 |
| Job Title |
|
Quality Manager - Dairy |
| Location |
|
Shropshire, West Midlands |
| Job Number |
|
117191976 |
| Posted |
|
21/05/2012 (11:23) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
Description
|
|
Our client is a successful and growing Dairy company in the Shropshire region and they are looking for a Quality Manager to cover all Quality and Technical issues on site.
The main responsibilities of the role will be to;
- prepare and deliver a Quality Strategy and Continuous Improvement Plan in line with the Company Business Plan and objectives.
- lead, manage and motivate the Quality team through a period of significant change and growth.
- lead site quality matters, hygiene standards, agreed customer expectations and certification standards.
You will work closely with the production director and head of HR to develop and implement a QA Strategy and Plan.
You will work closely with customers, ensuring all technical requirements are agreed and implemented, via customer audits and visits to site.
You will manage all quality and hygiene through internal audits, review of complaint reports, implementation of monitoring processes and maintaining Health & Safety requirements.
You will manage Quality across both production and the laboratory and be responsible for all Quality staff and the laboratory function, including team leader and QC analysts. You will manage the day to day performance of the quality team, offering support and guidance when needed. You will also be responsible for their learning and development.
You will be responsible for the resourcing and talent management of Quality and laboratory staff into the business through development of a recruitment plan and a continuous learning and development programme.
The successful candidate will have proven experience in a Quality Management role within the dairy industry. You will show exceptional management skills and will have both manufacturing and laboratory experience from both a quality and supervisory point of view. You will have worked closely with customers and suppliers, as well as industry agencies and have excellent communication and interpersonal skills.
For further information please contact Laura on 0845 680 5812 or apply online
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
 |
|
|
|
|
|
| Job Title |
|
Senior Analyst / Team Leader |
| Salary/rate |
|
£20000 - £25000/annum |
| Location |
|
East Yorkshire, Humberside |
| Job Number |
|
120259362 |
| Posted |
|
21/05/2012 (11:22) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
A new position has opened for a Senior Analyst/Team Leader within a pharmaceutical company in East Yorkshire.
The role will involve the use of analytical techniques, mainly HPLC and GC, to confirm the quality of solid dose generic pharmaceutical products produced in the companies manufacturing facilities outside of the UK.
The role will also involve supporting the laboratory manager in mentoring technicians and analysts, as well as facilitating and concluding laboratory investigations.
The successful candidate will have a BSc or equivalent in a chemistry based or relevant scientific subject, with previous experience of working in the pharmaceutical and/or chemical industry. Experience in the use of HPLC, GC, UV etc is essential, along with working to GMP/GLP standards. Knowledge and experience of implementing MHRA out of spec guidelines would be an advantage.
We are looking for a strong assertive individual who has either experience of leading/supervising a small team or has the skills required to do so. An individual who has an interest in quality; implementing continuous improvement plans and new procedures to improve lead times in the laboratory would be perfect for this role.
For more information please contact Laura Osta on 0845 680 5812 or apply online
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
QC analyst |
| Salary/rate |
|
£18000 - £21000/annum includes shift allowance |
| Location |
|
East Yorkshire, Humberside |
| Job Number |
|
120233305 |
| Posted |
|
21/05/2012 (11:21) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
We are looking for a QC analyst for a global pharmaceutical company based in East Yorkshire.
You will be working within a busy QC environment, supporting manufacturing in the testing of raw materials and final products using a variety of techniques including HPLC and GC and wet chemistry and physical testing techniques. Previous experience of working in a fast paced laboratory environment would be advantageous, however full training will be given.
The successful candidate will have a minimum of BSc or equivalent in a Chemistry based subject with previous laboratory experience. We are looking for someone with good attention to detail, who can work under pressure and is happy working within a manufacturing environment.
The contract will initial be a rolling contract but there is a good chance the role will become permanent for the right candidate.
The shift rotates between a week of 6am-2pm and a week of 2pm-10pm, Mon-Fri.
