The Company:
CK Group are recruiting for a Development Technologist, to join a multinational corporation, specialising in the development and production of advanced thermoset composite materials, at their site in Nottinghamshire, on a permanent basis, for a salary from £35,000 - £45,000pa.
Location:
This role is located in Nottinghamshire. The site is also easily commutable from Derbyshire and South Yorkshire.
Development Technologist Role:
To identify potential technological improvements and areas of potential R&D, in line with the company s business strategy and market plan.To deliver agreed R&D projects.Involvement in Product Launch and related marketing activities.Communicate the results of R&D projects through appropriate formats to a variety of audiences.Support the Product Development team as required in line with the R&D roadmap.Assist with the creation of the company s Product Development objectives.Your Background:
To be considered for this position, you will have the following qualifications, skills and experience:
Degree level qualification materials science / chemistry.Industry experience.Proven ability to develop resin formulations for prepreg applications.Good presentation skills.Knowledge of analytical techniques used for resin development.Project Management experience.Microsoft Office competent.
This is a fantastic opportunity for a Development Technologist to join this global brand that works with some of the biggest names in aerospace.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
INDCH
CK Group are recruiting for a QC Chemist, to join a company in the pharmaceutical industry, on a contract basis for 6 months.
Salary:
From £12.44 per hour PAYE.
Your Background:
Previous lab experience, prefereably within the pharmaceutical indusrty.Experience with arange of analytical techniques including Ph, conductivity, pipetting, dilutions.Knowledge of GMP and GDP.Flexibility to cover potential overtime at weekends.Any knowledge of aseptic technique would be an advantage.
QC Chemist Role:
Chemical testing of raw materials. stability samples and finished product.Performing calibrations and validation maintenance.Follow Good Manufacturing Processes (GMP) and Good Documentation Practice (GDP).Preperation of reagents.
Company:
Our client specialises in healthcare with a focus on vital organ therapies.
Location:
This role is based at our clients' site in Liverpool.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
INDKA
CK Group are recruiting for a Formulation Technical Readiness Lead, to join a global Consumer Healthcare company, who are based in Reading, on a contract basis for 12 months.
Company:
Our client is a global consumer healthcare business with well known household brands.
Location:
The role is based in Reading.
Role:
Act as an expert in all formulation and technology aspects across different forms (tablets, softgels, gummies, powders, liquids etc), ensuring technical rigour and compliance with internal and external EU and local regulations and requirements.Define learning plans with Contract Manufacturers (CMs) to address complex formulation and technology questions including product/formula preparation (e.g. physical determinations, product performance, product stability, etc.).Ensure Technical Product Development readiness of projects supporting the Personal Health Care portfolio is delivered in line with agreed business timings.Provide technology and formulation advice to other functions within medicinal product development projects in Europe.Perform product feasibility assessment and technical activities from product development with CMs.Determine product development strategy (internal and external) including due diligence, risk assessment, and IP strategy.Design and execute sound learning plans to evaluate technology introduction into products to deliver breakthrough benefits or for cost innovation where applicable.
Your Background:
Educated to degree level or above in Life science or a related field with proven experience in a similar formulation and technology role in consumer healthcare or a similar regulated industry.Previous experience of manufacturing and packaging processes within a regulated environment and knowledge of tablet, soft and hard gel capsule and oral liquid products is desirable.Strong project management skills: You will be responsible to ensure the readiness of the projects in line with timings and to the required standard.Proficient in applying scientific methods to build, execute and report technical learning plans initiatives i.e. Define the problem, gather data, form hypothesis, test hypothesis and report findings.Proficient in formulation and specification tools and systems.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
INDLS
CK Group are recruiting for a Business & Program Management Leader, to join a company in the pharmaceutical industry, on a contract basis for 12 months.
Salary:
Rates £650 - £750 LTD/UMB per day (outside IR35) or £419.61 - £484.13 PAYE per day.
Business & Program Management Leader role: Partner with the business accountable and team to drive development of new tools and processes that will enable the organisation to deliver their Vision. Using appropriate Project Management methodologies, as best fits the needs of the project team, scope, plan and execute the project to ensure solutions are adopted and intended value is realized within the agreed timeframe and in an iterative manner. Enable team norms, effective decision making, drive progress, meeting design/facilitation, simplifying processes/work & coaching for effective change leaders. Ensure the wider business is aware of the project and its impact, identifying concerns and opportunities early.
Your Background: You are an experienced Project and Program Leader with over 7 years experience in leading IT and Business solution delivery. Experience within a Pharmaceutical environment is highly preferred. You have a proven track record of delivering technical and business projects in complex and regulated environments to strict timelines, budget and scope. You have demonstrated the ability to successfully define, plan and execute enterprise level technology initiatives aligned with business objectives. Proven experience managing multi disciplinary teams from business, technical and data teams. You have excellent communication skills with the ability to translate technical concepts, activities and deliverables to non technical stakeholders You are skilled at balancing and ensuring technical delivery with stakeholder engagement, collaboration and communication.
Company:
Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.
Location:
This role is a hybrid position between home and our clients site in Welwyn Garden City.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
CK Group are recruiting for a QC Chemist, to join a company in the pharmaceutical industry, on a contract basis for 6 months.
Salary:
From £12.44 per hour PAYE.
Your Background:
Previous lab experience, prefereably within the pharmaceutical indusrty.Experience with arange of analytical techniques including Ph, conductivity, pipetting, dilutions.Knowledge of GMP and GDP.Flexibility to cover potential overtime at weekends.Any knowledge of aseptic technique would be an advantage.
