GMP Training Specialist – London – Competitive Package
This role is critical in ensuring that all employees involved in GMP-regulated activities receive the highest standard of training to maintain compliance, product quality, and patient safety.
Key Responsibilities:
Develop, implement, and maintain a GMP training program tailored for ATMP manufacturing, ensuring compliance with regulatory standards. Deliver engaging and effective GMP training sessions for new hires, operational teams, and senior staff. Create and update training materials, SOPs, and competency assessments to reflect the latest regulatory changes and best practices. Conduct training gap analyses to identify areas for improvement and ensure continuous enhancement of training programs. Maintain accurate training records in compliance with regulatory expectations (MHRA, FDA, EMA). Collaborate with QA, Manufacturing, and Regulatory teams to align training with quality and compliance objectives. Prepare the organization for regulatory inspections , ensuring employees are audit-ready regarding GMP training compliance. Support on-the-job training initiatives , working closely with team leaders and subject matter experts to reinforce best practices.
Requirements:
Experience in GMP training and compliance within a pharmaceutical or biotechnology environment, preferably in ATMPs, cell & gene therapy, or biologics . Strong knowledge of GMP regulations (MHRA, FDA, EMA, ICH, Eudralex) and training best practices. Excellent presentation, communication, and interpersonal skills, with the ability to engage diverse audiences. Experience with Learning Management Systems (LMS) and electronic training records is a plus. A proactive mindset, with strong attention to detail and organizational skills.
What is in it for you?
Be part of a groundbreaking biopharmaceutical company that is transforming patient care. Work in a dynamic ATMP environment , contributing to cutting-edge therapies. Competitive salary and benefits package, with opportunities for career growth. A supportive and collaborative team culture.
GMP Training Specialist – London – Competitive Package
This role is critical in ensuring that all employees involved in GMP-regulated activities receive the highest standard of training to maintain compliance, product quality, and patient safety.
Key Responsibilities:
Develop, implement, and maintain a GMP training program tailored for ATMP manufacturing, ensuring compliance with regulatory standards. Deliver engaging and effective GMP training sessions for new hires, operational teams, and senior staff. Create and update training materials, SOPs, and competency assessments to reflect the latest regulatory changes and best practices. Conduct training gap analyses to identify areas for improvement and ensure continuous enhancement of training programs. Maintain accurate training records in compliance with regulatory expectations (MHRA, FDA, EMA). Collaborate with QA, Manufacturing, and Regulatory teams to align training with quality and compliance objectives. Prepare the organization for regulatory inspections , ensuring employees are audit-ready regarding GMP training compliance. Support on-the-job training initiatives , working closely with team leaders and subject matter experts to reinforce best practices.
Requirements:
Experience in GMP training and compliance within a pharmaceutical or biotechnology environment, preferably in ATMPs, cell & gene therapy, or biologics . Strong knowledge of GMP regulations (MHRA, FDA, EMA, ICH, Eudralex) and training best practices. Excellent presentation, communication, and interpersonal skills, with the ability to engage diverse audiences. Experience with Learning Management Systems (LMS) and electronic training records is a plus. A proactive mindset, with strong attention to detail and organizational skills.
What is in it for you?
Be part of a groundbreaking biopharmaceutical company that is transforming patient care. Work in a dynamic ATMP environment , contributing to cutting-edge therapies. Competitive salary and benefits package, with opportunities for career growth. A supportive and collaborative team culture.
Validation Manager – North West – Competitive Package
BioTalent are delighted to be partnering with a pharmaceutical organisation who are looking to recruit for a Validation Manager to join the team on a permanent basis. This is a unique position with a great opportunity to either continue your career at management level, or make the step up into gaining management experience.
You will be responsible for maintaining the company’s validation policy and framework, spearheading compliance initiatives, and acting as the primary point of contact for validation during audits and meetings with regulatory bodies, clients, and notified bodies.
You will be responsible for:
Define and implement validation standards across the organisation, reporting performance to the quality SLT. Oversee the Qualification and Validation aspects of the Quality Management System, ensuring consistent and effective application. Deliver internal training on validation and qualification processes. Author and implement validation protocols, plans, and reports.
You will bring the following:
At least 3+ years’ experience working specifically in a validation related position within a pharmaceutical/Medical device organisation. Good leadership and communications – previous background line managing or overseeing a team would be advantageous. Skilled in leading audits and management reviews. CSV experience is also highly advantageous.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: Mobile: 03333076496
I look forward to hearing from you!
Validation Manager – North West – Competitive Package
BioTalent are delighted to be partnering with a pharmaceutical organisation who are looking to recruit for a Validation Manager to join the team on a permanent basis. This is a unique position with a great opportunity to either continue your career at management level, or make the step up into gaining management experience.
You will be responsible for maintaining the company’s validation policy and framework, spearheading compliance initiatives, and acting as the primary point of contact for validation during audits and meetings with regulatory bodies, clients, and notified bodies.
You will be responsible for:
Define and implement validation standards across the organisation, reporting performance to the quality SLT. Oversee the Qualification and Validation aspects of the Quality Management System, ensuring consistent and effective application. Deliver internal training on validation and qualification processes. Author and implement validation protocols, plans, and reports.
You will bring the following:
At least 3+ years’ experience working specifically in a validation related position within a pharmaceutical/Medical device organisation. Good leadership and communications – previous background line managing or overseeing a team would be advantageous. Skilled in leading audits and management reviews. CSV experience is also highly advantageous.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: Mobile: 03333076496
I look forward to hearing from you!