For further information about this role please contact Laura on 0845 680 5812 or apply online.
|
| Job Type |
|
Contract |
| Contract Length |
|
N/A |
| Start Date |
|
asap |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Product Compliance Head |
| Location |
|
North Lincolnshire, Humberside |
| Job Number |
|
120260449 |
| Posted |
|
11/05/2012 (19:24) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
We are looking for a Head of Product Compliance for a global pharmaceutical company in the North Lincolnshire area. Reporting into the QA site manager you will provide technical leadership on all product quality compliance related matters on site.
You will manage the compliance across the 3 production units, ensuring that all aspects of the handling, manufacturing and distribution of pharmaceutical products comply with the requirements of the Quality Manual and Policies and meet all relevant cGMP regulatory and legislative requirements.
You will ensure that the local quality system and SOPS are in place and compliant with cGMP and that high quality products are achieved through qualification and validation based upon quality risk analysis.
You will provide leadership, direction and support to the people within the QA Compliance area and ensure that they are qualified and competent.
You will maintain knowledge of local and international regulatory and legislative requirements to ensure provision of expert advice on quality related matters is available to the whole site.
You will manage all complaints, recalls and product tampering and ensure that release of products, packaging and materials is carried out in accordance with registered specifications.
The successful candidate will have a BSc or equivalent in a life science subject and have previous experience in Quality Assurance and Quality Control and/or in a manufacturing environment within the pharmaceutical industry.
Previous experience in API manufacture and associated ICH guidelines are preferred, however experience within secondary pharmaceutical manufacture will also be considered if you show the technical and managerial skills required for this role. You will have sound knowledge of pharmaceutical regulatory requirements and be familiar with international guidelines, including MHRA and FDA.
This is an excellent opportunity for an experienced QA specialist to develop in a senior position within a global pharmaceutical company. It offers the chance of international exposure across the quality structure of their sister sites.
For further information please contact Laura Osta on 0845 680 5812 or apply online
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Programme Manager - Medical Device |
| Location |
|
North Yorkshire |
| Job Number |
|
120240687 |
| Posted |
|
11/05/2012 (18:32) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
We are looking for a Senior Development Manager for a successful and growing medical device company in the North Yorkshire area.
You will be part of the senior management team reporting directly to the managing director. As Development Manager you will be responsible for organising and managing all development projects within agreed budgets and timelines.
Responsibilities of the role are outlined below but are not limited to these;
You will be responsible for planning, conducting and supervising all new and existing product development projects, both short and long term. You will develop and execute a programme to ensure all company commercial objectives are met.
You will manage a group of project leaders, ensuring project milestones are met by identifying project needs and assigning resources where needed. You will be responsible for motivating and developing your team through personal development plans and being on hand to offer technical advice and hands on support.
You will work closely with Business Development and manufacturing to identify, engineer and manufacture new products that fit identified markets and customer needs. You will evaluate (with Business Development) market reactions to existing products to ensure the timely adjustment of development strategy and new project opportunities.
You will ensure that the development department interfaces with clinicians and customers to gather new product information.
Working closely with Regulatory Affairs, Manufacturing & Quality Assurance/Quality Control you will ensure that the development of new products meets and/or exceeds company, EU and US quality standards.
The successful candidate will have a BSc or equivalent in a scientific discipline, preferably life science. You will have proven experience of working within teh medical device industry in a product development environment, managing multiple projects over varied timelines and budgets. You will have experience of managing a team, setting milestones and working with departments across the business.
The company focuses on biological medical device and is keen to find someone with a background in this sector, who is happy to be hands on whilst managing the overall project portfolio.
The individual will be extremely organised, be able to work under pressure and have experience of dealing with changing timelines and priorities.
For further information please contact Laura on 0845 680 5812 or apply online.
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
QA Expert |
| Location |
|
North Lincolnshire, Humberside |
| Job Number |
|
120260443 |
| Posted |
|
11/05/2012 (18:16) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
We are looking for a QA expert for a global pharmaceutical company in the North Lincolnshire area. Reporting into the product compliance head, the role will focus on providing technical leadership for product quality and quality improvements within one of the company Production Units.
You will ensure that the quality system and SOPS are in place and that operations are compliant with cGMP legal and regulatory requirements.
You will lead the quality improvement initiatives within the production unit and lead and improve visualisation of the quality systems.
