Project Manager - In-licensing Job at 360 Resourcing Solutions (East Kilbride or Burnopfield)

Director, Business Development & In-Licensing

The Director of Business Development & In‑Licensing will drive Theramex’s inorga...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Educated to degree level
an advanced degree is preferred
Experience in European pharmaceutical business development with an international remit
pan‑European exposure strongly preferred
Proactive, highly autonomous self‑starter who is comfortable rolling up their sleeves and driving work forward independently
Demonstrated track record of leading licensing transactions, supported by a clear, deal‑focused transaction sheet showcasing relevant in‑licensing deals
Strong understanding of EU pharmaceutical licensing frameworks, regulatory pathways, and commercial drivers across major European markets
Strong financial acumen, including valuation, forecasting, and business‑case development
Proven negotiation capabilities with a record of successfully concluding multiple deals
Ability to influence, collaborate, and build strong relationships across all levels within a matrix organisation, with an understanding of key functions such as pricing and market access, regulatory, legal, logistics, sales & marketing, and quality

Job Responsibility

Work closely with the Chief Corporate Development Officer (CCDO), Member of the Executive Leadership Team (ELT), to review, assess and acquire new in-organic growth opportunities for presentation to the Board (Private Equity owned)
Identify and assess relevant in-organic growth opportunities, including reviewing competitive landscape, evaluating macroeconomic trends, and working with IQVIA data and other industry sources, building business cases, performing valuations and preparing slides for Board decisions
Effectively source, identify and triage target opportunities and communicate the strategic and industrial logic of the relevant opportunity for the Theramex business to key stakeholders
Strong relationships and engagement with KOLs to assess areas of unmet need and, with the support of Medical, help run Advisory Boards to generate potential leads for evaluation
Negotiate new product-licensing opportunities with third parties which are in line with the company's geographic and therapeutic expansion goals
Together with the CCDO, participate in the negotiation and settlement of licensing deals
Be able to work with senior executives, including members of the ELT, key employees at Theramex, and investor representatives, Board Members and advisors and consultants engaged on particular projects
Work cross-functionally to review expansion opportunities with Theramex's existing portfolio (e.g., portfolio optimisation)
To extent necessary also support activities in relation to M&A or product acquisition

What we offer

A fast-paced environment, with broad exposure, where you can develop professionally – even outside your area of expertise
We support you as you grow and learn, and we love to celebrate success and recognize performance
We provide opportunities for driven and talented professionals who want to be part of our exciting journey

Fulltime

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This position is responsible for leading CMC regulatory activities for investiga...

Location

United States; Belgium; Italy; United Kingdom , Collegeville; Wavre; Durham; Siena; London; Waltham

Salary:

144375.00 - 240625.00 USD / Year

GSK

Expiration Date

Until further notice

Requirements

Bachelor's degree in Life Sciences or related field
Four or more years of experience in drug development and manufacturing and supply processes and may have a specialized area of expertise
Four or more years of experience interpreting and executing complex worldwide CMC regulatory requirements and demonstrated ability to influence the global internal/external regulatory environment
Two or more years of experience completing project management tasks.

Job Responsibility

Drives the CMC strategy coordinates the timely preparation and authors, as needed, technical (CMC) regulatory documents to support development/registration/lifecycle maintenance submission content, in accordance with the applicable regulatory & scientific standards, and taking into account the evolving regulatory requirements
Identifies risks to the business associated with submission data and information packages and provides and communicates well defined risk mitigation strategies
Mentors or trains staff
May have direct line management responsibility
Manages project activities for multiple complex projects and teams simultaneously, including those for reporting staff as appropriate
Provides strategic direction, data assessment and conclusions within and across departments
Able to establish organisational networks (internal and external understanding departmental constraints/pressure within a highly complex organisation
Engages and may lead CMC Subject Matter Expert activities, both internally (for increased compliance, harmonisation and efficiency) and externally (external advocacy and shaping the regulatory environment)
May deliver CMC regulatory strategy to support major inspections (e.g. PAI's) or quality incidents (PIRCs)
Has accountability for submission content

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays
Vacation

Fulltime

Director of External Research & Development

At Amgen, if you feel like you're part of something bigger, it's because you are...