QC Chemist Role:
Chemical testing of raw materials. stability samples and finished product.Performing calibrations and validation maintenance.Follow Good Manufacturing Processes (GMP) and Good Documentation Practice (GDP).Preperation of reagents.
Company:
Our client specialises in healthcare with a focus on vital organ therapies.
Location:
This role is based at our clients' site in Liverpool.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
INDKA
CK Group are recruiting for a QC Microbiologist, to join a company in the pharmaceutical industry, on a contract basis for 6 months.
Salary:
From £12.44 per hour PAYE.
Your Background:
Previous lab experience, prefereably within the pharmaceutical indusrty.Experience with a range of amicrobial techniquesKnowledge of GMP and GDP.Flexibility to cover potential overtime at weekends.Any knowledge of aseptic technique would be an advantage.
QC Microbiologist Role:
Micro testing of raw materials. stability samples and finished product.Total Viable Count (TVC), environmental monitoring and endotoxin testing.Follow Good Manufacturing Processes (GMP) and Good Documentation Practice (GDP).
Company:
Our client specialises in healthcare with a focus on vital organ therapies.
Location:
This role is based at our clients' site in Liverpool.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
INDKA
CK Group are recruiting for a QC Analyst, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a 1 year fixed term contract.
Role:
This job is responsible for ensuring that all materials are tested according to agreed specifications and procedures and within agreed lead times.
Key duties will include :
To test all materials according to agreed specifications and procedures.To qualify all laboratory equipment.To maintain and calibrate all laboratory equipment according to approved procedures.To maintain all laboratory Quality Systems and Quality Management Systems in compliance according to approved procedures.To write under supervision, all SOPs associated with QC support.To support the internal and external audit process and audit schedules as appropriate.To support the preparation and hosting of competent authority inspections.To raise and support the investigation of deviations and associated CAPA s.To support the collection of data for reporting Quality Assurance Performance Indicators.To support the implementation and management of stability programmesTo perform any other appropriate duties at the request of the QC HeadYour Background:
Ability to establish and maintain effective working relationships and communication links within affiliated organisations and other customersExtensive knowledge of Quality Control, Quality Assurance, Quality Systems, GMP, Regulatory Compliance and manufacture and packaging of pharmaceutical productsGood technical and scientific judgementAbility to interpret complex data and present key findingsComputer literate e.g. Word, Excel and PowerPointDemonstrated Knowledge, understanding and application of GMP Guidelines and Regulations
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
CK Group are recruiting for a Clinical Trial Supplies Manager, to join a global pharmaceutical company, on a contract basis, for 6 months initially.
Salary:
Up to £30.03 per hour PAYE.
Clinical Trial Supplies Manager Role:
Collaborates with internal Global Clinical Supply Chain (GCSC) teams, external Customers & Service Providers Medical to ensure all needs are met.Defines, plans, & communicates the clinical supply chain strategy in support of global clinical studies to promote optimal use.Demonstrates strong knowledge of GCSC processes when presenting at cross-functional meetings.Responsible for identifying and supporting strategies for continuous improvement.Influences clinical and development timelines, study design & country selection.Reviewing & providing input to draft clinical protocols, communicating timelines & investigational product strategies.
Your Background:
Degree in a relevant scientific subject or have equivalent working experience.Previous working experience in the pharmaceutical industry.Prior experience in a role focussed on Clinical Supplies/Development with global experience or equivalent experience.Strong knowledge of the global drug development process & global regulatory requirements.Strong knowledge of IVRS and CTMS systems.Company:
Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.
Location:
This role is remote with travel to the Uxbridge office 1-2 times a month.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
CK Group are recruiting for a Field Service Engineer, to join a diagnostics company, working in the regions of Hampshire & Dorset, on a contract basis for 12 months.
Salary:
Per Day: £200 - £230 PAYE or £265 - £305 Umbrella (Inside IR35).
Field Service Engineer Role:
Onsite handling of customer issues and enquiries liaising with other Business areas to provide support.Identification and troubleshooting of issues on site.Conducting installations, commissioning and go-live support.Conducting and design of internal and external training.
Your Background:
Degree educated, preferred (relevant biomedical discipline).Experience of mechanical / electrical engineering troubleshooting.Previous experience of working in a hospital / research laboratory.Proven track record of troubleshooting experience, fixing biochemistry equipment (such as large scale analyzers).Understanding of the Diagnostics industry / NHS hospital setting and familiar with hardware used in pathology particularly biochemistry/blood sciences.Full UK/EU (or equivalent) driving licence and own transport,Passport (required for overseas training).
Company:
Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK.
Location:
This role is field based, covering sites in both Hampshire and Dorset areas.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
INDKA
CK Group are recruiting for an experienced Senior Protein Scientist, with a background in antibody pre-clinical development and experienced in the use of Octet or Biacore systems, to join a growing biotechnology company, based in London, on a permanent basis.
The Company:
A global biotech company specialising within the field of immuno-oncology.
Location:
London.
The Role:
This is a lab-based role and a great opportunity to contribute to the innovation of all aspects of the company s pipeline and platforms, and to be involved in design and execution of experiments in the areas of antibody discovery/characterisation and pre-clinical development, furthering product discovery and development projects. You will also be involved in other laboratory activities.
Your Background:
PhD in biological/ biochemical science, with experience across academia and biotechnology industry (5 years+).Understanding of the biologic product discovery and antibody pre-clinical development process.Strong drug discovery background.Technical skills in the following: AKTA, protein expression from bacterial and mammalian host cells, protein purification and characterisation (affinity determination, cell binding etc.).Extensive experience using an Octet/ SPR or Biacore systems and a mammalian cell bioreactor (ESSENTIAL).
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
INDCP
