CSO Senior Technician

Bristol-Myers Squibb; Moreton; On-site; GBP 30,000 - 42,000; Full time

Job summary

Bristol Myers Squibb in the United Kingdom is seeking a Senior Technician for Clinical Trials Packaging and Labelling to deliver safe, compliant, right-first-time execution of clinical supply activities.

You will work with SOPs, batch records and SAP, operate GMP equipment, complete electronic batch records and support investigations, deviations, change control and internal audits.

Qualifications

• Must have GMP experience within a pharmaceutical packaging and labelling team.
• Clinical trial packaging and labelling, preferred

Responsibilities

• Maintain high standards of cGMP, safety, documentation and data integrity.
• Complete primary and secondary production operations per procedures.
• Operate GMP equipment to support production and perform in-process checks.
• Complete electronic batch records and SAP transactions accurately and timely.
• Work independently or as part of a team across general production tasks.
• Support investigations, deviation assessment and change control activities.

Skills

GMP experience

Independent worker

Quality mindset

Tools

SAP

Job description

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Position Summary

Senior Technician within Clinical Trials Packaging and Labelling operations, working to a high standard with increased independence to deliver safe, compliant, right-first-time execution of clinical supply activities. Demonstrate strong working knowledge of approved SOPs, Work Instructions, batch records, electronic systems and GMP requirements, supporting timely completion of process orders and escalation of issues Act as an experienced operational contributor by supporting problem solving, process discipline, continuous improvement, and the development of less experienced technicians.

Key Responsibilities

• Maintain high standards of cGMP, safety, documentation, data integrity and good housekeeping practices, actively identifying and escalating risks or abnormal conditions.
• Completion of Primary and Secondary production operations in accordance with approved procedures.
• Operate GMP equipment to support production, including set-up, in-process checks, basic troubleshooting, post-operation strip down and cleaning.
• Complete electronic batch records, equipment logbooks and associated production documentation accurately and in a timely manner, including relevant SAP transactions.
• Demonstrate the ability to work independently or as part of a team across general production operations and supporting tasks.
• Monitor production processes and equipment performance, resolve routine issues within training and authority, andescalate non‑routine issues appropriately.
• Apply a good working understanding of regulatory, GMP, safety and quality requirements relevant to clinical trial packaging and labelling, including when to stop, challenge orescalate work.
• Support investigations, deviation assessment, root cause analysis, corrective actions and change control activities where required, providing accurate operational input and evidence.
• Participate in internal audits, inspections, readiness activities, equipment validation or system user acceptance testing.
• Support continuous improvement by identifying opportunities to improve workflow, compliance, safety, quality, material flow or operational efficiency.
• Support training, coaching and mentoring of technicians by sharing technical knowledge, reinforcing procedural discipline and helping embed good GMP behaviours.
• Contribute to a respectful, inclusive and collaborative team environment, modelling accountability, clear communication and patient-focused decision making.
• Demonstrate a patient-focused mindset by recognising the importance of clinical supply activities to trial delivery, product quality and patient outcomes.

Required and Preferred Experience

Must have GMP experience within a pharmaceutical packaging and labelling team. Clinical trial packaging and labelling, preferred

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Bristol Myers Squibb is Disability Confident – Employer A UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [e-mail]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1605445 : CSO Senior Technician Data Privacy Link

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.