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Senior QC Analyst (Quality Manager / Pharmaceuticals)

Expired
  • Salary: £200 - £300 per day
  • Job type: Contract
  • Location: Haverhill, Suffolk
  • Sector: Science
  • Date posted: 07/03/2018
  • Job reference: J382858A

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We are looking for an experienced and talented Senior QC Analyst to join our client,on a 4 month contract, based in Haverhill.
This person will be brought i to act as a key contact and provide technical guidance for own value stream. They will be responsible for analysis (sample/ equipment), review and collation of experimental data against specifications laid down by the Quality Department
Pay rates are between £200-300 per day

Role responsibilities:
* Sampling, analysis and release of PPMs and drug products, ensuring all documented results are according to cGMP
* Review and collation of raw data, including generation of C of A's and release from QC where appropriate
* Ensures testing aspects of Stability programs controlled from Haverhill are maintained and fit for purpose
* Provides technical guidance for testing/ equipment within own area and has a broad understanding of other areas of QC
* Performs in depth statistical analyses, data mining and report generation as necessary
* Acts as the key contact for a specified customer group and builds strong working relations with those customers
* Has a good understanding of how all elements of the value stream work
* Leads investigations and identifies root causes and appropriate preventative actions including documentation for out of spec issues
* Responsible for delivery of projects to agreed timelines, as appropriate
* Actively seeks out EHS improvement opportunities
* Ensure Continued Professional Development (CPD) in area of expertise
* Training of staff where appropriate and providing technical support to less experienced staff
* Drives continuous improvement within the department
* Ensure that the laboratory is maintained in a safe and tidy manner at all times
* Complete all Events, CAPAs, Change Controls and ERs within the agreed timelines
* Maintain core training and prior to conducting any activity ensure you are trained in the current version
* Responsible for personal safety and that of others, reporting all accidents and unsafe acts and conditions
* Provides support for the LUNA system across site, as necessary

Knowledge Skills and Experience:
* Good understanding of the pharmaceutical regulatory process
* Demonstrated high level of competence in a variety of analytical techniques and skills
* Ability to implement, promote and adhere to laboratory health and safety practices
* Ability to build and develop good relations across the value streams and externally
* Proven experience in coaching less experienced colleagues
* Demonstrated ability to work consistently to quality policies and cGMP
* Demonstrated ability to successfully manage own workload to meet departmental targets

Education

Desirable:
* Degree level qualification (or equivalent) in a relevant science subject

Interested candidates should submit their CV in the first instance to Sophie . Garty @ experis . co . uk / 0161 924 3651

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