Process Development Chemist – North West

Hannah Milward at CK Science is currently recruiting for a Process Development Chemist to join a chemical manufacturer who specialise in the application of novel enzymatic systems and flow technologies join their team for the duration of 3 months with the view to go permanent. This role is based in the North West

Qualifications:

To be considered for this Process Development Chemist position you will have a good degree/PhD or equivalent in science, have sound knowledge of organic chemistry and be familiar with HPLC, GC and NMR techniques.

How to apply:

Apply online now

For more information or to apply for this Process Development Chemist role please contact Hannah Milward on 0114 2839956 or email hmilward@ckscience.co.uk. Please quote reference SH23939 in all correspondence.

Click here to see our other chemical industry jobs

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Sales Manager (Pharmaceutical, Biotechnology) Europe

Andrew Bolton at CK Science is currently recruiting for a Sales Manager to join a global provider in the supply of chemical products & contract research (CRO) services for customers in the pharmaceutical, biotechnology & agrochemical industries.  This is a field based role based role covering the UK & Europe.

Responsibilities:

This Sales Manager role is a key position within the organisation, you will be responsible for:

  • Developing & building relationships with both new & existing customers within the UK & Europe;
  • Delivery of new sales through the development of new customers & market opportunities
  • Key account management to understand customer requirements, negotiation of terms & instigating proposals as well as completion of all sales reports & strategies.

Qualifications:

To be considered for this Sales Manager role, you will have a successful proven sales track record of products and/or services to the Pharmaceutical, Biotechnology and/or Agrochemical industries.

Location:

The successful candidate for this Sales Manager role should ideally be based in one of the following regions: Oxfordshire, Buckinghamshire, Berkshire, Bedfordshire, Cambridgeshire and Northamptonshire.

How to apply:

Apply online now:

For more information or to apply for this Sales Manager role please contact Andrew Bolton on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST23867 in all correspondence.

Click here to see our other pharmaceutical jobs

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Compounding Laboratory Manager – East Midlands

Naynesh Mistry at CK Science is currently recruiting for a Compounding Laboratory Manager to join a pharmaceutical manufacturing company at their facility in the East Midlands

The facility:

As a Compounding Laboratory Manager the successful candidate will lead the unlicensed medicines manufacturing department. The department is at a well established business unit with an excellent track record of quality and value for money, currently manufactures ‘special’ medicines for the NHS, private hospitals and community pharmacies throughout the UK. The department consists of approximately twenty people including two registered pharmacists, and is supported by a small team of releasing pharmacists.

Responsibilities:

This Compounding Laboratory Manager role is a key position in the company and the person appointed will have the opportunity of growing the department to match the expectations of the customer base and placing this company in a position where they can effectively compete in a dynamic marketplace. In the first instance the Manager will report in to the Head of Non sterile production.

The role of Compounding Manager will include;

  • Planning and managing production schedules
  • Overseeing the formulation activity
  • Supervising the costing process
  • Managing the customer services function
  • Meeting with key customers in NHS hospitals
  • Analysing and reporting on profitability
  • Improving current manufacturing systems
  • Improving productivity
  • Implementing a programme of continuous improvement
  • Implementing appropriate staff training programmes
  • Appraising all staff in the department
  • Motivating the production team

Qualifications:

The ideal candidate for this Compounding Laboratory Manager role will have a degree in Pharmacy or equivalent, have line management experience and worked within a aseptic, sterile manufacturing environment.

How to apply:

Apply online now

For more information or to apply for this Compounding Laboratory Manager role please contact Naynesh Mistry on 0114 283 9956 or email nmistry@ckscience.co.uk.  Please quote reference SH23945 in all correspondence.

Click here to see other roles in the Midlands

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Compliance Officer – North East

Heather Deagle at CK Science is currently recruiting for a Compliance Officer to join a biotechnology company based in the North East of England.

Responsibilities:

As a Compliance Officer you will be responsible for ensuring that manufacturing documents are compliant with GMP, writing new manufacturing documents, providing assistance to the New Product Co-ordinator during manufacturing and perform document compliance reviews.

Qualifications:

The ideal candidate for this Compliance Officer role must be qualified to at least HND level in chemistry or equivalent subject or possess equivalent industrial experience and have prior knowledge of GMP and Quality issues. 

How to apply:

Apply online now

For more information or to apply for this Compliance Officer role please contact Heather Deagle on 0191 384 8905 or email hdeagle@ckscience.co.uk. Please quote reference DH23938 in all correspondence.

