Pharmaceutical regulatory affairs jobs in Teaneck, New Jersey (NJ) State

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...

We are seeking a highly skilled and experienced Real Estate and Construction Project Manager with. They will be responsible for coordinating and managing all project activities from inception to completion, ensuring that projects are completed on time, within budget, and to the highest quality st...

As the Associate Director of Finance, reporting directly to the VP of Finance, you will play a crucial role in overseeing and enhancing the financial reporting processes for this global manufacturing organization. ...

Compass Associates are excited to be working with a respected and established mental health provided in New Jersey for a new Director of Nursing. As the Director of Nursing you will be leading on the full operations of clinical/management of nursing being responsible for the quality, provision an...

Senior Manager, Energy & Sustainable Operations. Manage development and implementation of E&C operations to align with overall business objectives. Collaborate with regional & Global Workstreams leadership and regional FM operations organization to manage energy and conservation-related nuances a...

Want to work as a Technical Business Analyst at a public real estate investment trust company?. As the Technical Business Analyst, you will help assess and analyze the organization’s current IT platform capabilities and suggest solutions to improve the company’s systems and processes. Solid under...

Job Title: ServiceNow HRSD Business Analyst. Able to capture HRIS Business requirement and write SCRUm stories. ...

As the Director of Infrastructur, you will lead our organization's efforts in designing, building, and maintaining a robust and scalable data center infrastructure, while also overseeing our transition to cloud-based solutions. ...

Ensure program/project managers meet established schedules, help resolve technical and operational issues, and accomplishes delivery goals towards contract commitments - People care, including training, performance oversight, performance feedback, assessments, performance improvement planning & o...

Minimum of 5 years in a Business Analyst/System Analyst role. Looking for individuals with responsibilities to implement, maintain , and change business processes and application support to help drive further efficiency within the department. Oversee maintenance of existing platforms; SQL Server,...

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). ...

With over 10 years of construction project backlog, this firm is well-positioned to grow and provide lifetime careers for its people. Trust me, I have placed multiple people there who have told me so! This organization is looking to hire a Construction Code Specialist to provide management, overs...

Proven experience as a Technical Project Manager with a focus on Infrastructure or Software Development projects. We are seeking an experienced Technical Project Manager with a strong background in Infrastructure or Software Development. Utilize project management tools and methodologies to track...

Canada, Iris Software delivers technology services and solutions that help clients complete fast, far-reaching digital transformations and achieve their business goals. ...

We are seeking an experienced business analyst who can demonstrate strong analytical, problem-solving and communication skills. Deliver detailed business requirement/functional requirements/use cases/user stories/wireframes/ data mappings/training materials. Bachelor’s degree in Technology/Financ...

The Clinical SOP Writer edits and performs QC review of clinical procedures. The Writer may also eventually work with Process Owners, Subject Matter Experts (SMEs), and relevant stakeholders to develop new and revise existing clinical procedures. The Writer ensures procedures and associated forms...

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...

Iris's client, one of the world's largest multinational investment banking and financial services corporation is looking to hire a Senior Business Analyst (ERM-Enterprise Risk Management) for a Long Term opportunity. Canada, Iris Software delivers technology services and solutions that help clien...

Ability to author clear and concise regulatory documents (CMC authoring) with oversight of all documents for regulatory submissions and associated messaging. Job Title: Lead Regulatory Affairs. Ensure development programs are compliant with ICH regulatory requirements and all local country regula...

Strong hands on Internal/External Audit Experience.Strong Risk and Controls experience preferably in the financial services industry.Has relevant business expertise (Enterprise Risk Management) and sufficient technology literacy....

As the Director, Regulatory Affairs – Advertising, Promotion and Regulatory Compliance you will be responsible for leading a group of US Regulatory Affairs professionals responsible for advertising and promotion, compliance, labeling and submission operations within US RA. Coordinate regulatory p...

Responsibilities Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific meri...

As the Senior Manager, Regulatory Affairs you will be responsible for the development and execution of US regulatory strategy for projects within an assigned Therapeutic Area (“TA”). Develop and execute US regulatory strategy, with oversight as needed, and in conjunction with Global Regulatory Le...

As the Associate Director, Regulatory Affairs you will be responsible for leading the development and execution of US regulatory strategy for projects within an assigned Therapeutic Area (“TA”). Lead the development and execution of US regulatory strategy in conjunction with Global Regulatory Lea...