Jan
18
Domestic Appliance Engineer
January 18, 2025 | Construction Jobs | Comments Off on Domestic Appliance Engineer
Domestic Appliance Engineer
London
£32,000 - £37,000 Basic + Bonus + Monday-Friday + IMMEDIATE START
Are you an experienced Domestic Appliance Engineer looking for a role with great work-life balance and competitive pay? This growing company is looking for someone who enjoys working independently in the field, solving appliance issues, and delivering excellent customer service. Join a supportive, family-oriented team where you're respected and trusted to do your job.
With a strong reputation for quality service and rapid growth across London, we need skilled engineers to meet the increasing demand. If you're ready to use your expertise in fixing kitchen appliances and want to work for a company that values hard work and fosters a positive atmosphere, this is the role for you.
Your Role as a Domestic Appliance Engineer Will Include:
Covering a local patch and diagnosing / repairing kitchen appliances
Completing a minimum of 8 jobs a day, all within the same area.
Carrying out repairs and replacements of kitchen appliances to a high standard.
Maintaining professional customer relationships while delivering quality service.
As a Domestic Appliance Engineer You Will Need To Have:
Minimum of 2 years' experience in repairing and servicing kitchen appliances
Full UK driving license
Ability to diagnose faults and repair white goods appliances effectively
Local to East London and happy to cover the London area
If this sounds like you apply or call Masoud Hassan on 07537153909 for IMMEDIATE CONSIDERATION.
Keywords: field service engineer, white goods, appliances, engineer, kitchen, field service, London, East London, E13, domestic
This vacancy is being advertised by Future Engineering Recruitment Ltd. The services of Future Engineering Recruitment Ltd are that of an Employment Agency.
Future Engineering Recruitment Ltd can only accept applications from candidates who have a valid legal permit or right to work in the United Kingdom. Potential candidates who do not have this right or permit, or are pending an application to obtain this right or permit should not apply as your details will not be processed.
We will endeavour to respond to all applicants however due to the sheer volume of response, we can only guarantee that candidates who have been shortlisted will be contacted
Jan
17
Clinical Trial Scientist
January 17, 2025 | Construction Jobs | Comments Off on Clinical Trial Scientist
Clinical Trial Scientist
Based in Basildon (hybrid role: 3 days office, 2 days home per week)
Salary: Competitive + Benefits + Bonus
Permanent or FTC role
If you are an exceptional clinical trials professional looking for a new and varied role with a fast-growing international business, then we want to hear from you.
Join us to help improve peoples' lives and make healthcare better for everyone!
Why Pharmanovia?
Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines.
Our core behaviours are:
- We act decisively but we never compromise on quality.
- We keep our promises and do as we say.
- We value our heritage and foster an entrepreneurial spirit.
- We reinvest in our future - in our products, our brands, and our people.
- We give back to our communities.
Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, U.A.E., India, Singapore, Italy, Spain, and South Korea.
We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce.
Pharmanovia's therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.
About the role
Reporting to Head of Clinical Development, you will play a key role in the design, execution, and oversight of clinical trials across various phases (I-IV). This position collaborates with cross-functional teams, including Regulatory Affairs, Market Access, Strategic Marketing, Legal and Medical Affairs, to ensure scientific integrity and operational excellence in clinical trial planning and execution.
You will contribute to protocol development, data analysis, and scientific communication to drive clinical development strategies and achieve high-quality outcomes that meet regulatory and corporate standards. You will also act as the main point of interaction with external CROs, help in identifying best partners to appoint for trial execution and support, as well as ensuring each clinical study protocol is designed with scientific integrity with the endpoints clearly addressing the study objectives in line with the CDP and business needs and other regulatory standards of all trials including IITs.
The department has an ethos of continuous improvement, refining systems and creating efficiencies. This, along with the rapid growth of the business, leads to a varied and dynamic working environment.
Main responsibilities and duties
Clinical Trial Design:
- Develop and contribute to the design and writing of clinical trial protocols, investigator brochures, and related study documents.
- Collaborate with the clinical development team to establish study objectives, endpoints, and inclusion/exclusion criteria.
- Provide scientific input into trial design, statistical analysis, and risk management strategies.
