1,000+ matching jobs for “Audit Associate”

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Amgen

Senior Associate Software Engineer Salesforce

India - Hyderabad

Full time
Regular

Job Posting Title: Senior Associate Software Engineer Salesforce Workday Job Profile: Senior Associate Software Engineer Department Name: …

Added Oct 15, 2026

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Abbott Laboratories

Associate Director, Test Engineering

Alameda, California, United States

Pay posted by employer$148,700–$297,300

… best place to work for diversity, working mothers, female executives, and scientists. THE OPPORTUNITY This Associate Director, Test Engineering position can work out of Alameda, CA location. We are looking for a Director of …

Added Oct 16, 2026

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Analog Devices

Associate Analyst, Finance Planning

Limerick, Munster, Ireland

… allocation and claim calculations. Support eternal advisors and scope out model for apportionment Support audit readiness activities. Identify opportunities to improve process Implementation of systems and tools to …

Added Nov 3, 2026

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Northern Trust

Senior Associate, Security Development & Automation

Pune, Maharashtra, India

… of enterprise AI platforms. • Ability to deliver in a regulated environment with strong attention to audit-ready evidence, access controls, change management, testability, resiliency and production support. Nice to …

Added Oct 31, 2026

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Hartford Insurance Group

Associate, Finance Leadership Development Program

Hartford, Connecticut, United States

Hybrid
Regular

Pay posted by employer$66,400–$99,600

Associate, Finance LDP - FF08EE We’re determined to make a difference and are proud to be an insurance company that …

Added Nov 3, 2026

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Amgen

Senior Associate — Incentive Compensation Administration

India - Hyderabad

Full time
Regular

… your career. What you will do Let’s do this. Let’s change the world. In this vital role, the Senior Associate, Incentive Compensation Administration will independently manage the accurate and timely administration of …

Added Oct 15, 2026

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Amgen

Associate, Medicaid – Contracts & Pricing Execution (AIN)

India - Hyderabad

Full time
Regular

Associate, Medicaid – Contracts & Pricing Execution (AIN) Join Amgen’s Mission of Serving Patients At Amgen, if you …

Added Oct 15, 2026

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Ameriprise Financial

Operation Risk Management Associate

Gurugram, Haryana, India

Hybrid
Full time
Permanent

… and report them through ORM route. Handle Operational Risk Management ad-hoc requests related to audit and other regulatory requirements. Required Qualifications 1-3 years of relevant experience with master …

Added Nov 3, 2026

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Amgen

Associate - IC Plan Design

India - Hyderabad

Full time
Regular

… and Documentation Maintain documentation of IC plan rules, calculations, exceptions, and approvals for audit readiness. Track IC plan change requests and rationale over time. What We Expect Of You We are all …

Added Oct 15, 2026

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Amgen

Associate, Chargebacks – Contracts & Pricing Execution (AIN)

India - Hyderabad

Full time
Regular

Associate, Chargebacks – Contracts & Pricing Execution (AIN) Join Amgen’s Mission of Serving Patients At Amgen, if …

Added Oct 15, 2026

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Labcorp Holdings

Sample Handling Associate I - LPS

Singapore, Singapore

Full time
Regular

… contamination control requirements when handling biological and radioligand specimens. Maintain accurate audit trails, training records, and required documentation. Perform other duties as assigned. Minimum …

Added Oct 16, 2026

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Labcorp Holdings

Sample Handling Associate I

Bengaluru, India

Full time
Regular

… training Additional Responsibilities: Ensure received batches are timely processed. Generate an appropriate audit trail of all activities. Perform On-call and after-hours duties as needed. Ensure concerned SOPs are timely …

Added Oct 16, 2026

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Abbott Laboratories

Clinical Research Associate I

Alameda, California, United States

Pay posted by employer$73,900–$116,000

Clinical Research Associate I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your …

Added Oct 25, 2026

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Merck (MSD)

Associate Specialist, Global Fixed Asset

Petaling Jaya, Selangor, Malaysia

… financial services and processes across our company's business divisions and markets for the 3 regions. The Associate Specialist, Global Fixed Asset COE will be responsible for ensuring that the transactions of all the …

Added Oct 16, 2026

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Amgen

Associate Director, Development Analytical Reporting

India - Hyderabad

Full time
Regular

Associate Director, Analytical Reporting Department Name: Global Development Operations - Data Management Role GCF: …

Added Oct 15, 2026

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Merck (MSD)

Associate Specialist – Accounting to Reporting (AtR)

Petaling Jaya, Selangor, Malaysia

Associate Specialist – Accounting to Reporting (AtR) Our company is a global health care leader with a diversified …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate I/Clinical Research Associate II - Central Poland

Remote, Poland

Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Capital One Financial

Sr. Risk Associate, Commercial Bank

McLean, Virginia, United States +2 locations

… mitigate, and monitor compliance and operational controls. As a member of the Controls Team, the Sr. Risk Associate will be responsible for working with designated Commercial Bank business teams to uncover opportunities to …

