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public affairs specialist
3 weeks ago
Department of the Air Force - Agency Wide Los Angeles, United StatesSummary · Eligibilities being considered and other IMPORTANT information. · The primary purpose of this position is to carry out a variety of recurring precedented public affairs assignments that include elements of media operations, social media, community engagement, command/ ...
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Regulatory Affairs Specialist
3 weeks ago
PureTek Corp Los Angeles, United StatesJob Description · Job Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-be ...
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Regulatory Affairs Specialist
1 week ago
Curtis Food Recruiters Los Angeles, United StatesSimply Good Foods is seeking a Regulatory Affairs Specialist to support continued growth. This is a critical role for the organization, supporting the Quest and Atkins brands in complying with regulations and laws at the ingredient and trade levels. · Keys to success in this rol ...
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Regulatory Affairs Specialist
3 weeks ago
The Wonderful Company Los Angeles, United StatesThe Wonderful Company | · Los Angeles, CA | · Legal | · Associate | · Full-time | · Job ID: REF3516C · You may know us as Wonderful Pistachios, FIJI Water, POM Wonderful, Wonderful Halos Mandarins, JUSTIN Wine, and Teleflora, but we're all Wonderful – and we have a great opp ...
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Regulatory Affairs Specialist
2 days ago
Kindeva Drug Delivery Los Angeles, United States19901 Nordhoff St, Northridge, CA 91324, USA Req #98104 April 2024K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to imp ...
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Regulatory Affairs Specialist
1 week ago
Kindeva Drug Delivery Los Angeles, United States19901 Nordhoff St, Northridge, CA 91324, USA · Req #981 · 04 April 2024 · K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our custome ...
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Regulatory Affairs Specialist
3 weeks ago
SprintRay Inc. Los Angeles, United StatesLocation: On-SiteAt SprintRay, we are in a super-charged growth mode and are constantly looking for ways to maintain the quality of our products and processes while growing at a phenomenal pace. To help grow and maintain the regulatory and quality standards, we are seeking a Regu ...
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Regulatory Affairs Specialist
3 weeks ago
BioPhase Solutions Los Angeles, United StatesJob Description · Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Regulatory Affairs Specialist to work for a leading Greater Los Angeles area medical device comp ...
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Regulatory Affairs Specialist
2 weeks ago
INTELLECTT INC Los Angeles, United StatesPosition: Regulatory Affairs SpecialistLocation: Los Angeles, CAResponsibilitiesMaintain regulatory compliance of existing products for global customers.Manage regulatory compliance activities and customer product registrations.Provide strategic planning for regulatory changes.Ac ...
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Sr. Regulatory Affairs Specialist
4 weeks ago
Cypress HCM Los Angeles, United StatesSr. Regulatory Affairs Specialist · Location: Los Angeles, Ca · Company Size: 200/ Team Size: 15 · Duties & Responsibilities: · Manage all regulatory activities necessary to maintain and to grow the business. · Develop and implement regulatory strategies for new and existing pro ...
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Sr. Regulatory Affairs Specialist
2 days ago
Cypress Human Capital Management, LLC Los Angeles, United StatesSr. Regulatory Affairs Specialist · Location: · Los Angeles, Ca · Company Size : 200/ · Team Size : 15 · Duties & Responsibilities: · Manage all regulatory activities necessary to maintain and to grow the business. · Develop and implement regulatory strategies for new and exist ...
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Principal Regulatory Affairs Specialist
13 hours ago
Medtronic Los Angeles, United StatesCareers that Change Lives · Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better tha ...
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Principal Regulatory Affairs Specialist
3 weeks ago
Medtronic Los Angeles, United StatesCareers that Change Lives · Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than ...
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Sr. Regulatory Affairs Specialist
2 days ago
Cypress Human Capital Management Llc Los Angeles, United StatesSr. Regulatory Affairs SpecialistLocation: Los Angeles, CaCompany Size : 200/ Team Size : 15Duties & Responsibilities:Manage all regulatory activities necessary to maintain and to grow the business.Develop and implement regulatory strategies for new and existing products regulate ...
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Regulatory Affairs Specialist
1 week ago
Adecco Permanent Recruitment Los Angeles, United StatesAbout the OpportunityThe Regulatory Affairs Specialist is responsible for ensuring foreign and domestic compliance for regulated dental products adhering to Quality and Regulatory compliance. This role works in conjunction with the Quality and Regulatory team to create, maintain ...
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Regulatory Affairs Specialist
3 weeks ago
PureTek Los Angeles, United StatesJob Description Job DescriptionPureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being ...
