Immatics
Join Immatics and Shape the Future of Cancer Immunotherapy
Immatics is at the forefront of immunotherapy innovation, working to harness the power of T cells to transform cancer treatment. Immatics is an exceptional clinical-stage biopharmaceutical company active in the discovery and development of T cell redirecting cancer immunotherapies. We use these powerful T cells to develop groundbreaking immunotherapies that target cancer cells. We are dedicated to transforming cancer treatment and improving patient outcomes through cutting-edge research and advanced TCR technology. Why Join Us? Innovative Environment: Help to pioneer advancements in cancer immunotherapy. Collaborative Culture: Be part of a diverse team dedicated to your professional growth. Global Impact: Contribute to therapies that make a lasting impact on patients globally. Position Title: Associate Quality Control Manager
2nd Shift We are seeking an Associate Quality Control Manager
2nd Shift to support our Global Quality Control team. The main role of the Associate QC Manager is to provide oversight of QC personnel who conduct in-process and final product testing of Immatics' GMP products and manage the day-to-day scheduling and activities within the QC Department. Schedule: 12:30 PM
8:30 PM; Monday to Friday; On-site Reports to: Quality Control, Director What You'll Do: As an Associate QC Manager, you will play a key role in: Management Act as a role model for team members with respect to earning their trust by your own attendance, keeping your word, personal behaviors, transparent/frank communication, and execution of personal assignments. Hire team members that will fit the job, company culture, and team dynamics. Distribute work appropriately among team members. Organize and manage team members time/schedules and assignments, keep track that team members are utilizing their time in meaningful assignments that will move the company forward. Communicate frequently and regularly with team members assuring they have the information and tools to perform their functions. Resolve conflict between team members if any arises
be an active listener of your team members. Set goals, measure achievement progress, and assist team members in successful execution of their/team goals as well as coach and help develop team members into higher roles at Immatics if they so desire. Provide regular, meaningful (honest but emphatic) performance feedback, expertise, and coaching (5:1 positive to negative ratio) that will help team members grow and develop. Turn feedback into coaching moments and show your willingness to be a partner in team members career development at Immatics. Reward and give credit to team members when they so deserve
publicly and privately. At the same time, coach team members on the spot if corrections are needed (privately). Provide psychological safety to team members if they make mistakes but expect mistake corrections and improvements. Quality Control Organize the daily QC schedule and ensure appropriate staffing. Perform release assays for cell product identity and safety, which includes the use of different laboratory methods such as microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, and immunoassays. Review and support release assays for DNA isolation, PCR, sterility, endotoxin, and mycoplasma. Safely handle human biological specimens. Extract, compile, and analyze data. Generate, report, and track results. Conduct and document all activities consistent with cGMP/GxP, regulatory filings, and written procedures. Write study plans, validation plans, and reports for QC testing, assays, and equipment. Review and approve relevant audit reports, and related corrective action plans. Initiate, review, and approve relevant controlled documents. Analyze data and prepare technical reports summarizing quality control results. Manage, in collaboration with other team members, supply inventory. Manage, in collaboration with other team members, purchasing, receiving, formulating, testing, and release of materials and reagents. Manage, in collaboration with other team members, equipment and assay qualifications and validations. Perform routine equipment maintenance and troubleshooting. Maintain data integrity and logs for equipment. Lead quality documents and processes such as GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. Involved in the creation of systems used in quality control to maintain compliances with regulations. Secondary Functions: Transport human biological samples between manufacturing facility and QC laboratory. Transport controlled documents between OQS office and QC laboratory. Transport QA-released QC materials between QC laboratories. Required Experience and Education: BA or BS in any science-related field. Minimum five (5) years experience in a regulated laboratory environment. MS degree or specialized skill set may substitute for 3 years. Laboratory skills including any of the following: microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma. Preferred Experience and Education: BA or BS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering. Laboratory skills including more than one of the following: microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma. Experience writing GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. Prior management of direct reports is preferred. Competencies: Initiative Problem Solving Very detail oriented Strong analytical, technical writing, verbal communication, and interpersonal skills Ability to work independently and manage multiple projects with aggressive timelines Work Environment: This position works in a typical office and lab environment with moderate noise levels and uses phone, computer, office equipment and supplies on a regular basis. Other duties performed while outside of office and lab building could involve exposure to manufacturing operations, along with outdoor conditions (including highway traffic) and temperatures. While performing the duties of this job, the employee may be occasionally exposed to moving mechanical parts, fumes or airborne particles, pathogens, and toxic or caustic chemicals. This position requires handling of human biological specimens including human peripheral blood and human T cell products, as well as laboratory chemicals. Travel required:
Less than 10%, minimal Physical demands: Communicating Verbally
expressing or exchanging ideas by means of the spoken word to impart oral information to others to convey detailed spoken instructions or other workers accurately, loudly or quickly. Hearing
the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds. Keyboarding
entering data or text into a computer or other machine by means of a keyboard. Devices include a traditional keyboard, 10 key-pad, touch screens and others. Lifting
- raising or lowering an object (up to 25 lbs) from one level to another (includes upward pulling). Carrying is to transport an object
usually by holding it in the hands or arms but may occur on the shoulder. Near Visual Acuity
clarity of vision at approximately 20 inches or less (working with small objects, reading small print, including the use of computers). Pushing
