Referso Jobs

Senior Director, Content Strategy Head, Respiratory, Immunology and Inflammation (RIIRU)

GSK · Posted Nov 9, 2026

Open

United Kingdom
Hybrid
Full-time · Director

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Senior Director, Content Strategy Head, Respiratory, Immunology and Inflammation (RIIRU)

GSK · Posted Nov 9, 2026

Open

United Kingdom
Hybrid
Full-time · Director

Apply with Referso

Global Regulatory Lead

Excelya · Posted Nov 9, 2026

Open

Saclay, Île-de-France, France

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Lead global regulatory strategy and support product development and registration worldwide.

Responsibilities

Develop and maintain global regulatory strategies aligned with development and business objectives
Assess evolving regulatory requirements, competitor landscapes, and regulatory intelligence across major markets
Lead interactions with Health Authorities, including EMA, FDA, PMDA, and other key agencies
Drive regulatory activities related to registrations, lifecycle management, orphan drug designation, and market expansions
Design and oversee global submission plans in collaboration with regional regulatory teams and submission management

Requirements

Master's Degree
PharmD
PhD
MD
equivalent scientific qualification

Skills

global regulatory frameworks (ICH, EMA, FDA)product development submissions regulatory interactions with Health Authorities

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Senior Medical Writer

Thermo Fisher Scientific · Posted Aug 11, 2026

Open

Shanghai, China
On-site
Senior
8+ years

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Join Us as a Principal Medical Writing - Make an Impact at the Forefront of Innovation

Responsibilities

Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.
As the lead writer, review documents for the team and provide training and guidance to junior team members.
Provide advice on document development strategy, regulations and industry best practices.
Demonstrate subject matter and therapeutic area expertise.
Act as backup program manager.

Requirements

Bachelor's degree in a scientific discipline or equivalent
Advanced degree preferred

Skills

Significant knowledge of global, regional, national and other document development guidelines In-depth knowledge in one or more specialty areas such as preclinical, therapeutic, regulatory, submissions, communications Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills

QA Director

Scopely · Posted Nov 6, 2026

Open

Barcelona, Catalonia, Spain +1 more
Hybrid
Full-time · Senior
10+ years

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Lead and manage Scopely’s Mobile and Console QA & Deployment Program, ensuring quality, automation, and AI integration across all platforms.

Locations (2)

Barcelona, Catalonia, Spain
Dundee, Scotland, United Kingdom

Responsibilities

Collaborate with peers, senior management and external partners to align operations with strategic goals
Shape future QA & Deployment practices and product quality
Lead a multi-disciplinary QA & Deployment program across mobile and console
Provide leadership, technical expertise and career development for QA & Deployment project owners
Build and maintain team metrics for quality and operational excellence

Requirements

Nice to have: Console and PC deployment & compliance
Nice to have: Localization
Nice to have: LQA
Nice to have: Build distribution and submissions

Skills

Regulatory Affairs Manager SASSA

Elanco · Posted Nov 6, 2026

Open

Centurion, Gauteng, South Africa
On-site

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Support the maintenance of existing and registration of new animal health products, including therapeutics, feed additives, biocides and care products.

Responsibilities

Manage regulatory compliance and lifecycle activities for the existing and future portfolio, including submissions, variations, renewals and referrals to the South African Health Products Regulatory Authority and other relevant authorities.
Develop and implement regulatory strategies for export markets across the region, while building effective relationships with competent authorities and external regulatory partners.
Coordinate packaging development and artwork activities, including the release of production artwork through the Elanco Artwork System.
Review and approve promotional materials in PromoMats, and coordinate national regulatory issues, submissions and packaging updates.
Maintain regulatory information in systems such as Veeva Vault RIM, collaborate with internal and external stakeholders, and lead regional Regulatory Affairs projects as required.

Requirements

Pharmacist qualification
Nice to have: similar experience from the animal health industry
Nice to have: fluent English

Skills

regulatory compliance activities submissions

Regional Director, Corporate Affairs

Hypertec Group · Posted Nov 5, 2026

Open

Montreal, Quebec, Canada
Hybrid
Full-time · Manager
7–10 years

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Lead government relations, public affairs, media relations, and corporate reputation initiatives for Hypertec in Canada.

Responsibilities

Develop and implement Canadian government relations strategy
Build and maintain relationships with federal, provincial, and municipal officials
Represent Hypertec in government meetings and policy forums
Prepare government briefings, submissions, position papers
Manage media relations and crisis communication

Requirements

University degree in Political Science, Public Policy, Communications, Law, Business, or related field
Nice to have: experience in technology, infrastructure, energy, or industrial sectors

Skills

government relations public affairs corporate affairs briefing notes submissions position papers press releases

Regulatory Team Lead, Maintenance and CTA

Novartis · Posted Nov 5, 2026

Open

Barcelona, Catalonia, Spain
Hybrid
Full-time · Manager
€64K–€118K per year

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Lead and develop a global regulatory team responsible for delivering high-quality, compliant and timely clinical trial submissions and approvals.

Compensation

Expected Annual Base Salary Range for role: €63,600 to €118,000

Responsibilities

Lead and develop a global regulatory team delivering high-quality, compliant and timely clinical trial submissions and approvals.
Coach and support team members, building capability and enabling professional growth.
Allocate resources effectively across the assigned portfolio, balancing priorities and business needs.
Drive process improvement, simplification and automation to strengthen operational excellence.
Build strong, customer-focused relationships with key stakeholders and act on feedback.

Requirements

Bachelor’s or Master’s degree in a science-related discipline

Skills

regulatory experience global regulations guidelines processes people management

Underwriting Assistant, Financial Institutions

Ascot Group · Posted Nov 4, 2026

Open

New York, New York, United States
Hybrid
Full-time
$80K–$90K per year
5+ years

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Support the Financial Institutions underwriting team across the full lifecycle of an account, including new business, renewals, and ongoing servicing.

Compensation

Salary Range: $80,000 - $90,000

Responsibilities

Support the underwriting process for the Financial Institutions portfolio, including new business, renewals, and account servicing.
Assist with submission preparation, rating, referrals, quoting, binding, policy issuance, and endorsements within assigned authority.
Review submissions and maintain accurate underwriting files, rating information, and account documentation.
Partner with Underwriters, brokers, reinsurers, and internal teams to obtain required information and resolve outstanding subjectivities.
Coordinate policy issuance instructions, endorsements, forms, notices, certificates, and related documentation.

Requirements

High school diploma required; some college or a college degree preferred.
Nice to have: some college or a college degree preferred.

Skills

underwriting processes submissions rating

LCP & MSP Specialist

ForzaCare · Posted Nov 3, 2026

Open

Remote, United States
Remote
Full-time

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Coordinate and support MSP compliance services, Conditional Payments, Life Care Plans, and Medical Cost Projections for a predominantly remote team.

Responsibilities

Manage workflow from intake through completion
Review and process new referrals
Track case progress and follow up
Maintain accurate internal logs
Ensure compliance with CMS guidelines

Requirements

Active Registered Nurse license
Certified Rehabilitation Counselor (CRC) license with associated college degree
CCM certification
Life Care Planner certification
Certified Medicare Secondary Payer (CMSP) certification

Skills

Life Care Planning Medicare compliance Submissions Appeals Medical terminology Diagnosis Procedure familiarity

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