¿©·¯ºÐ¸¸ÀÇ Æ¯º°ÇÑ Àç´ÉÀ¸·Î ¸ÓÅ©¿Í ÇÔ²² ¸¶¹ýÀ» ÆîÃĺ¸¼¼¿ä!
Ä¿¸®¾î ¿©Á¤À» °è¼ÓÇؼ ŽÇèÇÏ°í, ¹ß°ßÇÏ°í, µµÀüÇÒ Áغñ°¡ µÇ¼Ì³ª¿ä? Ä¿¸®¾î¿¡ ´ëÇÑ ¿Á¤À¸·Î °¡µæÇÑ ¿©·¯ºÐó·³, ¸ÓÅ©µµ °Å´ëÇÑ Æ÷ºÎ·Î °¡µæÇÏ´ä´Ï´Ù! ¸ÓÅ©ÀÇ Àü ¼¼°è¿¡ ÀÖ´Â ±¸¼º¿øµéÀº °úÇÐ ±â¼úÀÇ Çõ½ÅÀ¸·Î ÇコÄɾî, »ý¸í°úÇÐ, ±×¸®°í ÀüÀÚ¼ÒÀç ºÎ¹®¿¡¼ »ç¶÷µéÀÇ »îÀ» dz¿ä·Ó°Ô ¸¸µé°í ÀÖ½À´Ï´Ù. ¸ÓÅ©ÀÇ ±¸¼º¿øµéÀº ÇѸ¶À½ÀÌ µÇ¾î °í°´, ȯÀÚ, Àηù, ´õ ³ª¾Æ°¡ Áö±¸ÀÇ Áö¼Ó °¡´ÉÇÔÀ» À§ÇØ Èû¾²°í ÀÖ½À´Ï´Ù. ±×°ÍÀÌ ¹Ù·Î ¸ÓÅ©°¡ È£±â½É °¡µæÇÑ ÀÎÀ縦 ¿øÇÏ´Â ÀÌÀ¯¶ø´Ï´Ù, È£±â½ÉÀº ¸ðµç °ÍÀ» »ó»óÇÒ ¼ö ÀÖ°Ô ¸¸µå´Â ¿øµ¿·ÂÀ̴ϱî¿ä.
Your role:
- Act as manufacturing engineering lead for new investment project in S. Korea for Merck Life Science. The candidate will be responsible for manufacturing equipment function from design, installation till commissioning, qualification, start-up, and future plant routine operation.
- Collaborate with cross-functional teams to design, develop, and implement manufacturing processes for the sterile manufacturing product line.
- Conduct analysis and optimization of manufacturing workflows to improve efficiency, productivity, and product quality.
- Identify and troubleshoot process issues, implement root cause analysis, and develop effective solutions to maximize manufacturing performance.
- Develop and maintain process documentation, including standard operating procedures (SOPs), work instructions, and manufacturing guidelines.
- Participate in equipment selection, process design, commissioning, and qualification activities for the manufacturing process, ensuring compliance with regulatory standards and quality requirements.
- Support the transfer of new products from giving site to receiving site production, ensuring seamless integration into the manufacturing process.
- Collaborate with quality assurance and validation teams to ensure compliance with regulatory requirements and facilitate process validation activities.
- Drive continuous improvement initiatives, identify opportunities for cost reduction, process optimization, and quality enhancement within the manufacturing process.
- Provide technical support and training to production operators and technicians, ensuring adherence to established procedures and safety guidelines.
- Stay updated with the latest industry trends, technologies, and best practices related to manufacturing engineering and share knowledge with the team.
Who you are:
- Bachelor¡¯s degree in manufacturing engineering, Mechanical Engineering, Industrial Engineering or a related field.
- +5 years equipment design/maintenance experience regarding pharmaceutical equipment, biopharmaceutical process line, or medical device assembly line.
- Knowledge of GMP and occupational safety / machine guarding
- CCM, Pharmaceutical, Single Use, Chemical Industry accepted.
- Good experience and knowledge of typical equipment used for bag, bottle, syringe assembly and bag making process.
- Experience in designing equipment package documentation.
- Ability to work effectively across the matrix organization interacting with global colleagues, design company, equipment vendor and cross functional teams.
- Good command in English and Korean in writing and speaking.
- Strong coordination, analytical, judgment, communication, and problem-solving skill.
