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Job Details

QC Analyst

Company: X4 Group
Location: Lancashire
Reference: LABQCA
Closing Date: 02 Dec 16
Type: Permanent
Salary (£): 20,000 - 30,000
Benefits:

Job Summary:

QC Analyst / Quality Control / Quality Control AnalystPositions: QC AnalystLocation: LancashireSalaries: £20,000 - £25,000 DOEA Pharmaceutical Company who manufacturer bespoke Pharma products based in the Lancashire area are currently seeking a QC Analyst to join their team on a permanent basis.Role and Responsibilities: Conduct checks on data to ensure Quality and consistency of the data. ...

Requirements:

QC Analyst / Quality Control / Quality Control Analyst

Positions: QC Analyst

Location: Lancashire

Salaries: £20,000 - £25,000 DOE

A Pharmaceutical Company who manufacturer bespoke Pharma products based in the Lancashire area are currently seeking a QC Analyst to join their team on a permanent basis.

Role and Responsibilities:

  • Conduct checks on data to ensure Quality and consistency of the data.
  • Carry out analysis of finished products, in-process samples, raw materials using traditional QC methods in particular HPLC, UV & IR
  • Interpret the measured data by use of laboratory software packages and calculation methods; record all such calculations and methods for working in laboratory work files and prepare the results in a format suitable for presentation to management.
  • Keep all equipment in calibration and carry out preventative maintenance of equipment.
  • Ensure that the procedures relating to the calibration of analytical systems are adhered to and that accurate records of these calibrations are maintained.
  • Follow all other administrative procedures and work instructions specified by the laboratory management systems (SOPs, STMs and protocols) so as to comply with the requirements of accredited Quality standards.
  • Be aware of safety considerations at all times and bring any perceived safety issues to the attention of management (or nominee) without delay.
  • QC analyst is expected to undertake any additional duties on line Managers or Departmental Manages discretion.
  • To perform method development, verification / validation of existing and new products.
  • Analyse all Finished Product batch samples within 24 hours of receipt.
  • All Raw Material analysis and document collation to be completed within 24 hours of receipt.
  • All stability trial samples to be analysed on time within the correct time points.
  • Stability trial trending to be performed on monthly basis.
  • Quality Control metrics to be trended on monthly basis.

Candidate Requirements:

  • Graduate with BSc in Chemistry or other related scientific aptitude
  • Analytical Chemistry and Spectroscopy
  • Extensive knowledge of HPLC is a must
  • Method development
  • Minimum of 1 years’ experience in Pharmaceutical Industry Quality Control/ Stability Department
  • Knowledge and experience of EU GMP and MHRA regulations
  • Knowledge and experience of Stability Trials
  • Knowledge of Health & Safety in the laboratory
  • Computer / IT Literate
  • Ability to work as part of a team using own initiative to ensure efficient work flow.
  • Good organisation and communication skills
  • Strict attention to detail
  • Good team player with sound interpersonal skills
  • Motivation, accuracy, discretion and helpfulness are critical to this position

Apply by sending your updated CV through to l.beckwith@x4group.co.uk and call me on 0207 812 7700 to discuss your application in further detail. Interviews for this role are already being arranged.

GMP / Quality / QC / QA / SOP / Pharma / Pharmaceutical / CAPA / HPLC / MHRA / Protocols / Validation / Batch / Chemistry / Spectroscopy

Apply for this job: QC Analyst

Contact Information:

Address:  Head Office
2nd Floor, Brettenham House
Lancaster Place,
London,
WC2E 7EN
England
Tel:  02078127700
Website:  Visit Our Web Site

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