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Global Life Science Hub

Global Life Science Hub is a pioneering organization focused on biotechnology and life sciences, offering a range of job openings across various roles in manufacturing, regulatory affairs, and biostatistics.

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Jobs at this company:

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🔥 Customer Success Manager
Posted 2024-11-20

đź“Ť United States

🔍 Life sciences and pharmaceutical industries

  • Proven background in customer success or account management.
  • Ideally within the life sciences or pharmaceutical sector.
  • Strong communication and relationship-building abilities.
  • Excellent problem-solving skills.
  • Client-focused, proactive mindset, and passion for helping clients achieve success.

  • Act as the primary point of contact for internal accounts.
  • Deliver exceptional client experience and support.
  • Build strong, trust-based relationships and proactively address client needs.
  • Monitor account health, identify growth opportunities, and drive client satisfaction.
  • Collaborate with internal teams to deliver tailored solutions and meet client goals.

Business DevelopmentBusiness developmentCommunication SkillsCollaborationProblem SolvingCustomer serviceOrganizational skillsWritten communication

Posted 2024-11-20
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🔥 QC Analyst
Posted 2024-11-20
Posted 2024-11-20
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🔥 QC Analyst
Posted 2024-11-18
Posted 2024-11-18
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🔥 Customer Success Manager
Posted 2024-11-18

đź“Ť Oregon, United States; Missouri, United States

🔍 Life sciences and pharmaceutical industries

  • Proven background in customer success or account management, ideally within the life sciences or pharma sector.
  • Strong communication, relationship-building, and problem-solving abilities.
  • Client-focused, proactive, and passionate about helping clients achieve success.

  • Act as the primary point of contact for our internal accounts, delivering exceptional client experience and support.
  • Build strong, trust-based relationships and proactively address client needs.
  • Monitor account health, identify growth opportunities, and drive client satisfaction.
  • Collaborate with internal teams to deliver tailored solutions and meet client goals.

GoCommunication SkillsAnalytical SkillsCollaborationProblem SolvingCustomer serviceNegotiationAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communicationMultitasking

Posted 2024-11-18
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🔥 Downstream Processing Scientist
Posted 2024-11-14

đź“Ť United States

🔍 Biopharmaceutical

  • Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences.
  • 2+ years of relevant experience in the biopharmaceutical industry.
  • Proven experience in GMP and aseptic manufacturing environments.
  • Proficiency with AKTA process skids or similar systems.
  • Familiarity with single-use manufacturing consumables, such as bags, tube sets, columns, and process manifolds.
  • Strong understanding of engineering and clinical batch execution.
  • Solid grasp of GMP documentation and compliance.

  • Execute downstream processes at multiple scales in a cGMP environment, including chromatography column packing, TFF operations, and data analysis.
  • Provide technical leadership in the development and execution of purification processes.
  • Utilize software tools to collect and analyze operating data, making real-time adjustments to optimize product yield and equipment performance.
  • Ensure timely execution of engineering and clinical batches, maintaining high-quality standards.
  • Collaborate with cross-functional teams and external vendors to troubleshoot technical issues and maintain production equipment.
  • Adhere to GMP guidelines and lead compliance with environmental health and safety policies.
  • Coordinate investigations and implement corrective actions for issues encountered during batch execution.
Posted 2024-11-14
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🔥 Upstream/Downstream Scientist
Posted 2024-11-14

đź“Ť United States

🔍 Biopharmaceutical

  • 1-2 years of experience in cell culture and bioreactor operations, including GMP and Aseptic Manufacturing experience for upstream roles.
  • Proficiency with single-use manufacturing consumables and prior experience in scale-up manufacturing activities.
  • At least 1-2 years of experience in Downstream Processing with expertise in TFF operations.
  • Hands-on experience in running chromatography systems and column packing, with knowledge in Unicorn software.
  • Familiarity with depth filtration processes and knowledge of cGMP regulations.

  • Execute mammalian cell culture processes to produce recombinant proteins for Biologics, managing cell culture batches up to 2000l.
  • Operate bioreactors and establish operating equipment specifications.
  • Collaborate with manufacturing associates and engineers, effectively interpreting and providing instructions.
  • Initiate batch records, protocols, and oversee investigations in a cGMP environment to ensure compliance.
  • Review and document manufacturing and packaging batch records, maintaining adherence to safety standards and GMP guidelines.
  • Perform purification processes for mammalian cell cultures, including handling purification volumes up to 2000l.
  • Operate AKTA purification skids and TFF operations, contributing to column packing and process troubleshooting.
  • Direct technical aspects of purification and collaborate with external vendors on equipment maintenance.
  • Ensure compliance with BLA requirements for clinical and engineering batches, following GMP policies and safety protocols.
  • Manage batch execution, ensuring efficient issue resolution and process improvements.
Posted 2024-11-14
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🔥 Manufacturing Scientist (USP)
Posted 2024-11-14

đź“Ť United States

🔍 Biopharmaceutical

  • Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences.
  • Minimum of 3+ years relevant experience in the biopharmaceutical sector.
  • Proficiency in planning, executing, analyzing, and documenting process development.
  • Strong foundational knowledge to manage engineering and clinical batches.
  • Previous experience in GMP and aseptic manufacturing settings.
  • Familiarity with single-use manufacturing consumables like bags, tube sets, and columns.

