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Job Details

Analytical Group Supervisor-133318

Company: PPD
Location: Europe, Middle East & Africa-Ireland-Westmeath-Ath
Reference: 133318
Closing Date: 09 Jan 19
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Our GMP laboratory based in Athlone, Ireland offers fully integrated solutions for product development and analytical development, including analytical testing services in method development, method validation, method transfer, release and stability studies. Our highly qualified GMP lab staff work with large and small molecules, including active pharmaceutical ingredients (API), drug products, inhaled products and other medical devices. ...

Requirements:

Our GMP laboratory based in Athlone, Ireland offers fully integrated solutions for product development and analytical development, including analytical testing services in method development, method validation, method transfer, release and stability studies. Our highly qualified GMP lab staff work with large and small molecules, including active pharmaceutical ingredients (API), drug products, inhaled products and other medical devices.

Due to further expansion of our site in Athlone, Ireland in 2018, we have a new opening for an Analytical Group Supervisor/Associate Group Leader in our BioPharm team.
 
About the Associate Group Leader position
 
PPD provides laboratory services that are designed to provide the best and highest level of service to our clients. Our lab employees are committed to quality results and strict compliance with regulatory standards. The role of Associate Group Leader is to provide support to our BioPharm department by providing management and direction to a group of laboratory staff and resources for project activities and needs, overseeing daily operations to monitor quality and project timeliness, and assist in preparation and implementation of company policies, quality systems and training programs. You will have ownership to ensure responsiveness to the client and overall client satisfaction.

Key responsibilities:

  • Management of a team of analysts
  • Allocation, scheduling and managing laboratory resources for group's project activities and updates LIMS for project status.  Reviews timesheet reports for billing accuracy.
  • Preparation, review and approval of study protocols, project status reports, final study reports and other project-related technical documents.
  • Designing experimental study and participates in technical troubleshooting.
  • Reviewing data for technical quality and compliance to protocols, methods and SOPs.  Review and approve laboratory investigations, deviations, QA facility and data audits.  Assists in client and regulatory authority audits.
  • Responding to client questions and needs; leads client technical meetings.
  • Assisting in preparation of proposals, project definition and pricing.
  • Coordinating and prioritizing project activities with internal functional groups (physical testing, analytical development, etc.) and support functions (QA, sample management, etc.)
  • Assisting senior group leaders and/or managers in their responsibilities.
  • Preparation and implementing SOPs and company operational policies. Ensuring adherence and making recommendations to quality system improvements.

Qualifications

Skills and experience:
  • Educated to a Bachelor's Degree level in a relevant area, ie chemistry, biochemistry
  • Management experience in the pharmaceutical, biotech or analytical contract laboratory industries
  • Stability/QC/analytical R&D/project and program management.
  • Direct supervision of technical staff.
  • Full understanding of GMP requirements, client SOPs, ICH guidelines, EP and USP requirements and EMEA and FDA guidance's.
  • Knowledge and experience of a wide range of techniques, HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA, spectrophotometry.
This role offers an excellent opportunity for someone who has previous GMP experience in a small molecule environment coupled with proven record of team leadership; who would now like to embrace a new technical environment/Biopharm specific techniques.   The successful candidate can look forward to job stability with a leading CRO that has experienced year-on-year growth. With future expansion plans, there is the opportunity to progress in your career with PPD at our Athlone labs. We offer a generous salary, medical insurance, pension, life insurance and relocation assistance to those qualified candidates based outside of the Republic of Ireland.

 

 

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Apply for this job: Analytical Group Supervisor-133318

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Website:  Visit Our Web Site

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