A Validation Manager is required for our Limerick based trailblazing
pharma client. This role is a leadership role and requires someone
with extensive Validation experience. Join a leading multinational
today.
ROLE OF THIS POSITION
* Leads cross-functional teams in developing Validation best
practices, standards and guidelines which includes exploring new
techniques, methods and other industry practices.
* Leads projects by developing appropriate plans, schedules,
resource loading and other project deliverables as required Execution
of validation projects and overseeing Validation projects as well as
junior-level staff. Based on engineering specification, performs
validation projects which include authoring protocols, executing
validation protocols and writing reports of validation results.
* Reviews and approves Validation protocols and summary reports
generated by the Validation staff against standard operating
procedures and policies as well provides guidance to Validation staff
writing protocols and final reports
* Prepares equipment for qualification studies and executes
qualification and validation studies according to approved protocols
and SOPs
* Leads team of Validations specialist who investigates and
troubleshoots problems which occur and determines solutions or
recommendations for changes and/or improvements.
* Provide direction and assign work to Validations Specialists to
meet goals and timings
JOB REQUIREMENTS
* Requires BS/BA degree in Life Sciences or related field and 5+
years of GMP experience, preferably in the pharmaceutical or
biotechnology industries.
JOB DESCRIPTION
A Validation Manager is required for our Limerick based trailblazing
pharma client. This role is a leadership role and requires someone
with extensive Validation experience. Join a leading multinational
today.
ROLE OF THIS POSITION
* Leads cross-functional teams in developing Validation best
practices, standards and guidelines which includes exploring new
techniques, methods and other industry practices.
* Leads projects by developing appropriate plans, schedules,
resource loading and other project deliverables as required Execution
of validation projects and overseeing Validation projects as well as
junior-level staff. Based on engineering specification, performs
validation projects which include authoring protocols, executing
validation protocols and writing reports of validation results.
* Reviews and approves Validation protocols and summary reports
generated by the Validation staff against standard operating
procedures and policies as well provides guidance to Validation staff
writing protocols and final reports
* Prepares equipment for qualification studies and executes
qualification and validation studies according to approved protocols
and SOPs
* Leads team of Validations specialist who investigates and
troubleshoots problems which occur and determines solutions or
recommendations for changes and/or improvements.
* Provide direction and assign work to Validations Specialists to
meet goals and timings
JOB REQUIREMENTS
* Requires BS/BA degree in Life Sciences or related field and 5+
years of GMP experience, preferably in the pharmaceutical or
biotechnology industries.
We need : English (Good)
Type: Permanent
Payment:
Category: Others
