Employer Profile:
Our Client discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, our Client was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient.
Job Description:
The Engineering Department at the Client’s plant in South co. Dublin is seeking to utilise the services of a process improvement engineer on a contract basis.
Profile:
The Engineer operates as part of a process team. Within this team they work alongside Technical, Engineering, Manufacturing and Quality colleagues.
Key Responsibilities: ?
Provide the expert process support necessary to identify, introduce and develop systems to support the site operations processes. ?
Responsible for translating those processes for each product into Electronic Batch Records (EBR) suitable for use in Production. ?
Involved in problem solving and troubleshooting with a focus on the use of Right First Time tools, including initiation and documentation of investigations ?
Has detailed operational and engineering knowledge of process equipment with a focus on reliability and optimisation as well as an understanding of how product flows through production process. ?
Plays a key role in the development of the manufacturing systems and will be responsible for continuous improvement initiatives. ?
Is responsible for the use, review, revision and upgrade of operational documentation including batch sheets, SOP?s, etc. ?
Is a champion for safe working practices and safety initiatives within their functional area. ?
Performs all tasks with due care and attention and in accordance with Good Manufacturing Practices and Amgen requirements, policies and procedures. ?
The job holder will be part of a learning and development programme which will include goal setting, annual performance reviews and individual development plans.
Requirements:
Basic Qualifications: ? Degree in Engineering/Science or equivalent ? Significant relevant process engineering industry experience
Key competencies: ? Analytical thinking ? Focus on quality ? Drive for results ? Initiative ? Planning and prioritisation ? Teamwork and Co-operation
Previous experience on ATEC or other stopper processing equipment is a distinct advantage
Excellent technical writing skills are essential
Good mechanical and process engineering skills
Ability to be self directed and operate to defined dead lines
Chemical engineering , mechanical engineering or biotechnology qualifications are distinct advantages however demonstrated experience in pharma or biopharma industry will be considered.
Understanding of sterilisation cycle development
Duration:
Minimum 6 months
Package:
€35-40/hour
Similar Jobs
Biotechnology Jobs
Job Title: Process Engineer -Dublin
Employer Profile:
Our Client discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, our Client was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient.
Job Description:
The Engineering Department at the Client’s plant in South co. Dublin is seeking to utilise the services of a process improvement engineer on a contract basis.
Profile:
The Engineer operates as part of a process team. Within this team they work alongside Technical, Engineering, Manufacturing and Quality colleagues.
Key Responsibilities: ?
Provide the expert process support necessary to identify, introduce and develop systems to support the site operations processes. ?
Responsible for translating those processes for each product into Electronic Batch Records (EBR) suitable for use in Production. ?
Involved in problem solving and troubleshooting with a focus on the use of Right First Time tools, including initiation and documentation of investigations ?
Has detailed operational and engineering knowledge of process equipment with a focus on reliability and optimisation as well as an understanding of how product flows through production process. ?
Plays a key role in the development of the manufacturing systems and will be responsible for continuous improvement initiatives. ?
Is responsible for the use, review, revision and upgrade of operational documentation including batch sheets, SOP?s, etc. ?
Is a champion for safe working practices and safety initiatives within their functional area. ?
Performs all tasks with due care and attention and in accordance with Good Manufacturing Practices and Amgen requirements, policies and procedures. ?
The job holder will be part of a learning and development programme which will include goal setting, annual performance reviews and individual development plans.
Requirements:
Basic Qualifications: ? Degree in Engineering/Science or equivalent ? Significant relevant process engineering industry experience
Key competencies: ? Analytical thinking ? Focus on quality ? Drive for results ? Initiative ? Planning and prioritisation ? Teamwork and Co-operation
Previous experience on ATEC or other stopper processing equipment is a distinct advantage
Excellent technical writing skills are essential
Good mechanical and process engineering skills
Ability to be self directed and operate to defined dead lines
Chemical engineering , mechanical engineering or biotechnology qualifications are distinct advantages however demonstrated experience in pharma or biopharma industry will be considered.
Understanding of sterilisation cycle development
Duration:
Minimum 6 months
Package:
€35-40/hour
Similar Jobs
Biotechnology Jobs
We need : English (Good)
Type: Permanent
Payment: package
Category: Pharmaceutical
