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The Company:
A world leading medical devices manufacturer with a small family feel
A rapidly growing orthopaedic implant sales company
A fantastic career opportunity
The Role of the Clinical Support Specialist:
Our client is one of the leading manufacturer of orthopaedic implants.
The main element of the role is to support, train theatre staff and assist in cases.
Supporting sales reps in the South West region.
Checking implants, doing audits within the NHS and private hospitals.
These are surgery products for the hips, knees and shoulders that are mainly implants.
- Both primary & revision surgery.
Liaising & supporting orthopaedic surgeons, consultants, nurses.
Ensuring that business is retained as they have some big contracts in the North London region - Around 6 sites you will be visiting.
Manage their own work load within the hospitals
Benefits of the Clinical Support Specialist
£40k-£45k Basic Salary
£10k Bonus
Car Allowance
All other benefits
The Ideal Person for the Clinical Support Specialist:
It is all about drive and motivation, there is a lot that the company can offer but must be earned by hard work and determination to achieve goals.
Someone with a couple of years working as a clinician (e.g.
ODP, Scrub Nurse, Theatre Nurse, ODA) wanting a step up and is extremely passionate about orthopaedics that has that get up and go.
- Must have hip & knee experience.
Will possibly consider shoulders.
The ideal candidate will already be working as a clinical support specialist in orthopaedics
Must have a goal of breaking into medical sales as this is the progression ahead.
Strong people skills.
Strong communication/presentation skills.
If you think the role of Clinical Support Specialist is for you, apply now!
Consultant: Rio Barclay
Email: riob@otrsales.co.uk
Tel no.
0208 397 4114
Candidates must be eligible to work and live in the UK.
About On Target
At On Target, we specialise in sales, technical and commercial jobs in the Engineering, Construction, Building Services, Medical & Scientific, and Commercial & Industrial Solutions sectors, enabling our consultants to become experts in their market sector.
We place all levels of personnel, up to Director across the UK and internationally. ....Read more...
Type: Permanent Location: Plymouth, Exeter, Newquay, Exmouth, England
Start: ASAP
Duration: Full-Time
Salary / Rate: £40000 - £45000 Per Annum Excellent Benefits
Posted: 2024-10-11 15:19:16
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The Company:
A world leading medical devices manufacturer with a small family feel
A rapidly growing orthopaedic implant sales company
A fantastic career opportunity
The Role of the Clinical Support Specialist:
Our client is one of the leading manufacturer of orthopaedic implants.
Due to the success the sales team is having in the London region they are looking for a Clinical Support Specialist
The main element of the role is to support, train theatre staff and assist in cases.
Supporting 3 Sales Reps in the London area (Within the M25).
Checking implants, doing audits within the NHS and private hospitals.
These are surgery products for the hips, knees and shoulders that are mainly implants.
- Both primary & revision surgery.
Liaising & supporting orthopaedic surgeons, consultants, nurses.
Ensuring that business is retained as they have some big contracts in the North London region - Around 6 sites you will be visiting.
Manage their own work load within the hospitals
Benefits of the Clinical Support Specialist
£40k-£45k Basic Salary
£10k Bonus
Car Allowance
All other benefits
The Ideal Person for the Clinical Support Specialist:
It is all about drive and motivation, there is a lot that the company can offer but must be earned by hard work and determination to achieve goals.
Someone with a couple of years working as a clinician (e.g.
ODP, Scrub Nurse, Theatre Nurse, ODA) wanting a step up and is extremely passionate about orthopaedics that has that get up and go.
- Must have hip & knee experience.
Will possibly consider shoulders.
The ideal candidate will already be working as a clinical support specialist in orthopaedics
Must have a goal of breaking into medical sales as this is the progression ahead.
Strong people skills.
Strong communication/presentation skills.
If you think the role of Clinical Support Specialist is for you, apply now!
Consultant: Rio Barclay
Email: riob@otrsales.co.uk
Tel no.
0208 397 4114
Candidates must be eligible to work and live in the UK.
About On Target
At On Target, we specialise in sales, technical and commercial jobs in the Engineering, Construction, Building Services, Medical & Scientific, and Commercial & Industrial Solutions sectors, enabling our consultants to become experts in their market sector.
We place all levels of personnel, up to Director across the UK and internationally. ....Read more...
Type: Permanent Location: Stanmore, Harrow, Watford, Borehamwood, England
Start: ASAP
Duration: Full-Time
Salary / Rate: £40000 - £45000 Per Annum Excellent Benefits
Posted: 2024-10-11 15:11:14
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We are currently looking for a QC Analyst to join a leading company based in the Essex area.