Click here for more biotechnology roles

Not quite what you’re looking for? Click here to register your CV with us today.

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Our Latest Science Jobs in the UK

Here is a list of the latest science jobs we have had in this week. Click on the links below to find out more and be the first to apply!

Rubber Chemist/ Rubber Technologist – South Wales

Microbiologist – Pharmaceutical, NE England

Test Rig Operator – Catalyst, Chemical, Oxford

Catalyst Coating Specialist – Oxfordshire

Formulation Scientist – Agrochemicals, West Mids

Process Technologist – County Durham

Sales Engineer – Oil & Gas, Waste Water, Essex

Quality Assurance Representative – North West

Product Development ScientistCentral Belt of Scotland

Stability Team Leader – PharmaceuticalNorth East

QA Manufacturing Support Engineer – Yorkshire

Production Operative – Herts

Shift Process Chemist – Oxfordshire

Regulatory Manager – East Anglia

Senior Chemist – UV Coatings, Greater London

Head of ProductionNorthern Ireland

Senior Chemist – Packaging, FMCG, Hertfordshire

Analytical Scientist – Herts

Shift Chemist – Teeside

Compliance OfficerNE England

Medical Devices Sterile SpecialistEast Midlands

Shift Chemist – Teeside

Microbiology AnalystTeeside

Not quite what you’re looking for? Click here to register your CV with us today.

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Regulatory Manager – East Anglia

Jason Johal at CK Science is currently recruiting for a Regulatory Manager to join a global Biopharma company in East Anglia and close to Cambridge

The Job:

The role of this Regulatory Manager job is to provide effective regulatory and strategic input during product development and product life cycle management to support manufacturing activities on site and to ensure regulatory compliance for final product release. This is a dual reporting role to the Director of Quality Operations and to the Director of RA CMC Europe.

Responsibilities:

As a Regulatory Manager  you will have responsibility for 5 Quality Assurance and Regulatory Affairs professional staff and a budget up to $1MM key responsibilities include:

  • Partnering with Global RA CMC to deliver the strategy and execution for the preparation of CMC components for investigational medicinal products, new marketing applications, MAA variations and responses to agency questions.
  • Evaluation of post-approval CMC changes that affect EU MAA and International filings. Good working knowledge of EMA centralized variation system and variation application form. Scientific assessment of all relevant product related documents in compliance with EU regulatory requirements. Preparation of the EU quality components for CMC variations and maintenance of CMC sections in CTD format for EU MAA.
  • Collecting and developing responses to questions from regulatory authorities in close cooperation with project team members in US and EU.
  • Developing and maintaining a knowledge and understanding of current regulatory requirements for manufacture of API and testing, release and distribution of licensed medicinal products.
  • Maintaining regulatory compliance system for therapeutic products to support final product release and distribution to market.
  • Maintaining a high quality standards and a continuous improvement approach in responding to the evolving regulatory environment.
  • Maintaining CMC regulatory documents and liaison with appropriate Regulatory Authorities. This includes Site Master Files and manufacturing licenses and other regulatory approvals are maintained and available for regulatory agency and Customer Inspections.

Qualifications and Skills:

This Regulatory Manager role will require good working relationships with internal customers from QA/QC/Production/ Materials Management to improve regulatory compliance and awareness as well as collaboration with global regulatory personnel to ensure best practices and knowledge of global activities are communicated to site.

The company require someone capable of working independently to achieve goals and objective and with the ability to prioritise and organise daily work to meet overall deadlines. They must be able to influence others in a positive way and to identify and manage their own projects to completion. They will need the following:

  • A good knowledge of Pharmaceutical manufacturing processes and cGMP is essential as is knowledge and experience of international regulatory affairs environment for product life cycle management.
  • Practical experience of European regulatory procedures and the EU centralized procedure both pre and post approval are expected as is a good understanding of global change control management and regulatory compliance.
  • The ability to work on a number of projects with tight timelines, good scientific writing skills and the ability to work independently with minimal guidance are also required.

How to apply:

Apply online now

For more information or to apply for this Regulatory Manager role please contact Jason Johal on 01438 723 500 or email jjohal@ckscience.co.uk.  Please quote reference ST23896 in all correspondence.

For more regulatory jobs click here

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Compliance Process Engineer – Oxfordshire

Jason Johal at CK Science is currently recruiting for a Compliance Process Engineer  to join a global, broad-based health care company at their site in Oxfordshire.

