UNKNOWN

ADAPTED_NOW

This role oversees maintenance staff to ensure the physical asset is well-maintained and safe, works closely with the leasing team to drive occupancy and resident satisfaction, and manages the property's budget and financial reporting to meet ownership and investor expectations. * Analyze monthly financial statements (income statements, variance reports, rent rolls) and provide clear explanations for budget variances.

Synerfac Technical Staffing

Property Manager

Currently has, or is in the process of obtaining one of the following with an expectation that the required degree will be obtained on or before the scheduled start date: A Bachelors or Master’s Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, Computer Engineering, Software Engineering, Mechanical Engineering, Information Systems or a related quantitative field), Business or Marketing. As a Senior Manager of Product Management at Capital One, you will report directly to the Director of the Migration domain and lead the domain responsible for ensuring that customer, account, product, and transactional data is migrated accurately, completely, and repeatedly.

YEAR

Discover Financial Services

Senior Manager, Product Manager-Data Analysis & Governance

Ivy Exec

Lennar is one of the nation's leading homebuilders, dedicated to making an impact and creating an extraordinary experience for their Homeowners, Communities, and Associates by building quality homes and providing exceptional customer service, giving back to the communities in which we work and live in, and fostering a culture of opportunity and growth for our Associates throughout their career. Tech-savvy with proficiency in Microsoft Office, Build Pro, Procore, and other construction management software, leveraging technology to streamline workflows, enhance project tracking, and improve overall efficiency.

Lennar Corporation

Construction Manager

This individual will provide 24 hour accountability and responsibility for excellence in the operational and cliniccal practice and delivery of Home Health care services within an ANCC Magnet® designated ChristianaCare HomeHealth team. This person will work in the office located on Avenue North, in North Wilmington, DE as well as spend time in the field with their staff and be responsible for committing to rotations for weekend, holiday, and on-call rotation.

HOUR

ChristianaCare

Clinical Manager | ChristianaCare HomeHealth

Capital Markets Placement_feed

FULL_TIME

FEED

Lennar Homes

The Senior Manager, Regulatory Affairs, CMC will primarily be responsible for managing regulatory CMC submissions and strategy for development and marketed products, for biologic/small molecules, from early development through late-stage (phase 3, registration and post-approval). Experience with global clinical trial and marketing applications, eCTD submissions, electronic document management systems (e.g., Veeva Vault platform), and Starting Point and Microsoft Word Templates.

Kaztronix is committed to the clients and employees we serve. Our mission is to provide the best and brightest industry talent, solutions, and services available. We have been working with various industries and clients across the United States for nearly 10 years.

Kaztronix

Sr Mgr, Regulatory Affairs CMC

jobdiva

You will coordinate regulatory submissions, product labelling activities and post-approval commitments while partnering with affiliates, global teams and regulatory authorities to maintain marketing authorisations and support continued product supply. As a (Senior) Regulatory Affairs Manager, EU Procedures, you will support regional registration activities for existing animal health products registered in two or more European Economic Area countries or the United Kingdom.

Elanco Animal Health Incorporated

(Senior) Regulatory Affairs Manager, EU Procedures

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Excellent knowledge required of regulatory and cGMP requirements, including in 21 CFR Part 11, Part 210, Part 211, Part 212, Part 314, and other relevant 21 CFR parts and regulatory guidance documents as applied to a sterile injectable drug and oral capsule manufacturing environment. Oversee and perform risk management reviews through products' life cycles and participate in change management internal processes, such as engineering and documentation change control and cross-functional project meetings.

Cardinal Health Inc

Manager, Regulatory Affairs

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This role coordinates technical reviews, permitting meetings, inspections, code compliance reviews, and approval processes with organizations including Richmond Planning & Development Review, Land Use Administration, Permits & Inspections Bureau, Fire Marshal's Office, Department of Public Utilities, Department of Public Works, Virginia DEQ, VDOT, Dominion Energy, and other applicable authorities. KBR is seeking a Regulatory & AHJ (Authority Having Jurisdiction) Coordination Manager to develop, manager, and maintain strategic relationships with all regulatory, inspection, and approval authorities involved in the planning, design, construction, commissioning, and startup of a multi-billion-dollar greenfield pharmaceutical manufacturing project.

