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Pharmaceuticals
QC Analyst
Bristol
DBS Not Required
Smart4Sciences are currently recruiting for a QC Analyst to join a Pharmaceutica...
Smart4Sciences are currently recruiting for a QC Analyst to join a Pharmaceutical company in the Bristol region
As a QC Analyst you will be responsible for testing finished products, raw materials and stability samples using a broad range of analytical techniques in a GMP accredited environment.
Key Responsibilities
Routine testing of Raw Materials, Active Ingredients and Finished Products
Ensure all work is completed 'right first time' in accordance with GMP, GLP and other in-house procedures
Support analytical development and validation activities
Manage your own day-to-day work load, prioritising tasks accordingly to ensure testing is completed within agreed time frames.
Key Requirements
BSc or equivalent industry experience
Hands on experience with analytical techniques including HPLC, GC, FTIR, UV-vis
Prior experience working with Pharmaceutical GMP conditions is strongly preferred
This QC Analyst position is an urgent requirement so please apply now if you are interested
As a QC Analyst you will be responsible for testing finished products, raw materials and stability samples using a broad range of analytical techniques in a GMP accredited environment.
Key Responsibilities
Routine testing of Raw Materials, Active Ingredients and Finished Products
Ensure all work is completed 'right first time' in accordance with GMP, GLP and other in-house procedures
Support analytical development and validation activities
Manage your own day-to-day work load, prioritising tasks accordingly to ensure testing is completed within agreed time frames.
Key Requirements
BSc or equivalent industry experience
Hands on experience with analytical techniques including HPLC, GC, FTIR, UV-vis
Prior experience working with Pharmaceutical GMP conditions is strongly preferred
This QC Analyst position is an urgent requirement so please apply now if you are interested
Pharmaceuticals
Formulation Scientist
Bristol
DBS Not Required
Smart4Sciences are currently working with a Pharmaceutical CRO in the South West...
Smart4Sciences are currently working with a Pharmaceutical CRO in the South West to recruit for a Formulation Scientist responsible for development of new Inhalation products and respiratory drugs
As a Formulation Scientist you will be working as part of a team tasked with delivering projects to design, develop and optimise a range of inhalation/respiratory formulations.
Key Responsibilities
Formulation of new and existing Inhalation products as per project requirements
Act as the primary technical contact for client communication
Execute projects to support formulation development activities, analysing and interpreting experimental data to optimise formulation plans
Key Requirements
PhD or equivalent industry experience is essential
Significant experience in Pharmaceutical Formulation Development (ideally Inhalation/respiratory products)
Experience in the development of Biologics products is desirable
Interviews for this Formulation Scientist position are imminent so please apply today if interested.
As a Formulation Scientist you will be working as part of a team tasked with delivering projects to design, develop and optimise a range of inhalation/respiratory formulations.
Key Responsibilities
Formulation of new and existing Inhalation products as per project requirements
Act as the primary technical contact for client communication
Execute projects to support formulation development activities, analysing and interpreting experimental data to optimise formulation plans
Key Requirements
PhD or equivalent industry experience is essential
Significant experience in Pharmaceutical Formulation Development (ideally Inhalation/respiratory products)
Experience in the development of Biologics products is desirable
Interviews for this Formulation Scientist position are imminent so please apply today if interested.
Pharmaceuticals
Validation Manager
Bristol
DBS Not Required
Smart4Sciences are currently working with a Pharmaceutical Manufacturer in the W...
Smart4Sciences are currently working with a Pharmaceutical Manufacturer in the West County who are looking to recruit a Validation Manager in a newly created position within the company.
As a Validation Manager you will have overall responsibility for Validation and Qualification activities across the site including the opportunity to develop, implement and maintain the site Validation Master Plan and Cleaning Validation Master Plan.
Responsibilities
Define and maintain the Site Validation Master Plan and Cleaning Validation Master Plan
Author, execute and report all qualification and validation activities across site.
Use Quality Risk Management principals to establish a risk based approach to validation
Lead the investigation and resolution of non-conformances encountered during validation, qualification and periodic review activities
Act as Validation SME during regulatory and customer inspections
Requirements
Significant experience of full life cycle validation activities with a GMP accredited Pharmaceutical/Medical Device environment including process, equipment, facilities, computer system and cleaning validation
Significant hands on experience authoring and executing validation and qualification protocols including URS, DQ, FAT, SAT, IQ, OQ and PQ
Line Management experience of a validation team is highly desirable
Interviews for this Validation Manager position are happening now so please apply now or contact Gareth Gooley at Science Solutions for more information
As a Validation Manager you will have overall responsibility for Validation and Qualification activities across the site including the opportunity to develop, implement and maintain the site Validation Master Plan and Cleaning Validation Master Plan.
Responsibilities
Define and maintain the Site Validation Master Plan and Cleaning Validation Master Plan
Author, execute and report all qualification and validation activities across site.
Use Quality Risk Management principals to establish a risk based approach to validation
Lead the investigation and resolution of non-conformances encountered during validation, qualification and periodic review activities
Act as Validation SME during regulatory and customer inspections
Requirements
Significant experience of full life cycle validation activities with a GMP accredited Pharmaceutical/Medical Device environment including process, equipment, facilities, computer system and cleaning validation
Significant hands on experience authoring and executing validation and qualification protocols including URS, DQ, FAT, SAT, IQ, OQ and PQ
Line Management experience of a validation team is highly desirable
Interviews for this Validation Manager position are happening now so please apply now or contact Gareth Gooley at Science Solutions for more information