At a Glance
- Tasks: Join us in transforming lives through clinical supply activities and innovative medicines.
- Company: Bristol Myers Squibb, a leader in biopharmaceuticals with a mission to improve patient outcomes.
- Benefits: Enjoy competitive benefits, flexible work options, and opportunities for personal and professional growth.
- Other info: Be part of a diverse team that values collaboration, accountability, and continuous improvement.
- Why this job: Make a real impact in patients' lives while developing your career in a supportive environment.
- Qualifications: GMP experience in pharmaceutical packaging and labelling is essential.
The predicted salary is between 34200 - 41800 £ per year.
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 c GMP, 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 adastaffingsupport@bms. com.
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 TAEnablement@bms. com.
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.
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CSO Senior Technician in Moreton employer: Bristol Myers Squibb
Bristol-Myers Squibb in Uxbridge is an exceptional employer, offering a dynamic work culture that prioritises collaboration and innovation. Employees benefit from extensive career growth opportunities, mentorship programs, and the chance to contribute meaningfully to life-changing clinical trials, all while enjoying a supportive environment that values data integrity and compliance.
StudySmarter Expert Advice🤫
We think this is how you could land CSO Senior Technician in Moreton
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Bristol Myers Squibb. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Bristol Myers Squibb.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Bristol Myers Squibb. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Bristol Myers Squibb is looking for. A tailored application can really make you stand out!
We think you need these skills to ace CSO Senior Technician in Moreton
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Bristol Myers Squibb!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Bristol Myers Squibb that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Bristol Myers Squibb!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Bristol Myers Squibb, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Bristol Myers Squibb
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Bristol Myers Squibb that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Bristol Myers Squibb’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.