We have other current jobs related to this field that you can find below
-
Regulatory Affairs Specialist II
2 months ago
Lake Forest, United States Source One Technical Solutions Full timeJob DescriptionJob DescriptionSource One is a consulting services company and we’re currently looking for the following individual to work as a consultant to our direct client, a global medical device company in Lake Forest, CA.Job Title: Regulatory Affairs Specialist II (Contract)Pay Rate Range: $42.86/hr - $48.57/hr (W-2)Initial Duration: 12 months with...
-
Regulatory Affairs Ops Specialist II
3 weeks ago
Round Lake, United States Experis Full timeOur client, one of the largest Healthcare companies in the U.S., is looking for a Regulatory Affairs Ops Specialist II which is Round Lake, IL. As a Regulatory Specialist you will be responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory...
-
Regulatory Affairs Operations Specialist II
5 days ago
Round Lake, Illinois, United States Experis Full timeOur client, a prominent player in the Healthcare sector, is seeking a Regulatory Affairs Operations Specialist II. In this role, you will be tasked with executing intricate global regulatory strategies, securing and upholding marketing authorizations for products, and conveying essential regulatory requirements to facilitate the licensing of...
-
Regulatory Affairs Specialist II
5 days ago
Lake Forest, Illinois, United States ICU Medical Full timePosition Overview The role involves providing essential regulatory support and direction related to the global and US registration of medical device products. This includes analyzing regulatory requirements and monitoring deliverables. Under supervision, the position aids in the implementation of global regulatory strategies and contributes to the...
-
Regulatory Specialist II
5 days ago
Lake Forest, United States Collabera Full time $33 - $36Job DescriptionJob Description· The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. · In this role you will prepare documentation for EU Technical Files and international product registrations. · This job description will be reviewed periodically and is...
-
Regulatory Specialist II
3 months ago
Lake Forest, United States Collabera Full timeJob DescriptionJob Description· The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. · In this role you will prepare documentation for EU Technical Files and international product registrations. · This job description will be reviewed periodically and is...
-
Regulatory Affairs Operations Specialist II
5 days ago
Round Lake, Illinois, United States Experis Full timePosition Overview:We are seeking a skilled Regulatory Affairs Operations Specialist II to support our healthcare initiatives. This role involves the execution of complex global regulatory strategies and the maintenance of marketing authorizations for various products.Key Responsibilities:Formulating and implementing intricate regulatory project...
-
Regulatory Affairs Specialist II
1 week ago
Lake Forest, United States Abbott Laboratories Full timeAbout AbbottDiagnostic testing is a compass, providing information that helps in the prevention, diagnosis, and treatment of a range of health conditions.Abbottâs life-changing tests and diagnostic tools give you accurate, timely information to better manage your health. Weâre empowering smarter medical and economic decision making to help...
-
Regulatory Affairs Specialist II
7 days ago
Lake Forest, United States Abbott Laboratories Full timeAbbott 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 and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.About...
-
Regulatory Affairs Specialist
2 months ago
Lake Forest, United States Astrix Full timeOur client is the world’s leading manufacturer of eye care products and medical devices! They are looking for a Regulatory Affairs Specialist to join their expanding team!Location: Lake Forest, CAPay: $40-$45/hrResponsibilities:Work with global partners and support worldwide registrations efforts.Works in close collaboration with internal customers and...
-
Regulatory Affairs Specialist
1 month ago
Lake Forest, United States Astrix Full timeOur client is the world’s leading manufacturer of eye care products and medical devices! They are looking for a Regulatory Affairs Specialist to join their expanding team!Location: Lake Forest, CAPay: $40-$45/hrResponsibilities:Work with global partners and support worldwide registrations efforts.Works in close collaboration with internal customers and...
-
Regulatory Affairs Specialist
4 weeks ago
Lake Forest, United States Astrix Inc Full timeOur client is the worlds leading manufacturer of eye care products and medical devices! They are looking for a Regulatory Affairs Specialist to join their expanding team! Location: Lake Forest, CA Pay: $40-$45/hr Responsibilities: Work with global partners and support worldwide registrations efforts. Works in close collaboration with internal customers...
