FORMUALTION DEVELOPMENT SCIENTIST | LOUGHBOROUGH | Competitive SalaryAn exciting pharmaceutical organisation are currently recruiting for a Formulation Development Scientist to join their facility based in Loughborough on a permanent basis due to consistent growth.Reporting to the Group Leader Formulation Development, you will directly involved in the formulation and process development of medicinal products, covering a range of dosage forms including tablets, capsules, controlled release systems, sachets, liquids and semi-solids. You will operate various equipment involved in the manufacturing process at laboratory and pilot scale, complete accurate process documentation in accordance with GMP, manage the transfer of technology from formulation development to production and liaise with relevant staff on the manufacture of clinical trial batches.In order to be considered for the role, candidates must have a Bachelors degree in a related Scientific / Technical discipline and have 2 years + of experience in formulation development of solid oral dosage forms with knowledge of some of the following processes: wet granulation, dry granulation, fluid bed coating / drying, encapsulation, tabletting and tablet coating. Candidates must have previous experience of optimising manufacturing processes. Working knowledge of cGMP clinical manufacturing would be advantageous, along with any previous experience in controlled release, statistical experimental design, QbD experience or regulatory submissions.As well as a competitive salary on offer, the role comes with opportunities for growth & promotion, working at state of the art facility.In order to apply for this role please forward your CV to melissa@blackfieldassociates.com or call Melissa on +44 (0) 2392 322 306 for further details.
STR Limited is acting as an Employment Agency in relation to this vacancy.....Read more...
We are currently looking for a QC Analyst to join a leading company based in the Kent area. As the QC Analyst you will be responsible for the analysis of pharmaceutical raw materials, APIs, and finished products to ensure compliance with internal and regulatory specifications. Daily tasks will involve general chemical analysis including stability testing, various laboratory support activities, documenting analytical data, writing reports and SOPs all in accordance with cGMP.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1. As a QC Analyst you will be involved in Performing analytical testing using GC, HPLC, KF, FTIR and other required techniques in accordance with written procedures.
2. You will be required to record data into appropriate records and notify the line manager of any OOS, OOT, OOE or questionable results
3. You will create and update documents in accordance with cGMP and company procedures
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 or related science discipline.
2. Proven industry experience in Pharmaceutical QC testing and GMP (ideally small molecule) and analytical testing using GC, HPLC, KF, FTIR.
3. Experience in completing OOS investigations, deviations, CAPA, and Change Controls
Key Words: GC / HPLC / TLC / FTIR / QC / Quality Control/ QC Scientist/ GMP / API / Raw materials / Chemistry / analytical /
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...
