Regulatory Compliance Professional

Job ResponsibilitiesThe successful candidate for the Director of Regulatory Compliance role will be responsible for overseeing the management of regulatory activities associated with planning, authoring, compiling, and submitting high-quality regulatory submissions to the FDA. This includes preparing and compiling new ANDAs, Amendments, Supplements, Annual...

About the RoleWe are currently seeking an experienced Regulatory Compliance Engineer to join our team at TK-CHAIN LLC. In this role, you will be responsible for ensuring that our software applications meet or exceed regulatory requirements. This includes developing releases on multiple platforms to ensure that all code released to production systems meet or...

About TK-CHAIN LLCWe are seeking a highly skilled Director, Regulatory Affairs to join our team at TK-CHAIN LLC. This individual will be responsible for integrating knowledge of pharmaceutical drug development into all aspects of our company's drug development policies and procedures.The annual salary for this position is approximately $195,000, based on...

Are you an experienced regulatory professional looking for a challenging role in the pharmaceutical industry? Look no further! TK-CHAIN LLC is seeking a highly skilled Director of Pharmaceutical Regulatory Compliance to join our team in Pine Brook, New Jersey.The estimated salary for this role is $130,000 - $190,000 per year, based on industry standards and...

TK-CHAIN LLC is a dynamic and innovative company that is looking for a highly skilled Compliance and Regulatory Strategy Lead to join our team in Pine Brook, New Jersey.The estimated salary for this role is $140,000 - $200,000 per year, based on industry standards and the candidate's qualifications.Job DescriptionWe are seeking a seasoned regulatory...

MSCCN is seeking a Regulatory Compliance Coordinator to join our team in Princeton, NJ. This role offers a competitive salary range of $40.00 to $45.30 per hour.As a Regulatory Compliance Coordinator at MSCCN, you will be responsible for ensuring that all documents and records are maintained in accordance with FDA regulations and ISO standards. Your duties...

Compensation and BenefitsWe offer a competitive salary range of $32.56 - $45.48 per hour, depending on experience, as well as a comprehensive benefits package, including health insurance, an incentive and recognition program, and 401K contribution.Why Work with Us?Opportunity to work with a leading medical device company in the Princeton, NJ area.Competitive...

About the JobWe are seeking an experienced Regulatory Labeling Associate to join our team at TK-CHAIN LLC. The successful candidate will be responsible for preparing, reviewing, and submitting high-quality regulatory labeling submissions to the FDA.This is a dynamic role that requires strong analytical and problem-solving skills, as well as excellent...

About Us:TK-CHAIN LLC is a pioneering pharmaceutical company committed to delivering innovative solutions that meet the evolving needs of patients and healthcare professionals. As a Senior Manager, Regulatory Affairs, you will play a vital role in shaping our regulatory strategy and ensuring compliance with regulatory requirements.">Job Summary:We are...

About the Role: We are seeking a skilled Documentation Specialist to join our team at MSCCN in Princeton, New Jersey. As a key member of our quality team, you will be responsible for managing quality system document control activities and ensuring compliance with FDA, ISO, and international regulations.

Job Title: Associate II Regulatory LabelingThe TK-CHAIN LLC is seeking a highly motivated and detail-oriented individual to join our team as an Associate II Regulatory Labeling. This role plays a critical part in ensuring the accuracy and compliance of our pharmaceutical products' labeling submissions to the FDA.About the Role:In this position, you will be...

Job Title:Senior Regulatory Content SpecialistOverviewWe are seeking a Senior Regulatory Content Specialist to provide strategic leadership and subject matter expertise in the development of clinical regulatory documents. The ideal candidate will have a strong background in medical writing, regulatory affairs, and experience working with cross-functional...

TK-CHAIN LLC is seeking an experienced Head of US Regulatory Strategy to join our team in Pine Brook, New Jersey. This role requires a minimum of 12 years of pharmaceutical industry experience, with at least 10 years in Regulatory Affairs and 6 years of managerial experience.You will be responsible for leading cross-functional teams to develop and implement...

Company OverviewTK-CHAIN LLC is a leading provider of innovative solutions in the pharmaceutical industry. We are committed to excellence and innovation, and we seek individuals who share our passion and values.About the JobThe Senior Associate Regulatory Operations CMC will play a critical role in ensuring the quality and compliance of our regulatory...

Gardner Resources Consulting, LLC is seeking a skilled Pharmaceutical Regulatory Affairs Expert to join our team. As a regulatory affairs expert, you will play a key role in ensuring compliance with US pharmaceutical industry and healthcare landscape guidelines.Estimated Salary: $120,000 per yearAbout the Job:This position requires a thorough understanding...

TITLE: Associate, Regulatory LabelingROLE RESPONSIBILITIESThe Associate, Regulatory Labeling will be responsible for preparing, reviewing, and submitting regulatory labeling submissions to the FDA.This includes preparing responses to labeling comments received from the US FDA and serving as the PRC Chair to review and approve advertising and promotional...

Job OverviewThe Chief Regulatory Affairs Strategist plays a pivotal role in TK-CHAIN LLC drug development programs, ensuring compliance with US regulatory guidelines and federal regulations.This position is responsible for integrating knowledge of pharmaceutical drug development into all aspects of the company's drug development policies and procedures,...

TITLE: Associate, Regulatory LabelingJOB SUMMARYThe Associate, Regulatory Labeling plays a critical role in ensuring compliance with FDA regulations and guidelines.This position involves preparing, reviewing, and submitting regulatory labeling submissions to the FDA, as well as providing guidance and support to internal and external customers.The ideal...

TITLE: Associate, Regulatory LabelingOVERVIEW OF THE COMPANYTK-CHAIN LLC is a dynamic company that values innovation and excellence in the pharmaceutical industry.We are committed to delivering high-quality products and services that meet the evolving needs of our customers.SALARY: $85,000 - $110,000 per yearJOB DESCRIPTIONThe Associate, Regulatory Labeling...

Job OverviewTK-CHAIN LLC seeks an experienced Regulatory Affairs Senior Manager to lead our regulatory submissions team. Reporting directly to the Director/Associate Director Regulatory Affairs, this role will be based in Pine Brook, New Jersey.In this challenging and dynamic position, you will oversee the planning, authoring, compiling, and submitting...