  • Optimize bioreactor performance and scale-up procedures to achieve production goals.
  • Develop and refine equipment specifications for upstream manufacturing techniques.
  • Collaborate with manufacturing associates and engineers for efficient batch execution.
  • Interpret and communicate instructions in various formats for clarity and compliance.
  • Follow GMP guidelines and maintain environmental health and safety policies.
  • Review batch records for accuracy and compliance.
  • Coordinate investigations for batch execution issues.
  • Perform additional functions to support team objectives.
Posted 2024-11-14
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🔥 Scientist Upstream/Downstream Manufacturing
Posted 2024-11-13

đź“Ť United States

🧭 Full-Time

🔍 Biopharmaceutical

  • Upstream: At least 1-2 years of experience in cell culture and bioreactor operations, including GMP and Aseptic Manufacturing experience.
  • Proficiency with single-use manufacturing consumables (e.g., bags, tube sets, columns) and prior experience in scale-up manufacturing activities.
  • Downstream: At least 1-2 years of experience in Downstream Processing with demonstrated expertise in TFF operations.
  • Hands-on experience in running chromatography systems and column packing, with knowledge in Unicorn software.
  • Familiarity with depth filtration processes and knowledge of cGMP.

  • Execute mammalian cell culture processes to produce recombinant proteins for Biologics, managing cell culture batches up to 2000l.
  • Operate bioreactors, establish operating equipment specifications, and enhance manufacturing techniques.
  • Collaborate with manufacturing associates and engineers, interpreting and providing instructions effectively.
  • Initiate batch records, protocols, and oversee investigations in a cGMP environment to ensure compliance.
  • Review and document manufacturing and packaging batch records and related documents, maintaining adherence to safety standards and GMP guidelines.
  • Perform purification processes for mammalian cell cultures, including handling purification volumes up to 2000l.
  • Operate AKTA purification skids and TFF operations, contributing to column packing, process troubleshooting, and data analysis.
  • Direct technical aspects of purification, collaborating with external vendors on production equipment maintenance.
  • Maintain compliance with BLA requirements for clinical and engineering batches, following GMP policies and safety protocols.
  • Manage batch execution, ensuring efficient issue resolution, batch documentation, and process improvements.
Posted 2024-11-13
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🔥 Upstream/Downstream Manufacturing
Posted 2024-11-07

đź“Ť United States

🧭 Full-Time

🔍 Biopharmaceutical

  • Masters or Bachelor degree in Chemistry, Biology, Biochemistry or a related field.
  • Relevant experience in a Biopharmaceutical organization.
  • Experience and knowledge in drug substance manufacturing (Fermentation and protein purification).
  • Experience in drug product manufacturing (aseptic processing areas).
  • Upstream or downstream background.
  • Must have worked in biologics for at least 2 years.

  • Writes and reviews SOPs.
  • Provides support to Quality and Compliance Departments during regulatory audits.
  • Accomplishes small projects independently and supports large projects.
  • Monitors bioreactor operation (70% of the total night shift).
  • Supports media or buffer preparation.
  • Supports downstream processes (cleaning of columns, sampling, etc.).
  • Performs logbook verification and document review.
  • Participates in cleaning activities per the cleaning validation program.
  • Compiles process data.
  • Calibrates/ verifies pH/conductivity meters, osmometers, and scales.
Posted 2024-11-07
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🔥 Downstream Scientist
Posted 2024-11-07

đź“Ť United States

🔍 Biopharmaceutical

  • Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences.
  • 2+ years of relevant experience in the biopharmaceutical industry.
  • Proven experience in GMP and aseptic manufacturing environments.
  • Proficiency with AKTA process skids or similar systems.
  • Familiarity with single-use manufacturing consumables (e.g., bags, tube sets, columns, and process manifolds).
  • Strong understanding of engineering and clinical batch execution.
  • Solid grasp of GMP documentation and compliance.

  • Execute downstream processes at multiple scales in a cGMP environment, including chromatography column packing, TFF operations, and data analysis.
  • Provide technical leadership in the development and execution of purification processes.
  • Utilize software tools to collect and analyze operating data, making real-time adjustments to optimize product yield and equipment performance.
  • Ensure timely execution of engineering and clinical batches, maintaining high-quality standards.
  • Establish and enhance equipment specifications, driving improvements in manufacturing techniques.
  • Collaborate with cross-functional teams and external vendors to troubleshoot technical issues and maintain production equipment.
  • Adhere to GMP guidelines and lead compliance with environmental health and safety policies.
  • Coordinate investigations and implement corrective actions for issues encountered during batch execution.
  • Perform additional duties as assigned to support team objectives and adhere to all company policies and standards.
Posted 2024-11-07
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