When you become part of the When you become part of the KBR team, your opportunities are endless. As a leading global technology, engineering, procurement and construction company serving the hydrocarbons and government services industries. For decades it has been the company that customers turn to for their most challenging assignments.
 
With operations in 40 countries, KBR has more than 25,000 people delivering services to customers in over 70 countries. Together they represent an unmatched reservoir of talent and experience in a wide range of markets.
 
Whatever the assignment, no matter how complex or demanding, KBR can marshal resources across every product line to respond quickly and effectively to changing markets and customer needs.
 
Whether it's providing the technology and consulting know-how to develop our customers' valuable assets; designing and constructing the infrastructure and facilities to develop energy resources in some of the world's more remote and challenging locations; providing support and services for men and women of their countries' armed forces; or navigating the intricacies of undertaking major projects in geopolitically or culturally sensitive environments, our clients depend on KBR because they know that We Deliver.
 
Join us and you'll be part of a dynamic, elite team of professionals who understand what it takes to get a job done and has the experience, knowledge and determination to succeed.”

KBR Inc

Regulatory & AHJ Manager

Ability to understand and apply technical materials and regulations, strong technical writing skills, knowledge of CMC, clinical and non-clinical pharmaceutical development, Possess a broad knowledge of biopharmaceutical manufacturing and operations. Provide regulatory guidance to cross-functional groups regarding all aspects of preclinical and clinical development and testing for products.

Prelude Therapeutics Inc

VP, Regulatory Affairs

Prelude Therapeutics

As the Associate Director Promotional Regulatory Affairs, you will ensure efficient and effective regulatory review and risk assessment of promotional material for all segments (HCP, Consumer, Managed Markets) and media (Print, broadcast and electronic), sales training, faculty training, Proactive Scientific Exchange by SciP, Corporate Affairs communications, and any other materials required to be reviewed through AZAP. The Associate Director Promotional Regulatory Affairs will work with a with a cross-functional review team and provide regulatory guidance and risk assessment to help business teams develop and deliver initiatives that are intended to comply with applicable laws, rules and regulations governing the advertising and promotion of pharmaceutical products in the US.

AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

AstraZeneca Plc

Associate Director, Promotional Regulatory Affairs

Accountabilities: Regulatory Promotion Review: Drive efficient and effective regulatory review and risk assessment for promotional materials across HCP, Consumer, and Managed Markets segments and all media types, including sales and faculty training, scientific exchange, and Corporate Affairs communications, through established systems. Training and Capability Building: Evaluate brand regulatory training needs and develop and deliver training in partnership with internal/external Learning teams or the PRA Skill Center, building regulatory acumen across the business.

Director Promotional Regulatory Affairs

This is a strategic, high-impact role designed for a professional with deep expertise in FDA promotional regulations, capable of delivering expert regulatory guidance across assigned brands and key business areas. As PRA Director, you will work independently with cross-functional teams, providing risk assessments, strategic advice, and leadership in the review of promotional materials through the MLR (Medical, Legal, Regulatory) Approval Process.

Director, Promotional Regulatory Affairs

AstraZeneca GmbH

The role: The purpose of the Advisor - Global Regulatory Affairs CMC Biologicals role is to work cross functionally with Elanco R&D, Manufacturing, Quality, and other Elanco departments in support of the authorization and maintenance of registrations with global regulatory agencies for the biological products. Lead CMC regulatory pre-submission preparation and proactively communicate CMC regulatory strategy, key issues and other critical topics throughout the product life cycle to interdisciplinary project teams, while applying the global strategy into submissions.

Advisor - Global Regulatory Affairs CMC Biologicals

Serves as project lead for deliverables of assigned complex and/or large medical writing projects, including, but not limited to, scheduling and leading internal project-specific team meetings, organizing project-specific requirements, and ensuring all information is distributed to the editorial team and implemented within the deliverable. •Copyedits assigned documents, applying correct grammar, punctuation, spelling, and style following AMA Manual of Style or various custom style guidelines as well as established medical writing internal checklists and best practices.

Syneos Health

Senior Medical Editor - Copy Editing + QC - Regulatory (EMEA Home Based)

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Our Staff Regulatory Affairs Specialist position is primarily focused on maintaining continued market access of our existing PreAnalytiX and Lab Specimen Management product portfolios, in addition to opportunities to provide regulatory support for new product development projects. Represent RA and demonstrate leadership in complex product development teams by identifying and interpreting relevant regulatory requirements, and providing actionable regulatory guidance throughout the product development cycle prior to regulatory submission.

