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TRAINING COORDINATOR

 

Company:

LOTUS TECHNICAL SERVICES
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Job Reference Number

14570566

Client ID:

RI/LTS TC C
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Posted On:

Feb 17 2012

Location:

CORK
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Job Type:

Contract

Salary:

COMPETITIVE
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Lotus Technical Services is a leading solutions provider offering a complete range of automation and technical services specifically designed to enhance productivity and efficiency, and to maximise the value of our customer's core business. We are currently recruiting a Training Coordinator based within the Biopharmaceutical industry.

Job Purpose:

As Training Coordinator you will be responsible for carrying out tasks, projects and activities within the Operations Department.

Responsibilities:

· Responsible and accountable for assuring the safe accomplishment of job activities, following good environmental practices and procedures.

· Carry out routine and non-routine tasks delegated by Manager/Team Leader according to appropriate procedures, values and standards.

· Report deviations promptly to the Manager/Team Leader to ensure compliance with EHS and GMP requirements.

· Participate in and lead Cross-Functional teams as necessary.

· Identify and plan for the present and future training & development requirements of the Operations Department (Perform Training Needs Analysis, as required)

· Schedule and co-ordination of trainers (internal and external), training rooms, training materials and other resources to meet Operations department training requirements

· Monitor quality of training, implementing continuous improvement strategies compliant with site procedures and cGMP/EHS requirements

· Ensure Operations documentation is reviewed and/or updated as necessary in accordance with site procedures

· Provide support and assistance to the Site Quality Training Team Leader

· Generation and review of documentation using eDocs and tracking of documents through review/approval cycle, Process Operations documentation through the site change control and approval cycle

· Develop systems to monitor quality of documentation and efficiency of documentation review, and develop and implement continuous improvement strategies

· Supports the development and management of compliance systems through tasks related to the management of document control in respect of SOPs and other GMP regulated documents

· Apply GMP regulations and other FDA and international guidelines to all aspects of the position.

Requirements:

· The successful candidate will have a third level qualification in a scientific/technical discipline with a minimum of 3 years experience in a related role within the biological and/or pharmaceutical industry.

· Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.

Lotus Technical Services is an Equal Opportunities Employer