GSK
Technology Associate
The Technology Associate will support managing certain elements (such as upstream or downstream etc.) of the transfer of primary (drug substance) biopharmaceutical production technologies from R&D, third party clients or Contract Manufacturing Organizations to UM Biopharm and from UM Biopharm to other biopharmaceutical manufacturing sites. Assist in supporting delivery of new biopharmaceutical applications and technologies as well as on delivering improvements to the existing supply chains supported by UM Biopharm and technology transfers between UM Biopharm & R&D. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Determine adequacy of plant to accept new technologies and appropriate actions to implement start of new process operations. Responsible for development and preparation of technology transfer/process validation protocols and "hands-on" startup of production processes with operators. Responsible for preparation and presentation of technology transfer/process validation reports or documentation. Define training program for operators as part of technology transfer and when required train process operators. Identify potential process problems, provide technical advice to Production and/or Quality Department to resolve process problems. Provide real-time and in-person process monitoring and technical oversight for a 24/7 manufacturing facility which will require off hours and weekend support as needed. Advise management as to possible opportunities for process improvements. Collect and track process trend data and monitor process trends. Determine causes of process variances and recommend corrective actions. Stay current with developments in the fields of biotechnology and bioprocessing. Responsible for learning and understanding process technologies under development within R&D. Demonstrate the use of GPS tools and philosophies. Why You? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Bachelors Degree in biotechnology or chemical engineering, biology, biochemistry or chemistry 1+ year of post-graduate industrial experience in technology/biopharmaceutical process development, technical project management and process transfer to production in a manufacturing environment Preferred Qualifications: Masters Degree in biotechnology or chemical engineering, biology, biochemistry or chemistry Knowledge in biopharmaceutical technologies such as large scale cell culture/microbial technology, biopreparations technologies, or pharmaceutical manufacturing of proteins. Basic understanding of analytical technologies related to the above. Strong interpersonal and leadership skills. Strong verbal and written communication skills. Strong analytical and critical thinking skills. Able to interact well with peers, subordinates, and senior personnel in scientific, quality, engineering and operational disciplines. Able to prioritize, and decide appropriate courses of actions. Effective at implementing decisions. Committed team player prepared to work in and embrace a team-based culture. Evidence of leading improvement activities with delivery of quantifiable business improvement Expert competency in project work Formal root causing and problem-solving techniques Confident in own ability. Makes timely decisions in a confident way with justification if necessary. Ensures others are very clear about own stance or position when uncertainty exists Ability to present technical concepts to end users as well as Senior level managers. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at
1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US) . GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
The Technology Associate will support managing certain elements (such as upstream or downstream etc.) of the transfer of primary (drug substance) biopharmaceutical production technologies from R&D, third party clients or Contract Manufacturing Organizations to UM Biopharm and from UM Biopharm to other biopharmaceutical manufacturing sites. Assist in supporting delivery of new biopharmaceutical applications and technologies as well as on delivering improvements to the existing supply chains supported by UM Biopharm and technology transfers between UM Biopharm & R&D. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Determine adequacy of plant to accept new technologies and appropriate actions to implement start of new process operations. Responsible for development and preparation of technology transfer/process validation protocols and "hands-on" startup of production processes with operators. Responsible for preparation and presentation of technology transfer/process validation reports or documentation. Define training program for operators as part of technology transfer and when required train process operators. Identify potential process problems, provide technical advice to Production and/or Quality Department to resolve process problems. Provide real-time and in-person process monitoring and technical oversight for a 24/7 manufacturing facility which will require off hours and weekend support as needed. Advise management as to possible opportunities for process improvements. Collect and track process trend data and monitor process trends. Determine causes of process variances and recommend corrective actions. Stay current with developments in the fields of biotechnology and bioprocessing. Responsible for learning and understanding process technologies under development within R&D. Demonstrate the use of GPS tools and philosophies. Why You? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Bachelors Degree in biotechnology or chemical engineering, biology, biochemistry or chemistry 1+ year of post-graduate industrial experience in technology/biopharmaceutical process development, technical project management and process transfer to production in a manufacturing environment Preferred Qualifications: Masters Degree in biotechnology or chemical engineering, biology, biochemistry or chemistry Knowledge in biopharmaceutical technologies such as large scale cell culture/microbial technology, biopreparations technologies, or pharmaceutical manufacturing of proteins. Basic understanding of analytical technologies related to the above. Strong interpersonal and leadership skills. Strong verbal and written communication skills. Strong analytical and critical thinking skills. Able to interact well with peers, subordinates, and senior personnel in scientific, quality, engineering and operational disciplines. Able to prioritize, and decide appropriate courses of actions. Effective at implementing decisions. Committed team player prepared to work in and embrace a team-based culture. Evidence of leading improvement activities with delivery of quantifiable business improvement Expert competency in project work Formal root causing and problem-solving techniques Confident in own ability. Makes timely decisions in a confident way with justification if necessary. Ensures others are very clear about own stance or position when uncertainty exists Ability to present technical concepts to end users as well as Senior level managers. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at
1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US) . GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.