Manufacturing Expansion Transition Technician – A Shift

Bard Pharmaceuticals Limited; Cambridge; On-site; GBP 30,000 - 42,000; Full time

Benefits offered by this job

Competitive salary

Fixed-term project role

Cambridge site

Job summary

Bard Pharmaceuticals Limited is seeking a Manufacturing Technician for a fixed-term project at our Cambridge site. The role supports routine manufacturing within legacy production areas, ensuring targets, quality and safety are met while the expansion project is underway.

The successful candidate will work with cross-functional teams to maintain continuity, perform routine equipment prep, and uphold GMP compliance within a highly regulated pharmaceutical setting.

Qualifications

• Experience in a GMP-regulated pharmaceutical environment.
• Strong understanding of GMP principles and quality systems.
• Background in 5S, TPM, and continuous improvement methods.

Responsibilities

• Support legacy manufacturing operations to maintain production targets.
• Prepare equipment, materials and changeover readiness for shifts.
• Collaborate with Engineering and Quality to resolve issues.
• Ensure documentation and batch records are accurate and complete.

Skills

GMP compliance

5S Workplace

Autonomous Maintenance

Problem solving

Effective communication

Education

GCSEs incl. Maths & English

A-Levels or equivalent

Job description

Manufacturing Technician (Fixed-Term Project Role) Location: Bard Manufacturing Facility Department: Manufacturing Operations Job Type: Fixed-Term (Project-Linked) Reports to: Shift Manager / Manufacturing Coordinator Join us and make a difference when it matters most! At Bard, we are committed to delivering high-quality medicines safely, efficiently, and consistently for patients who depend on them. As part of our commitment to operational excellence and continuous improvement, we are investing in the future expansion of our manufacturing capabilities while ensuring uninterrupted supply from our existing production operations. This fixed-term opportunity offers the chance to play a critical role in maintaining manufacturing continuity during a major business transformation project.

Role Summary

The Manufacturing Technician is a fixed-term, project-linked position created to support routine manufacturing operations within Bard's existing manufacturing suites during the Manufacturing Expansion Training Workstream. The role exists to ensure uninterrupted production while permanent technicians are released to participate in training activities associated with the new ADHD bead manufacturing unit and expansion assets. The successful candidate will be responsible for manufacturing processes within an assigned legacy production area, ensuring production targets, quality standards, and safety requirements are consistently achieved. The role is focused exclusively on existing manufacturing operations and does not include training, qualification, authorization, or deployment on any new expansion assets. This appointment is temporary and will conclude upon completion of the Manufacturing Expansion Training Workstream.

Role and Responsibilities

• Manufacturing Operations Support Cell Leads in achieving production targets within designated legacy manufacturing areas.
• Work collaboratively within the production team to ensure operational continuity and effective shift coverage.
• Prepare equipment, materials, and resources for incoming shifts to ensure efficient start-up and continuity of operations.
• Ensure components, materials, and changeover requirements are available and prepared in advance.
• Maintain operational readiness and support efficient manufacturing performance throughout the shift.

Production Performance & KPI Delivery

• Support delivery of key manufacturing performance indicators, including: Changeover time targets
• Production run rates
• Downtime reduction
• Yield performance
• Asset utilization
• Monitor process performance and elevate issues appropriately.

Continuous Improvement

• Participate in root cause investigations and problem-solving activities to support operational excellence.
• Contribute to Continuous Improvement initiatives focused on waste reduction, yield enhancement, and process optimization.
• Lead or support small Kaizen projects within the manufacturing area.
• Actively participate in Autonomous Maintenance programs and workplace improvement activities.

Quality & Compliance

• Ensure full compliance with Good Manufacturing Practice (GMP) requirements and site procedures.
• Maintain accurate production documentation and records.
• Demonstrate strong understanding of quality systems, batch records, and manufacturing documentation.
• Raise Documentation Change Requests (DCRs) as required to support operational efficiency and regulatory compliance.
• Support validation activities, including protocol execution and sampling requirements.
• Ensure all activities comply with internal quality standards and regulatory expectations.

Equipment & Asset Care

• Operate manufacturing equipment safely and effectively within approved procedures.
• Maintain machinery in a clean, safe, and operational condition.
• Support equipment cleaning, servicing, and basic maintenance activities.
• Work closely with Engineering teams to resolve equipment-related issues and atypical events.
• Assist with troubleshooting and corrective actions to minimize production disruption.

Cross-Functional Collaboration

• Collaborate closely with Engineering, Quality, and Manufacturing teams to resolve operational challenges.
• Communicate effectively across departments to ensure production objectives are achieved.
• Support Shift Managers and Coordinators through timely reporting of operational performance and downtime events.
• Contribute to a positive team environment that encourages collaboration and continuous improvement.

Workplace Management, Health & Safety

• Maintain high standards of workplace organization through effective 5S implementation.
• Take ownership of housekeeping, stock control, and workplace management processes.
• Ensure work areas remain compliant with GMP and Health & Safety requirements.
• Adhere to all site security, environmental, and safety procedures.
• Promote a culture of safety, accountability, and operational excellence.

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 qualifications.

Experience Minimum Required

• Experience working within a GMP-regulated environment.
• Experience cleaning, servicing, or operating production equipment.

Preferred Experience

• Experience within the pharmaceutical manufacturing industry.
• Experience supporting process equipment maintenance activities.

Knowledge and Skills

• Good understanding of GMP principles and pharmaceutical manufacturing practices.
• Knowledge of 5S, Workplace Management, Kaizen, and Continuous Improvement methodologies.
• Understanding of Total Productive Maintenance (TPM) and Autonomous Maintenance principles.
• Strong focus on quality, compliance, and operational excellence.
• Results-oriented with a proactive and accountable approach.
• Effective problem-solving and root cause analysis skills.
• Good organizational and time-management capabilities.
• Ability to communicate effectively across multiple organizational levels.
• Positive attitude with a commitment to learning, improvement, and change.
• Sound understanding of regulatory, quality, and business compliance requirements.
• Ability to work both independently and collaboratively within a team environment.

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 activities and repetitive movements. Regular stripping, cleaning, reassembly, and operation of manufacturing equipment. Shift-based working pattern as required by operational needs. Fixed-Term Project Information This position has been created solely to support continuity of routine manufacturing operations during the Manufacturing Expansion Training Workstream. Responsibilities are limited to activities within assigned legacy manufacturing areas and supporting processes required to maintain production output during the transition period. The role does not include training, qualification, authorization, deployment, or scheduling on the new ADHD bead manufacturing unit or any associated expansion asset. Employment within this role will conclude upon completion of the Manufacturing Expansion Training Workstream in accordance with the terms of the fixed-term employment agreement.

What We Offer in Return

• Competitive salary and benefits package.
• Opportunity to contribute to a significant manufacturing expansion project.
• Experience within a highly regulated pharmaceutical manufacturing environment.
• Exposure to Continuous Improvement and operational excellence initiatives.
• Supportive and collaborative team culture.
• Opportunities to develop manufacturing and GMP expertise during the project assignment.

Diversity and Inclusion

At Bard, we are committed to creating a workplace where everyone feels respected, valued, and included. We believe diversity drives innovation, strengthens our teams, and helps us achieve better outcomes for our employees, customers, and the patients we serve.

About Bard

Bard is committed 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 initiatives that improve healthcare outcomes for patients globally.

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