Study Execution and Oversight:
- Ensure trials are conducted in compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Oversee data collection, quality control, and data integrity throughout the trial lifecycle.
- Serve as a point of contact for clinical trial sites, supporting trial-related activities, troubleshooting, and monitoring patient safety.
Data Analysis and Reporting:
- Analyse and interpret clinical data, working closely with biostatistics and data management teams to ensure data accuracy.
- Contribute to the preparation of clinical study reports (CSRs), abstracts, posters, and manuscripts for internal and external presentations.
- Review study results for accuracy and consistency, identifying key findings relevant to product development.
Cross-Functional Collaboration:
- Partner with Medical Affairs, Regulatory Affairs, Market Access, and Pharmacovigilance to ensure alignment on study objectives and milestones.
- Provide scientific expertise in meetings with key stakeholders, including regulatory bodies, investigators, and partners.
- Contribute to project timelines, budget adherence, and risk management.
Regulatory Support:
- Assist in the preparation of regulatory submissions, including PIP and MAAs, by providing scientific insights and data.
- Stay current with regulatory guidelines, therapeutic area trends, and competitive landscape to inform clinical development strategies.
About you - what you will need to have
- Advanced degree (Ph.D. or equivalent) in life sciences, clinical research, or related field.
- Minimum 5+ years of experience in clinical trial management.
- High level of scientific and analytical ability to design and interpret complex clinical studies.
- Ability to work cross-functionally and foster strong partnerships within and outside the organization.
- Strong attention to protocol adherence, data accuracy, and scientific integrity.
- Effective problem-solving skills, with a proactive approach to identifying and addressing trial challenges.
- Strong knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Excellent communication and presentation skills, with an ability to translate complex scientific information for diverse audiences.
- Determined, driven to achieve results and business minded.
- Proven track record of working and leading a cross-functional team in a matrix environment.
- The ability to review both data and procedures in detail and the ability to see the greater overall picture.
What we offer
We offer a competitive salary plus bonus and rewards package including holiday, health & wellbeing program, employee recognition awards, social events, pension scheme and hybrid working.
`
By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible.
Jan
17
Clinical Trial Scientist
January 17, 2025 | Construction Jobs | Comments Off on Clinical Trial Scientist
Clinical Trial Scientist
Based in Basildon (hybrid role: 3 days office, 2 days home per week)
Salary: Competitive + Benefits + Bonus
Permanent or FTC role
If you are an exceptional clinical trials professional looking for a new and varied role with a fast-growing international business, then we want to hear from you.
Join us to help improve peoples' lives and make healthcare better for everyone!
Why Pharmanovia?
Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines.
Our core behaviours are:
- We act decisively but we never compromise on quality.
- We keep our promises and do as we say.
- We value our heritage and foster an entrepreneurial spirit.
- We reinvest in our future - in our products, our brands, and our people.
- We give back to our communities.
Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, U.A.E., India, Singapore, Italy, Spain, and South Korea.
We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce.
Pharmanovia's therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.
About the role
Reporting to Head of Clinical Development, you will play a key role in the design, execution, and oversight of clinical trials across various phases (I-IV). This position collaborates with cross-functional teams, including Regulatory Affairs, Market Access, Strategic Marketing, Legal and Medical Affairs, to ensure scientific integrity and operational excellence in clinical trial planning and execution.
You will contribute to protocol development, data analysis, and scientific communication to drive clinical development strategies and achieve high-quality outcomes that meet regulatory and corporate standards. You will also act as the main point of interaction with external CROs, help in identifying best partners to appoint for trial execution and support, as well as ensuring each clinical study protocol is designed with scientific integrity with the endpoints clearly addressing the study objectives in line with the CDP and business needs and other regulatory standards of all trials including IITs.
The department has an ethos of continuous improvement, refining systems and creating efficiencies. This, along with the rapid growth of the business, leads to a varied and dynamic working environment.
Main responsibilities and duties
Clinical Trial Design:
- Develop and contribute to the design and writing of clinical trial protocols, investigator brochures, and related study documents.
- Collaborate with the clinical development team to establish study objectives, endpoints, and inclusion/exclusion criteria.
- Provide scientific input into trial design, statistical analysis, and risk management strategies.
