HPLC Analyst, Pharmaceutical
Posted a week ago by Russell Taylor Group Ltd
HPLC Analyst, Pharmaceutical
Location: Greater Manchester
Type: Permanent
Hours: 37.5 hours per week. Site based role.
Typically 09:00 - 18:00 ( including 1 hour lunch and 2 x 15 minute breaks unpaid), there is some flexibility.
Our client, a pharmaceutical company are growing and looking to recruit an experience HPLC analyst within an GMP setting.
The Role:
Key Responsibilities:
• Carry out analysis of finished products, in-process samples, raw materials using traditional QC methods, in particular, HPLC, UV & FTIR.
• Conduct checks on data to ensure Quality and consistency of the data.
• Interpret and analyse the measured data via specific laboratory software packages. Calculate results via the specified calculation and record all calculations and methods for analysis in the appropriate files and prepare the results in a format suitable for presentation to management.
• 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, Worksheet and protocols) so as to comply with the requirements of accredited Quality standards.
• QC analyst is expected to undertake any additional duties online Managers or Departmental Managers discretion.
• To perform method development, verification/validation of existing and new products.
• Ensuring targets are met and our company's strategy is achieved through consistent development and coaching of staff.
• Undertaking relevant project work as required, involving improvement of QC systems and processes.
• Responsible for in-process and final release of pharmaceutical products ensuring compliance with current regulations and timely delivery to customers.
• To be the point of contact on the site for Health and Safety documentation and reporting ensuring that the Senior Leadership Team take responsibility and accountability for the H & S of their teams.
The Person:
• Will hold a degree in a Scientific discipline
• Experience in HPLC testing
• The ideal person will have worked in a GMP accredited setting with extended method dev/ validation experience but not essential
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
Location: Greater Manchester
Type: Permanent
Hours: 37.5 hours per week. Site based role.
Typically 09:00 - 18:00 ( including 1 hour lunch and 2 x 15 minute breaks unpaid), there is some flexibility.
Our client, a pharmaceutical company are growing and looking to recruit an experience HPLC analyst within an GMP setting.
The Role:
Key Responsibilities:
• Carry out analysis of finished products, in-process samples, raw materials using traditional QC methods, in particular, HPLC, UV & FTIR.
• Conduct checks on data to ensure Quality and consistency of the data.
• Interpret and analyse the measured data via specific laboratory software packages. Calculate results via the specified calculation and record all calculations and methods for analysis in the appropriate files and prepare the results in a format suitable for presentation to management.
• 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, Worksheet and protocols) so as to comply with the requirements of accredited Quality standards.
• QC analyst is expected to undertake any additional duties online Managers or Departmental Managers discretion.
• To perform method development, verification/validation of existing and new products.
• Ensuring targets are met and our company's strategy is achieved through consistent development and coaching of staff.
• Undertaking relevant project work as required, involving improvement of QC systems and processes.
• Responsible for in-process and final release of pharmaceutical products ensuring compliance with current regulations and timely delivery to customers.
• To be the point of contact on the site for Health and Safety documentation and reporting ensuring that the Senior Leadership Team take responsibility and accountability for the H & S of their teams.
The Person:
• Will hold a degree in a Scientific discipline
• Experience in HPLC testing
• The ideal person will have worked in a GMP accredited setting with extended method dev/ validation experience but not essential
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
- Type:
- Permanent
- Start Date:
- 26/06/2024
- Contract Length:
- N/A
- Contact Name:
- Login or register to view
- Job Reference:
- J91979715
- Job ID:
- 221902664
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