You will maintain knowledge of local and international regulatory and legislative requirements to ensure provision of expert advice on quality related matters is available to the whole site. You will also provide support to staff within the production unit, ensuring they are qualified and competent in all quality aspects of their role.
You will manage all complaints, recalls and product tampering and ensure that release of products, packaging and materials is carried out in accordance with registered specifications.
The successful candidate will have a BSc or equivalent in a life science subject and have previous experience in Quality Assurance and Quality Control and/or in a manufacturing environment within the pharmaceutical industry.
Previous experience in API manufacture and associated ICH guidelines would be preferable, however experience within secondary pharmaceutical manufacture will also be considered. You will have sound knowledge of pharmaceutical regulatory requirements and the ability to champion and implement improvements to internal quality systems and processes/equipment on the plant.
This is an excellent opportunity for an experienced QA specialist to work in a global pharmaceutical company. For the right candidate opportunities to development within the QA department and gain exposure internationally across other company sister sites are available.
For further information please contact Laura Osta on 0845 680 5812 or apply online
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Laboratory Scientist - Haematology |
| Salary/rate |
|
£28000 - £31000/annum Excellent package |
| Location |
|
Lancashire, North West |
| Job Number |
|
120260302 |
| Posted |
|
11/05/2012 (09:28) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
Our client is an international pharmaceutical company, specialising in the veterinary sector. They are looking to recruit a hardworking, highly motivated and professional individual capable of working within the fast-moving laboratory environment.
You will have sound working knowledge of haematology, practical laboratory skills and be capable of organising work schedules and analytical methods. You will have a degree or HNC in a relevant discipline.
As the successful applicant you will report to the Laboratory Manager and your duties will be primarily be to provide supervision for the haematology section, assisting other sections when required. You will have the skills to evaluate methods, reagents and equipment and be able to maintain stocks and ensure correct storage. You will be required to authenticate results, prepare cytological examination of body fluids and aspirates and participate in and monitor performance in external and internal quality assurance schemes.
You must be up to date with current advances and concepts and dedicated to both your personal development and that of your team. You will have high standards and work with the haematology operating procedure manual, keeping work areas clean and safe in compliance with the Health and Safety at Work Act.
For further information please contact Laura Osta on 0845 680 5812 or apply online.
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Supply Microbiology Manager |
| Salary/rate |
|
£38000 - £45000/annum plus benefits |
| Location |
|
East Yorkshire, Humberside |
| Job Number |
|
120259367 |
| Posted |
|
02/05/2012 (13:53) |
| Agency/Employer |
|
Agenda 1 Scientific Training & Recruitment |
| Description
|
|
We are looking for a Supply Microbiology Manager to work within the manufacturing/factory areas of a leading FMCG company in the East Yorkshire area.
You will report into the site Quality Manager and be responsible for minimising microbiological risk in the production environments, as well as leading and assisting in microbiological and quality investigations.
Key responsibilities include;
- Ensuring microbiological contamination issues are fully investigated with preventative measures put in place to stop a repeat occurrence of the issue.
- Ensuring new projects and equipment are installed with microbiological control in place
- Supporting quality department on regulatory and internal audit
- Micro risk awareness of hazards through training and education of staff
- Use of risk assessments to reduce potential micro contamination
- Control of the sites waters supply via the site water group to maintain quality of purified and WFI supply loops
- Assist quality team in their investigations when required
- Support other departments on site as the micro specialist
- Assist external compliance with auditing of microbiologically sensitive products or raw materials
- Work with R&D on microbiologically sensitive projects affecting the Hull site
The successful candidate will have a BSc or equivalent in Microbiology with experience of working within a pharmaceutical or cosmetic manufacturing environment. Non-sterile liquid dose form and CIP cleaning experience is essential. Auditing experience is preferred.
You will also be required to train staff so proven experience in this area would be advantageous. The site works at a very fast pace with a focus on continual manufacturing. The ability to communicate potential risks and microbial contamination to both key decision makers and manufacturing staff is essential.
For further information please contact Laura Osta on 0845 680 5812 or apply online
|
| Job Type |
|
Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