The Role:

This aim of this Compliance Process Engineer job is to coordinate and direct compliance issues within the Operations Engineering department of a global, broad-based health care company devoted to the discovery, development, manufacture and marketing of pharmaceuticals and medical products, including nutritionals, devices and diagnostics. They will ensure a consistent approach is taken to resolving quality issues including ERs, CAPAs, Calibration Alerts and Post Investigations.

Responsibilities:

The responsibilities of this Compliance Process Engineer role will include:

  • Providing technical support to the calibration department to ensure that all calibration activities meet divisional and corporate requirements.
  • Supporting the introduction of new products and / or equipment through effectively managing the engineering document change process.
  • Seeking new ways of improving the efficiency of the Engineering Compliance group. Actively promoting the use of continuous improvement programs.
  • Developing strong links within Operations department to ensure service provided meets business requirements.
  • Understanding regulatory and corporate requirements to ensure the Operations Engineering department continues to meet cGMP and leading teams to deliver compliance projects and quality initiatives.

The successful incumbent will be expected to develop projects from concept through to implementation with the aim of continually improving Engineering processes including preventative and demand maintenance programs. They will also be responsible for authoring, reviewing and updating Operations Engineering documents to ensure compliance with regulatory, site and corporate requirements and for providing SME support to internal and external audits as required.

Qualifications and skills:

The ideal candidate for this Compliance Process Engineer job will have experience within a regulated industry, preferably medical devices or pharmaceutical along with a proven knowledge of engineering and calibration processes. They will also have:

  • The ability to take prompt action to accomplish objectives and to work under their own initiative.
  • A proven track record of technical report authoring and of delivering assigned projects / goals to on time, within budget and ensuring that internal customer requirements are meet.
  • Experience of working within a high volume highly regulated manufacturing environment with full membership of a recognised professional Engineering or Quality body is desirable.

How to apply:

Apply online for this role

For more information or to apply for this Compliance Process Engineer role please contact Jason Johal on 01438 743 047 or email jjohal@ckscience.co.uk. Please quote reference ST23812 in all correspondence.

 

Register your CV with us now

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Senior R&D Scientist – North West

Naynesh Mistry at CK Science is currently recruiting for a Senior R&D Scientist to join a leading manufacturer and supplier of clinical microbiology instrumentation in their product development team on a permanent basis in the North West

 

Job Summary:

This Senior R&D Scientist role will be to conduct research into and develop a wide range of new products for diagnostic microbiology with an emphasis on establishing novel molecular diagnostics.

 

Purpose/Objective:

As a Senior R&D Scientist you will carry out investigations related to both the improvement of existing products, and the improvement of manufacturing procedures and resolution of manufacturing problems, as well as working towards the achievement of recognition of significant new products through publication and presentation of external evaluations.

The primary focus of research will be the development of novel targets and probes for pathogenic micro-organisms with an emphasis on pathogens in human clinical disease.

The successful applicant will be expected to play a leading role in the development of a portfolio of molecular assays integrating a novel platform with forefront diagnostic assay. 

 

Qualifications and skills required:

The ideal candidate for this Senior R&D Scientist role will have a knowledge of nucleic amplification and extraction techniques is essential, combined with experience in conventional microbiological diagnostic methods.  Experience of primer design and bioinformatics software and databases would be advantageous

Ideally, candidates should have MSc or PhD in appropriate discipline or equivalent, as well as experience in commercial and/or academic research facilities, and be committed to continuous learning and professional development.

 

How to apply:

For more information or to apply for this Senior R&D Scientist role please contact Naynesh Mistry on 0114 2839956 or email nmistry@ckscience.co.uk. Please quote reference SH23878 in all correspondence.

 

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Analytical Chemist, Biotechnology–North of England

Heather Deagle at CK Science is currently recruiting for several Analytical Chemist’s (more senior roles available too) to join a major biotechnology company at their site in the North East of England. These roles will be on a temporary contract for initially 6-12 months with a strong possibility of becoming permanent.

Skills required:

The ideal candidate for this Analytical Chemist role will have proven experience in working in an analytical laboratory type role involving method qualification or validation, release testing of drug substances or stability testing.

Qualifications:

The successful candidate for this Analytical Chemist role ideally will be qualified to Degree level or similar in a relevant scientific discipline and have some experience gained with in a GMP setting.

How to apply:

Apply online for this role

For more information or to apply for this Analytical Chemist role please contact Heather Deagle at CK Science on 0191 384 8905 or email hdeagle@cksicience.co.uk. Please quote reference DH23844 in all correspondence.

