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» Job Vacancy

QC Analytical Specialist


Hours:
Salary: £34000 - £47000/annum
Category: Medical/Pharmaceutical/Scientific,
Location: Haverhill, Suffolk, United Kingdom

Mar 14th
days old


views


applied




Description
QC Analytical Specialist - Contract Role - Haverhill £34,000 to £47,000 per annum

Our client is a leading pharmaceutical company based in Haverhill with over 40 years' experience in the industry. They are currently looking to recruit a QC Analytical Specialist to cover a contract until 29th March 2019

Your role will be to act as a key contact and provide technical guidance for QC and external parties. You will be responsible for analysis (sample/ equipment), review and collation of experimental data, against specifications laid down by the Quality Department. Our QC Analytical specialist will need to have a background in a supervisory role as you will be responsible for between 6-7 analysts and be accountable for ensuring all the scheduled work is completed to strick timelines. You will have strong communication skills and be influential to your team and other departments.

As QC Analytical Specialist your duties will include:

* Sampling, analysis and release of raw materials, drug substances and drug products, ensuring all documented results are according to cGMP.
* Collation and release of analytical data and generation of certificates of analysis
* Responsible for project implementation and ongoing administration as required
* Leads projects with significant technical requirement
* Provides analytical support to other projects and laboratories, both internally and externally
* Responsible for delivery of departmental projects to agreed timelines
* Support the introduction of new products, procedures and processes into the department or other departments
* Experiemental design and testing of non-standard work
* Keeps up to date on regulatory guidelines and ensures GWP across QC
* Has a good understanding of how all elements of the value stream work
* Lead investigations and identifies root causes and appropriate corrective actions
* Ensure the lab is maintained in a safe and tidy manner at all times
* 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
* Complete all corrective and preventative actions within the agreed timelines
* Maintain core training and prior to conducting any activity ensure you are trained in the current version

We are looking for a QC Analytical Specialist that can demonstrate the following in order to be able to carry our this role effectively, along with the ability to meet departmental objectives within the deadlines stipulated:

* Good understanding of the pharmaceutical regulatory process
* Demonstrates 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
* Proven ability to successfully manage and lead projects
* Demonstrated ability to work consistently to quality policies and cGMP.

Ideally you will have a degree level qualification (or equivalent) in a relevant science subject, ideally microbiology.

If you feel this role is for you and you are happy with the contract duration until March 2019, then please forward your CV in Word for consideration
Company
Company: CV Library Ltd

Further Information
Reference: 207535714/j4m621296
Posted: 14 Mar 2018, 15:34
Visa Required: Applicants must be eligible to work in the specified location








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