Team Leader – Molecular Biology

Reference Number: JO-2504-549914
Team Leader – Molecular Biology
Rate: Negotiable
Job Type: Contract
Location: Cambridge

Job Title: Team Leader – Molecular Biology

Location: Cambridge

Pay rate: Up to £50 per hour

Contract Duration: 12-month contract

Cpl Life Sciences is working exclusively with a biotech company committed to advancing human health and scientific discovery. They are seeking an accomplished Team Leader in Molecular Biology to drive cutting-edge research and innovation within their advanced biopharmaceutical division. This role is crucial in shaping and integrating strategies, guiding high-impact projects, and mentoring a team of industry-leading scientists.

Key Responsibilities:

• Define and execute the molecular biology strategy, aligning with business goals to accelerate therapeutic development.
• Lead, mentor, and grow a high-performing team of scientists, fostering innovation, technical excellence, and career progression.
• Oversee the development and validation of novel molecular biology methodologies, ensuring scientific proficiency and industry-leading innovation.
• Drive automation, data-driven approaches, and next-generation sequencing (NGS) to enhance molecular biology capabilities.
• Work closely with departments including Bioinformatics, Process Development, and Clinical Research to drive integrated solutions.
• Ensure all molecular biology processes align with GMP, GLP, and regulatory expectations from the FDA, EMA, and other governing bodies.
• Represent the company in scientific conferences, regulatory discussions, and strategic partnerships to advance molecular research impact.

Minimum Qualifications:

• PhD in Molecular Biology, Biochemistry, Biotechnology, or a related field.
• Over 6-8 years of experience in molecular biology R&D, with a strong track record in senior roles within biotech or pharmaceutical organizations.
• Deep expertise in gene editing, synthetic biology, CRISPR, mRNA technology, plasmid DNA manufacturing, and cell-based assays.
• Experience in working within GMP/GLP-regulated environments and knowledge of global regulatory frameworks.
• Strong leadership and people management skills with experience building and leading large scientific teams.
• Proven ability to translate research into commercial and clinical applications.
• Excellent communication, stakeholder engagement, and project management skills.