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QC Analyst

Job LocationBretby
EducationNot Mentioned
SalarySalary negotiable
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

We are collaborating with a specialist contract manufacturer for solid dose pharmaceuticals. They are forecasting a growth period with several new customer relationships. They are well known for exceeding customer expectations. You will contribute to thecompany performance as a QC Analyst by performing analytical tests in the laboratory using HPLC, AAS, FT-IR and related techniques.The PositionYou will be part of the twelve-person team in the laboratory and be cross trained developing knowledge of stability studies, method development, dissolution studies and QA requirements. They have invested in robust training opportunities and one-to-one meetingswith your manager to set clear goals to develop you into the professional you want to be. The development and progression of their current staff and management show how they put this approach to effective use.You will have:

  • Commercial/industrial experience using HPLC in a GMP or ISO 17025 environment. (Essential)
  • Knowledge or experience with solid dosage pharmaceutical testing such as stability testing, dissolution studies, grind studies, particle size study, disintegration studies and other related studies (Desirable)
  • Experience of Chromeleon 7.2 software or other related software packages (Desirable)
  • Commercial/industrial experience with techniques such as FT-IR, AAS, LC, MS (Desirable)
This role offers you an opportunity to develop rapidly and be supported in the journey to senior analyst, QA Officer or specialise into a specific area of pharmaceutical development and manufacturing. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Keyskills :
GMPHPLCPharmaceuticalcGMPAASFT-IRISO17025QC Analyst

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