Regulatory Affairs Manager
$106.1k - $197kRoche
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. At Roche Global Regulatory Affairs we strive to be the world's best Regulatory organization, championing patient access to the world's best diagnostics. Our team is tasked with regulatory projects as well as overarching regulatory topics with specific focus in Companion Diagnostics. You can expect an open-minded work environment, where you will be working closely with colleagues in other departments and other counties. The Opportunity You oversee regulatory document and submission compilation, which includes the development of submission/product registration dossiers of more complex products/programs. You develop and manage parts of comprehensive global regulatory submissions and registration plans. You interface with external management. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders. You build effective and enduring external relationships and apply effective stakeholder management practices. You contribute to audits by supporting preparation, execution and follow up You lead the organization to adapt to the evolving regulatory environment and requirements. You have an understanding of external environmental changes, precedents, to navigate complex situations and influence strategies and decision making. You have the ability to interpret and apply understanding of the regulators' thinking to projects and apply strategies to the different needs of different regions without significant guidance. You proactively create unique/innovative regulatory strategies and influencing approaches to avoid regulatory obstacles and accelerate worldwide approvals You effectively partner with external and internal stakeholders to understand and provide best solutions. You take initiative to address problems or opportunities and involve collaborators for best solutions. You develop relationships that significantly influence the current and future direction for Roche and our products. You have courage to make decisions even outside of scope/comfort zone and proactively initiate activities independently. You embrace good decision making principles You model VAAC Leadership and agility. You identify opportunities to develop VACC competency. You act with integrity, courage, passion and honor commitments and contribute to an inclusive environment You are able to pull people together around a common goal and seek to understand and build on different perspectives to enhance outcomes. You address and resolve conflict by creating an atmosphere of openness and trust. You bring out the best in people and teams Who You Are You have a Bachelor's / Master degree in Life Science, Data Science or related subject or equivalent experience. Advanced degree preferred You have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs or equivalent You have demonstrated experience and knowledge of Daily Management and Continuous Improvement best practices You have knowledge of the European, US, China and other international regulations and demonstrated ability to adequately interpret and implement quality standards considered an advantage You have demonstrated the ability to manage more complex work and/or at parts of global projects Preferred Qualifications Experience in Companion Diagnostics. Experience with systems and software. Locations You are local to Tucson, Indianapolis or Branchburg. No relocation benefits are available for this position. The expected salary range for this position based on the primary location of Arizona is $106,100 and $197,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Who we are A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law. #J-18808-Ljbffr Roche
$71.25k - $116k
...alignment with GxP requirements, data integrity principles and regulatory expectations. The IT Compliance analyst helps enable business... ...adherence to lifecycle controls: Change Control Incident / Problem Management CAPA management Periodic Reviews System Retirement Confirm...SuggestedTemporary workWork experience placementRelocation packageFlexible hoursShift work$184k - $230k
...Compliance member of the Medical, Legal, and Regulatory review committee; ensure promotional and... ...analytical, organizational, and project-management skills; able to manage competing... ...with Legal, Regulatory, Quality, Medical Affairs, Commercial, Finance, IT, and HR. Working...SuggestedContract workTemporary workFor contractorsFixed term contractWork at officeFlexible hours3 days per week- ...medical device company focused on vascular access and medication management. Our mission is to improve the lives of patients worldwide... ...and an entrepreneurial mindset. Role Description: The Regulatory Affairs Manager is a seasoned professional responsible for...SuggestedWork at officeLocal areaRemote workWorldwide
- ...site Responsibilities: Provide global oversight of EHS regulatory compliance. Own the Global EHS Regulatory Monitoring and Impact... ...reports. Govern the global EHS incident investigation and management process. Develop and enhance business systems that support...SuggestedFull timeTemporary workLocal area
- ...site Responsibilities: Provide global oversight of EHS regulatory compliance. Own the Global EHS Regulatory Monitoring and Impact... ...reports. Govern the global EHS incident investigation and management process. Develop and enhance business systems that support...SuggestedTemporary workLocal area
- ...Process Outsourcing (RPO) Back-office Services Application Design and Development Website Design and Development Program/Project Management Our Domain Strength With currently over 1000+ staff serving over 49 clients worldwide including “Fortune” companies, LanceSoft serves...Permanent employmentTemporary workWork at officeWorldwide
- ...Job Title Responsibilities: # Compiling data in support of Quarterly Executive Management Review. # Developing PowerPoint presentation with input from global business owners. # Collaborating to complete deliverables with global Quality Teams. # Reviewing...