Register your CV with us now

Search for more biotechnology roles now

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Medical Devices Auditor Job (Active Devices)

Andrew Bolton at CK Science is currently looking for a Medical Device Auditor to join a world leading auditing & certification consultancy, which provides specialist services to the medical device & related technology industries. This role will initially be based between their sites in Hampshire & Germany during the training period, with the option to be field based thereafter.

Responsibilities:

As a Medical Device Auditor, you will be involved in:

  • Planning & conducting audits (ISO, IVD, MDD, FDA, MRA, CE Marking) of customer’s active medical devices, facilities & quality management systems (QMS)
  • Testing of active medical devices in line with relevant electrical standards
  • Reviewing & approval of technical file / design dossiers, significant change notifications and other technical documentation.

Within this role, you will be required to travel to customer sites within the UK, Europe, USA & Asia.

Qualifications and skills:

To be considered for this Medical Device Auditor role, you will have the following:

  • Degree in electrical engineering, physics or a related discipline (or equivalent)
  • Working knowledge of quality systems relating to medical devices (CE Marking, ISO 13485:2003 & ISO 9001:2008
  • Demonstrated experience involved in audits (internal or external).

Knowledge of another European language and/or experience as an Auditor in Medical Devices would be advantageous, but it is not essential.

Benefits:

This Medical Device Auditor role is an outstanding opportunity to join a leading auditing & certification consultancy for the medical device industries. In return they offer a competitive salary & excellent benefits.

How to apply:

Apply online for this role

For more information or to apply for this Medical Device Auditor role please contact Andrew Bolton on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST23810 in all correspondence.

Click here to register your cv with us now

Search here for more Medical Device roles

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Our latest science jobs in this week

Here is a list of the latest science jobs we have had in this week. Click on the links below to find out more and be the first to apply!

Asbestos Surveyor – P402, Southampton

Development Chemist – Coatings & Polymers, N West

Calibration Technician – Oil & Gas, Aberdeen

Administrator – Environmental

Sample Management Scientist, Temp, 36982

Meter Proving Technician – Oil & Gas, Aberdeen

Analytical Chemist

Field Based Immunology Sales Consultant

Medical Devices Auditor – Active Devices

Analytical Chemist – Pharmaceutical, NE England

Project Engineer – Oxfordshire

Compliance Process Engineer – Oxon

Support Engineer – Oxfordshire

Analytical Team Leader

Analytical Chemist

Polymer Chemist – Material Testing, North London

 

Not quite what you’re looking for? Click here to register your CV with us today.

Follow us on Twitter @CKScienceJobs to receive more industry news and CK jobs of the week updates

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Wales-based Pharma Company Set for £14m Expansion

As reported by  Penn Pharma, The Wales-based Pharmaceutical Manufacturing company, Penn Pharma is set to invest £14million on expanding it’s specialist facilities at their Gwent headquarters.

The investment is part of the company’s plan to expand their specialist facilities with a new 15,000 sq ft development which will manufacture tablets and capsules which meet the highest international Quality Standards. Speaking of the announcement, Dr Richard Yarwood, Chief Executive of Penn Pharma stated, “We are delighted to announce this significant investment in the UK pharmaceutical manufacturing sector at a time when the established industry remodels itself and out-sourcing is on the increase.”

Penn Pharma, based in the Welsh market town of Tredegar has also received funding and training support from the Welsh Assembly Government.

Penn, who currently employ 280 highly skilled staff, believe that people are at the heart of their success and are keen to keep highly skilled jobs within Wales. Yarwood stated, “Over recent years we have witness strong growth in our development and manufacturing services, we are expecting this to continue at an increasing rate post completion of the new facility. We wouldn’t have achieved such great year on year success if it wasn’t for the hard work of our skilled personnel.”

Penn Pharma is one of the longest established pharmaceutical services companies and has over 30 years experience in providing drug development, clinical trial supply and manufacturing services to the international healthcare industry.

Click here to search our current science jobs in Wales now.

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Our latest science jobs – 28th February 2012

Here is a list of the latest science jobs we have had in today. Click on the links below to find out more and be the first to apply!

Field Chemist – Oil & Gas – North Scotland

Senior Scientist – API – Kent

QC Technician – Teesside

Design Engineer x4 – Plastics, Polymers & Material – North West

Senior QC Analyst – North East

UKAS Technical Manager-Metrology, Balance & Weigh – East Midlands

Physical Properties QC Analyst – London/Kent

Application Support Team Leader – Polymer, Coating – Oxfordshire

Technical Specialist – Analytical Chemist – North East

Restricted Substances Manager – Chemical – London

Not quite what you’re looking for? Click here to register your CV with us today.

