QA Manager, GCP
$112K - $153K/yr
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
$112K - $153K/yr
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
$112K - $153K/yr
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
Boston, MA · On-site
$160K - $240K/yr
Opportunity Overview As the Associate Director, GCP/GLP/GVP QA, you will oversee GCP activities, ensure compliance and quality execution of clinical studies. You will assist in the development and ...
Boston, MA · On-site
$160K - $240K/yr
Opportunity Overview As the Associate Director, GCP/GLP/GVP QA, you will oversee GCP activities, ensure compliance and quality execution of clinical studies. You will assist in the development and ...
Raleigh, NC · On-site
$112K - $153K/yr
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
Raleigh, NC · On-site
$112K - $153K/yr
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
Raleigh, NC · On-site
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
Quick apply
Raleigh, NC · On-site
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi ...
Boston, MA · On-site
Provide QA GCP review and feedback on regulatory submissions. * Lead and participate in inspection readiness activities for regulatory inspections - both internally and at clinical sites. * Interface ...
Boston, MA · On-site
Provide QA GCP review and feedback on regulatory submissions. * Lead and participate in inspection readiness activities for regulatory inspections - both internally and at clinical sites. * Interface ...
San Diego, CA · On-site
$175K - $215K/yr
Provide ongoing GCP quality oversight and support to ensure adherence to global GCP, quality and ... Provide Clinical QA oversight for CROs, laboratories, and other clinical vendors. Ensure ...
Quick apply
San Diego, CA · On-site
$175K - $215K/yr
Provide ongoing GCP quality oversight and support to ensure adherence to global GCP, quality and ... Provide Clinical QA oversight for CROs, laboratories, and other clinical vendors. Ensure ...
San Diego, CA · On-site
$175K - $215K/yr
Provide ongoing GCP quality oversight and support to ensure adherence to global GCP, quality and ... Provide Clinical QA oversight for CROs, laboratories, and other clinical vendors. Ensure ...
San Diego, CA · On-site
$175K - $215K/yr
Provide ongoing GCP quality oversight and support to ensure adherence to global GCP, quality and ... Provide Clinical QA oversight for CROs, laboratories, and other clinical vendors. Ensure ...
Summary The Director, GCP & GLP QA, reporting to the Executive Director, Quality, is responsible for leading quality assurance oversight across clinical and nonclinical programs to ensure compliance ...
Summary The Director, GCP & GLP QA, reporting to the Executive Director, Quality, is responsible for leading quality assurance oversight across clinical and nonclinical programs to ensure compliance ...
Boston, MA · On-site
$185K - $235K/yr
Provide QA GCP review and feedback on regulatory submissions. * Lead and participate in inspection readiness activities for regulatory inspections - both internally and at clinical sites. * Interface ...
Boston, MA · On-site
$185K - $235K/yr
Provide QA GCP review and feedback on regulatory submissions. * Lead and participate in inspection readiness activities for regulatory inspections - both internally and at clinical sites. * Interface ...
Boston, MA · On-site
$171K - $256K/yr
Summary The Director, GCP & GLP QA, reporting to the Executive Director, Quality, is responsible for leading quality assurance oversight across clinical and nonclinical programs to ensure compliance ...
Boston, MA · On-site
$171K - $256K/yr
Summary The Director, GCP & GLP QA, reporting to the Executive Director, Quality, is responsible for leading quality assurance oversight across clinical and nonclinical programs to ensure compliance ...
In this role, you will design and execute risk-based GCP quality oversight strategies, lead ... Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across ...
In this role, you will design and execute risk-based GCP quality oversight strategies, lead ... Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across ...
San Diego, CA · Remote
$172K - $195K/yr
In this role, you will design and execute risk-based GCP quality oversight strategies, lead ... Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across ...
Quick apply
San Diego, CA · Remote
$172K - $195K/yr
In this role, you will design and execute risk-based GCP quality oversight strategies, lead ... Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across ...
As a key member of the Quality Assurance leadership team, this person will partner with relevant clinical development and operations teams to execute GCP, GLP, GVP, and CDx strategies and participate ...
Quick apply
As a key member of the Quality Assurance leadership team, this person will partner with relevant clinical development and operations teams to execute GCP, GLP, GVP, and CDx strategies and participate ...
San Diego, CA · On-site
$172K - $195K/yr
In this role, you will design and execute risk-based GCP quality oversight strategies, lead ... Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across ...
San Diego, CA · On-site
$172K - $195K/yr
In this role, you will design and execute risk-based GCP quality oversight strategies, lead ... Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across ...
As a key member of the Quality Assurance leadership team, this person will partner with relevant clinical development and operations teams to execute GCP, GLP, GVP, and CDx strategies and participate ...
Quick apply
As a key member of the Quality Assurance leadership team, this person will partner with relevant clinical development and operations teams to execute GCP, GLP, GVP, and CDx strategies and participate ...
San Diego, CA · On-site +1
Reporting to the Chief Operating Officer, the Senior or Executive Director Quality Assurance GCP will lead GCP activities and have responsibility for strategic and tactical oversight and ...
San Diego, CA · On-site +1
Reporting to the Chief Operating Officer, the Senior or Executive Director Quality Assurance GCP will lead GCP activities and have responsibility for strategic and tactical oversight and ...
