Laboratory Technician
Full Job Posting
Qualifications
- Education
- Minimum Required
- Minimum of 5 GCSEs (Grade C / Level 4 or above), including Mathematics and English, or equivalent qualifications.
- Preferred
- A-Level qualifications, ideally in a scientific discipline, or equivalent vocational qualification.
- Degree or higher education qualification in Science, Supply Chain, Logistics, Business Administration, or a related field.
- Experience working within a logistics, administrative, inventory management, warehouse, laboratory support, or regulated operational environment.
- Experience managing documentation and records with a high level of accuracy.
- Experience coordinating activities involving internal and external stakeholders.
- Experience within the pharmaceutical, healthcare, laboratory, or life sciences industry.
- Experience using Laboratory Information Management Systems (LIMS).
- Experience using Oracle or similar inventory management systems.
- Experience supporting import/export activities and regulated shipments.
- Experience working with contract laboratories, third-party logistics providers, or regulatory authorities.
- Knowledge of controlled drug handling and transportation requirements.
- Good understanding of GMP, GxP, and quality system requirements.
- Knowledge of sample management, inventory control, and laboratory support processes.
- Strong organizational and planning skills with the ability to manage multiple priorities.
- Excellent attention to detail and documentation accuracy.
- Proficient in Microsoft Office applications, including Word, Excel, Outlook, and Teams.
- Effective communication skills with the ability to collaborate across multiple functions and external organizations.
- Ability to follow SOPs, policies, and regulatory requirements consistently.
- Strong problem-solving and analytical skills.
- Ability to work independently while contributing effectively within a team environment.
- High level of accountability and ownership of assigned responsibilities.
- Understanding of import/export documentation and logistics processes.
- Commitment to quality, compliance, and patient safety.
- Demonstrated reliability, flexibility, and willingness to learn.
- Working Conditions
- Office and laboratory support environment.
- Frequent interaction with laboratory personnel, logistics providers, and external testing partners.
- Regular use of computerized laboratory and inventory management systems.
- Handling and coordination of controlled drug samples, reference standards, and laboratory materials.
- Occasional manual handling associated with sample packaging and shipment preparation.
- Requirement to comply with GMP, Health & Safety, and security procedures.
- Participation in audits, inspections, and compliance reviews as required.
- Fixed-Term Project Information
- This role has been created to support analytical testing and batch disposition activities during the Manufacturing Expansion Programme.
- The successful candidate will play a critical role in ensuring uninterrupted analytical sample flow between Bard and external testing laboratories, supporting timely product release and continuity of patient supply throughout the project period.
- This position is offered as a 2-year fixed-term contract, and successful candidates must be able to commit to the full contract period. Employment in this position will conclude upon completion of the project in accordance with the terms of the fixed-term contract.
- What You Get in Return
- Competitive salary and benefits package.
- Flexible benefits programme.
- Opportunity to gain experience in a highly regulated pharmaceutical environment.
- Exposure to laboratory operations, quality systems, and supply chain processes.
- Development of GMP, logistics, and compliance expertise.
- Opportunity to contribute to a major business transformation programme.
- Supportive and collaborative working environment.
- Training and development opportunities to build technical and operational knowledge.
- Experience working with international laboratories and global regulatory requirements.
- The opportunity to directly support product quality, compliance, and continuity of patient supply.
- GB Cambridge
- 2026-10-19
- Fixed Term Contract (Fixed Term)
Knowledge and Skills
- Good understanding of GMP, GxP, and quality system requirements.
- Knowledge of sample management, inventory control, and laboratory support processes.
- Strong organizational and planning skills with the ability to manage multiple priorities.
- Excellent attention to detail and documentation accuracy.
- Proficient in Microsoft Office applications, including Word, Excel, Outlook, and Teams.
- Effective communication skills with the ability to collaborate across multiple functions and external organizations.
- Ability to follow SOPs, policies, and regulatory requirements consistently.
- Strong problem-solving and analytical skills.
- Ability to work independently while contributing effectively within a team environment.
- High level of accountability and ownership of assigned responsibilities.
- Understanding of import/export documentation and logistics processes.
- Commitment to quality, compliance, and patient safety.
- Demonstrated reliability, flexibility, and willingness to learn.
- Working Conditions
- Office and laboratory support environment.
- Frequent interaction with laboratory personnel, logistics providers, and external testing partners.
- Regular use of computerized laboratory and inventory management systems.
- Handling and coordination of controlled drug samples, reference standards, and laboratory materials.
- Occasional manual handling associated with sample packaging and shipment preparation.
- Requirement to comply with GMP, Health & Safety, and security procedures.
- Participation in audits, inspections, and compliance reviews as required.
- Fixed-Term Project Information
- This role has been created to support analytical testing and batch disposition activities during the Manufacturing Expansion Programme.
- The successful candidate will play a critical role in ensuring uninterrupted analytical sample flow between Bard and external testing laboratories, supporting timely product release and continuity of patient supply throughout the project period.
- This position is offered as a 2-year fixed-term contract, and successful candidates must be able to commit to the full contract period. Employment in this position will conclude upon completion of the project in accordance with the terms of the fixed-term contract.
What You Get in Return
Competitive salary and benefits package.
Flexible benefits programme.
Opportunity to gain experience in a highly regulated pharmaceutical environment.
Exposure to laboratory operations, quality systems, and supply chain processes.
Development of GMP, logistics, and compliance expertise.
Opportunity to contribute to a major business transformation programme.
Supportive and collaborative working environment.
Training and development opportunities to build technical and operational knowledge.
Experience working with international laboratories and global regulatory requirements.
The opportunity to directly support product quality, compliance, and continuity of patient supply.
Additional Job Description:
Primary Location:
GB Cambridge
Job Posting Date:
2026-10-19
Job Type:
Fixed Term Contract (Fixed Term)
Preferred Qualifications
- Preferred
About Mundipharma
Global healthcare company focused on cancer pain management and specialty care for practitioners, caregivers, and patients worldwide.
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