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Our latest jobs – 28th of February 2012

 

Be the first to apply for our latest  jobs in science! Click on the links below to find out more and apply!

Restricted Substances Manager – Chemical, London

Technical Specialist – Analytical Chemist

Application Support Team Leader – Polymer, Coating

Physical Properties QC Analyst – London

UKAS Technical Manager-Metrology, Balance & Weigh

Senior QC Analyst

Design Engineer x4 – Plastics, Polymers & Material

QC Technician

Field Chemist – Oil & Gas

Senior Scientist – API, Kent

Not quite what you’re looking for? Click here to register your CV with us now.

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Technical Specialist (Analytical Chemist) – North East England

Barney Smith at CK Science is currently recruiting for a Technical Specialist in analytical chemistry to join a company that provides analytical services for the oil, gas, environmental and petrochemical industries to be based in the North East of England.

Responsibilities:

As a Technical Specialist with extensive knowledge and experience in analytical instrumentation such as GC, GC-MS, ICP, AA, UV, IR and KF, you will provide technical support and troubleshooting in instrumentation installation, validation, method development and maintenance to laboratories UK wide.  You will work with company Laboratory, Technical and QA Managers on instrumentation projects and provide technical support to other departments.

Qualifications and skills:

The successful candidate for this Technical Specialist role must be qualified to minimum HNC/HND in chemistry or related subject or possess equivalent commercial experience.  It is essential that you have an in-depth knowledge and proven track record in method development, validation and instrumentation maintenance within analytical chemistry.

How to apply:

Apply on line for this role now

For more information or to apply for this Technical Specialist role please contact Barney Smith on 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference DH23780 in all correspondence.

Click here to register your cv with us now

Click here to search for more roles in science now

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Formulation Development Scientist Jobs x 2 – Northern Ireland

Naynesh Mistry at CK Science is currently looking to recruit 2 x Formulation Development Scientists to join an international pharmaceutical organisation to work at their site in Northern Ireland on a permanent basis.

Responsibilities:

As a Formulation Development Scientist, the post holder will be directly involved in the development of all aspects of the processes used in the manufacture of new and existing drug products (dosage forms will include tablets and capsules)

The post holder will:

  • Assume direct involvement in the process development for the manufacture of medicinal products based in a range of dosage forms including tablets, capsules, controlled release systems, liquids and semi-solids.
  • Operate the various pieces of equipment involved in the process, at laboratory, pilot and commercial scale
  • Complete accurate process documentation in accordance with GMP, to include manufacturing documents and preparation of reports
  • Participate in transfer of technology from formulation development to production; liaising with production to ensure smooth transfer of information
  • Liaise with production in relation to manufacture of clinical trial batches
  • Participate in critical interpretation of experimental data
  • Participate in practical problem solving in relation of on-going and new projects

Qualifications and skills required:

The ideal candidate for this Formulation Development Scientist role would have a Bachelors degree (or equivalent) in a Scientific/Technical discipline.

Essential requirements are as follows:

  • Experience in solid dosage manufacturing
  • Previous experience of pharmaceutical drug product manufacturing techniques such as dry powder blending, granulation, encapsulation and tablet compression
  • Previous experience of completing batch processing instructions in accordance with GMP
  • Experience in cGMP audits and knowledge of Microsoft Office (Word, Office, Excel etc)

How to apply:

Apply online for this role now

For more information or to apply for these Formulation Development Scientist roles please contact Naynesh Mistry on 0114 283 9956 or email nmistry@ckscience.co.uk. Please quote reference SH23782 in all correspondence.

Not quite what you were looking for? Click here to register your cv today?

Click here to search for more Formulation jobs

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New Science Jobs in this Week!

Here is a list of our latest science jobs new in this week.  Please click on the links below to find out more and apply!

Science Jobs in North West UK

Science Jobs in South UK

Science Jobs in Yorkshire

Science Job in Scotland

 

Science Jobs in Midlands UK

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Analytical Services Business Manager – East Midlands

Naynesh Mistry at CK Science is currently seeking to recruit an Analytical Services Business Manager to join a major healthcare organisation on a permanent basis.

