Top 15 Regulatory affairs specialist Jobs in Livermore Ca

Sr Regulatory Affairs Specialist, Global Market
Kelly Services —Sunnyvale, CA
- $47 - $51 an hour
- Full-time
- Remote
- 3 years
- Master's degree
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
4d
Regulatory Affairs Specialist
Abbott Laboratories —Pleasanton, CA
- $73,900 - $116,000 a year
- Full-time
- 18 years or older
- No experience needed
- Research
- Health insurance
- Tuition reimbursement
Regulatory Affairs Specialist II
The Clorox Company —Pleasanton, CA
- $75,800 - $170,100 a year
- Full-time
- Bachelor of Science
- Office
- Bachelor's degree
- Health insurance
- Adoption assistance
Specialist, Regulatory Affairs Operations Publishing
Taiho Oncology, Inc. —Pleasanton, CA
- $86,700 - $102,000 a year
- Full-time
- Hybrid work
- Mid-level
- Organizational skills
- Fair chance
- Paid time off
- Parental leave
Quick Apply
Senior Regulatory Affairs Specialist – Heart Failure (on-site)
Abbott Laboratories —Pleasanton, CA
- $90,000 - $180,000 a year
- Full-time
- Word processing
- Writing skills
- Office
- Health insurance
- Tuition reimbursement
Regulatory Affairs Specialist II
Thermo Fisher Scientific —Fremont, CA
- $72,000 - $96,000 a year
- Full-time
- Background check
- No experience needed
- Mid-level
- Commuter assistance
- Paid parental leave
Regulatory Affairs Specialist III
Thermo Fisher Scientific —Fremont, CA
- $90,900 - $121,200 a year
- Full-time
- Background check
- Pass drug screening
- Office
- Commuter assistance
- Paid parental leave
Senior Regulatory Affairs Specialist
Abbott Laboratories —Santa Clara, CA
- $90,000 - $180,000 a year
- Full-time
- 18 years or older
- 3 years
- Master's degree
- Health insurance
- Tuition reimbursement
Staff Regulatory Affairs Specialist
PROCEPT BioRobotics Corporation —San Jose, CA
- Full-time
- 6 years
- Bachelor of Science
- Analysis skills
- Opportunities for advancement
Quick Apply
Regulatory Affairs Specialist - Vascular (on-site)
Abbott Laboratories —Santa Clara, CA
- $81,500 - $141,300 a year
- Full-time
- Mid-level
- Office
- Master's degree
- Health insurance
- Tuition reimbursement
Principal Regulatory Affairs Specialist – Vascular (on-site)
Abbott Laboratories —Santa Clara, CA
- $100,000 - $200,000 a year
- Full-time
- 6 years
- Bachelor's degree
- Product management
- Health insurance
- Tuition reimbursement
Senior Regulatory Affairs Specialist – Vascular (on-site)
Abbott Laboratories —Santa Clara, CA
- $90,000 - $180,000 a year
- Full-time
- Office
- 3 years
- Master's degree
- Health insurance
- Tuition reimbursement
Senior Regulatory Affairs Specialist
PROCEPT BioRobotics Corporation —San Jose, CA
- Full-time
- Bachelor of Science
- Analysis skills
- Bachelor's degree
- Opportunities for advancement
Quick Apply
11d
Principal Regulatory Affairs Specialist
PROCEPT BioRobotics Corporation —San Jose, CA
- Full-time
- Microsoft Excel
- 11+ years
- Research
- Opportunities for advancement
Quick Apply
11d

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Sr Regulatory Affairs Specialist, Global Market
Kelly Services —Sunnyvale, CA
Ensure proper filing and organization of all documents and correspondence supporting market protection regulatory assessments. This is a remote position.
$47 - $51 an hour
Quick Apply
4d
Regulatory Affairs Specialist
Abbott Laboratories —Pleasanton, CA
Interacts with regulatory affairs team members and other cross functional team members for regulatory submissions, product licensing and relevant documentation.
$73,900 - $116,000 a year

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Sr Regulatory Affairs Specialist, Global Market

Kelly Services -
Sunnyvale, CA

Quick Apply

Job Details

Full-time
$47 - $51 an hour
4 days ago

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Vision insurance
Retirement plan
Paid sick time

Qualifications

Quality management standards in production
ISO standards
Biomedical regulatory compliance

Full Job Description

Sr Regulatory Affairs Specialist, Global Market Protection
Location: Remote
Shift: M-F, standard working hours
Pay: $47/hr-$51/hr
1 year contract role

Overview:
The Regulatory Affairs Senior Specialist is responsible for serving as the RA lead on product lifecycle management project teams. This role includes completing regulatory reporting assessments for anticipated manufacturing, facility, product, and packaging changes to global regulatory agencies. The position offers the opportunity to advise project teams on regulatory impacts, devise compliance strategies, and liaise with regulatory bodies during audits. This is a remote position.

Responsibilities:

Serve as the lead on product lifecycle management project teams, supporting cross-functional stakeholders in reporting assessments for product and facility changes.
Act as the lead for QMS/Compliance activities, such as audits, Post Market Surveillance, Nonconformances (NC), Corrective and Preventative Actions (CAPA), Field Actions, and complaints.
Collaborate cross-functionally to understand changes, impacts, and implementation requirements in global regions and with the WHO to meet business priorities.
Identify project deliverables and contribute to developing project schedules.
Ensure proper filing and organization of all documents and correspondence supporting market protection regulatory assessments.
Work independently with minimal guidance.
Act as a resource for less experienced colleagues.
Solve complex problems using new perspectives and existing solutions, exercising judgment based on multiple information sources and maintaining a continuous improvement mindset.
Review and approve change orders for anticipated manufacturing, facility, product, and packaging changes in the Product Lifecycle Management Software.
Serve as a business partner for manufacturing, operations, and supply chain to advise on the regulatory impact of product and facility changes.

Requirements:

Bachelor’s degree with 5+ years of related work experience OR Master’s degree with 3+ years of related work experience.
Understanding of Regulatory Affairs concepts and regulations/guidelines governing the development of IVD diagnostic products.
Knowledge of US-IVD, CE-IVDD, CE-IVDR governance for IVD diagnostic products.
Familiarity with QMS, ISO standards, including ISO 13485.

Preferred Requirements:

Prior knowledge of Agile PLM system, SAP ERP system, and Salesforce-based applications.
Experience in project management.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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Refine Your Search

regulatory affairs specialist jobs in livermore ca

Sr Regulatory Affairs Specialist, Global Market

Regulatory Affairs Specialist

Regulatory Affairs Specialist II

Specialist, Regulatory Affairs Operations Publishing

Senior Regulatory Affairs Specialist – Heart Failure (on-site)

Regulatory Affairs Specialist II

Regulatory Affairs Specialist III

Senior Regulatory Affairs Specialist

Staff Regulatory Affairs Specialist

Regulatory Affairs Specialist - Vascular (on-site)

Principal Regulatory Affairs Specialist – Vascular (on-site)

Senior Regulatory Affairs Specialist – Vascular (on-site)

Senior Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

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