Clinical Trials Packaging and Labelling Technician

Atrium (EMEA); Wirral; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Clinical Trials Packaging and Labelling Technician for an initial 12-month contract. The role involves executing clinical trial packaging, ensuring quality standards and compliance with GMP, while working independently and as part of a team. Interested candidates should possess relevant skills and a strong background in GMP environments.

Qualifications

• Typically educated to A level standard, preferably in subjects relating to sciences or IT.
• Experience of packaging and labelling in a GMP environment.
• Working knowledge in SAP.

Responsibilities

• Ensure compliance with GMP requirements for clinical trial packaging.
• Perform primary packaging of oral dosage forms and assembly of trial supplies.
• Conduct basic troubleshooting of equipment and resolve production problems.

Skills

Problem-solving

Communication

Interpersonal skills

Ability to meet deadlines

Knowledge sharing

Education

A level standard in sciences or IT

Tools

SAP

Job description

Clinical Trials Packaging and Labelling Technician

Clinical Trials Packaging and Labelling Technician

Direct message the job poster from Atrium (EMEA)

Senior Recruitment Manager at Atrium (EMEA) - 0208 773 7657

Clinical Trials Packaging and Labelling Technician

Duration: Initial 12 months contract

Location: Moreton, Wirral

Work Schedule: Monday to Friday – 2 shifts available

Key Responsibilities

• Start-up, execute, cleaning and completion clinical trial packaging operations in accordance with appropriate Standard Operating Procedures.
• Primary packaging (bottle filling) of oral dosage forms using a range of equipment
• Labelling and assembly of clinical trials supplies, including automated labelling and walleting equipment
• Working independently and as part of a team, on equipment or process projects
• Control and monitor production process and equipment; resolve problems or correct abnormal conditions, conduct basic troubleshooting, and escalate problems appropriately.
• Develop and apply a working knowledge of relevant electronic systems, including SAP.
• Complete electronic batch documentation, equipment logbooks and other documentation relevant all stages of production.
• Understand and follow GMP requirements and defined procedures to maintain the requirements of quality standards in the packaging environment.
• Work safely in packaging environment, understanding personal responsibility for Health, Safety and the Environment and principles of risk management.
• Understand and comply with procedures relevant to COSHH.
• Participate in internal audits.
• Passionate about quality and customer service.
• Participate in continuous process improvement.

Required Skills and Qualifications

• Typically educated to A level standard, preferably in subjects relating to sciences or IT
• Problem-solving skills and ability to work effectively with colleagues to resolve problems
• Communication and interpersonal skills
• Ability to work accurately to deadlines
• Ability to develop and share knowledge

Required Knowledge and Experience

• Experience of packaging and labelling environment in a GMP environment, preferably within clinical trials.
• Working knowledge in SAP
• Basic knowledge of clinical trial operations

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Contract

Job function

• Job function

  Manufacturing

• Industries

  Pharmaceutical Manufacturing

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