Quality Assurance & Safety category and Biotechnology & Pharmaceuticals industry jobs

<< previous | Displaying 1-20 of 20 results | next >>
Catalent Pharma Solutions - Bathgate, EH48 2FY(13 hours ago)
Catalent Pharma Solutions are looking to recruit an experienced Quality SpecialistsII to join the team to undertake batch review, internal audit and release of incoming materials at our Bathgate facility. This role will see you join the dedicated and Quality function that are an integral part of our success here at Catalent. In this role you will be responsible for the movement, control and tracki...
full job description
A manufacturing company require a Head of Quality to join its management team. You will be responsible for setting, managing and delivering on key operational quality targets. As part of the management team, you will be an integral part of the company's growth strategy and be responsible for establishing and growing the quality systems across all company sites. You must have significant experience...
full job description
A Pharmaceutical Company based in Berkshire is currently looking for a Quality Officer (GMP Pharma) to join their team on a permanent basis. QA Officer (GMP Pharmaceuticals) – Key Responsibilities: •Technology Transfer of new products • Handling of market complaint investigations. •Review and approval of Master Batch manufacturing/packing records, Finished product specification and method of analy...
full job description
Are you looking for a dynamic and growing international organisation that will provide you with the perfect platform for career development? Biotage are now recruiting a Quality, Health & Safety and Environmental (QHSE) Manager to join our Management Team at our site in Ystrad Mynach. Who we are: Biotage is a knowledge-driven organization where the aptitude and scope for innovation is an important...
full job description
Cranleigh Scientific - Alton, South East/Southern, GU342PP(1 day ago)
A leading manufacturer of nutrition, health and beauty products require a Regulatory Affairs Officer to join its Technical Information team. As a junior Regulatory Affairs Officer you will provide support to the company's nutritional product range. You will ideally be educated to degree level in chemistry or a nutrition related subject. You will also have knowledge and/or experience within regulat...
full job description
REACH Regulatory Specialist An excellent opportunity has arisen for a career driven REACH Regulatory Specialist / Product Stewardship Manager to join a global leader operating in the chemical industry. As a key member of the global team you will Lead Product Stewardship activities and EHS support for one or more designated business units, coordinating chemical registrations and handling complex cu...
full job description
We have two exciting opportunities for two experienced Validation Specialists to join a Biopharmaceutical company near Oxfordshire area has become available. Each role as the Validation Specialist, will be responsible for being the subject matter expert for new filling equipment being brought into the new facility. You will be hands on, yet operate at a senior level with experience working with Is...
full job description
Hyper Recruitment Solutions are currently looking for a GMDP Quality Auditor to join a leading Global Pharmaceutical company based in the Cambridgeshire area. As the GMDP Quality Auditor you will be responsible for ensuring continued GMDP compliance across the companies broad product portfolio. KEY DUTIES AND RESPONSIBILITIES: Your duties as the GMDP Quality Auditor will be varied however the key ...
full job description
Job Title: Senior Quality Assurance Officer Job Type: Permanent, Full-Time Location: Berkshire Salary: D.O.E Quality – Manufacturing – Production – FMCG – GMP – Assurance – QA – Quality Assurance – Audit – ISO – Pharmaceutical – SOP – QMS – IPQA – Q.A A Berkshire based manufacturer are looking to recruit for a Senior Quality Assurance Officer on a permanent, full-time basis. The Senior Quality Ass...
full job description
Hyper Recruitment Solutions - South East England, South East/Southern(2 days ago)
We are currently looking for a Quality Officer to join a leading pharmaceutical company based in the South East. As the Quality Officer, you will be responsible for developing and maintaining the site QMS, ensuring GMP compliance throughout. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Quality Officer will be varied. However, the key duties and responsibilities are as follows: 1. You will r...
full job description
Hyper Recruitment Solutions - South East England, South East/Southern(2 days ago)
We are currently looking for a Technical Manager of Quality Assurance to join a leading pharmaceutical company based in the South East. As the Technical Manager of Quality Assurance, you will be responsible for the Quality Operations day-to-day management of the Quality Systems across site. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Technical Manager of Quality Assurance will be varied. H...
full job description
Hyper Recruitment Solutions are currently looking for a QC Section Head to join a leading Pharmaceutical company based in the Wiltshire area. As the QC Section Head you will be responsible for ensuring GxP compliance is maintained through effective QC operations. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Section Head will be varied however the key duties and responsibilities are as fo...
full job description
Hyper Recruitment Solutions are currently looking for a QC Manager to join a leading Pharmaceutical company based in the Wiltshire area. As the QC Manager you will be responsible for providing leadership to a large QC Function and supporting other business areas. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Manager will be varied however the key duties and responsibilities are as follows...
full job description
Hyper Recruitment Solutions - West Sussex, South East/Southern(2 days ago)
Hyper Recruitment Solutions are currently looking for a QC Chemistry Manager to join a leading Pharmaceutical company based in the West Sussex area. As the QC Chemistry Manager you will be responsible for ensuring that all laboratory activities are conducted in a GxP compliant manner. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Chemistry Manager will be varied however the key duties and...
full job description
We are currently looking for a QA Associate to join a leading company based in the Greater London area. As the QA Associate, you will be responsible for: KEY DUTIES AND RESPONSIBILITIES: Your duties as the QA Associate will be varied, however, the key duties and responsibilities are as follows: 1. As the QA Associate, you will coordinate the review and approval of controlled and QA documentation, ...
full job description
A growing consultancy require a Quality Assurance Officer to support their compliance team. You will have the opportunity to liaise with a range of clients within the medical device sector and support across a broad range of quality assurance activities. You will be educated to degree level in a scientific subject and have previous experience in either a QC, or preferably a QA role. Due to the loc...
full job description
An innovative medical device company have an exciting opportunity for a Quality and Regulatory Affairs Manager to help continue its growth. You will be responsible for leading maintenance, management and improvement of certified ISO 13485 quality system across two UK sites. You must have proven experience in a QA/RA function at management level within another medical device organisation. Purpose o...
full job description
Quality Operations Manager needed for one of the world's leading biopharmaceutical organisations in Surrey. Join this well known and reputable company on an initial 6 month contract to serve as Subject Matter Expert in the GDP Quality Management System. My client specialises in the manufacture and distribution of over 160 different vaccines, medicines and other consumer healthcare products worldwi...
full job description
We are seeking an experienced Quality Assurance Auditor for our Safety Assessment group site located in Tranent. The Quality Assurance Unit (QAU) supports the above sectors by monitoring scientific studies, procedures and reports for compliance with Good Laboratory Practice (GLP), and Good Clinical Practice (both human and veterinary). A career as a QA professional at Charles River means you get a...
full job description
We are seeking a Scientific Quality Auditor for our Safety Assessment group site located in Tranent. The Quality Assurance Unit (QAU) supports the above sectors by monitoring scientific studies, procedures and reports for compliance with Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and Good Clinical Practice (both human and veterinary). Quality Assurance is the framework that...
full job description
<< previous | Displaying 1-20 of 20 results | next >>