Talent.com

Regulatory affairs manager Jobs in Fremont, CA

Last updated: 12 hours ago
  • Promoted
Manager, Regulatory Affairs- Body Contouring

Manager, Regulatory Affairs- Body Contouring

Orange County Regulatory Affairs Discussion Group (OCRA)Pleasanton, CA, US
Full-time
Manager, Regulatory Affairs- Body Contouring.Manager, Regulatory Affairs- Body Contouring.Submissions, development and lifecycle maintenance. Plans and prepares complex regulatory documents for US a...Show moreLast updated: 14 days ago
  • Promoted
Regulatory Affairs Specialist

Regulatory Affairs Specialist

ACE PartnersFremont, CA, United States
$100,000.00–$120,000.00 yearly
Full-time
Position : Regulatory Affairs Specialist - $100k - $120k.My client, an innovative company that specializes in developing specialty surgical solutions. They’ve collaborated with healthcare professiona...Show moreLast updated: 6 days ago
  • Promoted
Manager / Director Regulatory Affairs - Pleasanton, CA

Manager / Director Regulatory Affairs - Pleasanton, CA

Tbwa Chiat / Day IncPleasanton, CA, US
$150,000.00–$220,000.00 yearly
Full-time
Manager / Director Regulatory Affairs - Pleasanton, CA.The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condi...Show moreLast updated: 14 days ago
  • Promoted
Regulatory Affairs Manager - Heart Failure (on-site)

Regulatory Affairs Manager - Heart Failure (on-site)

Abbott LaboratoriesPleasanton, CA, US
Full-time
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 10 days ago
  • Promoted
Senior Manager Regulatory Affairs CMC

Senior Manager Regulatory Affairs CMC

VirtualVocationsFremont, California, United States
Full-time
A company is looking for a Senior Manager / Associate Director in Regulatory Affairs CMC.Key ResponsibilitiesContribute regulatory CMC expertise to product development and registration for small mole...Show moreLast updated: 2 days ago
  • Promoted
Regulatory Affairs Manager - Heart Failure (on-site)

Regulatory Affairs Manager - Heart Failure (on-site)

AbbottPleasanton, CA, United States
$112,000.00–$224,000.00 yearly
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 18 days ago
  • Promoted
Manager / Director Regulatory Affairs - Pleasanton, CA

Manager / Director Regulatory Affairs - Pleasanton, CA

CalyxoPleasanton, CA, US
$150,000.00–$220,000.00 yearly
Full-time
The company was founded in 2016 to address the profound need for improved kidney stone treatment.Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resourc...Show moreLast updated: 26 days ago
Senior Manager, Regulatory Affairs

Senior Manager, Regulatory Affairs

Innova SolutionsRemote, California, United States
$70.00–$75.00 hourly
Remote
Full-time
Innova Solutions has a client that is immediately hiring for a.Position type : Full time Contract.Senior Manager, Regulatory Affairs. The Senior Manager supports Regulatory leadership in the developm...Show moreLast updated: 17 days ago
  • Promoted
Director of Regulatory Affairs

Director of Regulatory Affairs

Benitec Biopharma Inc. (NASDAQ; BNTC)Hayward, CA, United States
Full-time
Our commitment to patients drives our passion for excellence and innovation in drug development.As the Director of Regulatory Affairs, you will lead and oversee the regulatory strategy and executio...Show moreLast updated: 11 days ago
  • Promoted
Director of Regulatory Affairs

Director of Regulatory Affairs

MeetFremont, CA, United States
Full-time
Hybrid Opportunity - 2-3x per week onsite in South San Francisco, CA.Meet has partnered with a clinical-stage, pre-IPO biotech focused in treatments for rare hematology / oncology indications.They ar...Show moreLast updated: 11 days ago
  • Promoted
Associate Director, Regulatory Affairs :

Associate Director, Regulatory Affairs :

Ascendis Pharma A / SPalo Alto, CA, United States
$190,000.00–$215,000.00 yearly
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease an...Show moreLast updated: 16 days ago
  • Promoted
Manager, Regulatory Affairs- Body Contouring

Manager, Regulatory Affairs- Body Contouring

AbbViePleasanton, California, United States
$103,500.00–$197,000.00 yearly
Full-time
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable i...Show moreLast updated: 30+ days ago
Senior Manager, Regulatory Affairs

Senior Manager, Regulatory Affairs

R&D PartnersCalifornia, CA
R&D Partners is seeking to hire a.Senior Manager, Regulatory Affairs III.Your main responsibilities as a.Senior Manager, Regulatory Affairs III : . Responsible for preparation of the Quality sections ...Show moreLast updated: 30+ days ago
  • Promoted
Associate Director, Regulatory Affairs :

Associate Director, Regulatory Affairs :

Ascendis PharmaPalo Alto, CA, United States
$190,000.00–$215,000.00 yearly
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease an...Show moreLast updated: 11 days ago
  • New!
Regulatory Affairs Specialist

Regulatory Affairs Specialist

cGxPServeCA, United States
Full-time
Quick Apply
MessageBody"> Responsibilities : Prepare drug listings and lot distribution reports for biologics.Compile documentation and send certificate of phar...Show moreLast updated: 12 hours ago
  • Promoted
Digital Tech Manager - Regulatory Affairs