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Regulatory Affairs Specialist
3 weeks ago
The Wonderful Company Los Angeles, United StatesThe Wonderful Company | Los Angeles, CA | Legal | Associate | Full-time | Job ID: REF3516C · You may know us as Wonderful Pistachios, FIJI Water, POM Wonderful, Wonderful Halos Mandarins, JUSTIN Wine, and Teleflora, but were all Wonderful and we have a great opportunity for a Re ...
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Regulatory Affairs Specialist
2 weeks ago
Adecco Permanent Recruitment Los Angeles, United StatesAbout the Opportunity · The Regulatory Affairs Specialist is responsible for ensuring foreign and domestic compliance for regulated dental products adhering to Quality and Regulatory compliance. This role works in conjunction with the Quality and Regulatory team to create, mainta ...
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Regulatory Affairs Specialist
3 weeks ago
The Wonderful Company Los Angeles, United StatesThe Wonderful Company | Los Angeles, CA | Legal | Associate | Full-time | Job ID: REF3516CYou may know us as Wonderful Pistachios, FIJI Water, POM Wonderful, Wonderful Halos Mandarins, JUSTIN Wine, and Teleflora, but were all Wonderful and we have a great opportunity for a Regula ...
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Regulatory Affairs Specialist
2 weeks ago
Simply Good Foods Los Angeles, United StatesAre you a detail-oriented professional with a passion for regulatory compliance? Do you excel in ensuring products meet the highest standards? If so, Simply Good Foods is looking for you · As a Regulatory Affairs Specialist, you will be a key player in our R&D team, ensuring our ...
Regulatory Affairs Specialist - Los Angeles, United States - PureTek
Description
Job DescriptionJob Description
PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products.
With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers.
Join our team and contribute to our mission of creating high-quality healthcare and beauty solutions.Job Description:
We are currently seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team.
As a Regulatory Affairs Specialist, you will be pivotal in ensuring compliance with regulatory requirements for our pharmaceutical and cosmetic products.
Your responsibilities will include preparing and submitting regulatory documents, coordinating with regulatory authorities, and keeping abreast of evolving regulations to support our product development and commercialization efforts.
Responsibilities:
Collaborate with cross-functional teams to ensure regulatory compliance throughout the product lifecycle, from development to commercialization.
Prepare and submit regulatory documents, such as product registration dossiers, technical files, and labeling requirements, to regulatory authorities in compliance with applicable regulations.
Support the compilation and maintenance of product regulatory files, ensuring the accuracy and completeness of all required documentation.Conduct regulatory assessments of product formulas, packaging, and labeling to ensure compliance with local and international regulations.
Stay updated on changes in regulatory requirements for pharmaceutical and cosmetic products, communicate these changes to internal stakeholders, and develop strategies for compliance.
Assist in the coordination and preparation of regulatory submissions and product variations, as applicable.Interact and communicate effectively with regulatory authorities to address inquiries, respond to queries, and provide necessary information to support product registrations and approvals.
Collaborate with quality assurance and R&D teams to ensure compliance with applicable Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards.
Participate in regulatory audits and inspections, providing necessary documentation and support to regulatory authorities.Qualifications:
Bachelor's degree in a scientific discipline or a related field (advanced degree preferred).
Minimum of 3 years of experience in regulatory affairs within the pharmaceutical and/or cosmetic industry.
Strong understanding of local and international regulatory requirements for pharmaceutical and/or cosmetic products.
Experience with the preparation and submission of regulatory documents, such as product registration dossiers and technical files.
Familiarity with regulatory guidelines, including the FDA, and other relevant authorities.
Detail-oriented mindset with excellent analytical and problem-solving skills.
Effective communication and interpersonal skills to collaborate with internal teams and regulatory authorities.
Ability to work independently, prioritize tasks, and manage multiple projects simultaneously.
Proficiency in relevant software applications and databases used in regulatory affairs.
Company Description Family-run in the USA, PureTek is the contract manufacturer behind several of America's top brands of personal care, supplement, and Prescription & OTC products.
Our commitment, consistent dependability and adherence to the industry standards produces only the safest, highest quality products - with no exceptions.
All PureTek products, including personal care and over-the-counter items, are manufactured to pharmaceutical standards, making PureTek unique in the market of contract manufacturing.
Company Description
Family-run in the USA, PureTek is the contract manufacturer behind several of America's top brands of personal care, supplement, and Prescription & OTC products.
Our commitment, consistent dependability and adherence to the industry standards produces only the safest, highest quality products - with no exceptions.
All PureTek products, including personal care and over-the-counter items, are manufactured to pharmaceutical standards, making PureTek unique in the market of contract manufacturing.
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