$40 - $48 per hour
Piper Companies is currently looking for an experienced Quality Control Specialist in Branchburg, New Jersey (NJ) to work for a pharmaceutical cell therapy company. Must have experience with Flow Cytometry experience. Responsibilities for the Quality Control ...$83.71k - $109.87k
...quality, compliance, and adherence to global standards as well as regulatory requirements. Support Level I/II QALC by overseeing the... ...Compliance oversight of all QC operations. Support the supervisor in managing cross‑functional projects with QC Functional Area Owners....Permanent employmentFull timeTemporary workFor contractorsWork experience placementWork at officeLocal areaImmediate startFlexible hours- ...Job Description Job Description [Job Summary] The General Affairs Associate ensures smooth day-to-day office operations by managing facilities, procurement, assets, vendors, and administrative services. This role maintains a safe, efficient, and compliant workplace...Contract workWork at officeLocal areaRelocation
$62k - $71k
...create a warm, inspiring environment, while keeping parents informed and engaged. As a Director, you will: * Be a leader! Manages school staff by planning work schedules, evaluating staff performance, and developing performance improvement plans. Assists with...Bi-weekly payDaily paidFull time$150k - $180k
...and function of the Area Chief of Staff is to lead, develop and manage associate veterinarians in their hospitals to ensure Banfield... ...reviews. Hospital operations must meet all local, state and federal regulatory requirements including but not limited to compliance with...Full timeTemporary workPart timeLocal areaFlexible hoursShift work$19 - $22 per hour
...who want to take this journey with us! Get a sneak peek into life at ADESA! [ Role and Team * Reporting to the Reconditioning Manager or other designated manager, assures the quality of the Detail Shop process “First Time Right” is applied by Detailers. Communicate...Immediate startVisa sponsorship$83.71k - $109.87k
...ensure quality, compliance, and adherence to global standards and regulatory requirements. Support Level I/II QALC by overseeing spot‑... ...compliance oversight of all QC operations. Assist the supervisor in managing cross‑functional projects with QC functional area owners....Temporary workWork experience placementWork at officeWorldwideFlexible hours- ...employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. At Keenova, we believe that no one should be alone in their...
- ...Job Summary Our FP&A Manager, reporting to the Director of FP&A, will be responsible for leading the financial planning and analysis function, providing strategic insights to senior leadership to drive financial performance. This role manages the budgeting, forecasting...
$150k - $300k
...their merit. Job Function Technology Product & Platform Management Job Sub Function Technical Product Management Job Category... ...design decisions; lead prioritization decisions to balance regulatory, operational, and strategic initiatives while maximizing...Full timeLocal areaImmediate start$275k - $300k
...Females Together). Said quite simply, the culture is amazing! Position Overview Manages independent audits of operational processes and financial reporting in order to ensure regulatory compliance and that internal controls are appropriately designed and functioning...Full timeShift work$240k - $265k
...Director, Global Medical Affairs Lead, Neurodegeneration Location: Raritan, NJ Type: Full-Time Salary: $240,000 - $265,000... ...PhaseIIIb or PhaseIV studies, including appropriate staffing and management of budget. Work with relevant Disease Area Leadership Teams...Full timeLocal areaImmediate startRemote workWorldwide$45k - $50k
...professional development, entrepreneurial insight, and practical working experience inside a legacy brand. You will be challenged to manage people, systems, and processes in a fast-paced, high-performance environment where ownership and accountability matter. Completion...Full timeWork experience placementFlexible hoursShift work- ..., community programs, and local organizations. Partner with the Executive Director and leadership team to achieve occupancy goals. Manage leads, referrals, and follow-up activity using CRM tools. Monitor local market trends and identify opportunities to grow community...Work at officeLocal area
- ...manufacturing environment for personalized cell therapy products. You will lead timely, robust investigations, ensure CAPAs, support regulatory inspections, and collaborate with Manufacturing Operations, Technical Support, Maintenance, and Supply Chain to drive continuous...
- ...Peapack-Gladstone, NJ to serve as the strategic finance leader for the Engagement Solutions service line. The successful candidate will manage financial controls, lead a team of Client Finance Managers, and ensure financial integrity throughout project lifecycles. This...
- ...Role Overview FinPro, Inc is a management consulting firm specialized in financial institutions, with a focus on digital analytics... ...Preferred experience as a commissioned examiner at a state or federal regulatory agency. Strong drive, attitude, and willingness to thrive...Full timeNight shift
- ...degree in therapeutic recreation preferred or completion of NAAP/NCCAP Basic and Advanced Management Course for Activity Professionals Certification in accordance with regulatory agencies governing the center by the National Certification Council of Activity...
- Description Brandywine Living, a premier provider of quality senior living, is seeking a Life Enrichment Director! As the Life Enrichment Director, you will be responsible for planning and oversight of the Life Enrichment programming in the community, including...Full timeTemporary workLocal area
- ...for external manufacturers and strategic partners, ensuring consistent delivery of pharmaceutical products that meet safety and regulatory standards. In this role you will review quality systems, drive CAPA plans, and support tech transfer and new product introductions...
$32 per hour
...specifications) to full compliance to Quality, Food Safety and Regulatory requirements. This position is responsible for the creation... ...auditing and verification: Promote compliance with the Management System requirements and other applicable Standards. Support...Hourly pay$30 - $32 per hour
...development to ensure full compliance with Quality, Food Safety, and Regulatory requirements. The position is located in Bridgewater, NJ, with... ...and Regulatory requirements. Promote compliance with Management System requirements and other applicable standards....Full timeContract workTemporary workMonday to Friday- Recordati Rare Diseases, Inc. (RRD), North America, is seeking a Medical Science Liaison to act as a field-based scientific expert focusing on Cushing's Syndrome, Cushing's Disease, and Acromegaly. The MSL will build strong relationships with key opinion leaders and facilitate...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Manager. Be the first to apply!





