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Technical Trainer for QC

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Technical Trainer for QC

Posted :2 years ago
Job location
Galway, Ireland
Job type
Full time
Job Descriptions



The Opportunity:

This is an opportunity to be part of a dynamic team within the QC Department. We are looking for an individual who will support and drive Chanelle Pharma’s vision to be the most valued global provider of high quality, competitively priced pharmaceutical products and to provide excellent services and support to our customers.

In this role you will report to the QC Manager

KEY RESPONSIBILITIES:

  • Train New and Existing Analysts in both Departments on Good Laboratory Techniques.
  • Train New and Existing Analysts in both Departments on Good Manufacturing Practice.
  • Liaise with the HR Department to ensure a smooth transition into the Company for new Analysts.
  • Responsibility for the Training Records of Analysts in both departments (Maintenance and Updating).
  • Responsible for the Training Matrix of both departments.
  • Ensure training is done in each department by either the technical trainer or the SME of that particular area.
  • Co-ordinate with relevant SME’s on regular refresher training programs (GMP, Manual Handling etc).
  • Responsible for updating the training program that is already in place.
  • Responsible for updating the training records already in place.
  • Responsible for regular training on GMP documentation (OOS, Deviations, SOP writing)
  • Review and Revise Training Documentation.
  • Develop and present training programs which support the company training plans.
  • Evaluate and implement continuous improvement on design, delivery, and evaluation of training.
  • Provide ongoing support to all areas to ensure compliance to the highest GMP standards.
  • Perform Manual Handling Training for new hires.  
  • Perform Annual GMP training.
  • Perform/Co-ordinate training on updates to procedure or processes.
  • Adherence to health and safety procedures
  • Ensure compliance to documented procedures and GMP requirements as outlined in company procedures.
  • Maintenance of hygiene / housekeeping standards in the QC / R&D area’s.
  • Comply to terms and conditions outlined in your contract of employment.

Competencies:

  • Organizational skills, personal efficiency, time management skills and the ability to prioritize competing demands are key communication skills.
  • Ability to train a team and manage diverse personalities and viewpoints.
  • Ability to build relationships and collaborate with others is vital.
  • Strategic decision-making within the business as an influencer.
  • Demonstrate and lead on the values, initiatives, and culture of an organization. Professional expertise.
  • A strong working knowledge of best practice processes, change management implementation, coaching and mentoring.
  • Practical, action-orientated approach to managing priorities and teams.
  • Possesses knowledge of lean management principles and has a keen interest in the benefits of lean management systems.
  • Communicates in clear, effective, timely, concise, and organized manner, is articulate and persuasive in presenting, soliciting complex or sensitive data                
  • Requires minimal supervision, consistently promotes, and maintains a harmonious/productive work environment
  • Strong computer skills in MS office, Operating systems, and a wide variety of software suites.
  • Practical thinker who enjoys problem solving and solution development.

QUALIFICATIONS:

  • Experience working within a pharmaceutical Environment; with knowledge of EU, GMP and US FDA Guidelines
  • Degree in Scientific Area
  • Excellent written and verbal communication skills
  • Strong computer skills

PHYSICAL DEMANDS: Health & Safety requirements (eg. Manual Handling Training)

· To take reasonable care for their own safety, health and welfare at work and that of any other person that may be affected by their acts or omissions while at work.

· To cooperate with Realoch or any of its representatives that will enable the company to comply with the relevant health and safety statutory provisions.

· Adheres to safety regulations by ensuring correct usage of PPE in the lab area

· Reports to the supervisor or health and safety representative without unreasonable delay any defects in plant, equipment, place of work, system of work which might endanger safety, health or welfare of themselves or any employee, contractor or visitor to the company.

· Keeps work area safe, clean and tidy

· Not too intentionally or reckless interfere with or misuse any appliance, protective clothing, convenience, equipment or other means or thing provided.

· Required training:

  • Manual Handling training,
  • Glove removal and disposal training,
  • Working with chemicals
  • Disposal of waste
  • Working on PC

WORK ENVIRONMENT: (eg. Office, Production)

· Laboratory




Qualifications

Third Level Qualification in science

Skills
  • Strong Computer Literacy
  • Excellent written and verbal communication skills
Experience
  • 1 year
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