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Gcp Qa Jobs (NOW HIRING)

QA Manager, GCP

San Diego, CA ยท On-site

$112K - $153K/yr

Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Guide and support from a quality perspective the GCP/GCLP and GPP related activities ...

QA Manager, GCP

Raleigh, NC ยท On-site +1

$112K - $153K/yr

Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Guide and support from a quality perspective the GCP/GCLP and GPP related activities ...

This leader provides insight and partners with both GCP QA staff and Clinical Operations Quality Management (OQM) to address day-to-day clinical trial operations activities focused on deviations ...

Manager - Quality GCP

Boston, MA ยท On-site

$95K - $145K/yr

... QA GCP reviews of selected regulatory documents and submissions to ensure accuracy and compliance, as applicable. โ€ข Participate in and support inspection readiness activities as well as regulatory ...

The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the ... Oversees GCP compliance for all clinical activities, including monitoring, data management, and ...

The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the ... Oversees GCP compliance for all clinical activities, including monitoring, data management, and ...

Clinical Quality Lead

$152K - $209K/yr

Provide QA input during the creation/revision of argenx clinical procedural documents for GCP compliance * When assigned as "QA Approver" in ARGO or PhoeniQS, act as QA approver for GCP area. * Act ...

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Gcp Qa information

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$38K

$118.1K

$179K

How much do gcp qa jobs pay per year?

As of Jun 10, 2026, the average yearly pay for gcp qa 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.

What is a GCP QA job?

A GCP QA (Good Clinical Practice Quality Assurance) job involves ensuring compliance with regulatory guidelines in clinical research. Professionals in this role conduct audits, review protocols, and ensure clinical trials adhere to industry standards such as FDA and ICH guidelines. They work to identify, report, and mitigate risks to maintain the integrity of clinical data. GCP QA specialists collaborate with regulatory agencies, clinical teams, and sponsors to ensure ethical and quality-driven research practices.

What are the key skills and qualifications needed to thrive in the Gcp Qa position, and why are they important?

To thrive as a GCP QA, you need a strong understanding of Good Clinical Practice (GCP) guidelines, clinical research processes, and quality assurance methodologies, often backed by a degree in life sciences or a related field. Experience with audit tools, electronic data capture (EDC), and certifications such as RQAP-GCP or similar are highly advantageous. Excellent attention to detail, communication skills, and the ability to work collaboratively stand out as essential soft skills. These capabilities ensure compliance, data integrity, and the smooth execution of clinical trials within regulatory frameworks.

What are some of the typical responsibilities of a GCP QA throughout a clinical trial?

GCP QA professionals are responsible for planning, conducting, and documenting quality audits of clinical trial processes, ensuring compliance with Good Clinical Practice guidelines and regulatory requirements. They review study documentation, identify compliance gaps, and work closely with clinical project teams to implement corrective actions. GCP QA specialists regularly communicate with sponsors, investigators, and regulatory agencies. Their oversight ensures data integrity and subject safety throughout the clinical trial lifecycle, which is vital for successfully bringing new therapies to market.

More about Gcp Qa jobs
What cities are hiring for Gcp Qa jobs? Cities with the most Gcp Qa job openings:
What are the most commonly searched types of Gcp Qa jobs? The most popular types of Gcp Qa jobs are:
What states have the most Gcp Qa jobs? States with the most job openings for Gcp Qa jobs include:
Infographic showing various Gcp Qa job openings in the United States as of June 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 78% Physical, 7% Hybrid, and 15% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.

QA Manager, GCP

Sobi

San Diego, CA โ€ข On-site

$112K - $153K/yr

Full-time

Posted 14 days ago


Job description

Company Description

Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application!

At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.

Our mission and culture at Sobi North America get us excited to come to work every day, but here are a few more reasons to join our team:

  • Competitive compensation for your work
  • Generous time off policy
  • Opportunity to broaden your horizons by attending popular conferences
  • Emphasis on work/life balance
  • Collaborative and team-oriented environment
  • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments
Job Description

The QA Manager, GCPย is responsible for:ย ย 

  • Ensuring quality oversight and quality assuranceย and quality by designย activities related to GCP/GCLPย areaย 

  • Guide and support from a quality perspective the GCP/GCLPย and GPP related activities within Sobi,ย includingย audits,ย inspectionย andย supportย ofย and riskย assessmentย of the BLA/NDA/IND/CTA submissionsย under global umbrella.ย 

  • Support the collection of the data needed for Audit program riskย assessmentย 

  • Support from quality perspective the clinical studies related activities across Sobiย ย 

  • Ensure qualification of global and local ESP, as applicable,ย in GCP regulated area per Sobi proceduresย 

  • The employee will in this role work with relevant stakeholders across the Sobi organization.ย 

Key responsibilities:

  • Ensure GCP Audits management excellence of theย end to endย audit management process and overview of the assigned audits, as plannedย 

  • Assesย and approve from quality perspective the GCP deviations (global and local, as applicable),ย GCPย related CAPAs.ย 

  • Prepare regular status report on performed audits, auditย trending,ย  deviationย ternding,ย  CAPAsย trending and agreed upon metrics to ensure Quality oversight.ย ย 

  • Contributeandย supportย the GCP auditย riskย assesmentย according to SOPs.ย ย 

  • Ensureย active contribution in the cross-functional team with procurement, business owners forย GxPย and Quality requirements andย documented qualification of GCP service providers and review provisionsย in contracts/Quality agreements, as applicableย 

  • QA representativeย duringย GCPย inspectionsย global and siteย level, as applicableย and contribute to the Inspection Readiness framework and promote continuously quality mindset across Sobi.ย 

  • Authoring GCP QA related processes, reviewย and give guidanceย under global umbrella.ย 

Qualifications

Required:ย ย 

  • Universityย degreeย ย orย similarย in Life Sciences or related discipline.ย ย 

  • At least 5ย years experienceย from the pharmaceutical industryย inย Clinical Quality Assurance or in the operational conduct of clinical trials and the application of GCPย audit and/or Quality Assurance experience.ย ย 

Technical skills:ย ย 

  • Excellent knowhow of theย applicable ICH GCP guidelines, industry best practices andย FDA,ย EMAย and ROWย regulatory requirements.ย 

  • Quality assurance activities principles andย know-howย 

  • Documented education/experience in QA systems and preferably auditingย 

Soft skills:ย 

  • Structured with focus on results and detail orientedย ย 

  • Strong interpersonal skills with communicative and flexible attitudeย ย 

  • Proactive and collaborative mindsetย 

  • Strong multi-tasking abilities with high resilienceย at stressย and adaptative skillsย 

Additional Information

Compensation and Total Rewards at Sobi

At Sobi, we are dedicated to providing our employees with a comprehensive and industry-competitive total rewards package. Our compensation philosophy is designed to recognize and reward talent, ensuring that your contributions are valued and reflected in your overall rewards.

The base salary range for this role isย $112,000-$153,000. Each individual offer will be determined based on several factors, including your experience, qualifications, and location. Additionally, this role is eligible for both short-term and long-term bonuses, as outlined in the plan details.

All Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership. Are you ready to be on the Sobi team? Come join a culture that empowers every person to be the person that makes a difference for rare disease.

Why Join Us?
We are a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we're ready to take on the world's diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others' lives because that's exactly what we do here. If you're seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you.
We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff.
Sobi Culture
At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them.
As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can't change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth.

An Equal Opportunity Employer
Sobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity, protected veterans and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status or protected groups by the laws or regulations in the locations where we operate.

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to [emailย protected]ย ย 

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