Clinical Supply Operations (CSO) Technician Full Time NEW

Are you detail-oriented with a passion for quality in a fast-paced GMP environment? We are seeking a dedicated and organized Clinical Supply Operations (CSO) Technician to support critical packaging activities within our dynamic clinical operations team. This operational role offers the opportunity to contribute to groundbreaking clinical trials, ensuring the safe and accurate packaging of investigational medicinal products.

What You’ll Do

• Execute start-up, routine, and completion activities for clinical trial packaging in accordance with SOPs, GMP standards, and EHS guidelines.
• Perform primary packaging tasks such as bottle filling of oral dosage forms, and assemble and label supplies including syringes, vials, and wallets using automated and manual equipment.
• Maintain accurate electronic batch records, equipment logbooks, and documentation throughout all production stages.
• Monitor and control production processes, troubleshoot equipment issues, and escalate concerns as needed to ensure consistent quality.
• Collaborate with team members and operate independently to meet daily production targets.
• Participate in internal audits and contribute to continuous process improvements, always prioritizing safety, quality, and customer service.

Required Skills

• Prior experience in GMP packaging and labelling, preferably within clinical trial environments.
• Familiarity with electronic systems such as SAP.
• Proven ability to follow SOPs, GMP practices, and health and safety requirements.
• High attention to detail and accuracy.
• Strong problem-solving, communication, and teamwork skills.
• Computer literacy and willingness to learn and share knowledge.

Nice To Have Skills

• Clinical trial packaging experience.
• Experience with automated labelling and walleting equipment.
• Knowledge of clinical trial operations beyond packaging.

Preferred Education And Experience

• A-levels or equivalent, preferably in sciences or IT-related subjects.
• Prior experience in a GMP environment with exposure to clinical packaging operations.

Other Requirements

• This is a full-time, on-site role based in Merseyside
• Ability to work safely, adhere to COSHH regulations, and participate in internal audits.
• The position is initially contracted for 12 months, with potential for extension.

If you’re eager to make a meaningful impact in clinical research through meticulous and compliant packaging operations, we encourage you to apply now. Take the next step in your career and join a team committed to excellence and innovation in healthcare.