Regulatory Affairs Project Manager (Contract, Bahrain Relocation Opportunity) Bahrain, Middle East Up to $11,000 per month Plus Accommodation, Flights, Benefits Package Our client specialises in working in practical implementation based projects with their customers around the world. They have been appointed to lead a project in the Gulf region, and as such, they are now on the lookout for a Regulatory Affairs Project Ma...
Our client is a market leader in the production and manufacturing of flavours and fragrances. Overview: Responsible for supervising the maintenance of Quality Management Systems standards and SHE Advisor in conjunction and support with the SHE Officer Reports to: Regulatory Affairs Manager - Food Europe and QMS Officer(s) Key Interfaces: Site Manager/s Operations Manag...
Job Title: REGULATORY AFFAIRS MANAGER Location: Bedford (Kempston based) Salary: up to £37,000pa Closing date: 21st June 2013 The organisation is the professional association for Chartered Legal Executive lawyers and other members working in the legal sector. It regulates its members in the public interest. Our client provides education, training and the development of skills for its members, an...
ACTIVE DEVICES EXPERT - MEDICAL DEVICES - UK - 45-60k Industry: Medical Devices & Healthcare Job Title: Scheme Manager - Technical Specialist - Medical Device Expert - Certification Manager Location: UK Salary: 45-60k Type: Permanent Organisation: a Notified Body for the Medical Device Industry. Reason: Future growth for 2013/14. Typical: Today you are working from home rev...
Superb, brand new opportunity for a competent Regulatory and Quality Affairs Manager to join this rapidly growing, global radiotherapy equipment developer. As an experienced Regulatory and Quality Affairs Manager you will assist in extending the company’s expansion into new markets and territories. The Company: Our highly successful North London based client is a fast growing 3D imaging medical technology company speci...
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Date: 6 days ago
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Wembley, Middlesex
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£50,000 - £65,000 per annum, negotiable, pro-rata, inc benefits
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3 applications
QP/QA Manager - Pharma - Middlesex - Circa 60k Type: Permanent Benefits: 23 days + Bank Holidays, Employee Discount PURPOSE: To ensure effective Quality Management Systems are maintained within the Group incorporating all aspects of quality assurance and quality control. The role also ensures effective coordination of the required work flow within the RA department, and that applicable regulatory compliance is strictl...
Regulatory Affairs Manager / Executive - Croydon Opportunity : Are you looking for a new job in pharmaceutical regulatory affairs (RA)? Do you have experience of conducting and reviewing marketing authorisation applications? Not quite found what you are looking for? Yes, then please read on as this is a role you do not want to miss out on This is a fantastic pharmaceutical Regulatory Affairs Manage...
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Date: 31 May
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Croydon, Surrey
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£35,000 - £50,000 per annum, pro-rata
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2 applications
Regulatory Affairs Manager / Executive - Croydon Opportunity : Are you looking for a new job in pharmaceutical regulatory affairs (RA)? Do you have experience of conducting and reviewing marketing authorisation applications? Not quite found what you are looking for? Yes, then please read on as this is a role you do not want to miss out on This is a fantastic pharmaceutical Regulatory Affairs Manage...
Our client is an API and intermediate manufacturer based in Hertfordshire. They are currently looking for a Regulatory Affairs Officer to join their regulatory department. Responsibilities: - You will assist in the compilation, assembly and submission of Drug Master Files and Certificate of Suitability for our clients existing and new Active Pharmaceutical Ingredients. - To assist in...
This well established family owned Japanese Pharmaceutical business in Slough, that has seen rapid growth over the past year to eighteen months, is seeking an experienced Regulatory Affairs officer to help take them forward to the next stage of their development. Roles and Responsibility - Liaising with MHRA (Medicines and Healthcare products Regulatory Agency) and EMEA. - Obtain information of regulatory a...
Job Title: Quality Assurance and Regulatory Affairs Manager (QARA) Approaching its 25th anniversary, Hunt Developments (UK) Ltd, based in Midhurst, West Sussex, have grown to become a prestigious organisation providing a range of specialised sub-contract assembly and packing services to the medical device and healthcare industry. With a quality management system certified to ISO 13485 and ISO 9001, the company operates state-o...
Technical Manager (Pharmaceutical, Pharmacy, Chemistry) BLUT7544 Chippenham £40,000 to £50,000 Founded in 1998, our client is an international publicly owned pharmaceutical group listed on AIM, part of the London Stock Exchange, and has its headquarters in the UK. Their principal activities are the acquisition and licensing of mature pharmaceutical products and th...
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Date: 5 June
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Ilford, Essex
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£22,000 - £29,800 per annum
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13 applications
STRANDHAVEN LIMITED Requires OPERATIONS MANAGER For their generic arm Somex Pharma The candidate must be able to manage the business including product development, Quality Assurance, registration and packaging. He/She will be required to design and develop packaging for Somex products, identifying and sourcing from product manufacturers in Asian countries and provide guidance on manufacturing costs ...
21 jobs matching this search were posted in the last week
Organisation Description Leading global life sciences organisation Job Description This role requires a seasoned Regulatory Affairs Manager who has excellent people management skills. Based in Dubai you will manage a large team responsible for the registration of pharmaceutical products for all Gulf countries. As a key stakeholder you will ensure that products are regi...