Validation Manager – North West – Competitive Package
BioTalent are delighted to be partnering with a pharmaceutical organisation who are looking to recruit for a Validation Manager to join the team on a permanent basis. This is a unique position with a great opportunity to either continue your career at management level, or make the step up into gaining management experience.
You will be responsible for maintaining the company’s validation policy and framework, spearheading compliance initiatives, and acting as the primary point of contact for validation during audits and meetings with regulatory bodies, clients, and notified bodies.
You will be responsible for:
Define and implement validation standards across the organisation, reporting performance to the quality SLT. Oversee the Qualification and Validation aspects of the Quality Management System, ensuring consistent and effective application. Deliver internal training on validation and qualification processes. Author and implement validation protocols, plans, and reports.
You will bring the following:
At least 3+ years’ experience working specifically in a validation related position within a pharmaceutical/Medical device organisation. Good leadership and communications – previous background line managing or overseeing a team would be advantageous. Skilled in leading audits and management reviews. CSV experience is also highly advantageous.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: Mobile: 03333076496
I look forward to hearing from you!
Validation Manager – North West – Competitive Package
BioTalent are delighted to be partnering with a pharmaceutical organisation who are looking to recruit for a Validation Manager to join the team on a permanent basis. This is a unique position with a great opportunity to either continue your career at management level, or make the step up into gaining management experience.
You will be responsible for maintaining the company’s validation policy and framework, spearheading compliance initiatives, and acting as the primary point of contact for validation during audits and meetings with regulatory bodies, clients, and notified bodies.
You will be responsible for:
Define and implement validation standards across the organisation, reporting performance to the quality SLT. Oversee the Qualification and Validation aspects of the Quality Management System, ensuring consistent and effective application. Deliver internal training on validation and qualification processes. Author and implement validation protocols, plans, and reports.
You will bring the following:
At least 3+ years’ experience working specifically in a validation related position within a pharmaceutical/Medical device organisation. Good leadership and communications – previous background line managing or overseeing a team would be advantageous. Skilled in leading audits and management reviews. CSV experience is also highly advantageous.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: Mobile: 03333076496
I look forward to hearing from you!
Capital Expenditure (CapEx) Planner – Contract Position
Location: Just outside Glasgow, Scotland
Duration: May 2025 - February 2026 (10 months)
Hours: Full-time
About the Role We are seeking an experienced Capital Expenditure (CapEx) planner to join our team on a contract basis. In this role, you will be responsible for managing our capital investment planning, scheduling, and tracking processes during a key period of strategic development. Key Responsibilities Develop and maintain detailed capital expenditure schedules and forecasts Coordinate with department heads to collect, analyze, and prioritize capital spending requests Monitor and report on capital project statuses, highlighting variances and risks Support the financial planning team with budget preparation and regular reviews Create clear documentation and reports for management decision-making Implement best practices for capital spending management and control
Capital Expenditure (CapEx) Planner – Contract Position
Location: Just outside Glasgow, Scotland
Duration: May 2025 - February 2026 (10 months)
Hours: Full-time
About the Role We are seeking an experienced Capital Expenditure (CapEx) planner to join our team on a contract basis. In this role, you will be responsible for managing our capital investment planning, scheduling, and tracking processes during a key period of strategic development. Key Responsibilities Develop and maintain detailed capital expenditure schedules and forecasts Coordinate with department heads to collect, analyze, and prioritize capital spending requests Monitor and report on capital project statuses, highlighting variances and risks Support the financial planning team with budget preparation and regular reviews Create clear documentation and reports for management decision-making Implement best practices for capital spending management and control
Capital Expenditure (CapEx) Planner – Contract Position
Location: Just outside Glasgow, Scotland
Duration: May 2025 - February 2026 (10 months)
Hours: Full-time
About the Role We are seeking an experienced Capital Expenditure (CapEx) planner to join our team on a contract basis. In this role, you will be responsible for managing our capital investment planning, scheduling, and tracking processes during a key period of strategic development. Key Responsibilities Develop and maintain detailed capital expenditure schedules and forecasts Coordinate with department heads to collect, analyze, and prioritize capital spending requests Monitor and report on capital project statuses, highlighting variances and risks Support the financial planning team with budget preparation and regular reviews Create clear documentation and reports for management decision-making Implement best practices for capital spending management and control
Validation Manager – Midlands – Competitive Package
BioTalent are delighted to be partnering with a pharmaceutical organisation who are looking to recruit for a Validation Manager to join the team on a permanent basis. This is a unique position with a great opportunity to either continue your career at management level, or make the step up into gaining management experience.
You will be responsible for maintaining the company’s validation policy and framework, spearheading compliance initiatives, and acting as the primary point of contact for validation during audits and meetings with regulatory bodies, clients, and notified bodies.
You will be responsible for:
Define and implement validation standards across the organisation, reporting performance to the quality SLT. Oversee the Qualification and Validation aspects of the Quality Management System, ensuring consistent and effective application. Deliver internal training on validation and qualification processes. Author and implement validation protocols, plans, and reports.
You will bring the following:
At least 3+ years’ experience working specifically in a validation related position within a pharmaceutical/Medical device organisation. Good leadership and communications – previous background line managing or overseeing a team would be advantageous. Skilled in leading audits and management reviews. CSV experience is also highly advantageous.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: Mobile: 03333076496
I look forward to hearing from you!
