Manufacturing Expansion Transition Technician – B Shift

Bard Pharmaceuticals Limited; Cambridge; On-site; GBP 27,000 - 36,000; Full time

Benefits offered by this job

Competitive salary

Job summary

Bard Pharmaceuticals Limited in Cambridge is seeking a Manufacturing Technician on a fixed-term project. You will support legacy production areas, ensure GMP compliance, and maintain continuity of supply during the manufacturing expansion programme.

This role focuses on safe operations, accurate documentation, quality control, and teamwork, with training for new expansion assets handled separately. The position ends with the completion of the project.

Qualifications

• Minimum 4 GCSEs (Maths and English) or equivalent.
• A-Level qualifications or equivalent preferred.
• Experience in GMP-regulated manufacturing environment.
• Knowledge of process equipment maintenance and validation activities.
• Strong attention to detail and documentation accuracy.

Responsibilities

• Support daily production targets across legacy manufacturing areas.
• Ensure activities are completed safely and per procedures.
• Prepare equipment and areas for shift handovers and readiness.
• Maintain production continuity through teamwork and prioritisation.
• Raise issues affecting production quality or performance promptly.

Skills

GMP compliance

5S

Kaizen

TPM

Problem-solving

Documentation

Education

GCSEs incl Math & English

A-Levels preferred

Job description

Manufacturing Technician (Fixed-Term Project Role) Location: Bard Manufacturing Facility Department: Manufacturing Operations Job Type: Fixed-Term (Project-Based) Reports to: Shift Manager Join us and make a difference when it matters most! At Bard, we are committed to delivering high-quality medicines safely, efficiently, and reliably to patients who depend on them. As part of our ongoing manufacturing expansion programme, we are investing in new capabilities while maintaining excellence within our existing operations. This role offers a unique opportunity to contribute to a critical business initiative by ensuring continuity of supply during a period of operational transformation.

Role Summary

The Manufacturing Technician is a fixed-term, project-linked position established to support manufacturing operations within Bard's legacy production suites during the Manufacturing Expansion Training Workstream. The role will ensure uninterrupted production while permanent manufacturing technicians undertake training and knowledge-transfer activities associated with the new ADHD bead manufacturing facility and related expansion assets. The post-holder will be responsible for delivering production, quality, safety, and operational performance targets within an assigned legacy manufacturing area, ensuring compliance with GMP requirements and Health & Safety standards. This role is restricted to existing manufacturing operations and does not include training, qualification, authorization, or deployment on the new expansion facilities.

Role and Responsibilities

• Manufacturing Operations Support Cell Leads in delivering daily production targets across assigned manufacturing areas.
• Ensure manufacturing activities are completed safely, efficiently, and in accordance with approved procedures.
• Prepare equipment, materials, and production areas to ensure smooth shift handovers and operational readiness.
• Maintain production continuity through effective teamwork and support of operational priorities.
• Proactively identify and elevate issues that may affect production performance or product quality.

Production Performance & Continuous Improvement

• Contribute to the achievement of key manufacturing performance indicators, including production output, equipment efficiency, changeover performance, and downtime reduction.
• Participate in root cause investigations and problem-solving activities to improve process understanding and operational performance.
• Support Continuous Improvement initiatives focused on waste reduction, yield improvement, and process optimization.
• Champion small-scale Kaizen projects and contribute to site improvement programmes.
• Participate in Autonomous Maintenance activities to support equipment reliability and performance.

Quality & Compliance

• Ensure all activities are performed in accordance with Good Manufacturing Practice (GMP) standards and company procedures.
• Complete manufacturing documentation accurately and in a timely manner.
• Support validation activities, including protocol execution, sampling activities, and associated documentation.
• Maintain a strong understanding of quality requirements, production records, and compliance expectations.
• Raise Documentation Change Requests (DCRs) for batch records, procedures, and controlled documents as required.
• Support ongoing regulatory compliance through adherence to approved processes and procedures.

Equipment & Asset Management

• Operate manufacturing equipment safely and effectively within designated production areas.
• Maintain machinery and production equipment in a clean, safe, and operational condition.
• Support routine cleaning, inspection, and servicing activities.
• Work collaboratively with Engineering and Quality teams to investigate and resolve equipment or process-related issues.
• Assist with troubleshooting activities to minimize operational disruptions.

