Hub Labeling Manager
Posted on Jun 23, 2026 by CV-Library
Tadworth, Surrey, United Kingdom
Pharmaceutical
Immediate Start
£17 - £20.9 Hourly
Temporary
Hub Labeling Manager (Multilingual)
Type: Temporary
Duration: 12 months initially
Location: Tadworth, Surrey (Hybrid - minimum 2.5 days onsite)
Rate: (INSIDE IR35)
- up to 20.90 per hour (PAYE)*
SRG are seeking a detail-oriented Hub Labeling Manager to support regulatory labeling activities across multiple markets with a leading pharmaceutical company. This is an exciting opportunity to contribute to compliance, digital innovation, and cross-functional collaboration within a global regulatory environment.
Fluency in English, French, and German is essential for this role.
Key Responsibilities
Prepare and maintain regulatory labeling documents (LPDs, LLDs, PLDs) in line with internal procedures and external requirements.
Develop and compile submission-ready labeling documentation, including annotated labels, change histories, and comparison tables.
Manage labeling systems and workflows, ensuring accuracy, completeness, and data integrity.
Perform quality control (QC) reviews of labeling outputs to ensure compliance and consistency.
Collaborate with cross-functional teams and provide regulatory expertise to support submissions and responses to regulatory authorities.
Contribute to process improvements, digital initiatives, and the adoption of new tools and technologies for labeling activities.Skills & Experience Required
Degree in life sciences, pharmacy, or equivalent professional experience.
Fluency in English, French, and German (written and spoken) is required.
Strong understanding of regulatory labeling principles and applicable local/global guidelines.
Experience working with structured data and systems (e.g., Excel, SharePoint, document management tools).
Excellent analytical, problem-solving, and attention-to-detail skills with the ability to manage multiple priorities.
Proven ability to work collaboratively across international teams and quickly adapt to new systems and processes.This role suits a proactive professional with a passion for regulatory excellence, digital innovation, and working in a multilingual, global environment.
To Apply
Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed)
*Umbrella also possible - please enquire for more information
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Type: Temporary
Duration: 12 months initially
Location: Tadworth, Surrey (Hybrid - minimum 2.5 days onsite)
Rate: (INSIDE IR35)
- up to 20.90 per hour (PAYE)*
SRG are seeking a detail-oriented Hub Labeling Manager to support regulatory labeling activities across multiple markets with a leading pharmaceutical company. This is an exciting opportunity to contribute to compliance, digital innovation, and cross-functional collaboration within a global regulatory environment.
Fluency in English, French, and German is essential for this role.
Key Responsibilities
Prepare and maintain regulatory labeling documents (LPDs, LLDs, PLDs) in line with internal procedures and external requirements.
Develop and compile submission-ready labeling documentation, including annotated labels, change histories, and comparison tables.
Manage labeling systems and workflows, ensuring accuracy, completeness, and data integrity.
Perform quality control (QC) reviews of labeling outputs to ensure compliance and consistency.
Collaborate with cross-functional teams and provide regulatory expertise to support submissions and responses to regulatory authorities.
Contribute to process improvements, digital initiatives, and the adoption of new tools and technologies for labeling activities.Skills & Experience Required
Degree in life sciences, pharmacy, or equivalent professional experience.
Fluency in English, French, and German (written and spoken) is required.
Strong understanding of regulatory labeling principles and applicable local/global guidelines.
Experience working with structured data and systems (e.g., Excel, SharePoint, document management tools).
Excellent analytical, problem-solving, and attention-to-detail skills with the ability to manage multiple priorities.
Proven ability to work collaboratively across international teams and quickly adapt to new systems and processes.This role suits a proactive professional with a passion for regulatory excellence, digital innovation, and working in a multilingual, global environment.
To Apply
Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed)
*Umbrella also possible - please enquire for more information
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Reference: 225282456
https://jobs.careeraddict.com/post/113451400
Hub Labeling Manager
Posted on Jun 23, 2026 by CV-Library
Tadworth, Surrey, United Kingdom
Pharmaceutical
Immediate Start
£17 - £20.9 Hourly
Temporary
Hub Labeling Manager (Multilingual)
Type: Temporary
Duration: 12 months initially
Location: Tadworth, Surrey (Hybrid - minimum 2.5 days onsite)
Rate: (INSIDE IR35)
- up to 20.90 per hour (PAYE)*
SRG are seeking a detail-oriented Hub Labeling Manager to support regulatory labeling activities across multiple markets with a leading pharmaceutical company. This is an exciting opportunity to contribute to compliance, digital innovation, and cross-functional collaboration within a global regulatory environment.
Fluency in English, French, and German is essential for this role.
Key Responsibilities
Prepare and maintain regulatory labeling documents (LPDs, LLDs, PLDs) in line with internal procedures and external requirements.
Develop and compile submission-ready labeling documentation, including annotated labels, change histories, and comparison tables.
Manage labeling systems and workflows, ensuring accuracy, completeness, and data integrity.
Perform quality control (QC) reviews of labeling outputs to ensure compliance and consistency.
Collaborate with cross-functional teams and provide regulatory expertise to support submissions and responses to regulatory authorities.
Contribute to process improvements, digital initiatives, and the adoption of new tools and technologies for labeling activities.Skills & Experience Required
Degree in life sciences, pharmacy, or equivalent professional experience.
Fluency in English, French, and German (written and spoken) is required.
Strong understanding of regulatory labeling principles and applicable local/global guidelines.
Experience working with structured data and systems (e.g., Excel, SharePoint, document management tools).
Excellent analytical, problem-solving, and attention-to-detail skills with the ability to manage multiple priorities.
Proven ability to work collaboratively across international teams and quickly adapt to new systems and processes.This role suits a proactive professional with a passion for regulatory excellence, digital innovation, and working in a multilingual, global environment.
To Apply
Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed)
*Umbrella also possible - please enquire for more information
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Type: Temporary
Duration: 12 months initially
Location: Tadworth, Surrey (Hybrid - minimum 2.5 days onsite)
Rate: (INSIDE IR35)
- up to 20.90 per hour (PAYE)*
SRG are seeking a detail-oriented Hub Labeling Manager to support regulatory labeling activities across multiple markets with a leading pharmaceutical company. This is an exciting opportunity to contribute to compliance, digital innovation, and cross-functional collaboration within a global regulatory environment.
Fluency in English, French, and German is essential for this role.
Key Responsibilities
Prepare and maintain regulatory labeling documents (LPDs, LLDs, PLDs) in line with internal procedures and external requirements.
Develop and compile submission-ready labeling documentation, including annotated labels, change histories, and comparison tables.
Manage labeling systems and workflows, ensuring accuracy, completeness, and data integrity.
Perform quality control (QC) reviews of labeling outputs to ensure compliance and consistency.
Collaborate with cross-functional teams and provide regulatory expertise to support submissions and responses to regulatory authorities.
Contribute to process improvements, digital initiatives, and the adoption of new tools and technologies for labeling activities.Skills & Experience Required
Degree in life sciences, pharmacy, or equivalent professional experience.
Fluency in English, French, and German (written and spoken) is required.
Strong understanding of regulatory labeling principles and applicable local/global guidelines.
Experience working with structured data and systems (e.g., Excel, SharePoint, document management tools).
Excellent analytical, problem-solving, and attention-to-detail skills with the ability to manage multiple priorities.
Proven ability to work collaboratively across international teams and quickly adapt to new systems and processes.This role suits a proactive professional with a passion for regulatory excellence, digital innovation, and working in a multilingual, global environment.
To Apply
Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed)
*Umbrella also possible - please enquire for more information
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Reference: 225282456
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