Location

United States , Thousand Oaks; South San Francisco; Cambridge

Salary:

191355.40 - 258892.60 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree in a scientific field & 4 years of experience in drug development industry and/or biopharma business development
Master's degree in a scientific field & 7 years of experience in drug development industry and/or biopharma business development
Bachelor's degree in a scientific field & 9 years of experience in R&D and/or biopharma business development

Job Responsibility

Lead Amgen's business development efforts in identifying and evaluating innovative therapeutics being developed outside of Amgen within the Inflammation/autoimmune therapeutic space for potential in-licensing, M&A, or collaborations
Develop and nurture a network of key industry and academic contacts to ensure robust communication of ideas, interests and information between the external community and internal groups
Proactive efforts to manage the search and identification of opportunities through networking and reviews of the external landscape and assessing prioritizing based on Amgen's therapeutic area strategy
Lead the technical evaluations of opportunities by creating and managing cross-functional review teams, providing recommendations based on robust scientific and drug industry knowledge, and ensuring appropriate and efficient decision-making processes
Ensure efficient reviews and engage in business negotiations and work with legal to execute contractual agreements for certain projects
Lead strategic discussions and presentations, collaborating closely with senior management, R&D, and Commercial to develop a set of priorities for licensure or M&A
Support of out-licensing activities

What we offer

Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Head of Business Development

Lead strategic growth initiatives in Japan's dynamic pharmaceutical market – hyb...

Location

Japan , Tokyo

Salary:

20000000.00 - 28000000.00 JPY / Year

Randstad

Expiration Date

July 22, 2026

Requirements

Bachelor's degree in Life Sciences, Pharmacy, or a related field
MBA or advanced degree preferred
8+ years of experience in business development within the pharmaceutical or biotech industry
Strong understanding of drug development and commercialization processes
Proven track record of successful deal-making and strategic partnerships
Excellent negotiation, communication, and leadership skills
Ability to manage multiple high-impact projects simultaneously
Fluency in Japanese and English
Experience working in a global pharmaceutical company is highly desirable
Experience with market access and pricing strategies

Job Responsibility

Develop and execute the Japan business development strategy
Lead deal sourcing, due diligence, negotiation, and execution of strategic transactions
Build and maintain strong relationships with key industry stakeholders
Collaborate with cross-functional teams to assess and develop new opportunities
Support pricing and market access strategies for in-licensed or acquired products
Develop business cases and financial models
Assess risks and mitigation strategies for potential deals
Represent the company at industry events

What we offer

健康保険
厚生年金保険
雇用保険
土曜日
日曜日
祝日

Fulltime

Senior Corporate Counsel

Baxter is seeking a Senior Corporate Counsel for Australia and New Zealand to pr...

Location

Australia , Old Toongabbie, New South Wales

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Tertiary Degree in Law from a well-regarded Australian university
Admitted to practice as a solicitor in a State or Territory of Australia
Approximately 6 to 10 years of post-admission experience
Significant experience in a well-regarded law firm and, preferably, additional experience as in-house legal counsel
Strong contract drafting, negotiation, and advisory skills
Knowledge of competition and consumer laws is preferred but not essential
Knowledge of local privacy laws is preferred but not essential
Proficiency in interpreting and applying legislation, regulations, codes of conduct, and corporate policies
Knowledge of modern slavery laws and sustainable procurement requirements is preferred but not essential
Excellent communication and multicultural interpersonal skills

Job Responsibility

Partner with the AGC to identify and manage legal risks across the business, including managing medium to high risks with minimal supervision
Draft, negotiate and advise on a range of commercial contracts with business partners in both the private and public sectors, including customers, suppliers and research institutions
Support local and global business development activities, including acquisitions, divestments, integrations and in-licensing
Support the AGC in advising on competition and consumer law risks
Advise on marketing and educational initiatives
Partner with the global Privacy team to advise on privacy issues
Partner with the regional Ethics & Compliance team to manage anti-bribery risks
Support the AGC in the development, implementation and continuous improvement of local policies, processes and compliance programmes, including those relating to contract lifecycle management, competition and consumer law, whistleblowing and modern slavery
Assist in the creation, upkeep, and application of global policies and procedures
Develop and deliver training on global and local policies and local laws

Senior Corporate Counsel

Are you a seasoned legal professional ready to make an impact in a dynamic, purp...

