Regulatory affairs specialist jobs in Teaneck, New Jersey (NJ) State

Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus 2 years of related experience. Prior experience must include: Develop the regulatory submission strategies for products in commercial and developmen...

Director, Technical Program Manager - Generative AI SystemsAre you interested in leading programs that deliver on critical business goals and build large scale products & platforms?About Capital One: At Capital One, we’re changing banking for good. In addition to the technical program, you will a...

Director, Technical Program Manager - Generative AI SystemsAre you interested in leading programs that deliver on critical business goals and build large scale products & platforms?About Capital One: At Capital One, we’re changing banking for good. In addition to the technical program, you will a...

Comcast brings together the best in media and technology.We drive innovation to create the world's best entertainment and online experiences.As a Fortune 50 leader, we set the pace in a variety of innovative and fascinating businesses and create career opportunities across a wide range of locatio...

Comcast brings together the best in media and technology.We drive innovation to create the world's best entertainment and online experiences.As a Fortune 50 leader, we set the pace in a variety of innovative and fascinating businesses and create career opportunities across a wide range of locatio...

The Associate, Regulatory Affairs - Labeling position is responsible for the preparation of various regulatory Labeling submissions. Electronically search for new regulatory guidelines and regulations. Minimum 1-3 years regulatory experience in the generic pharmaceutical industry. Solid written c...

The Associate, Regulatory Affairs - Labeling position is responsible for the preparation of various regulatory Labeling submissions. Electronically search for new regulatory guidelines and regulations. Minimum 1-3 years regulatory experience in the generic pharmaceutical industry. Solid written c...

The Associate, Regulatory Affairs - Labeling position is responsible for the preparation of various regulatory Labeling submissions. Electronically search for new regulatory guidelines and regulations. Minimum 1-3 years regulatory experience in the generic pharmaceutical industry. Solid written c...

The Associate, Regulatory Affairs - Labeling position is responsible for the preparation of various regulatory Labeling submissions. Electronically search for new regulatory guidelines and regulations. Minimum 1-3 years regulatory experience in the generic pharmaceutical industry. Solid written c...

Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA with the following requirements: Bachelor’s degree in a scientific field or foreign academic equivalent plus 4 years of related experience. Required skills: Ability to work with firm deadlines and adapt quickly to chan...

Prior experience must include: Vendor and Client Management for Regulatory Operations – Manage relationships with vendors and clients for various regulatory operations services; Identify and evaluate potential eCTD submission vendors based on their experience, expertise, cost-effectiveness, and t...

DutiesWHAT IS THE SMALL BUSINESS/SELF EMPLOYED (SBSE) DIVISION?A description of the business units can be found at: https://www.Vacancies will be filled in the following specialty areas: Small Business Self Employed Field ExaminationThe following are the duties of this position at the full workin...

For the HR Compliance Specialist position, this role will require creating and maintaining policies and procedures. The position will plan, direct, or coordinate activities for the company to ensure compliance are within ethical and regulatory standards including ACA, HIPAA, and more. Collaborate...

Our client, a Reputable, Global Pharmaceutical Company, is seeking a Regulatory Affairs Strategy professional at the Director level. The position will report directly into the VP of Regulatory Affairs. Develop and implement Regulatory Affairs strategy for Oncology programs. Regulatory Affairs Str...

Joining an established & small Medical Device company, within quality team with both sustaining and new product activities in the pipeline, the Senior Design Assurance Engineer position will give someone the opportunity to lead and mentor quality members, and take the reigns on all design quality...

As a Senior Project Manager, you will play a crucial role in overseeing multiple projects simultaneously from Commercial to Public Sector projects, ensuring they are completed on time, within budget, and to the highest standards. Proven experience as a Project Manager in the construction industry...

Role: Quality Engineer - Mobile Testing (. ...

Opportunity to join a global medical device company currently going through a transition and investing heavily into the Quality team. Develop and improve inspection methods to analyze product quality. Improve product quality by making recommendations for change. Ensure products adhere to company ...

The Quality Engineer is responsible for ensuring optimal production quality performance by addressing quality issues, implementing corrective actions, and maintaining adherence to quality management systems. We are working with a global sing-use medical device company looking for a Quality Engine...

The Quality Engineer is an essential member of our Quality Assurance Department responsible for ensuring that quality systems are properly established and maintained for effective and efficient internal compliance and customer satisfaction. The responsibilities of the Quality Engineer will comple...

Manages and oversees the administration of a Behavioral Health Services (BHS) program, including the appropriate utilization and management of staff and the quality of program participants care with an emphasis upon an inter-disciplinary team approach to the delivery of care. Monitors the program...

Manager of Regulatory Affairs Strategy to join their team. Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. We are currently partnered with a growing biopharmaceutical company in need of a Manager/Sr. This role...

The ideal candidate will come with a strong background in Regulatory Affairs from within the Medical Device industry. At least 5 years of Regulatory Affairs experience working with Medical Devices (Class I-III). ...

The Regulatory Affairs Specialist (F&B) will be responsible to independently provide Symrise Inc. The Regulatory Affairs Specialist may provide support to the retrieval of revenue paid for the use of tax paid Distilled spirits in finished product materials and support other TTB related activities...