Associate General Counsel at AGC Biologics

Copenhagen, Denmark

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Biopharmaceuticals, Biotechnology, PharmaceuticalsIndustries

Requirements

Master of Laws (LL.M.) or equivalent law degree
Qualified to practice law in Denmark
A minimum of 7 years of relevant legal experience, preferably with in-house experience in the biotech, pharmaceutical, or CDMO industry
Extensive experience drafting and negotiating complex commercial agreements, such as manufacturing, supply, and licensing agreements
Proven ability to manage complex legal matters and support cross-functional projects
Strong negotiation skills with a proven track record of handling high-value, complex agreements, preferably in the life sciences industry
A strategic mindset with the ability to translate complex legal issues into actionable business advice
Demonstrated ability to work effectively across a global, matrixed organization, collaborating with stakeholders in Business Development, Operations, and Quality
Solid expertise in Danish and EU law, corporate compliance, and regulations relevant to the pharmaceutical/biotech industry
Excellent communication and interpersonal skills, with the ability to advise and build trust at all levels of the organization
High integrity, professional judgment, and discretion in handling sensitive and confidential matters
Preferred
Experience gained from a major international law firm with a focus on life sciences or corporate transactions
In-house experience supporting a manufacturing site or operational facility in a regulated environment
Track record in managing corporate compliance and risk management programs

Responsibilities

Lead the negotiation and drafting of complex commercial agreements, including Development & Manufacturing Services Agreements, Commercial Supply Agreements, and technology transfer agreements
Serve as a key legal partner for the Copenhagen and Heidelberg site leadership, providing practical, solution-oriented legal counsel on a variety of business matters
Support the development, implementation, and management of corporate governance and compliance programs, ensuring adherence to local and global regulations and company policies
Investigate potential compliance violations, document findings, and recommend corrective actions
Work closely with the Senior Employee Relations Partner to develop policies, manage employee relations issues, and ensure compliance with Danish and EU labor laws
Manage and oversee legal disputes and litigation matters related to the Copenhagen and Heidelberg sites, engaging and directing external counsel as needed
Monitor evolving regulatory landscapes in the pharmaceutical and biotech industries, advising on potential impacts and assisting in policy adjustments
Draft, review, and negotiate a wide variety of legal documents and commercial contracts critical to the company’s operations

Skills

Contract Negotiation

Commercial Agreements

Development Agreements

Manufacturing Services Agreements

Supply Agreements

Technology Transfer Agreements

Corporate Governance

Regulatory Compliance

Compliance Investigation

EU Law

Danish Law

Employee Relations

AGC Biologics

Contract development and manufacturing for biopharmaceuticals

About AGC Biologics

AGC Biologics specializes in the development and manufacturing of therapeutic proteins, plasmid DNA, viral vectors, and genetically engineered cells for the biopharmaceutical industry. The company provides end-to-end solutions, assisting clients from the initial development stages to full-scale production. Their services are particularly focused on fast-tracking projects for orphan drugs and rare diseases, which often require quicker timelines. AGC Biologics operates a network of advanced facilities across the U.S., Europe, and Asia, all adhering to strict quality regulations known as current Good Manufacturing Practices (cGMP). What sets AGC Biologics apart from competitors is its commitment to continuous innovation and its recent expansion to enhance capabilities in cell and gene therapy. The company's goal is to support biopharmaceutical companies in bringing new treatments to market efficiently and effectively.

Bothell, WashingtonHeadquarters

2001Year Founded

$613MTotal Funding

ACQUISITIONCompany Stage

Biotechnology, HealthcareIndustries

1,001-5,000Employees

Risks

Restructuring and layoffs in Colorado indicate potential financial instability.

Leadership changes may disrupt ongoing projects and affect client trust.

Significant investment in Japan could strain financial resources and divert focus.

Differentiation

AGC Biologics specializes in therapeutic proteins, plasmid DNA, and viral vectors.

The company offers fast-track project capabilities for orphan drugs and rare diseases.

AGC Biologics operates globally with facilities in the U.S., Europe, and Asia.

Upsides

Increased demand for plasmid DNA boosts AGC's gene therapy and vaccine services.

Partnership with BioConnection enhances biodrug development capabilities, attracting more clients.

Expansion in Yokohama aligns with growing mRNA and cell therapy demand.

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