Senior Regulatory Affairs Manager, Chemistry Manufacturing and Controls
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 just now — 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 23h ago
The date the source published, not the day we noticed it (2026-10-12). Last seen at its source just now.
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
$106.4k–159.6k/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 just now · last seen just now
The listing
GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.Job Description
Key Responsibilities include
- To provide CMC related strategic regulatory input for the assigned projects/products.
- Build, or provide input to, submission strategy documents by defining variation type, data required to support submission, and submission documents required for the submission package. Review and approve published output.
- In conjunction with the Global Regulatory Lead (GRL), guide the project team in the project planning phase so that the correct data (and level of detail) to suit the needs of all markets is collected and submitted.
- Review and, if necessary, write and edit individual CMC submission documents/CMC dossier sections to support regulatory submissions.
- Maintain registration tracking information and assist in the development of good document management practice standards.
- Work closely with global RA and, regional RA’s to address questions from regulatory authorities.
- In support of key brand CMC variations, proactively provide CMC related regulatory advice and assessment of impact to product dossiers. Advise project teams accordingly.
- To support QA during audits and inspections as required.
- To keep oneself updated on CMC related guidelines.
Qualifications/Requirements
- Bachelor's Degree and 6+ years of experience.
- Experience in a diagnostic, pharmaceutical, or medical device industry.
- Ability to prioritize, plan & evaluate deliverables to established strategic goals.
- Demonstrated experience of operating in a highly-regulated environment. Capable of applying analytical skills in a CMC regulatory environment.
- Demonstrated knowledge & experience in scientifically related field e.g. pharmaceutical sciences, chemistry and analytical sciences.
- Experience in electronic document management and Quality management systems.
- Knowledge of international CMC regulatory requirements.
Desired Characteristics
- Master's Degree
- Experience in pharmaceutical CMC regulatory or QA environment particularly with experience with injectable diagnostic or pharmaceutical products.
- Has experience working within a matrix organization and has strong interpersonal and influencing skills to work across disciplines. Has the capability to influence managers and help drive decisions at a project level.
- Experience with Veeva RIM or other registration tracking tools.
- Demonstrated experience of prioritizing conflicting demands from multiple business entities in an extremely fast paced environment.
- Strong problem solving and negotiation skills.
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