Global Quality Assurance Auditor, Pharmacovigilance
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 2d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 7d ago
The date the source published, not the day we noticed it (2026-10-27). Last seen at its source 6h ago.
We have tracked this listing since 27 Oct 2026 (6 days). The employer's own board has carried it every time we have read it, most recently 6 hours ago.
Is it remote?
Remote, Remote, Remote, Remote, Remote, Remote, Remote, Remote, Remote, Remote, Remote
That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.
Who may apply?
Not stated
The description states no restriction of its own. This is the source's own tag.
Pay
$102.3k–153.5k/yr
Read out of the job description by us, not from a structured field. Shown in the posting's own currency and period; we never convert.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Workday employer's own board first seen 6d ago · last seen 6h ago
The listing
The role will perform audits on behalf of CQA with a focus on PV. In this role insights and industry trends are to be proactively shared within the organization to ensure continued compliance and early identification of areas for continuous improvement.
This role will provide analyses of audits / trends and support in the assessment and promotion of compliance within PV QA. This role will be aware of changes to regulations, guidelines, and provide support and QA oversight for any necessary updates to operating procedures, risk assessments and change controls for process changes as well as productivity / efficiency improvement initiatives.Job Description
Roles and Responsibilities
- Support a program (plan, prepare and execute) of internal and external audits for QRA.
- Ensure all identified actions / observations are appropriate to remediate the deficiency and are completed in a timely manner and complete reviews to ensure effectivity.
- Work with the customer to undertake risk analysis of systems and processes, to propose process / functional audits.
- Support regulatory inspections and customer audits as a functional QA subject matter expert.
- Conduct trend analysis of audit and other quality related data, provide to internal / external stakeholders as agreed.
- Assure completion of vendor qualification and surveillance activities performed and documented as defined in global and functional procedures.
- Participates in the quality management system (QMS) improvements.
- Provide guidance and ensure that ‘CAPA’s are correctly set up to capture risk assessment, effective corrective and preventive actions and have the required evidence. Perform QA approvals of Quality Event records.
- Keep up to date with latest guidelines from MHRA, FDA, EMEA and other Regulatory bodies. Monitor legislation, implementing changes, and informing the company of any relevant changes.
- Provide Quality Assurance support, guidance, and management of Quality Issues, as assigned.
Required Qualifications
- Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 8 years of experience in pharmaceutical industry.)
- 6+ years of experience in the pharmaceutical industry
- Previous Auditing experience required.
- Experience interfacing with global regulatory agencies.
- Ability to comprehend and communicate key regulatory requirements and expectations
- Experience in collaboration, negotiation & conflict resolution skills
- Knowledge of GPvP, cGMP, and GDP
Desired Characteristics
- Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.
- Demonstrated experience with applying classic Quality tools
- Experience interfacing with global regulatory agencies
- Change agent with energy, passion & enthusiasm to drive change
- Demonstrated effective interpersonal, teamwork & networking skills
- Ability to influence. Determine a position and argue it effectively within the business context.
GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.
Relocation Assistance Provided: No