As the QC Analyst you will be responsible for conducting Quality Control testing and documenting laboratory testing in accordance with the MHRA and EU GMP Guidelines.
As the QC Analyst will also be responsible for performing and assisting in the OOS investigations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1.
As the QC Scientist you will be competing analysis of Pharmaceutical products using analytical techniques such as HPLC, UV-Vis, GC and IR.
2.
You will comply with cGMP and carrying out routine tasks accurately and following strict methodologies to carry out analyses.
As well as complying with company Health & Safety Policy and Procedures.
3.
As the QC Analyst you will perform method validations and method transfers where needed, whilst maintaining and operating standard laboratory equipment, for example titrators, pH meters etc.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1.
Relevant degree in a .chemistry discipline or equivalent industry experience.
2.
Proven industry experience in working with a GMP or GLP environment within a pharmaceutical, chemical or food laboratory.
3.
A working knowledge and practical experience with HPLC as well as other analytical methods such as GC, IR and UV-VIS.
Key Words: HPLC, QC, Quality Control, GMP, GLP, Pharmaceuticals, Essex, GC, ICH, MHRA.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves.. ....Read more...
Type: Permanent Location: Essex,England
Start: 11/10/2024
Salary / Rate: £25000 - £32000 per annum
Posted: 2024-10-11 10:05:35
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Senior QC Systems Technical Specialist (1 year FTC) | HERTFORDSHIRE | Competitive SalaryBlackfield Associates are currently supporting a global pharmaceutical manufacturing organisation at their site based in the Hertfordshire area, to recruit for a Senior QC Systems Technical Specialist to join the organisation initially on a 1 year FTC basis.
The position has been created to support the implementation of a new LIMS system.You will provide expert technical support for QC laboratory electronic systems (LIMS, CDS), manage master data, resolve system issues, and ensure compliance with GMP and Data Integrity standards during this critical project.Key Responsibilities:
Manage and maintain QC electronic system data, particularly in the new LIMS implementation.
Troubleshoot system issues and support system enhancements.
Assist in the deployment, validation, and qualification of new systems.
Create and update SOPs and training materials.
Ensure compliance with regulatory and internal procedures.
Collaborate with internal teams and external vendors.
Support continuous improvement initiatives.
Skills and Qualifications:
Degree in a science discipline or equivalent experience.
At least 2 years' experience with LIMS/CDS in a QC setting.
Strong knowledge of GMP guidelines and data integrity.
Excellent communication and problem-solving skills.
Ability to work independently and manage multiple tasks.
STR Limited is acting as an Employment Agency in relation to this vacancy. ....Read more...
Type: Permanent Location: Hertfordshire, England
Duration: 12-months
Posted: 2024-10-10 15:43:15
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We are currently looking for an Associate Director, QC Stability to join a leading Biopharmaceutical company based in the Oxford.
As the Associate Director, QC Stability you will be responsible for setting up and maintaining a compliant stability program and regulatory submissions in both clinical and commercial settings.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Associate Director, QC Stability will be varied however the key duties and responsibilities are as follows:
1.
Oversee routine and non-routine stability studies, ensuring all data reports and documentation to support regulatory submissions are available on schedule.
2.
Manage and maintain a compliant stability program, including sample management, identifying stability studies, authoring stability protocols and reports, and maintaining trending of all stability activities.
3.
Provide technical expertise for laboratory investigations, troubleshooting assays, and ensuring acceptably low invalid rates.
4.
Lead the QC Stability team, including recruitment, leadership, and direction, as well as managing external vendors and contract testing facilities.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Associate Director, QC Stability we are looking to identify the following on your profile and past history:
1.
Relevant degree in Chemistry, Biochemistry, Microbiology, or a related science.
2.
Extensive industry experience in a GLP/GMP-regulated environment, with a focus on laboratory-based testing and management.
3.
A working knowledge and practical experience with stability testing, regulatory submissions, and continuous improvement processes.
Key Words: Associate Director | QC Stability | Biopharmaceutical | Stability program | Regulatory submissions | Clinical | Commercial | GLP | GMP | Laboratory testing | Continuous improvement | Quality Control | QC |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer.
We welcome applications from anyone who meets the role requirements.
HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career. ....Read more...
Type: Permanent Location: Oxford,England
Start: 10/10/2024
Salary / Rate: Competitive
Posted: 2024-10-10 11:16:05
