1,000+ matching jobs for “Audit Associate”How results work Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.
… products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Sr Associate Tax What you will do As the Sr Associate Tax, you will report to the Transfer Pricing Manager and …
Added Oct 15, 2026
We are seeking an Associate Software Engineer to support the configuration, development, integration, testing, deployment, validation, …
Added Oct 22, 2026
Pay posted by employer $64,600–$88,800
… a variety of Employee Resource Groups (ERGs) to support employees. How you will make history here... The Associate Analyst Specialist – Commercialization is responsible for supporting the successful execution of new …
Added Oct 27, 2026
Pay posted by employer $35,900–$74,800
… We Are Looking For: High School Diploma or equivalent (some CAP/CLIA laboratory locations may require an Associate Degree in laboratory science or medical laboratory technology) Proficiency with pipetting techniques and …
Added Oct 15, 2026
+2 locations
Principal Associate , Accounting At Capital One, data is at the center of everything we do. As part of our newly formed …
Added Oct 27, 2026
Role Description: The Senior Associate , Benefits supports the administration, compliance, and daily operations of the EMEA benefits programs. This …
Added Oct 15, 2026
Associate Software Engineer What you will do Let’s do this. Let’s change the world. As an Associate Software Engineer …
Added Oct 15, 2026
… activities, including license entitlement reconciliation, usage analysis, compliance reviews, publisher audit support, and risk-based remediation planning. Analyze asset utilization, lifecycle status, renewal …
Added Oct 27, 2026
In person Full time Regular Pay posted by employer $89,800–$143,700 USD
Job Summary: The Associate Manufacturing Supervisor provides direct supervision to the production personnel and assures the effective …
Added Oct 29, 2026
… Visitに関連した資料の準備を支援する場合がある 日本の要件に基づき、データベースロックの期限遵守に向けた調整を支援する場合がある シニアレベルの期待事項 （Senior Clinical Research Associate に適用） 施設レベルおよび国レベル双方において、潜在的な問題を主体的に特定・解決する Clinical Trial Managerおよび／またはLine managerと連携し、より複雑な課題の解決を支援する …
Added Oct 15, 2026
+3 locations
involves interaction with various units locally and overseas. The Senior Associate should possess the ability to learn new skills, embrace change and communicate effectively. Effective …
Added Oct 27, 2026
… and regulatory requirements. Support the Quality Compliance Supervisor in maintaining the site in a stable, audit -ready, and inspection-prepared state. Manage personal priorities and assigned compliance activities while …
Added Oct 16, 2026
Pay posted by employer $107,800–$148,200
… a variety of Employee Resource Groups (ERGs) to support employees. HOW YOU WILL MAKE HISTORY HERE As the Associate Credit Manager, you will play a critical role in protecting Campbell's financial health while enabling …
Added Oct 27, 2026
… Compliance & Safety Ensure compliance with Amgen policies, EH&S standards, statutory requirements, and audit expectations. Support internal and external audits. Maintain required documentation, SOPs, and operational …
Added Oct 15, 2026
+1 location
… time and subject to any necessary consultation processes. We are searching for the best talent for MQSA Associate Scientist, located in West Chester, PA USA or Palm Beach Gardens, FL USA. As an MQSA Associate Scientist , …
Added Oct 18, 2026
+3 locations
Senior Associate , Accounting (Hybrid) Does the idea of working with professional, highly trained accountants inspire you? …
Added Oct 27, 2026
Pay posted by employer $76,500–$87,400 per year
… business trends Accounting: Participate in the external financial reporting process, including the external audit process and OSFI reporting Prepare accurate and timely reports, schedules and documentation Perform …
Added Oct 27, 2026
+2 locations
… ● Support quarterly Earnings and reporting cycle as necessary ● Support control processes and engage with audit and compliance groups as necessary ● Support ad-hoc research projects, peer analysis, and disclosure update …
Added Oct 27, 2026
Job Description: Study Delivery Senior Associate (SDSA) Role Name: Study Delivery Senior Associate Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of …
Added Oct 15, 2026
2 postings
Role Name: Study Delivery Senior Associate ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and …
Added Oct 15, 2026
About this opportunity Original employer description Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. Our dedication to quality and safety drives everything we do, fostering a dynamic environment where your role is crucial in advancing healthcare solutions.
What You Will Achieve
In this role, you will:
Serve as a key resource within the Quality Compliance organization, supporting site inspection readiness and ensuring compliance with Pfizer and regulatory requirements. Support the Quality Compliance Supervisor in maintaining the site in a stable, audit-ready, and inspection-prepared state. Manage personal priorities and assigned compliance activities while taking accountability for delivering accurate, timely, and effective results. Support the execution of the Internal Audit Program, including self-assessments, internal audits, walkthroughs, report preparation, and follow-up of corrective and preventive actions. Contribute to maintaining the site Inspection Readiness Program and support internal audits, external inspections, customer audits, and regulatory authority inspections. Assist departments in implementing improvements resulting from audit findings, inspection observations, and compliance gap assessments. Support supplier quality management activities, including supplier qualification, maintenance of approved supplier lists, quality agreement review, and supplier audits. Prepare and monitor Quality Compliance metrics and dashboards to evaluate quality system performance and drive continuous improvement. Support implementation and continuous improvement of the site's Data Integrity Program, ensuring compliance with ALCOA+ principles and Pfizer requirements. Participate in investigations, perform root cause analyses, and support development of effective corrective and preventive actions (CAPAs). Monitor commitments, CAPAs, effectiveness checks, and quality actions to ensure timely implementation and sustainable closure. Actively support IMEx initiatives and contribute to Structured Gemba activities and quality performance reporting. Here Is What You Need (Minimum Requirements)
Bachelor's Degree (BAC+3) or Master's Degree (BAC+5) in Quality Management for Bio-industries, Pharmacy, Chemistry, Biology, Biotechnology, Engineering, or a related scientific discipline. Recent graduates and candidates with internship, apprenticeship, or initial professional experience in the pharmaceutical, biotechnology, or regulated manufacturing industry are encouraged to apply. Basic knowledge of Good Manufacturing Practices (cGMP) and pharmaceutical quality systems. Understanding of quality compliance principles, including audits, inspections, CAPA management, Change Control, and Quality Risk Management. Awareness of Data Integrity principles and regulatory expectations related to electronic records and documentation. Strong analytical and problem-solving skills with the ability to identify issues and propose practical solutions. Excellent communication and interpersonal skills. Ability to work effectively in a cross-functional team environment. Strong organizational skills and attention to detail. Ability to manage multiple priorities and work independently when required. Proficiency in Microsoft Office applications (Word, Excel, PowerPoint). Willingness to learn and develop expertise in quality compliance systems and regulatory requirements. Bonus Points If You Have (Preferred Requirements)
Internship, apprenticeship, or first professional experience in Quality Assurance, Quality Control, Quality Compliance, or pharmaceutical manufacturing. Exposure to GMP-regulated environments through academic projects, internships, or work experience. Knowledge of Data Integrity concepts and ALCOA+ principles. Familiarity with quality systems such as Deviations, CAPAs, Change Controls, Risk Management, and Document Management. Experience with electronic quality management systems such as PDOCS, QTS, SMS, Vault, TrackWise, or equivalent platforms. Participation in internal audits, inspection readiness activities, or continuous improvement projects. Knowledge of Quality Risk Management tools such as FMEA. Strong presentation, training, and facilitation skills. Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity. Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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Quality Assurance and Control
Why this result? · Employer labels Keywords also found in description
Fixed Term (Fixed Term) Full time Quality Assurance and Control
