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Contact Info
Libby O'Donoghue
Life Science

+353 1 507 9254
[email protected]
Connect with me on
VP of R&D
Galway
Program Manager
Westmeath
GMP Inspector
Dublin
Regulatory Affairs Specialist
Republic of Ireland
Process Engineer
Limerick
R&D Engineer
Galway
Quality Engineer
Limerick
Risk Manager
Dublin
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Details

Process Scientist-Associate Manager LO(A008014)


Reference:A008014 Location: Limerick
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Scientist

Summary:Lead a team to manage all activities to ensure that manufacturing processes are supported. Responsible to support the Process Sciences Department through Process Validation, manufacturing floor support, product impact assessments, investigations, and technical evaluation as required. Active member of the Process Sciences management team.

Essential Duties and Responsibilities include, but are not limited to, the following:
• Lead a team and manage all activities to assure that manufacturing processes are supported.
• Responsible for developing a team such as development plans, upskilling and team forming.
• Write, review and approve Process Validation protocols and reports.
• Identification of process parameters and appropriate ranges to be included in process validation.
• Provide on the floor support to Manufacturing (Cell culture and Purification)
• Lead/Participate Process and Quality risk assessments.
• Lead troubleshooting activities associated with the manufacturing process.
• Provide technical support for manufacturing personnel to improve understanding of both cell culture and purification operations.
• Review and approve manufacturing documentation such as manufacturing records, SOPs and batch sheets.
• Develops/writes/plans and reviews protocols and activities for manufacturing support.
• Serves as a subject matter expert (SME) for data trending and manufacturing support.
• Presents and reviews process monitoring data to IOPS Management as necessary.
• Investigates and reviews OOS and OOL IPCs investigations.
• Performs, reviews and approves product impact assessment.
• Performs, reviews and approves scientific investigations (EOE & DNF).
• Communicate information on current process data and other IOPS initiatives which may impact process development and/or technology transfer.
• Support the site through regulatory audits by providing technical expertise.
Work efficiently and effectively in a fast-paced team-oriented environment to ensure maximum and high-quality output.

Education and Experience:
• BS/BA in a related field with 6+ years of related experience in a GMP environment. Previous experience in biological drug substance (DS) manufacturing.

For more information please contact Libby O'Donoghue on 0871897333 or [email protected]