Senior Cell Therapy Supply Chain Specialist

ImmaticsHouston, TX
30dOnsite

About The Position

Join Immatics and shape the future of cancer immunotherapy; one patient at a time! 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 cells 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. We are seeking a Senior Cell Therapy Supply Chain Specialist to support our Global Patient Supply team. The Senior Cell Therapy Supply Chain Specialist will be responsible for overseeing the patient's journey from screening through treatment across TCR-based immunotherapy platforms. This role will work cross functionally to ensure therapies reach patients in the shortest possible time by working cross functionally with internal and external stakeholders. FLSA Classification: Salary, Exempt Schedule: 8:00 AM – 5:00 PM; Monday to Friday; On-site Reports to: Associate Director, Global Patient Supply Location: 13203 Murphy Road Suite 100 Stafford, TX 77477

Requirements

  • A bachelor's or an associate degree in relevant discipline (or equivalent experience)
  • 4 years of work experience or the equivalent combination of education and experience
  • Previous industry experience in a biotech or pharma company
  • Experience with cell therapies

Nice To Haves

  • Proficient verbal & written communication and presentation skills
  • Strong ability to identify, deeply analyze & communicate problems
  • High ability to anticipate future risks and establish a mitigation plan
  • Comprehensive understanding of impact on broader scope (e.g. beyond own team/department)
  • Proficient ability to develop & independently implement solutions (within own area of responsibility or across teams/departments)
  • Highly pro-active attitude and strong sense of responsibility beyond own scope
  • Main driver of innovation & development in own area of expertise
  • Matrix leadership skills
  • Ability to analyze straightforward problems and develop possible solutions using technical experience and judgment; may escalate unusual or complex problems
  • Proven experience to effectively balance customer expectations with internal/team expectations
  • Ability to apply knowledge of applicable regulations (e.g., GMP, GCP, Part 11) including cold chain logistics practices
  • Works effectively across departments and levels, building and maintaining productive relationships
  • Proficient in Microsoft Office applications (i.e. Word, Excel, PowerPoint, etc.)
  • Demonstrated ability to manage own workload and lead/guide others on the team
  • Strong written and verbal communication skills to exchange information cross functionally (internal) as well as with external partners
  • Ability to work with minimal supervision for routine tasks and limited supervision for non-standard tasks
  • Clear and efficient verbal communication, ability to identify, deeply analyze and communicate problems
  • Common courtesy
  • Regular interaction with other teams or departments
  • Basic presentation skills (efficient presentation of own work to small groups/own team)
  • Advanced reflection on standard & non-standard processes and advanced ability to develop & pro-actively propose suitable solutions
  • Basic ability to anticipate future risks
  • High degree of initiative & intrinsic motivation to exceed expectations on own tasks and responsibilities
  • Intermediate organizational skills required to structure own tasks according to predefined work packages, schedule
  • Good understanding of priorities within own scope requiring limited interaction with supervisor
  • Actively reflect on and suggest trainings supporting professional development within or beyond current area of responsibility

Responsibilities

  • Work cross functionally between clinical operations, manufacturing, and quality to effectively manage patient products from leukapheresis collection through drug product infusion
  • Develop and improve SOPs, work instructions, and training materials which are used to ensure seamless end to end patient journey
  • Manage logistics providers which are responsible for transportation of patient material (starting material, intermediates, and final product)
  • Ensure chain of custody (COC) and chain of Identity (COI) measures are maintained throughout all patient journey activities
  • Support CMO activities which includes logistics support for all patient related material including CMO storage capacity management
  • Manage auxiliary medicinal products (AxMPs) as applicable for support of current clinical trials
  • Oversee collection kit materials which will be used for starting material collections including inventory management at clinical sites
  • Support clinical site onboarding through initial training (SIV) and re-training of any applicable processes for existing clinical sites
  • Manage initial application and maintaining applicable certifications, licenses, and permits related to import and export of patient related material
  • Support clinical sites as primary point of contact (POC) for scheduling and general inquiries regarding patient journey activities

Benefits

  • Competitive rates for Health, Dental, and Vision Insurance
  • 4 weeks of Paid Time off, granted up front each year and prorated for first and last year of employment.
  • Sick Time Off – 56 hours
  • 12 Paid Holidays
  • 100% Employer-Paid Life Insurance up to at 1x annual salary
  • 100% Employer Paid Short- and Long-Term Disability Coverage
  • 401(k) with Immediate Eligibility & company match… You are eligible for 401(k) plan participation as of your first paycheck. The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
  • Partially paid Parental Leave for eligible employees. (3 weeks)
  • Additional voluntary employee paid coverages including Accident, Hospital Indemnity, and Critical Illness
  • Employee Paid Identity Theft Protection and Pet Insurance.
  • Opportunities to work with leading experts in the field of T-cell immunotherapy.
  • Company provided learning and development opportunities
  • Fast paced, high demand collaborative and dynamic environment.
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