Kedrion Biopharma is recruiting for a Technical Trainer to join the Training department to play a pivotal role in ensuring that our team members possess the necessary knowledge and skills to maintain compliance with GMP standards in all aspects of manufacturing processes. You will design, develop, and deliver training programs tailored to meet the needs of employees working in a GMP-regulated environment. Your expertise will be instrumental in cultivating a culture of quality, safety, and continuous improvement within our organization.

Our site is not easily accessible by public transport so please take this into consideration when applying as this role is fully on-site.

Duties & Responsibilities:

Responsible for but not limited to the following:

Training Program Development:

• Design comprehensive training programs covering various aspects of GMP regulations, procedures, and best practices.
• Collaborate with subject matter experts, training coordinators and departmental leaders to identify training needs and develop relevant content.
• Create engaging and effective training materials, including presentations, manuals, and multimedia resources.
• Assessing training needs and creating customized training materials to address specific areas of improvement.

Training Delivery:

• Conduct engaging training sessions for employees at all levels, including new hires, existing staff, and cross-functional teams.
• Employ a variety of instructional techniques, such as lectures, group discussions, hands-on activities, and simulations, to maximize learning outcomes.
• Adapt training delivery methods to accommodate diverse learning styles and preferences among participants.
• Take part in the learning and development supporting activities, i.e., H&S activities etc.
• Provide guidance and support to employees regarding training compliance issues and best practices.
• Work collaboratively with training coordinators / facilitators, team leaders and area management to ensure staff training compliance is maintained at the expected level.

GMP Compliance:

• Ensure that training programs align with current GMP regulations, industry standards, and company policies.
• Emphasize the importance of adherence to GMP principles in all training materials and sessions.
• Monitor and evaluate employee performance to identify areas for improvement and reinforce compliance with GMP requirements.

Documentation and Reporting:

• Maintain accurate records of training activities, including attendance, evaluations, and certifications.
• Prepare reports summarizing training effectiveness, participant feedback, and compliance metrics for management review.
• Collaborate with quality assurance teams to support audit preparations and address any training-related findings or recommendations.
• Update training materials and content to reflect changes in regulations, industry standards, and best practices.

Continuous Improvement:

• Proactively seek feedback from trainees and stakeholders to identify opportunities for enhancing training programs and processes.
• Stay abreast of developments in GMP regulations, industry trends, and training methodologies to ensure the ongoing relevance and effectiveness of training initiatives.
• Participate in cross-functional teams and projects aimed at improving overall quality, efficiency, and compliance within the organization.

Training Centre:

• Onboarding of new starters, as required.
• Deliver “Manufacturing Essentials” – onboarding programme for production.
• Maintain stock levels of consumables and raw material required for training.
• Ensure all equipment is adequately maintained.

Individual Accountability:

• Ensure training records are maintained and managed in line with BPL’s quality standards and requirements.
• Contribute to continuous improvement of the technical training programme delivered at the Training centre and on the job.

Skills & experience to help you within the role –

Able to work within a team environment.
Adaptable & flexible with a logical & systematic approach to problem solving.
Able to communicate ideas & build effective relationships with colleagues at all levels within the organisation.
Ability to design, develop & deliver training content.
Good communication and presentation skills.
Ability to evaluate & measure training compliance.
Planning and prioritisation of tasks / activities to achieve the required outputs.
Resilient to change within a dynamic work environment.
Computer literate, proficient with MS Office (Excel, Word, PowerPoint, etc.).
Good knowledge of cGMP and regulatory compliance.
Good knowledge and experience (at least 1 years) working within a Pharmaceutical GMP manufacturing environment.
Experience developing and delivering training content.
Practical experience operating laboratory-based equipment. E.g. pH meters, Balances, Chromatography columns etc
BTec, degree or equivalent professional qualification in a relevant science or education discipline.

In return we offer -

• Competitive salary
• Annual bonus scheme
• 25 days holiday (plus bank holidays)
• Pension
• Life insurance
• On-site parking
• Employee assistance programme
• Virtual GP
• Cycle to work scheme
• Subsidised canteen
• Employee discounts and cash back
• Gym membership discounts
• Family friendly policies
• Employee recognition programme 
• Loyal service awards

Kedrion Biopharma is a biopharmaceutical company headquartered in Italy dedicated to collecting and fractionating blood plasma to produce and distribute plasma-derived therapies worldwide. These treatments help manage and prevent rare, ultra-rare, and debilitating conditions, including Coagulation and Neurological Disorders, Immunodeficiencies, and Rh sensitization. 

The Kedrion group has numerous legacies within its brand; your employer will be Bio Products Laboratory Ltd, doing business as Kedrion Biopharma UK. Our plant is based in Elstree and counts nearly 1000 colleagues across various departments.

Since its foundation, Kedrion has experienced consistent growth, backed by strong performance indicators. Today, the company employs 5,200 people globally who work collaboratively on our portfolio of 38 life-enhancing plasma-derived products distributed in over 100 countries.