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Technical Product
2 weeks ago
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Technical Product (Transfer) Manager Client: Perrigo
Location: Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: (Not Provided)
Job Views: 83
Posted:
Expiry Date:
Job Description: Description Overview Do you enjoy working with multiple stakeholders and managing/organising technical projects?
Do you have experience with process validation activities and are you considering growing your career with a role as a technical product transfer manager at Perrigo?
In this role you will work on our medicinal product projects and provide technical expertise to our business to deliver selfcare for everyone.
Scope of the Role Collaborate as part of a multidisciplinary team to resolve complex product development/manufacturing issues.
Provide technical support to internal and third party departments.
Lead technology transfer and NPI projects (mainly medicines) to contract manufacturing organisations in a pharmaceutical environment.
Support/lead technical risk assessments, Q3D assessments, nitrosamine assessments.
Provide technical review of process, packaging and analytical validation protocols and reports.
Liaise across all business functions to promote effective delivery of business goals.
Develop solid relationships with customers and service providers.
Review and propose continuous improvements both internally and externally.
Plan and manage projects involving modifications/upgrades/technology transfer of medicinal products within the outsourced manufacturing supply chain in line with GMP requirements.
Gather, evaluate and analyse a wide variety of data and information to support external technical operation function.
Conduct technical studies relating to a variety of technical operation activities (validation, etc.).
Maintain current product manufacture by providing technical support to internal and third party departments.
Provide expert technical advice, review and approval of changes, documentation approval and management.
Maintain accurate records to ensure all regulatory and internal company procedures are adhered to and work in line with GMP requirements.
Remain compliant with Standard Operating Procedures (SOPs).
Comply with the Perrigo Safety Policy and Procedures, to ensure a health and safety culture is supported in the areas for which you are responsible.
Undertake such other reasonable duties as may be required from time to time in order to support the Perrigo business.
Experience Required Degree in Chemistry/Pharmaceutical Science or equivalent.
Three plus years' experience in the pharmaceutical industry process validation, formulation development or analytical validation.
Knowledge of and experience with technology tools to support the business including excellent computer skills in Microsoft Suite environment.
Good communication skills and ability to make effective contributions to meetings with all personnel at all levels within the organization.
Organized and able to coordinate multiple tasks, as well as effectively communicate written and verbal information with the appropriate sense of urgency.
High level of accuracy and an eye for detail.
Goal-orientated and driven to achieve results to agreed timescales.
Effective team player.
Understand, recommend and progress continuous improvement strategies.
We are an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.
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