- High troubleshooting ability
- Good customer focus and teamwork coordination
- Experienced user of Office software as well as data bases
- Experience within gamma irradiation processes is a plus
- Experience of FMEA as a design engineer is a plus
•¿©·¯ºÐÀÌ Ã£°í °è½Ã´Â ä¿ë Æ÷Áö¼ÇÀÌ ¾øÀ¸½Å°¡¿ä? ±×·¸´Ù¸é ÀÎÀçÇ®(Ŭ¸¯)¿¡ ¿©·¯ºÐÀÇ À̷¼¸¦ µî·ÏÇØÁÖ¼¼¿ä! ÇâÈÄ Àη ¼ö¿ä°¡ ÀÖÀ» °æ¿ì ÃÖ¿ì¼±À¸·Î ¾È³»µå¸®°Ú½À´Ï´Ù¡±
•Áö¿ø ¼øÀ¸·Î ÀüÇüÀÌ ÁøÇàµÇ¸ç, ÀûÇÕÇÑ Èĺ¸ÀÚ ¹ß°ß ½Ã ä¿ëÀÌ ¹Ù·Î ¸¶°¨µÇ¿À´Ï Áö¿øÀǻ簡 ÀÖÀ¸½Å ºÐµéÀº ºü¸¥ Áö¿ø ¹Ù¶ø´Ï´Ù.
•¼¹ö ¾ÈÁ¤¼ºÀ» À§ÇØ, ÀÎÅÍ³Ý ÀͽºÇ÷η¯°¡ ¾Æ´Ñ ±¸±ÛÅ©·Ò, ȤÀº ¸¶ÀÌÅ©·Î¼ÒÇÁÆ® ¿§Áö¸¦ ÅëÇÑ Áö¿ø ¹Ù¶ø´Ï´Ù.
•º¸ÈÆ´ë»óÀÚ ¹× Ãë¾÷º¸È£´ë»óÀÚ´Â °ü·Ã¹ý¿¡ ÀÇ°ÅÇÏ¿© ¿ì´ëÇÕ´Ï´Ù.
•Áö¿ø¼ÀÇ ±âÀç»çÇ×ÀÌ »ç½Ç°ú ´Ù¸¥ °ÍÀ¸·Î È®Àεǰųª Reference from previous employer »ó¿¡ ä¿ë»óÀÇ °á°Ý»çÀ¯°¡ È®À뵃 °æ¿ì ÇÕ°Ý ¶Ç´Â ä¿ëÀÌ Ãë¼ÒµÉ ¼ö ÀÖ½À´Ï´Ù
•(The company reserves the right to withdraw the offer, it if discovers subsequently that a candidate has given false information in application or has provided false or fraudulent documentation in support of his/her application. The offer is conditional upon satisfactory results of reference checks.)
•¸ÓÅ©¿Í Ä«Ä«¿ÀÅå Ä£±¸¸¦ ¸Î¾î ÃֽŠä¿ë ¼Ò½ÄÀ» ¹Þ¾Æº¸¼¼¿ä! (»óÀ§ QRÄÚµå Ŭ¸¯ ȤÀº ¸µÅ© Ŭ¸¯: http://pf.kakao.com/_wWuUb)
¸ÓÅ©´Â ±¸¼º¿øµé¿¡°Ô ¾Æ·¡¿Í °°Àº ÇýÅÃÀ» Á¦°øÇÏ°í ÀÖ½À´Ï´Ù. ¸ÓÅ©¿¡¼´Â ¸ðµÎ È£±â½ÉÀ» ¹ÙÅÁÀ¸·Î ¼·Î ´Ù¸¥ ¹è°æ°ú °¡Ä¡°ü, ±×¸®°í °æÇèÀ» °¡Áø ´Ù¾çÇÑ ±¸¼º¿øµé°ú ÇÔ²² ¼ºÀåÇÒ ¼ö ÀÖ½À´Ï´Ù. ¸ÓÅ©´Â ´Ù¾ç¼ºÀ» ¼ÒÁßÈ÷ ¿©±â¸ç, À̸¦ ÅëÇØ Å¹¿ùÇÑ ¼º°ú¿Í Çõ½ÅÀ» À̲ø¾î³» °úÇÐ ±â¼úÀÇ ¹ßÀü¿¡ °øÇåÇÏ°í ÀÖ½À´Ï´Ù. ¸ÓÅ©´Â ±¸¼º¿ø ¸ðµÎ º»Àθ¸ÀÇ ¼Óµµ·Î ¹ßÀüÇÏ°í ¼ºÀåÇÒ ¼ö ÀÖµµ·Ï Ä¿¸®¾î °³¹ßÀÇ ±âȸ¸¦ Á¦°øÇÕ´Ï´Ù. ¸ÓÅ©ÀÇ ±¸¼º¿øµéÀº ¼·Î µ½´Â °Ç°ÇÑ ±â¾÷ ¹®È¸¦ Á¶¼ºÇÏ°í ÀÖ½À´Ï´Ù. ¸ÓÅ©¿¡¼ ¿©·¯ºÐ¸¸ÀÇ Æ¯º°ÇÑ Àç´ÉÀ¸·Î ÀηùÀÇ Áøº¸¸¦ ½ÇÇöÇÏ´Â ¸¶¹ýÀ» ÆîÃĺ¸¼¼¿ä!
´Ù¾ç¼ºÀ¸·Î °¡µæÇÑ ¸ÓÅ©ÀÇ ±¸¼º¿øÀÌ µÇ¾îÁÖ¼¼¿ä!