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[Lead the improvement projects and or program setting in DS/DP manufacturing Operation]
- cGMP ½ÂÀÎ project manage teamÀÇ manager
- Apply cGMP knowledge to drive multiple site improvement projects and actions in the vaccine manufacturing plant
- Manage multiple, small to medium complexity cross-functional GMP process improvement projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns with the overall site QE timeline
- Serve as a project manager, tracking overall project timeline and its elements to ensure that functional deliverables are completed on time and according to quality standard
- Proactively identify project risks and work with the team and a group of SMEs to develop a contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of collaboration, cooperation, execution, effective communication and cross-functional problem-solving to enable high-performance team
[Lead the improvement projects and or program setting in Quality Management Systems]
- cGMP ½ÂÀÎ project manage teamÀÇ manager
- Apply cGMP knowledge to drive multiple site improvement projects and actions in the vaccine manufacturing plant
- Manage multiple, small to medium complexity cross-functional GMP process improvement projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns with the overall site QE timeline
- Serve as a project manager, tracking overall project timeline and its elements to ensure that functional deliverables are completed on time and according to quality standard
- Proactively identify project risks and work with the team and a group of SMEs to develop a contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of collaboration, cooperation, execution, effective communication and cross-functional problem solving to enable high-performance team
[Lead the improvement projects and or program setting in Facilities & Equipment on site]
- cGMP ½ÂÀÎ project manage teamÀÇ manager
- Apply cGMP knowledge to drive multiple site improvement projects and actions in the vaccine manufacturing plant
- Manage multiple, small to medium complexity cross-functional GMP process improvement projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns with the overall site QE timeline
- Serve as a project manager, tracking overall project timeline and its elements to ensure that functional deliverables are completed on time and according to quality standard
- Proactively identify project risks and work with the team and a group of SMEs to develop a contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of collaboration, cooperation, execution, effective communication and cross-functional problem-solving to enable high-performance team
[Lead the improvement projects and or program setting in Laboratory Operations]
- cGMP ½ÂÀÎ project manage teamÀÇ manager
- Apply cGMP knowledge to drive multiple site improvement projects and actions in the vaccine manufacturing plant
- Manage multiple, small to medium complexity cross-functional GMP process improvement projects with small to medium size group (2 to 10)
- Develop and manage project timeline that aligns with the overall site QE timeline
- Serve as a project manager, tracking overall project timeline and its elements to ensure that functional deliverables are completed on time and according to quality standard
- Proactively identify project risks and work with the team and a group of SMEs to develop a contingency plan
- Prepare a routine project status report
- Promote a quality-based GMP culture of collaboration, cooperation, execution, effective communication and cross-functional problem-solving to enable high-performance team
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[Lead the improvement projects and or program setting in DS/DP manufacturing Operation]
- Çз : Çлç ÀÌ»ó
- °æ·Â : 5³â ÀÌ»ó
- Àü°ø : »ý¸í°øÇÐ, »ý¹°ÇÐ, ¹Ì»ý¹°ÇÐ, ÈÇÐ µî À¯°üÇаú
- ¿µ¾î ´ÉÅëÀÚ
- Must have experience in DS/DP/Aseptic processing in manufacturing operations
- Technical ¿µ¾î ¹®¼ ÀÛ¼º °¡´ÉÀÚ FDA/EMA ½Ç»ç ´ëÀÀ °æÇèÀÚ as an SME
- Cgmp ½ÂÀÎ ÇÁ·Î¼¼½º °æÇèÀÚ
- Must have experience in leading projects
- Must have excellence organization and time management skills
- Experienced with regulated GMP environment
- Must have highly organization skills with the ability to manage multiple tasks in parallel
- Must have experience working with cross-functional team
[Lead the improvement projects and or program setting in Quality Management Systems]
- Çз : Çлç ÀÌ»ó
- °æ·Â : 5³â ÀÌ»ó
- Àü°ø : »ý¸í°øÇÐ, »ý¹°ÇÐ, ¹Ì»ý¹°ÇÐ, ÈÇÐ µî À¯°üÇаú
- ¿µ¾î ´ÉÅëÀÚ
- Must have hands on experience in Quality Assurance (example: deviation handling/ batch release process / product complain handling / change control process etc.)
- Technical ¿µ¾î ¹®¼ ÀÛ¼º °¡´ÉÀÚ
- FDA/EMA ½Ç»ç ´ëÀÀ °æÇèÀÚ as an SME
- cGMP ½ÂÀÎ ÇÁ·Î¼¼½º °æÇèÀÚ
- Must have experience in leading projects
- Must have excellence organization and time management skills
- Experienced with regulated GMP environment
- Must have highly organization skills with the ability to manage multiple tasks in parallel
[Lead the improvement projects and or program setting in Facilities & Equipment on site]
Çз : Çлç ÀÌ»ó
- °æ·Â : 5³â ÀÌ»ó
- Àü°ø : »ý¸í°øÇÐ, »ý¹°ÇÐ, ¹Ì»ý¹°ÇÐ, ÈÇÐ µî À¯°üÇаú
- ¿µ¾î ´ÉÅëÀÚ
- Must have hands on experience in Facilities & Equipment (example: HVAC, utility equipment, DS/DP manufacturing equipment and maintenance and calibration program)
- Technical ¿µ¾î ¹®¼ ÀÛ¼º °¡´ÉÀÚ
FDA/EMA ½Ç»ç ´ëÀÀ °æÇèÀÚ as an SME
- cGMP ½ÂÀÎ ÇÁ·Î¼¼½º °æÇèÀÚ
- Must have experience in leading projects
- Must have excellence organization and time
management skills
- Experienced with regulated GMP environment
- Must have highly organization skills with the ability to manage multiple tasks in parallel
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- Experienced in cGMP computer system management is a plus
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