A leading Chemical company are looking for a QC Analyst to join their team in the Durham area.
Salary and Benefits of QC Analyst
Salary up to £28,000
Permanent Role
Skills and Qualifications needed for QC Analyst
Awareness of GMP Standards
Chemistry Degree
2 Years Experience in a relevant role
Fine Chemistry / Pharmaceutical Experience
HPLC and GC Experience
Responsibilities of the QC Analyst
The role of QC Analyst consists of Plan and prioritises own work with guidance from Senior Analyst or Manager. Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements and to carry out minor analytical method development to improve analysis, including HPLC, GC, spectrophotometric techniques and titrations
Additional Responsibilities of the QC Analyst:
Maintain the flow of documents within the department ensuring they are complete, accurate and compliant with procedures or guidelines
Carry out basic equipment maintenance and calibration of laboratory equipment following approved methods and procedures on assigned pieces of equipment
Write and review SOPs, Work Instructions and testing procedures for raw materials, intermediates and finished products
Monitor and maintain stock levels of reagents and consumables
For more information and to apply for the role of QC Analyst direct, please click the link below!....Read more...
This permanent and days based QC Analyst (Quality Control) is working with a globally leading pharmaceutical manufacturing company which is present in more than 20 countries world-wide, and over 20,000 employees globally. This company is willing to invest heavily into the successful candidate to promote their career and personal development. The QC Analyst role is offering between £25,000 - £30,000 base salary, with a competitive pension, private healthcare plan, up to 15% performance related annual bonus, annual pay review, flexible working opportunity, 25.5 days annual leave plus bank holidays (with an additional day after 5, 10 and 15 years’ service), 4 weeks full sick pay, income protection, business and personal travel insurance, life assurance up to 4x base salary, cycle to work scheme and more!Taking this opportunity as QC Analyst would mean working for a leading global producer of API’s (Active Pharmaceutical Ingredients). This role would include opportunities to advance your career, skillset, and education.Responsibilities of the QC Analyst will include:
Interpret, document and report critical analytical data.
Observe and monitor calibrations of analytical apparatus, dealing with troubleshooting issues, as well as maintaining the upkeep of the laboratory.
Prepare documentation in relation to customer standards.
Comply with all regulations including GMP.
Analysis of raw materials and product to established SOP’s.
Comply with all COSHH regulations and safe lab practices.
The QC Analyst Perform daily/weekly calibrations/monitoring of analytical apparatus.
Utilise analytical laboratory techniques such as GC (Gas Chromatography) and HPLC.
To be successful in this position as QC Analyst , you will hold an either a HNC/HND or a degree in a relevant Analytical, Chemical or Pharmaceutical subject, with an established technical Laboratory background including proven experience of GC (Gas Chromatography) and HPLC. Experience dealing with analytical reports and instrumental trouble shooting on a GMP site is also essential.Please apply directly for this QC Analyst role.....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...
