Assoc Regulatory Affairs Spec
Collabera
About Collabera Collabera is the largest minority‑owned Information Technology (IT) staffing firm in the U.S., with more than $525 million in sales revenue and a global presence that represents approximately 10,000 professionals across North America (U.S., Canada), Asia Pacific (India, Philippines, Singapore, Malaysia) and the United Kingdom. We support our clients with a strong recruitment model and a sincere commitment to their success, which is why more than 75% of our clients rank us amongst their top three staffing suppliers. Not only are we committed to meeting and exceeding our customer’s needs, but we are committed to our employees’ satisfaction as well. We believe our employees are the cornerstone of our success and we make every effort to ensure their satisfaction throughout their tenure with Collabera. As a result of these efforts, we have been recognized by Staffing Industry Analysts (SIA) as the “Best Staffing Firm to Work For” for four consecutive years since 2012. With over forty offices globally and a presence in seven countries, Collabera provides staff augmentation, managed services and direct placement services to Global 2000 Corporations. Collabera is ranked amongst the top 10 IT staffing firms in the U.S., and for the past 24 years we have continued to grow rapidly year after year. For consultants and employees, Collabera offers an enriching experience that promotes career growth and lifelong learning. Visit to learn more about our latest job openings. Awards and Recognitions Best Staffing Firm to Work For (2015, 2014, 2013, 2012) Largest U.S. Staffing Firms (2015, 2014, 2013) Largest Minority Owned IT Staffing Firm in the US Job Description Looking for someone who has international background with good regulatory affairs knowledge, very detail oriented and capable of working under pressure. Position summary: The Regulatory Affairs Admin/Coordinator is a key position in regulatory affairs as this individual will provide the necessary administrative and coordination support to the Global Regulatory Affairs department at Covidien Neurovascular. The responsibilities of this role cannot be emphasized strongly enough as the support required will directly influence the successful preparation, submission, receipt and maintenance of all Covidien Neurovascular product registrations and regulatory intelligence globally. The Regulatory Affairs Admin/Coordinator will be the face and voice of the Regulatory Affairs department to internal as well as external customers. As such, this role requires an individual with demonstrated skills in communication and professionalism. Principal accountabilities: Manage regulatory global dashboard Regulatory Document Legalization Acquire necessary Notarizations and Authentications needed for regulatory filings from appropriate US and foreign government Offices Regulatory Submission Assembly/Shipping Coordinate regulatory submission publishing for efficiency Assist team with electronic and hard‑copy submission compilation, assembly and shipping Shipping Release Authorization (SRA/GTS) Coordinate and manage SRA process from regulatory perspective Coordinate timely opening and closing of GTS regulatory tables and ensure compliance to approval evidence Qualifications Experience: Knowledge and understanding global regulations and requirements for medical devices, desired. Proficiency in use of Microsoft Office Suite computer software Proficiency in the use of Adobe Acrobat Professional computer software Strong written and verbal communication skills, including ability to communicate with individuals who do not speak English as their primary language High attention to detail and accuracy Skill in obtaining facts that assure information is complete and accurate. Ability to plan and prioritize work and balance multiple projects Skill in the completion and follow through of projects Ability to maintain satisfactory working relationships Notary Public or desire to obtain Education: Experience in Regulatory Affairs preferred. Additional Information To know more about this position, please contact: #J-18808-Ljbffr
- ...Job Title: Global Regulatory Affairs Principal Specialist Location: Fort Worth, TX, Johns Creek, GA, or Lake Forest, CA Summary of Position... ...of directly related experience (or high school +13 yrs; ~ Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs) ~ The ability to fluently...SuggestedVisa sponsorshipRelocation package
- ...provide sponsorship at this moment". Job Title: Principle Regulatory Affairs Strategy Associate Location: Lake Forest, CA - ONSITE... ...years of directly related experience (or high school +15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs) ~ The ability to fluently read...SuggestedContract workLocal area
- ...ready to join us? This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance... ...years of directly related experience (or high school +15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs) ~ The ability to fluently read...SuggestedHourly payLocal areaRelocation packageFlexible hours
- ...This role is part of Alcon's Quality & Regulatory Affairs organization, which ensures our products comply with global, regional, and internal... ...of directly related experience (or high school +15 yrs.; Assoc.+11 yrs.; M.S.+4 yrs.; PhD+3 yrs.) ~ The ability to fluently...SuggestedTemporary workRelocation packageFlexible hours
- ...metrics to project current and future business needs. Align and maintain communication channels with Medical, Marketing, Regulatory, Legal, and Public Affairs; identify process/policy improvements and lead initiatives. Assist with departmental budget management; identify and...SuggestedTemporary work
- ...Regulatory Affairs Manager Santa Ana, CA Part-time Employee Salary depending on experience. About Huisong Founded in 1998, Huisong Pharmaceuticals specializes in the R&D and manufacturing of premium-quality natural ingredients for world-leading companies in the pharmaceutical...Part timeFixed term contract
$28 - $33 per hour
...organizational skills, attention to detail, and familiarity with regulatory and payer specificrequirements. This role is essential for... ...Provide regular status reports to the Director of Regulatory Affairs on licensing and payer credentialing, and contracting progress...Hourly payCasual workWork at officeMonday to Friday$141.5k - $268.5k
...Associate Director, Regulatory Affairs US Advertising and Promotion 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...Temporary workWork at officeImmediate startRemote workMonday to Friday- ...Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S... ...of international product registrations and related regulatory affairs activities, including execution of procedures and systems...Work at office
- ...medical technology or similar. ~5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the... ...and written communication skills. ~ Thorough knowledge of policies, practices and procedures related to Regulatory Affairs....