Job Purpose: 

The purpose if this Analytical Services Business Manager is too:

  • To lead the Analytical Services Team and grow the business in line with the Strategic Position Assessment (SPA) and business plan.
  • Lead for excellent customer service (for internal and external customers) across Analytical Services to ensure a business brand that facilitates the retention of existing business and creation of new business.
  • Ensure the business operates compliantly to customer and regulatory requirements

Main responsibilities:

The main responsibilities of this Analytical Services Business Manager role are:

  • To deliver the sales and profit line of the business plan
  • Define and lead a marketing strategy for Analytical Services to drive growth in all areas of the AS business and deliver the strategy to the agreed budget.
  • Lead the Analytical Services team, providing focus, direction and performance leadership to enable them to meet the plan.
  • Ensure the right levels of customer service are delivered to new and existing customers
  • Ensure that all customer and regulatory compliance requirements are met
  • Develop partnerships with other companies/academia to broaden the Analytical Services offer and present business proposals to the Executive on potential business development opportunities.
  • Own the Analytical Services customer relationships on behalf of client by developing long term relationships with current non-group customers, developing relationships with group customers, including those not currently customers of Analytical Services.

Skills and Qualifications:

The successful candidate for this Analytical Services Business Manager role would be degree qualified in Science or equivalent, and have experience in a commercial pharmaceutical or analytical environment. The ideal candidate will also have an in depth knowledge of testing and legislative requirements and have experience of delivering financial targets with a track record of business delivery

Essential skills required are as follows

  • In depth knowledge of analytical testing market and analytical techniques
  • High level of impact and influencing skills which has been demonstrated through successful stakeholder management at a senior level, and engaging of others
  • Leadership of a team and delegation
  • Commerciality

How to apply:

Apply online for this role now

For more information or to apply for this Analytical Services Business Manager please contact Naynesh Mistry on 0114 283 9956or email nmistry@ckscience.co.uk. Please quote reference SH23764 in all correspondence.

 

Click here to register your cv with us now

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Technical Support Coordinator – Waste, Yorkshire

Victoria Walker at CK Science is currently recruiting for a Technical Support Coordinator to join a waste management and used oil company based in South Yorkshire in their Waste Services team.

Responsibilities:

The main roles and responsibilities of this Technical Support Coordinator position will be to ensure the smooth flow and processing of all information coming into and out of the sales department. This will include providing a regular point of telephone contact for the field sales force, clients and prospective clients, continually delivering high levels of customer service.

It will be your responsibility to identify, classify and label wastes and also dealing with requests for support and services from the field sales force. You will liaise and co-ordinate with the sales and operational functions on a daily basis which will include tracking orders and enquiries, arranging jobs (including sub-contracted works), checking availability of transport etc. Handling all incoming telephone calls from clients and potential clients, you will be expected to deal with technical queries and other administrative duties as required. You will also ensure that weekly and monthly reports are produced.

Qualifications:

To be considered for this Technical Support Coordinator role, as you will hold a minimum HNC qualification (ideally HND) or equivalent in Chemistry. This is imperative and is a legal requirement for the position. Experience within the waste industry is highly desired as knowledge of waste legislation, consignment notes, etc. is integral to the role. Significant experience within chemical manufacturing may also be considered. You will also possess good computer skills and will be able to work on your own initiative. A self-motivator, you will be confident in dealing with people with an excellent telephone manner and will also be able to work well in a team.

Please note that HNC/ HND level Chemistry or above is an essential requirement for this position.

How to apply:

Apply online for this role now

For more information or to apply for this Technical Support Coordinator role please contact Victoria Walker on 0114 283 9956 or email vwalker@ckscience.co.uk. Please quote reference SH23722 in all correspondence.

 

Click here to search for more jobs in the waste industry

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Shift Manager Jobs – Central Belt of Scotland

Barney Smith at CK Science is currently recruiting for a number of Shift Managers to join a food manufacturer based in the Central Belt of Scotland. Due to a company restructure and increase in workload they have a number of vacancies for shift managers to run production lines.

Responsibilities:

As a Shift Manager you will be responsible for:

  • Managing the efficient running of the designated areas of production
  • Assisting in implementation of plans
  • Achieving KPI targets,
  • Manage and train staff and contribute to continuous improvement initiatives.
  • There are positions available for night shift or for a rotation of earlies and back shift.

Skills required:

The successful candidate for these Shift Manager positions will have a proven track record in production management within the food industry and in managing production teams.

How to apply:

Apply online for this role now

For more information or to apply for one of  these Shift Manager jobs please contact Barney Smith on 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference DH23724 in all correspondence.

Click here to search for more jobs in the food industry

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