Location

Australia , Old Toongabbie

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Tertiary Degree in Law from a well-regarded Australian university
Admitted to practice as a solicitor in a State or Territory of Australia
Approximately 6 to 10 years of post-admission experience
Significant experience in a well-regarded law firm and, preferably, additional experience as in-house legal counsel
Strong contract drafting, negotiation, and advisory skills
Proficiency in interpreting and applying legislation, regulations, codes of conduct, and corporate policies
Excellent communication and multicultural interpersonal skills
Ability to role model integrity and build trust
Manage key stakeholders and collaborate effectively to develop creative solutions
The ability to manage a wide range of competing demands

Job Responsibility

Partner with the AGC to identify and manage legal risks across the business, including managing medium to high risks with minimal supervision
Draft, negotiate and advise on a range of commercial contracts with business partners in both the private and public sectors, including customers, suppliers and research institutions
Support local and global business development activities, including acquisitions, divestments, integrations and in-licensing
Support the AGC in advising on competition and consumer law risks
Advise on marketing and educational initiatives
Partner with the global Privacy team to advise on privacy issues
Partner with the regional Ethics & Compliance team to manage anti-bribery risks
Support the AGC in the development, implementation and continuous improvement of local policies, processes and compliance programmes, including those relating to contract lifecycle management, competition and consumer law, whistleblowing and modern slavery
Assist in the creation, upkeep, and application of global policies and procedures
Develop and deliver training on global and local policies and local laws

New

Head of IT Architecture & Data

We are looking for a Head of IT Architecture and Data to lead the firm's enterpr...

Location

United Kingdom , Leeds

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Proven enterprise architecture leadership experience, including data architecture
Experience defining strategy, standards, governance and roadmaps in a complex environment
Strong understanding of business, application, data, integration and technology architecture
Experience designing scalable, resilient and supportable solutions across cloud and SaaS environments
Good knowledge of data governance, AI governance, risk, assurance and control
The ability to explain complex topics clearly and influence senior stakeholders with credibility
Experience in a regulated or professional services environment would be advantageous.

Job Responsibility

Define and maintain enterprise architecture principles, standards, roadmaps and governance
Lead the firm's data strategy, governance, quality and management approach
Guide solution design for major initiatives, supporting simplification, resilience and reduction of technical debt
Set governance and design guardrails for AI-enabled and emerging technologies
Work closely with IT leadership, business stakeholders and suppliers to shape roadmaps and support informed decisions
Lead and develop the Solutions Architect and Data Architect, building capability and improving ways of working

What we offer

Competitive Salary & Benefits

Fulltime

New

Head of Platforms

Reporting to the Director of Technology and Innovation, the Head of Platforms is...

Location

United Kingdom , Leeds

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Senior platforms or enterprise technology leadership experience, ideally in legal or professional services
Track record of owning platform strategy, service improvement, lifecycle management and roadmap delivery
Experience leading software development, both on-shore and off-shore, testing and AI-related teams
Strong understanding of enterprise legal platforms, AI, cloud and SaaS environments and how they are governed and supported at scale
Experience with Microsoft SharePoint, Power Platform, Microsoft 365, Azure and Microsoft Entra, with a focus on standardisation and improved user experience
Strong understanding of software engineering lifecycle disciplines, including source control, testing, release controls and documentation
Good understanding of security, risk, resilience and compliance considerations relevant to platform ownership
Practical experience working within ISO 27001 and CyberEssentials+ aligned environments
Experience defining code governance, repository controls, engineering standards and release disciplines
Excellent stakeholder management and communication skills, with the ability to explain complex matters clearly to technical and non-technical audiences

Job Responsibility

Define and maintain platform strategy, standards, lifecycle plans and roadmaps for core platforms including DMS, CMS, Microsoft SharePoint and Power Platform, ensuring alignment with architecture, data, security and wider strategy
Own the platform estate, identifying priorities for optimisation, consolidation, modernisation, value realisation, risk and technical debt
Establish governance, including development and testing standards, code storage, version control, release disciplines and documentation
Work with Operations and Security to improve lifecycle management and documentation, resilience, performance, patching, configuration control, backup, recovery and platform health
Ensure platform changes are integrated, supportable and aligned to enterprise standards throughout the SDLC
Lead software development and testing capability, embedding quality practices and standards
Support assessment, adoption and governance of AI-related platforms, tooling and capabilities
Work with stakeholders, IT leadership and service teams to understand priorities, shape roadmaps and communicate direction, threats and opportunities
Maintain relationships with key suppliers and partners, working with Operations to drive service performance
Build and mature platform capability, including team structure, service ownership, governance, tooling, automation and operational documentation

Fulltime

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Project Manager - In-licensing

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