficiency and compliance.

What are popular job titles related to Quality Operations Manager jobs in Perth Amboy, NJ?

For Quality Operations Manager jobs in Perth Amboy, NJ, the most frequently searched job titles are:

What job categories do people searching Quality Operations Manager jobs in Perth Amboy, NJ look for?

The top searched job categories for Quality Operations Manager jobs in Perth Amboy, NJ are:

What cities near Perth Amboy, NJ are hiring for Quality Operations Manager jobs?

Cities near Perth Amboy, NJ with the most Quality Operations Manager job openings:

Quality Operations Manager jobs near you
Infographic showing various Quality Operations Manager job openings in Perth Amboy, NJ as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $93,558 per year, or $45 per hour.

Senior Clinical Quality Operations Manager

Eikon Therapeutics

Jersey City, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position
In partnership with the Director of Process Management for Clinical Research & Development, the Senior Clinical Quality Operations Manager (Sr. CQOM) is accountable for the execution of operational quality management and inspection readiness activities across Eikon's clinical development programs, to whom this role reports. The Sr. CQOM oversees clinical quality operations across assigned clinical programs, embedding quality-by-design principles, risk-based quality plans, and vendor oversight into Eikon's clinical trials. In partnership with Clinical Quality Assurance (CQA), the CQOM drives disciplined execution of quality plans and operational standards, enabling study teams to be inspection ready. This includes ensuring consistent execution of quality-by-design (QBD) principles across assigned clinical development programs and facilitating identification of Critical to Quality (CtQs) factors and associated risk assessments, establishing, and actively maintaining study-specific quality plans throughout the study lifecycle using a risk-based approach. The Sr. CQOM is accountable for the overall strategy to maintain inspection readiness through disciplined execution of risk assessments, quality plans and operational standards, in collaboration with Clinical Quality Assurance (CQA) on inspection preparation, management and follow-up activities.The successful candidate will work closely with cross-functional Clinical Research & Development teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support operational excellence and world-class in-house clinical study management.
This role requires onsite presence at minimum 3 days per week to support effective management, operational excellence, and high-performance delivery of clinical studies and expected team growth & collaboration.
About You
You are a collaborative, hands-on leader who enjoys working alongside clinical study teams to strengthen consistency, embed quality and drive disciplined trial execution. You bring credibility through deep knowledge of GCP and strong clinical operations expertise and are energized by cross-functional partnership. You are excited about the opportunity to shape a new function in a growing organization.
What You'll Do
  • Ensures consistent execution of 'quality by design' principles in assigned clinical trials. Reviews Risk Assessment and Categorization Tools (RACTs), quality plans, and study-specific procedures with Study Management Teams to confirm accuracy, compliance with Sponsor requirements, and inspection-readiness.
  • Facilitates TA-level review of CtQs, quality plans and risk mitigation approaches to identify inconsistencies, emerging signals, and trends and to provide relevant feedback to the Head of Clinical Study Management and Director of Process Management for Clinical R&D, as appropriate.
  • Works with Clinical R&D peers to analyze data across Eikon's clinical trials to identify signals and trends and translate findings into actionable process improvement strategies.
  • In partnership with the Director of Process Management for Clinical R&D, the Head of Clinical Data Analytics and Reporting and the Head of Clinical Study Management, builds proficiency in leveraging technology and data to recognize and respond to new and emerging risks across the clinical portfolio, including how GCP applies to digital data management and novel trial technology.
  • Partners with cross-functional study teams to ensure vendor and CRO performance is documented in vendor and CRO oversight plans and monitored against quality expectations, escalating compliance, or inspection-readiness risks to Clinical R&D functional area Heads, as necessary.
  • Builds and enables effective working relationships with key stakeholders to ensure and maintain role clarity and business effectiveness. This will include ongoing partnership with Clinical R&D Clinical Quality Assurance (CQA) and acting as the link between Clinical R&D functional areas, clinical study teams, enterprise business functions, and regional study management.
  • Contributes to the standardization of Clinical Quality Operations procedures, tools, and templates to ensure consistency and seamless progression throughout the study lifecycle.

Inspection Preparation and Management
  • Maintains current, in-depth knowledge of global GCP inspection practices - including requirements from FDA, EMA, MHRA, and other established and emerging authorities - to effectively support GCP inspections worldwide. May serve as point of contact for a specific regulatory area (e.g., FDA, EMA, NMPA). Is responsible for monitoring, interpreting, and communicating relevant regulatory developments.
  • Maintains current awareness of filing schedules, potential future inspections, and ongoing inspection preparation activities.
  • Supports CQA in developing, updating, and maintaining GCP inspection procedures and guidelines within Clinical Development Operations and Clinical R&D functional areas.
  • Contributes to the development and/or revision of Eikon policies, SOPs, and training materials.
  • Ensures the operational foundation supports favorable inspection outcomes and that study teams execute consistently against study plans and operational standards.
  • Partners with CQA to ensure the Clinical R&D functional areas are fully informed and prepared to support Regulatory Health Authority inspections led by CQA, worldwide.
  • Escalates potentially significant compliance risks/impact to Clinical R&D functional area Heads, as necessary.

CAPA Management Support
  • Leads CAPA implementation for CQA-sponsored internal audits, partnering with study teams and functions to translate findings into process changes.
  • For external audits and Regulatory Health Authority inspections, partners with study teams to develop CAPA responses and implement CQA-approved corrective actions requiring process, tool, or workflow changes.
  • Coordinates education and training for study teams on process changes resulting from CAPAs, ensuring changes are understood, adopted, and sustained in practice.

Other Activities
  • Provides RACT completion status, quality plan metrics, and other operational data to CQA for inclusion in GCP Quality Council meetings.
  • Assesses and provides input to strengthen company programs/strategies with an aim to increase inspection readiness.
  • Leads, drives, facilitates and/or supports remediation, prevention activities as process improvement and training, as needed.

Qualifications
  • Minimum of 8+ years of related experience with a Bachelor's degree; or 6+ years with a post graduate degree. Additional certifications such as lean six sigma or PMP are preferred but not required.
  • In-depth knowledge of GCP, ICH E6(R3) guidelines and other relevant regulations and guidelines.
  • Demonstrated experience with CAPA management, including root cause analysis, preventive action development, translating CAPA findings into operational changes and tracking commitments to completion.
  • Experience with risk management tools and quality planning in clinical development, including Quality by Design and risk-based approaches.
  • Proven ability to work cross-functionally with clinical operations, quality assurance, regulatory, data management, and other clinical development teams in a matrixed environment.
  • Superior oral and written communication skills in an international environment with the ability to influence at all levels.
  • Excellent teamwork and leadership skills, including conflict resolution expertise.
  • Ability to analyze, interpret and solve complex problems.
  • Ability to think strategically and objectively while applying creativity and innovation.
  • Ability to synthesize findings and deliver lessons learned.
  • Experience with Veeva or similar document and quality management systems is a plus.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
  • 401k plan with company matching
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
  • Mental health and wellness benefits
  • Weeklong summer and winter holiday shutdowns
  • Generous paid time off and holiday policies
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
  • Enhanced parental leave benefit
  • Daily subsidized lunch program when on-site

The expected salary range for this role is $157,000 to $189,000 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

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