Regulatory Affairs Manager It’s a terrifically exciting time to be working at this global pharmaceutical company. Would you like to do a regulatory affairs role where you really get to work at a Global level? This role offers exceptional, above average financial benefits Do you have the following experience? • A university Degree in a Scientific discipline. • At least 5 years or more of regulatory...
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Date: 3 June
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Germany,
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€65,000 - €72,000 per annum, negotiable, pro-rata, inc benefits
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1 application
ACTIVE DEVICES EXPERT - MEDICAL DEVICES - GERMANY Industry: Medical Devices & Healthcare Location: Germany Salary: 60-70k Euros Type: Permanent Organisation: a Notified Body for the Medical Device Industry. Reason: Future growth for 2013. Typical: Today you are working from home reviewing fatigue test data on a new drug eluting stent design of one of your customers. Tomorrow you a...
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Date: 7 June
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Sittingbourne, Kent
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£60,000 - £70,000 per annum, negotiable, pro-rata, inc benefits
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2 applications
QUALITY SYSTEMS PROJECT LEAD - PHARMA - KENT - Circa 60-70k TYPE: CONTRACT LOCATION: KENT REPORTS TO: DIRECTOR OF QUALITY SALARY: Attractive Salary + Benefits, South East England SUMMARY: This role not only supports the manufacture of active pharmaceutical ingredients and finished products for commercial, investigational and specials use in a rapidly growing oper...
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Date: 30 May
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Rochdale, Lancashire
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£40,000 - £46,000 per annum, negotiable, pro-rata, inc benefits
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10 applications
QMS AUDITOR - MEDICAL DEVICES - NORTH UK - 45k Type: Permanent Location: Home based, NORTH UK (M60/61/62/65 Corridor) Travel: Yes (Company car provided for) Work from Home: Yes (Plan you own diary and work schedule) Salary: 40-45K + 10% Bonus, company car, and excellent benefits. Training: Yes, investment from employer to become Lead Auditor Industry: Medical...
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Date: 30 May
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Leeds, West Yorkshire
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£40,000 - £46,000 per annum, negotiable, pro-rata, inc benefits
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8 applications
QMS AUDITOR - MEDICAL DEVICES - NORTH UK - 45k Type: Permanent Location: Home based, NORTH UK (M60/61/62/65 Corridor) Travel: Yes (Company car provided for) Work from Home: Yes (Plan you own diary and work schedule) Salary: 40-45K + 10% Bonus, company car, and excellent benefits. Training: Yes, investment from employer to become Lead Auditor Industry: Medical...
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Date: 30 May
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Manchester, Lancashire
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£40,000 - £46,000 per annum, negotiable, pro-rata, inc benefits
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5 applications
QMS AUDITOR - MEDICAL DEVICES - NORTH UK - 45k Type: Permanent Location: Home based, NORTH UK (M60/61/62/65 Corridor) Travel: Yes (Company car provided for) Work from Home: Yes (Plan you own diary and work schedule) Salary: 40-45K + 10% Bonus, company car, and excellent benefits. Training: Yes, investment from employer to become Lead Auditor Industry: Medical...
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Date: 30 May
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Oxford, Oxfordshire
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£40,000 - £46,000 per annum, negotiable, pro-rata, inc benefits
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4 applications
QMS AUDITOR - MEDICAL DEVICES - SOUTH WEST - >45k Type: Permanent Location: Home based, South UK Travel: Yes (Company car provided for) Work from Home: Yes (Plan you own diary and work schedule) Salary: 40-45K + 10% Bonus, company car, and excellent benefits. Training: Yes, investment from employer to become Lead Auditor Industry: Medical Devices & Hea...
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Date: 31 May
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China,
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£40,000 - £70,000 per annum, negotiable, pro-rata, inc benefits
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13 applications
PRODUCT SPECIALIST - MEDICAL DEVICES - CHINA - NEGOTIABLE Job Title: EU Notified Body Medical Device Product Specialist China Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: Shanghai/Shenzhen, China Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification ...
Senior GCP QA Auditor - Pharma - Cambridge - 40-48k Type: Permanent The position and responsibilities: COMPANY: An excellent opportunity has arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company. PURPOSE & RESPONSIBILITIES: As a Senior Clinical Quality Assurance Auditor within a multi-disciplined company, you will utilise your GCP auditing exper...
An excellent opportunity has opened for a Global Project Manager to join one of the most established and most credible market research agencies in the UK. The successful candidate for this role will handle the account of a large FMCG business and deliver a state of the art Global harmonized data, reporting and visualizations. Your responsibilities as the Global Project Manager will include: Ensure the delivery of s...
Pharmaceutical Senior Compliance Manager - Croydon Opportunity : This is a great opportunity for someone who has good pharmaceutical quality assurance and regulatory affairs compliance experience to join a growing pharmaceutical manufacturing company in Croydon. Your role as a Senior Compliance Manager will involve leading and managing quality assurance, regulatory affairs and compliance projects. Th...