Workplace Management & Operational Support

• Take ownership of workplace organization and housekeeping standards through effective implementation of 5S principles.
• Maintain appropriate stock levels of materials, consumables, and production components.
• Support Shift Managers and Coordinators through accurate operational reporting, including downtime recording and system updates.
• Manage workload effectively while maintaining flexibility to support business priorities.
• Ensure work areas remain inspection-ready and compliant with GMP and Health & Safety requirements at all times.

Health, Safety & Compliance

• Adhere to all site Health & Safety, security, and environmental requirements.
• Promote a culture of safety, quality, and continuous improvement.
• Ensure all manufacturing activities are conducted in accordance with company policies and regulatory expectations.
• Undertake any other reasonable duties required to support operational performance, product quality, and patient supply.

Qualifications

Education Minimum Required Minimum of 4 GCSEs (Grade C / Level 4 or above), including Mathematics and English, or equivalent qualifications.

Preferred A-Level qualifications or above, or equivalent vocational qualification.

Experience

Minimum Required Experience working within a GMP-regulated manufacturing environment.

Experience operating, cleaning, or servicing production equipment.

Preferred Experience within the pharmaceutical manufacturing industry.

Knowledge of process equipment maintenance activities.

Experience supporting quality, compliance, or validation activities within a regulated environment.

Knowledge and Skills Knowledge of GMP, 5S, Workplace Management, Kaizen, and Continuous Improvement principles. Understanding of Total Productive Maintenance (TPM) and equipment care practices. Strong focus on quality, compliance, and patient safety. Results-oriented with a proactive approach to achieving operational goals. Effective problem-solving and analytical skills. Good organizational and time-management abilities. Strong attention to detail and documentation accuracy. Positive attitude with a commitment to teamwork and continuous learning. Sound understanding of regulatory and business compliance requirements. Effective communication skills with the ability to work across multiple functions and organizational levels.

Working Conditions

• Manufacturing environment with exposure to hot and humid production suite conditions.
• Regular use of Personal Protective Equipment (PPE) and Respiratory Protective Equipment (RPE).
• Exposure to approved cleaning chemicals and pharmaceutical active ingredients.
• Frequent manual handling and equipment changeover activities.
• Physical tasks involving equipment dismantling, cleaning, inspection, and reassembly.
• Shift-based working arrangements as required by operational requirements.

Fixed-Term Project Information

• This role has been created specifically to support continuity of manufacturing operations during the Manufacturing Expansion Training Workstream.
• Responsibilities are limited to legacy manufacturing areas and associated production activities required to maintain product supply during the transition period.
• The successful candidate will not be trained, qualified, authorized, deployed or scheduled to work on the new ADHD bead manufacturing unit or any new expansion assets.
• Employment in this position will conclude upon completion of the Manufacturing Expansion Training Workstream, in accordance with the terms of the fixed-term contract.

What We Offer in Return

• Competitive salary and benefits package.
• Opportunity to contribute to a major manufacturing transformation programme.
• Experience within a highly regulated pharmaceutical environment.
• Exposure to Continuous Improvement and operational excellence initiatives.
• Supportive and collaborative working environment.
• Opportunities to further develop GMP and manufacturing expertise.

Diversity and Inclusion

At Bard, we are committed to fostering an inclusive workplace where everyone is treated with dignity, fairness, and respect. We value diverse backgrounds, experiences, and perspectives and believe they strengthen our ability to innovate and serve patients.

About Bard

Bard is dedicated to manufacturing high-quality medicines through operational excellence, innovation, and continuous improvement. Our teams play a vital role in ensuring reliable supply, maintaining the highest standards of quality and compliance, and supporting better outcomes for patients worldwide.

Additional Job Description

Primary Location: GB Cambridge Job Posting Date: 2026-08-17 Job Type: Fixed Term Contract (Fixed Term) Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe and debilitating disease areas. Our guiding principles, centered around Integrity and Patient-Centricity, are at the heart of everything we do. For more information visit www.mundipharma.com. For more information about Mundipharma's guiding principles and commitment to diversity and inclusion visit: www.mundipharma.com/people