-
Associate II, Regulatory Affairs
4 weeks ago
Lake Forest, United States ICU Medical Full timeDescription Position Summary Provides regulatory support and guidance associated with global and US registration of device products, including analysis of the requirements and tracking of deliverables. With oversight, supports execution of global regulatory strategies and assists in creation and maintenance of global registration dossiers. Assures full...
-
Regulatory Specialist II
1 month ago
Lake Forest, United States Randstad Life Sciences US Full timeAs a Regulatory Affairs Specialist, you are responsible for unleashing the full potential of our people and culture while simultaneously achieving timely and cost-effective manufacturing of high-quality medical devices. You are responsible for providing administrative support in ensuring compliance with all FDA and other U.S. and global regulatory...
-
Regulatory Specialist II
2 months ago
Lake Forest, United States Randstad Life Sciences US Full timeAs a Regulatory Affairs Specialist, you are responsible for unleashing the full potential of our people and culture while simultaneously achieving timely and cost-effective manufacturing of high-quality medical devices. You are responsible for providing administrative support in ensuring compliance with all FDA and other U.S. and global regulatory...
-
Regulatory Compliance Specialist
5 days ago
Lake Forest, California, United States Astrix Inc Full timeCompany Overview:Astrix Inc. is a prominent leader in the manufacturing of innovative eye care solutions and medical devices. We are currently seeking a Regulatory Affairs Specialist to enhance our dedicated team.Position Overview:As a Regulatory Affairs Specialist, you will play a crucial role in ensuring compliance with global regulations while supporting...
-
Global Regulatory Affairs Specialist
4 weeks ago
Salt Lake City, United States USANA Health Sciences Full timeWho We Are Looking For We are looking for a meticulousindividual to join USANA as a global regulatory affairs specialistto ensure compliance with domestic and international regulations across all assigned markets. In this role, you will be responsible for executing various regulatory affairs functions, maintaining the highest standards of procedural...
-
Regulatory Compliance Specialist II
5 days ago
Lake Forest, Illinois, United States ICU Medical Full timePosition Overview The role involves providing regulatory assistance and expertise related to the global and US registration of medical device products. This includes evaluating requirements and monitoring deliverables. Under supervision, the position supports the implementation of global regulatory strategies and aids in the development and upkeep of global...
-
Regulatory Affairs Associate
3 months ago
Lake Forest, United States PSG Global Solutions Full timeDescription We're looking for a Regulatory Affairs Associate , working in Biotechnology/Medical Devices industry in 100 Abbott Park Road, Lake Forest, Illinois, 60064, United States . Job description: Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental...
-
Sr Specialist, Regulatory Affairs
3 weeks ago
Round Lake, United States Baxter Full timeThis is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in...
![Randstad](https://media.trabajo.org/img/noimg.jpg)
Regulatory affairs specialist ii
2 months ago
job summary:
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you
location: Lake Forest, California
job type: Contract
salary: $40.00 - 48.57 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Work with global partners and support worldwide registrations efforts.
- Works in close collaboration with internal customers and supports multiple projects to align on regulatory strategy to achieve business objectives.
- Manages requests from regions and countries, provides responses and requested documentation (CFG's, FSC, certifications, Letter of Authorization, etc.) in a timely manner.
- Prepares supporting documentation and arrange for legalizations, as required by country regulations.
- Support communications with US and international affiliates and regulatory personnel.
- Ensures compliance with global regulatory requirements and adherence to internal policies and processes.
- Provides high quality regulatory support for assigned products/projects.
- Develops documents that are clear, concise, and complete to facilitate and maintain registration renewal, tenders, and licenses.
- Prepare, consolidate, response and follow-up on change assessments for global regulatory strategies.
- Review and approve labeling to ensure accuracy of content.
- Maintain a current knowledge of global medical device regulations pertaining to the distribution of products, which include facility registration and device listing.
- Maintain documentation and a historical record for regulatory submissions.
- Notarize regulatory registration documents as necessary. Willing to obtain notary license in California.
- Bachelor's Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6 yrs; M.S.+0 yrs)
- The ability to fluently read, write, understand, and communicate in English
- 2 Years of Relevant Experience
skills: GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Regulatory Briefing Documents, Submissions, ICH Regulations
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.