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QC Chemist

Employer
Thornshaw Recruitment
Location
Waterford (County), Munster (IE)
Salary
DOE
Start date
17 Sep 2020
Closing date
13 Oct 2020

View more

Discipline
Quality, QC Analyst, R & D , Chemistry
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

QC Chemist
On behalf of my client I am recruiting for a QC Chemist. The successful candidate will be responsible for ensuring all raw materials, packaging, finished products and Stability samples are analysed in accordance with cGxP
Responsibilities:
• To test and complete write up of QC raw material, packaging, finished product and stability samples in a timely & efficient manner.
• To support all other on-going laboratory functions & requirements.
• To prepare and review stability summary sheets where required.
• To ensure that all work carried out follows the required standards conforming to company, cGxP, SOPs, regulatory regulations and guidelines, safety and environmental guidelines.
• To identify and make recommendations for improvements as part of a team within or outside the department in order to ensure continuous improvement.
• Check own work and that of others for accuracy.
• To assist in the preparation for internal / customer/ regulatory inspections.
• Involved in internal investigations e.g. Out of Specifications, Incidents & Deviation investigations etc
• Draft, review or revise documentation management system
• Report any Deviations/Out of Specifications to Senior Chemist and complete in a timely manner
• Health & Safety:
a. Implement safety requirements as per site documentation including SOPs, Safety Statement and COPs
b. Report any defects
Qualifications:
• Qualified to a minimum of honours degree level in Analytical Chemistry, Pharmaceutical science or related discipline.
• At least two years’ experience working in a related position (not including academic experience).
• Proficient in the use of HPLC & associated problem solving, and dissolution testing
• Strong analytical ability and quality orientation
• Knowledge & proficiency of Microsoft products including, Excel, Word & Powerpoint.
• Strong attention to detail is critical and excellent time management
• Adaptability – maintain effectiveness in varying environments and with different tasks, responsibilities and people
• Broad understanding of regulatory requirements for submission of dossiers in EU, USA, Japan and other jurisdictions
• Analysis – secure relevant information and identify key issues and relationships from a base of information; relate and compare data from different sources, identifying cause-effect relationships

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

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For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
Website

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