Site Lead – Clinical Packaging & Labelling
We're partnering with a leading global provider of clinical trial supply and patient access solutions to recruit a Site Lead for their clinical packaging and labelling facility in Raleigh, NC.
This is an excellent opportunity for someone with hands-on experience in clinical packaging, labelling or GMP warehouse operations who enjoys leading from the front. You'll be responsible for the day-to-day operation of the site, ensuring production activities are completed safely, efficiently and in full compliance with GMP and regulatory requirements.
This is a highly visible role where you'll supervise operational teams, drive continuous improvement and play a key part in delivering critical medicines to patients around the world.
What you'll be doing
- Lead and supervise the daily operations of a GMP clinical packaging and labelling facility.
- Manage warehouse, packaging and labelling activities to ensure projects are delivered on schedule.
- Coach, mentor and develop production and warehouse personnel.
- Ensure compliance with GMP, GDP, SOPs and all quality standards.
- Monitor productivity, workflow and resource planning across the site.
- Work closely with Quality, Supply Chain, Project Management and Customer Services to ensure seamless project execution.
- Support investigations, deviations, CAPAs and change controls where required.
- Drive continuous improvement initiatives to improve efficiency, quality and operational performance.
- Ensure a strong culture of safety, compliance and accountability across the site.
What we're looking for
- Experience supervising or leading teams within a clinical packaging, clinical labelling or pharmaceutical manufacturing environment.
- Strong understanding of GMP and regulated pharmaceutical operations.
- Experience working within warehouse, packaging or production environments supporting clinical trials or pharmaceutical products.
- Proven ability to motivate teams and manage day-to-day operational performance.
- Comfortable working cross-functionally with Quality, Supply Chain and Project teams.
- Strong organisational, communication and problem-solving skills.
- Experience supporting audits, inspections or quality investigations would be advantageous.
Ideal background
We're particularly interested in candidates from:
- Clinical Trial Supply organisations
- Pharmaceutical packaging and labelling companies
- CDMOs
- Pharmaceutical manufacturing facilities
- Comparator sourcing and clinical supply providers
Why apply?
- Join a growing global organisation supporting life-changing clinical research.
- Take ownership of a critical operational leadership position.
- Work in a collaborative, quality-focused environment.
- Excellent opportunity for career progression within an expanding international business.