The Clinical Quality Assurance Manager is responsible for the strategic leadership, oversight, and ... Provide cross-functional oversight of the GCP Quality Management System to ensure compliance with ...
The Clinical Quality Assurance Manager is responsible for the strategic leadership, oversight, and ... Provide cross-functional oversight of the GCP Quality Management System to ensure compliance with ...
Boston, MA · On-site
$137K - $206K/yr
This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support ...
Boston, MA · On-site
$137K - $206K/yr
This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support ...
The Clinical Quality Assurance Manager is responsible for the strategic leadership, oversight, and ... Provide cross-functional oversight of the GCP Quality Management System to ensure compliance with ...
The Clinical Quality Assurance Manager is responsible for the strategic leadership, oversight, and ... Provide cross-functional oversight of the GCP Quality Management System to ensure compliance with ...
San Diego, CA · On-site
Provides Quality Assurance ("QA") expertise, leadership and training to ensure adherence with ... Lead, plan, conduct, and oversee GCP audits (e.g., vendor, clinical investigator site, internal ...
San Diego, CA · On-site
Provides Quality Assurance ("QA") expertise, leadership and training to ensure adherence with ... Lead, plan, conduct, and oversee GCP audits (e.g., vendor, clinical investigator site, internal ...
$14.90 - $18.40
17% of jobs
$19.78 is the 25th percentile. Wages below this are outliers.
$18.40 - $21.90
20% of jobs
$21.90 - $25.39
4% of jobs
The median wage is $27.72 / hr.
$25.39 - $28.89
13% of jobs
$28.89 - $32.39
13% of jobs
$33.93 is the 75th percentile. Wages above this are outliers.
$32.39 - $35.88
18% of jobs
$35.88 - $39.38
4% of jobs
$39.38 - $42.88
4% of jobs
$42.88 - $46.37
3% of jobs
$46.37 - $49.87
2% of jobs
$49.87 - $53.37
1% of jobs
$14
$31
$53
| Aspect | Internship Gcp Qa | Gcp Qa |
|---|---|---|
| Credentials | Typically pursuing or recent graduate, some certifications | Professional certifications like GCP certifications often required |
| Work Environment | Entry-level, training-focused, internship setting | Full-time, professional QA environment in cloud projects |
| Employer & Industry | Tech companies, cloud service providers, startups | Established tech firms, cloud service providers, enterprise IT |
The main difference is that an Internship Gcp Qa is an entry-level, training position aimed at gaining experience, while a Gcp Qa is a full-time professional role requiring more expertise and certifications. Internships serve as a stepping stone toward a full Gcp Qa career.
Cities with the most Internship Gcp Qa job openings:
The most popular types of Gcp Qa jobs are:
For Internship Gcp Qa jobs, the most frequently searched job titles are:
Raleigh, NC
$112K - $153K/yr
Full-time
Re-posted 16 days ago
At Sobi, we believe diversity drives innovation and inclusion creates stronger teams. We are committed to building a workplace where everyone feels valued and empowered to contribute.
If this role excites you but you're unsure if you meet every requirement, we encourage you to apply. Your unique perspective and experiences could be exactly what we need. We look forward to hearing from you!
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:
Due to the hybrid nature of the job, candidates must reside within commuting distance to Raleigh, NC
The QA Manager, GCP is responsible for:
Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area
Providing quality guidance and support for GCP/GCLP and GPP-related activities within Sobi, including audits, inspections, and risk assessment of BLA/NDA/IND/CTA submissions under the global umbrella.
Support the collection of the data needed for Audit program risk assessment
Support clinical studies-related activities from a quality perspective across Sobi
Ensure qualification of global and local ESP, as applicable, in GCP-regulated areas per Sobi procedures
The employee will in this role work with relevant stakeholders across the Sobi organization.
Key responsibilities:
Ensure GCP audit management excellence of the end-to-end audit management process and overview of the assigned audits, as planned
Asses and approve from quality perspective the GCP deviations (global and local, as applicable), GCP related CAPAs.
Prepare regular status report on performed audits, audit trending, deviation ternding, CAPAs trending and agreed upon metrics to ensure Quality oversight.
Contributeand support the GCP audit risk assesment according to SOPs.
Ensure active contribution in the cross-functional team with procurement, business owners for GxP and Quality requirements and documented qualification of GCP service providers and review provisions in contracts/Quality agreements, as applicable
QA representative during GCP inspections global and site level, as applicable and contribute to the Inspection Readiness framework and promote continuously quality mindset across Sobi.
Authoring GCP QA related processes, review and give guidance under global umbrella.
Required:
University degree or similar in Life Sciences or related discipline
5+ years of pharmaceutical industry experience in Clinical Quality Assurance or in the operational conduct of clinical trials and the application of GCP audit and/or Quality Assurance experience.
Technical skills:
Excellent knowhow of the applicable ICH GCP guidelines, industry best practices and FDA, EMA and ROW regulatory requirements.
Quality assurance activities principles and know-how
Documented education/experience in QA systems and preferably auditing
Soft skills:
Structured with focus on results and detail oriented
Strong interpersonal skills with communicative and flexible attitude
Proactive and collaborative mindset
Strong multi-tasking abilities with high resilience at stress and adaptative skills
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 is $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 [email protected]
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