Study Execution and Oversight:
- Ensure trials are conducted in compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Oversee data collection, quality control, and data integrity throughout the trial lifecycle.
- Serve as a point of contact for clinical trial sites, supporting trial-related activities, troubleshooting, and monitoring patient safety.
Data Analysis and Reporting:
- Analyse and interpret clinical data, working closely with biostatistics and data management teams to ensure data accuracy.
- Contribute to the preparation of clinical study reports (CSRs), abstracts, posters, and manuscripts for internal and external presentations.
- Review study results for accuracy and consistency, identifying key findings relevant to product development.
Cross-Functional Collaboration:
- Partner with Medical Affairs, Regulatory Affairs, Market Access, and Pharmacovigilance to ensure alignment on study objectives and milestones.
- Provide scientific expertise in meetings with key stakeholders, including regulatory bodies, investigators, and partners.
- Contribute to project timelines, budget adherence, and risk management.
Regulatory Support:
- Assist in the preparation of regulatory submissions, including PIP and MAAs, by providing scientific insights and data.
- Stay current with regulatory guidelines, therapeutic area trends, and competitive landscape to inform clinical development strategies.
About you - what you will need to have
- Advanced degree (Ph.D. or equivalent) in life sciences, clinical research, or related field.
- Minimum 5+ years of experience in clinical trial management.
- High level of scientific and analytical ability to design and interpret complex clinical studies.
- Ability to work cross-functionally and foster strong partnerships within and outside the organization.
- Strong attention to protocol adherence, data accuracy, and scientific integrity.
- Effective problem-solving skills, with a proactive approach to identifying and addressing trial challenges.
- Strong knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Excellent communication and presentation skills, with an ability to translate complex scientific information for diverse audiences.
- Determined, driven to achieve results and business minded.
- Proven track record of working and leading a cross-functional team in a matrix environment.
- The ability to review both data and procedures in detail and the ability to see the greater overall picture.
What we offer
We offer a competitive salary plus bonus and rewards package including holiday, health & wellbeing program, employee recognition awards, social events, pension scheme and hybrid working.
`
By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible.
Jan
17
Associate Director – Quantity Surveyor
January 17, 2025 | Construction Jobs | Comments Off on Associate Director – Quantity Surveyor
ASSOCIATE DIRECTOR - QUANTITY SURVEYOR Central London | £80-95k + Excellent Benefits
My client is a leading construction consultancy in Central London, seeking an exceptional Associate Director to join their thriving cost management team.
About The Client:
The client is one of London's most respected medium-sized construction consultancies, known for their work on prestigious projects across commercial, residential, and hospitality sectors. They've built an enviable reputation for excellence while maintaining a culture that sets them apart from their larger competitors.
With a portfolio of high-profile projects and a commitment to staff development, they've achieved an impressive 95% staff retention rate over the past three years. Their recent investment in state-of-the-art offices and digital transformation demonstrates their commitment to staying at the forefront of the industry.
The Opportunity:
This is a key appointment within the business, offering the successful candidate the chance to:
- Lead major projects across London's most exciting developments
- Head a team of quantity surveyors while managing personal project responsibilities
- Join the senior leadership team with a clear path to Director level
- Influence the strategic direction of a growing consultancy
Requirements:
- MRICS qualified with 5+ years' post-qualification experience
- Proven track record managing projects valued £50m+
- Strong commercial acumen and team leadership abilities
- Excellent client relationship skills
- Experience in business development
Package & Benefits:
- Base salary £80-95k depending on experience
- Performance-related bonus scheme
- Private healthcare and life insurance
- 27 days annual leave plus bank holidays
- Flexible working arrangements
- Comprehensive training and development programme
The client offers a refreshing alternative to the larger consultancies. Their size means you'll have direct access to the senior leadership team while working on major projects that compete with the industry's biggest names. Their commitment to internal promotion is evidenced by their current leadership team, where over 60% started with the company as graduates.
The modern office environment promotes collaboration while providing quiet spaces for focused work. Their approach to hybrid working demonstrates their trust in their team members to deliver excellence while maintaining work-life balance.
For a confidential discussion about this opportunity, please contact Andreea Hudson.