Becton Dickinson and Co

Staff Regulatory Affairs Specialist

Your role in our success: The Enterprise Compliance, Ethics & Risk Manager is responsible for developing, coordinating, and monitoring enterprise-wide compliance programs that support the company's regulated natural gas, propane, and electric utility operations. Monitor regulatory and legislative developments affecting natural gas, propane, and electric utility operations, including requirements related to pipeline safety, public utility regulation, environmental compliance, workplace safety, customer service, records retention, and ethics.

Chesapeake Utilities Corporation is a diversified energy company focused on delivering outstanding service and attaining sustainable growth that generates long-term value for our employees, customers, investors, and other stakeholders. Our success in these efforts is due to our employees&rsquo; relentless commitment to excellence, our comprehensive strategic planning and our disciplined financial analysis of growth opportunities.&nbsp; For more than 100 years, the Company has successfully delivered safe, secure, reliable and efficient solutions that are environmentally and economically smart. Chesapeake positions itself for long-term growth that creates superior value.&nbsp; Chesapeake Utilities Corporation genuinely cares while turning aspirations into reality every day. We make meaningful connections with our peers, customers, communities, shareholders and partners.
We strive to provide operational excellence and positive experiences for our customers and the communities we serve. Chesapeake&rsquo;s regulated energy businesses include natural gas distribution and transmission operations on the Delmarva Peninsula and in Florida, and electric distribution operations in Florida. Chesapeake&rsquo;s unregulated energy businesses include its natural gas marketing subsidiary, its propane distribution operations, and its propane wholesale marketing subsidiary.
We have a talented workforce made of experienced professionals with diverse backgrounds who take pride in the work they do at Chesapeake. They are hard working people, who generously get involved in their communities because they care about them. At Chesapeake, we believe our employees make the difference, and we care about every one of them &ndash; every day. One way we show gratitude to our employees is through our Chesapeake Cares Program that focuses on employee morale and a satisfying work environment. One day each month we conduct an event focused on employee fun and fellowship. We recognize our employees&rsquo; contributions with a rewards and recognition program geared towards continuous growth and career development within the company.

Chesapeake Utilities Corp

Enterprise Compliance Manager

Basic Qualifications: Currently has, or is in the process of obtaining one of the following with an expectation that the required degree will be obtained on or before the scheduled start date: A Bachelor's or Master's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, Computer Engineering, Software Engineering, Mechanical Engineering, Information Systems or a related quantitative field), Business or Marketing. As a Product Manager within Enterprise Payments, you'll join a thriving product management community, where you'll have the opportunity to define customer experiences, implement cutting-edge technology, and navigate the complex regulatory requirements through AI to scale customer insights and harness data-driven decision making, while accelerating speed to market.

Regulatory Manager Jobs in Delaware

Property Manager Synerfac Technical Staffing

Senior Manager, Product Manager-Data Analysis & Governance Discover Financial Services

Construction Manager Lennar Corporation

Clinical Manager | ChristianaCare HomeHealth ChristianaCare

Construction Manager Lennar Homes

Sr Mgr, Regulatory Affairs CMC Kaztronix

(Senior) Regulatory Affairs Manager, EU Procedures Elanco Animal Health Incorporated

Manager, Regulatory Affairs Cardinal Health Inc

Regulatory & AHJ Manager KBR Inc

VP, Regulatory Affairs Prelude Therapeutics Inc

VP, Regulatory Affairs Prelude Therapeutics

Associate Director, Promotional Regulatory Affairs AstraZeneca Plc

Director Promotional Regulatory Affairs AstraZeneca Plc

Director, Promotional Regulatory Affairs AstraZeneca Plc

Director, Promotional Regulatory Affairs AstraZeneca GmbH

Advisor - Global Regulatory Affairs CMC Biologicals Elanco Animal Health Incorporated

Senior Medical Editor - Copy Editing + QC - Regulatory (EMEA Home Based) Syneos Health

Staff Regulatory Affairs Specialist Becton Dickinson and Co

Enterprise Compliance Manager Chesapeake Utilities Corp

Manager, Product Manager - EP Payments Capital One Financial Corp

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