$80k - $100k
...The Regulatory Affairs Specialist is responsible for investigating and supporting regulatory policy necessary to obtain regulatory approval for the organization's products. Work with RA Leadership and other members of the RA team to set strategy for regulatory approval...Full timeWork at officeLocal areaMonday to FridayAfternoon shift- ...Regulatory Affairs Specialist (Labeling) Contract through May 2026 – NO C2C, W2 ONLY. A leading medical device team is seeking a Regulatory Affairs Specialist to support global and EU labeling compliance across a wide range of projects. What You’ll Do: Own regulatory...Contract work
- ...Support the Senior Director in developing and executing regional regulatory strategies for QOL initiatives within specific regions.... ...degree preferred. 5+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with a focus on...
- ...visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary,...Temporary workLocal area
$80k - $100k
...A leading medical technology company is seeking a Regulatory Affairs Specialist in Irvine, California. The role involves preparing regulatory submissions, supporting product approvals, and maintaining compliance documentation. Candidates should have a Bachelor's degree...Casual workMonday to FridayAfternoon shift- ...for Clinical Research (SCRC), the Supervisor, Study Startup and Regulatory is responsible for all startup and regulatory matters in... ...primary responsibility for overseeing startup and regulatory affairs coordinators who are responsible for creating, negotiating, and...
- ...systematic enhancements are implemented while adhering to all regulatory requirements and timelines. Turn complex compliance requirements... ...international / global logistics support services, regulatory affairs, government relations and distribution operations 3+ years of...
$90k - $140k
...Regulatory Strategy Lead Execute on regulatory strategy of De Novo submissions for AI/ML-based Software as a Medical Device (SaMD) product, including AidaBreast. Serve as regulatory lead for novel oncology diagnostic technologies integrating genomic and proteomic...$160.5k - $305k
...Director Regulatory Affairs, Device 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 impact on people's lives across...Work at officeImmediate startRemote workWorldwideMonday to Friday$85k - $95k
...powersports industry across all 50 states. This role focuses on regulatory compliance and customer protection, leading testing to ensure... .... Irvine, CA $72,000.00-$102,000.00 1 week ago Regulatory Affairs Specialist- APAC/LATAM Irvine, CA $230,000.00-$250,000.00 2 weeks...16 hoursFull timeWork at officeRemote work$165k - $220k
...health, and we believe we are well positioned to continue leading the advancement of eye health in the future. The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product...Temporary workWork visa- ...A staffing and recruiting firm is seeking a Regulatory Affairs Specialist to plan and implement regulatory submissions. Responsibilities include demonstrating knowledge of healthcare regulations, preparing submissions, and interacting with regulatory bodies to facilitate...Contract work
- ...Responsibilities: Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for non-medical devices, and medical devices. Assess the acceptability...
$84.72k - $120k
...registrations and submissions (510(k), PMA) to FDA and other regulatory bodies. Maintains company registrations and device listings... ...ISO 13485 Standards. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good...- ...A leading eye care company in Lake Forest, California, is seeking a Director of Regulatory Affairs Strategy. This role involves leading regulatory teams, developing and executing strategies for product approvals, and ensuring adherence to global regulatory requirements...
$45 - $50 per hour
...What You Bring Bachelor’s degree in biochemistry, biology, medical technology or a related field. 3–5 years of experience in regulatory affairs, QA, R&D, manufacturing or project management in the IVD industry. Knowledge of FDA and CE marking requirements for IVD products...Hourly payTemporary work- ...A leading company in pharmaceuticals seeks a Regulatory Affairs Specialist to ensure compliance with FDA and DEA regulations. This role involves preparing submissions, maintaining licenses, and coordinating audits while working closely with regulatory agencies. Ideal...
$89.2k - $169.5k
...Boston Scientific is seeking a Senior Regulatory Affairs Specialist to join our team in Irvine, CA. The role involves supporting regulatory compliance and submissions for our active implantable device portfolio. Candidates should have a Bachelor's Degree in a scientific...$170k - $200k
...Would you like to be part of our story? Don't hesitate, come and join us! About this opportunity - Senior Principal Regulatory Affairs Specialist Description The Sr. Principal Regulatory Affairs Specialist is a seasoned expert, responsible for completing...- ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the...Work at officeLocal area3 days per week
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