Clinical Supplies Technician

Bristol Myers Squibb; Wirral; On-site; GBP 25,000 - 30,000; Full time

Job summary

Join a leading company as a Clinical Supplies Technician, where you will ensure precision in clinical trial packaging within a GMP-regulated environment. Collaborate with a dynamic team to foster innovation and excellence in healthcare solutions, while enjoying competitive benefits and opportunities for growth.

Benefits

Competitive benefits

Qualifications

• Experience in a GMP packaging and labelling environment.
• Ability to work accurately to deadlines.
• Computer literate.

Responsibilities

• Execute clinical trial packaging operations according to SOPs.
• Control and monitor production processes and equipment.
• Complete electronic batch documentation.

Skills

Problem-solving

Communication

Interpersonal

Attention to detail

Education

A level standard in sciences or IT

Tools

SAP

Job description

1 day ago Be among the first 25 applicants

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.

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 .

Join our dynamic team as a Clinical Supplies Technician, where your passion for quality, attention to detail and customer service will drive the advancement of critical healthcare solutions.

In this pivotal role, you'll be working in a team to produce clinical trial kits within a GMP-regulated environment, ensuring precision and compliance in clinical trial packaging.

As a vital team member, you'll have the opportunity collaborate on projects, fostering innovation and excellence in everything you do.

Key Responsibilities

• Start-up, execute, cleaning and completion clinical trial packaging operations in accordance with appropriate Standard Operating Procedures.
• Primary packaging (bottle filling) of oral dosage forms using a range of equipment
• Labelling and assembly of clinical trials supplies, including automated labelling and walleting equipment
• Working independently and as part of a team, on equipment or process projects
• Control and monitor production process and equipment; resolve problems or correct abnormal conditions, conduct basic troubleshooting, and escalate problems appropriately.
• Develop and apply a working knowledge of relevant electronic systems, including SAP.
• Complete electronic batch documentation, equipment logbooks and other documentation relevant all stages of production.
• Understand and follow GMP requirements and defined procedures to maintain the requirements of quality standards in the packaging environment.
• Work safely in packaging environment, understanding personal responsibility for Health, Safety and the Environment and principles of risk management.
• Understand and comply with procedures relevant to COSHH.
• Participate in internal audits.
• Passionate about quality and customer service.
• Participate in continuous process improvement.

Required Skills and Qualifications

• Typically educated to A level standard, preferably in subjects relating to sciences or IT
• Problem-solving skills and ability to work effectively with colleagues to resolve problems
• Communication and interpersonal skills
• Ability to work accurately to deadlines
• Computer literate
• Ability to develop and share knowledge
  
  

Required Knowledge and Experience

• Experience of packaging and labelling environment in a GMP environment, preferably within clinical trials.
• Working knowledge in SAP
• Basic knowledge of clinical trial operations
  
  

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

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.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb is Disability Confident - Employer

A UK Government scheme

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Management and Manufacturing

• Industries

  Pharmaceutical Manufacturing

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