Aldwych Consulting values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Jan
17
Associate Director – Quantity Surveyor
January 17, 2025 | Construction Jobs | Comments Off on Associate Director – Quantity Surveyor
ASSOCIATE DIRECTOR - QUANTITY SURVEYOR Central London | £80-95k + Excellent Benefits
My client is a leading construction consultancy in Central London, seeking an exceptional Associate Director to join their thriving cost management team.
About The Client:
The client is one of London's most respected medium-sized construction consultancies, known for their work on prestigious projects across commercial, residential, and hospitality sectors. They've built an enviable reputation for excellence while maintaining a culture that sets them apart from their larger competitors.
With a portfolio of high-profile projects and a commitment to staff development, they've achieved an impressive 95% staff retention rate over the past three years. Their recent investment in state-of-the-art offices and digital transformation demonstrates their commitment to staying at the forefront of the industry.
The Opportunity:
This is a key appointment within the business, offering the successful candidate the chance to:
- Lead major projects across London's most exciting developments
- Head a team of quantity surveyors while managing personal project responsibilities
- Join the senior leadership team with a clear path to Director level
- Influence the strategic direction of a growing consultancy
Requirements:
- MRICS qualified with 5+ years' post-qualification experience
- Proven track record managing projects valued £50m+
- Strong commercial acumen and team leadership abilities
- Excellent client relationship skills
- Experience in business development
Package & Benefits:
- Base salary £80-95k depending on experience
- Performance-related bonus scheme
- Private healthcare and life insurance
- 27 days annual leave plus bank holidays
- Flexible working arrangements
- Comprehensive training and development programme
The client offers a refreshing alternative to the larger consultancies. Their size means you'll have direct access to the senior leadership team while working on major projects that compete with the industry's biggest names. Their commitment to internal promotion is evidenced by their current leadership team, where over 60% started with the company as graduates.
The modern office environment promotes collaboration while providing quiet spaces for focused work. Their approach to hybrid working demonstrates their trust in their team members to deliver excellence while maintaining work-life balance.
For a confidential discussion about this opportunity, please contact Andreea Hudson.
Aldwych Consulting values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Jan
17
Associate Director – Quantity Surveyor
January 17, 2025 | Construction Jobs | Comments Off on Associate Director – Quantity Surveyor
ASSOCIATE DIRECTOR - QUANTITY SURVEYOR Central London | £80-95k + Excellent Benefits
My client is a leading construction consultancy in Central London, seeking an exceptional Associate Director to join their thriving cost management team.
About The Client:
The client is one of London's most respected medium-sized construction consultancies, known for their work on prestigious projects across commercial, residential, and hospitality sectors. They've built an enviable reputation for excellence while maintaining a culture that sets them apart from their larger competitors.
With a portfolio of high-profile projects and a commitment to staff development, they've achieved an impressive 95% staff retention rate over the past three years. Their recent investment in state-of-the-art offices and digital transformation demonstrates their commitment to staying at the forefront of the industry.
The Opportunity:
This is a key appointment within the business, offering the successful candidate the chance to:
- Lead major projects across London's most exciting developments
- Head a team of quantity surveyors while managing personal project responsibilities
- Join the senior leadership team with a clear path to Director level
- Influence the strategic direction of a growing consultancy
Requirements:
- MRICS qualified with 5+ years' post-qualification experience
- Proven track record managing projects valued £50m+
- Strong commercial acumen and team leadership abilities
- Excellent client relationship skills
- Experience in business development
Package & Benefits:
- Base salary £80-95k depending on experience
- Performance-related bonus scheme
- Private healthcare and life insurance
- 27 days annual leave plus bank holidays
- Flexible working arrangements
- Comprehensive training and development programme
The client offers a refreshing alternative to the larger consultancies. Their size means you'll have direct access to the senior leadership team while working on major projects that compete with the industry's biggest names. Their commitment to internal promotion is evidenced by their current leadership team, where over 60% started with the company as graduates.
The modern office environment promotes collaboration while providing quiet spaces for focused work. Their approach to hybrid working demonstrates their trust in their team members to deliver excellence while maintaining work-life balance.
For a confidential discussion about this opportunity, please contact Andreea Hudson.
Aldwych Consulting values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.