Digital Tech Manager - Regulatory Affairs

The Clorox CompanyPleasanton, CA, US
$101,600.00–$200,100.00 yearly
Full-time
Clorox is the place that’s committed to growth – for our people and our brands.Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can ma...Show moreLast updated: 14 days ago
  • Promoted
Regulatory Affairs Manager

Regulatory Affairs Manager

BioTalentFremont, CA, United States
Full-time
Regulatory Affairs Manager – Medical Devices.Lead regulatory strategy and submissions for medical device products, including FDA 510(k), Q-subs, and international market approvals.Oversee regulator...Show moreLast updated: 11 days ago
Manager, Regulatory Affairs

Manager, Regulatory Affairs

Thermo Fisher ScientificFremont, California, United States of America
Full-time
Lead a team to contribute in establishing strategy for worldwide product approval submission activities, directly responsible for submission activities and for ensuring regulatory compliance.Implem...Show moreLast updated: 30+ days ago
Regulatory Affairs

Regulatory Affairs

The Judge GroupPalo Alto, CA
$68.00 hourly
Our client is currently seeking a Regulatory Affairs for a 12 month + contract.Hybrid position, 2 days in office (Palo Alto, CA). Position Description : •Perform the coordination and preparation of r...Show moreLast updated: 30+ days ago
  • Promoted
Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Accordance Search GroupPleasanton, CA, United States
Full-time
Principal Regulatory Affairs Specialist.As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient a...Show moreLast updated: 11 days ago
Manager, Regulatory Affairs- Body Contouring

Manager, Regulatory Affairs- Body Contouring

Orange County Regulatory Affairs Discussion Group (OCRA)Pleasanton, CA, US
14 days ago
Job type
  • Full-time
Job description

Manager, Regulatory Affairs- Body Contouring

Company : AbbVie

Position : Manager, Regulatory Affairs- Body Contouring

Location : Pleasanton, CA

Posted : January 24, 2025

Pleasanton, CA

Full-time

Salary Min : 103500

Salary Max : 197000

Company Description

Job Description

  • Submissions, development and lifecycle maintenance
  • Plans and prepares complex regulatory documents for US and ROW product approvals with minimum supervision.
  • Resolves submission problem areas with team.
  • Prepares clear and accurate internal and external complex administrative and scientific documents, under minimal supervision.
  • Prepares complex expository and technical documents, logically constructed and comprehensive in content.
  • Prepares documentation that is complete, accurate, and on time.
  • Plans and implements regulatory activities that support lifecycle management.
  • Reviews labeling and packaging components to ensure accuracy and compliance with government regulations. Submits product labeling in compliance with legal / regulatory requirements and communicates planned / approved changes with operations, commercial, medical affairs and marketing.
  • Advisory Responsibilities
  • Participates in global teams and provides regulatory strategy and guidance to global product development teams.
  • Under minimal supervision develops US regulatory filing strategy. Provides regulatory strategy and guidance to global teams. Makes recommendations to shape the global strategy in line with regional / commercial objectives.
  • Critically reviews complex reports, validations, etc. for scientific merit and regulatory appropriateness. Works collaboratively with cross-functional team to resolve project issues.
  • Has recognized regulatory expertise and extensive knowledge of regulatory requirements and regulations with ability to strategically interpret and communicate requirements.
  • Ensures planned device development activities comply with US and global regulatory guidelines, and, in cases where they do not, provide a critical analysis of the risks and issues.
  • Ensures that teams and functional groups are provided with clear, constructive regulatory advice and intelligence to assist planning and issue resolution during product development and registration.
  • Communications and Business Support :
  • Maintains professional relationships within the regulatory groups and with functional areas outside regulatory.
  • Conveys information on team timelines and status to supervisor.
  • Delivers presentations within the Company, as required.
  • Establishes relationships with US colleagues as well as global regulatory team to ensure local RA activities are in line with global business priorities.
  • Performs peer review of complex regulatory documents.
  • Provides leadership and development support to the Regulatory team.
  • As appropriate, supervises and ensures training and development for Regulatory staff to ensure execution of all duties in a timely and efficient manner.
  • Process and Organizational Effectiveness
  • Take personal responsibility for the Notification of Regulatory activities and related database entry / data accuracy for allocated projects.
  • Maintains a performance.
  • Ensure roles and responsibilities for external services within a project are clearly defined and documented.
  • Proactively resolve issues related to outsourced activities.
  • Updates and maintains appropriate SOPs for the departments.

Qualifications

  • BS or BA in engineering, biology or other health sciences; plus five-year experience in regulatory affairs.
  • At least three-year experience working in a medical device manufacturing company, preferably with capital medical equipment, highly desired.
  • Knowledge of FDA QSR, ISO 13485 and other regulations / standards.
  • Ability to focus on and achieve scheduled milestones, including contingency planning.
  • Strong team-working and communications skills. A drive to get the job done in the face of obstacles and time constraints, and a willingness to jump in wherever needed.
  • Competent using office software including MS Word, Excel, PowerPoint, and Outlook.
  • This position is based in Pleasanton, CA.

    ADDITIONAL REQUIREMENTS :

  • Domestic travel up to 15%.
  • Additional Information

    Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law :

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical / dental / vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.
  • This job is eligible to participate in our long-term incentive programs.
  • Note : No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

    AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

    US & Puerto Rico applicants seeking a reasonable accommodation.

    J-18808-Ljbffr