Added Oct 27, 2026

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Pfizer

Supply Operations Quality Senior Associate

Viet Nam - Ho Chi Minh

Full time
Regular

The SOQ Senior Associate will be responsible for supporting, maintaining, and implementing the Quality Management System (QMS) at …

Added Oct 16, 2026

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Amgen

Senior Associate, LCM Execution

India - Hyderabad 2 postings

… timely resolution with key stakeholders. Ensure accurate project documentation, execution records and audit readiness. Cross-Functional Collaboration Partner with Product Lifecycle Teams (PLTs), Regional Operations …

Added Nov 5, 2026

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Pfizer

Supply Operations Quality Senior Associate

Viet Nam - Ho Chi Minh

Full time
Regular

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About this opportunity

Original employer description

The SOQ Senior Associate will be responsible for supporting, maintaining, and implementing the Quality Management System (QMS) at the Pfizer Country Offices (PCOs) to ensure compliance with both Pfizer and Regulatory Authority expectations.

The SOQ Senior Associate will work closely with relevant local stakeholders, such as Global Regulatory Sciences (GRS), Global Supply Chain (GSC), Medical, and PGS sites or ESOQ to ensure that the appropriate quality standards and systems are implemented and maintained for the product supply operation of the Pfizer Vietnam business.

The SOQ Senior Associate is appointed as the Chief Pharmacist or to manage delegated duties of Chief Pharmacist for Vietnam Good Storage Practice License

Assists with the timely implementation of applicable quality management systems (SOPs) within the PCO.
Assists with ensuring initial and continuous training programs are implemented and maintained for all relevant PCO colleagues.
Assists planned, permanent & temporary changes of GMP/GSP related activities & systems are managed & documented appropriately. Ensures change actions are completed as per agreed timelines.
Collects key quality performance indicators, evaluates and highlights any significant trends and identifies actions.
Assists in the monitoring of Key Performance Indicators (KPIs) of the QMS, evaluate and highlight significant trends, and identify actions. Leads and/or participates in Quality Review Meetings as required.
Provides support in the preparation and coordination of any Health Authority (HA) inspection and/or internal Pfizer audits of GMP/GSP activities in the PCO.
Work with local cross functional team to define appropriate action plans to address the inspection/audit observation and tracks action implementation within the agreed timelines.
Participates in the self-inspection program as an auditor and/or auditee, as required.
Participates in the Quality Risk Management program for the consistent application, documentation and communication of risks to product quality/patient safety in support of GxP activities under the remit of SOQ.
Assists in the local release process of Products under the PCOs distribution licence, as required
Supports the coordination of all Product repackaging and/or relabelling activities in the PCO and at the third-party packaging site. Review and approve documentation related to the repackaging and/or relabelling of Pfizer Product, as required.
Assists in Actions Quarantine Alert Notifications promptly, as needed.
Ensures quarantine shipments are managed compliantly according to procedures, as required.
Provides support for any market action operation in the PCO, as required.
Complaint Handling – Perform Intake and Triage, assist in the issuance of correspondence letter as required. Acts as a contact point for Regulatory Agency/reporter in the PCO, as required.
Participate in deviation investigations using appropriate tools and works with cross-functional teams to implement CAPAs.
Notify Management of significant concerns or deviations within the QMS which have the potential to impact product, regardless of release status. Where issues originate in the PCO, assist with the preparation of QRT meetings, where required. Assist with the implementation of local actions identified during QRT.
Assists in the Management of relevant corrective and preventative actions (CAPA)

Execute tasks associated with the management of GxP Suppliers including qualification, quality oversight in accordance with internal and regulatory requirements for GxP activities.
Assists with ensuring appropriate customer screening processes are in place to align with Pfizer and local regulations, as required.
Assist with the coordination of RQA audits at the Supplier.

Assists in the development and execution of objectives / projects consistent with SOQ Purpose Blueprint.
Assists in the development and Maintenance of Quality culture, within the team and organisation.

JOB REQUIREMENTS

A minimum Tertiary Education in Pharmacy
A minimum of 5 years in the pharmaceutical industry in a quality role
Demonstrated ability to influence, when necessary, particularly with stakeholders and external parties.
Experience in Vietnam Pharmacy Law 2016, GMP, GDP, Vietnam GSP and QMS.
Technical writing and reporting
Registered Pharmacist with Vietnam Pharmacy Board with a valid pharmacy practice certificate (“chứng chỉ hành nghề dược”) and the scope of export and import, storage service of pharmaceuticals and/or vaccines
Fluent in English (written & verbal) – business proficiency
Fluent in Vietnam (written & verbal) – business proficiency
Experience in Quality administered systems.
Excellent computer system skills – Word and Excel essential.
Experience with electronic documentation control systems advantageous.
Previous use of Trackwise®, eQMS beneficial.

Work Location Assignment: Hybrid

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Important Notice for Applicants
At Pfizer, we value your privacy and security. Please note:

All job applications must be submitted only through our official channels:
Pfizer Careers Website: Careers | Pfizer
Verified LinkedIn page: https://www.linkedin.com/
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If you receive suspicious messages or job offers outside these channels, please report them immediately to [[email protected]]

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

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Keywords also found in description

Full time
Quality Assurance and Control
Regular

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