-
Immatics is at the forefront of immunotherapy innovation, working to harness the power of T cells to transform cancer treatment. Immatics is an exceptional clinical-stage biopharmaceutical company active in the discovery and development of T cell redirecting cancer immunotherapies. We use these powerful T cells to develop groundbreaking immunotherapies that target cancer cells. We are dedicated to transforming cancer treatment and improving patient outcomes through cutting-edge research and advanced TCR technology. Why Join Us? Innovative Environment: Help to pioneer advancements in cancer immunotherapy. Collaborative Culture: Be part of a diverse team dedicated to your professional growth. Global Impact: Contribute to therapies that make a lasting impact on patients globally. Position Title: Associate Quality Control Manager
2nd Shift We are seeking an Associate Quality Control Manager
2nd Shift to support our Global Quality Control team. The main role of the Associate QC Manager is to provide oversight of QC personnel who conduct in-process and final product testing of Immatics' GMP products and manage the day-to-day scheduling and activities within the QC Department. Schedule: 12:30 PM
8:30 PM; Monday to Friday; On-site Reports to: Quality Control, Director What You'll Do: As an Associate QC Manager, you will play a key role in: Management Act as a role model for team members with respect to earning their trust by your own attendance, keeping your word, personal behaviors, transparent/frank communication, and execution of personal assignments. Hire team members that will fit the job, company culture, and team dynamics. Distribute work appropriately among team members. Organize and manage team members time/schedules and assignments, keep track that team members are utilizing their time in meaningful assignments that will move the company forward. Communicate frequently and regularly with team members assuring they have the information and tools to perform their functions. Resolve conflict between team members if any arises
be an active listener of your team members. Set goals, measure achievement progress, and assist team members in successful execution of their/team goals as well as coach and help develop team members into higher roles at Immatics if they so desire. Provide regular, meaningful (honest but emphatic) performance feedback, expertise, and coaching (5:1 positive to negative ratio) that will help team members grow and develop. Turn feedback into coaching moments and show your willingness to be a partner in team members career development at Immatics. Reward and give credit to team members when they so deserve
publicly and privately. At the same time, coach team members on the spot if corrections are needed (privately). Provide psychological safety to team members if they make mistakes but expect mistake corrections and improvements. Quality Control Organize the daily QC schedule and ensure appropriate staffing. Perform release assays for cell product identity and safety, which includes the use of different laboratory methods such as microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, and immunoassays. Review and support release assays for DNA isolation, PCR, sterility, endotoxin, and mycoplasma. Safely handle human biological specimens. Extract, compile, and analyze data. Generate, report, and track results. Conduct and document all activities consistent with cGMP/GxP, regulatory filings, and written procedures. Write study plans, validation plans, and reports for QC testing, assays, and equipment. Review and approve relevant audit reports, and related corrective action plans. Initiate, review, and approve relevant controlled documents. Analyze data and prepare technical reports summarizing quality control results. Manage, in collaboration with other team members, supply inventory. Manage, in collaboration with other team members, purchasing, receiving, formulating, testing, and release of materials and reagents. Manage, in collaboration with other team members, equipment and assay qualifications and validations. Perform routine equipment maintenance and troubleshooting. Maintain data integrity and logs for equipment. Lead quality documents and processes such as GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. Involved in the creation of systems used in quality control to maintain compliances with regulations. Secondary Functions: Transport human biological samples between manufacturing facility and QC laboratory. Transport controlled documents between OQS office and QC laboratory. Transport QA-released QC materials between QC laboratories. Required Experience and Education: BA or BS in any science-related field. Minimum five (5) years experience in a regulated laboratory environment. MS degree or specialized skill set may substitute for 3 years. Laboratory skills including any of the following: microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma. Preferred Experience and Education: BA or BS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering. Laboratory skills including more than one of the following: microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma. Experience writing GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. Prior management of direct reports is preferred. Competencies: Initiative Problem Solving Very detail oriented Strong analytical, technical writing, verbal communication, and interpersonal skills Ability to work independently and manage multiple projects with aggressive timelines Work Environment: This position works in a typical office and lab environment with moderate noise levels and uses phone, computer, office equipment and supplies on a regular basis. Other duties performed while outside of office and lab building could involve exposure to manufacturing operations, along with outdoor conditions (including highway traffic) and temperatures. While performing the duties of this job, the employee may be occasionally exposed to moving mechanical parts, fumes or airborne particles, pathogens, and toxic or caustic chemicals. This position requires handling of human biological specimens including human peripheral blood and human T cell products, as well as laboratory chemicals. Travel required:
Less than 10%, minimal Physical demands: Communicating Verbally
expressing or exchanging ideas by means of the spoken word to impart oral information to others to convey detailed spoken instructions or other workers accurately, loudly or quickly. Hearing
the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds. Keyboarding
entering data or text into a computer or other machine by means of a keyboard. Devices include a traditional keyboard, 10 key-pad, touch screens and others. Lifting
- raising or lowering an object (up to 25 lbs) from one level to another (includes upward pulling). Carrying is to transport an object
usually by holding it in the hands or arms but may occur on the shoulder. Near Visual Acuity
clarity of vision at approximately 20 inches or less (working with small objects, reading small print, including the use of computers). Pushing
-