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?
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Innovative Environment: Help to pioneer advancements in cancer immunotherapy.
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Collaborative Culture: Be part of a diverse team dedicated to your professional growth.
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Global Impact: Contribute to therapies that make a lasting impact on patients globally.
We are seeking an Senior Quality Control Analyst to support our Global Quality Control team. This candidate will execute bio-analytical, cell-based, and/or molecular methods for product release and stability in the Quality Control laboratory. This role will also actively participate in method transfer, qualification and validation activities.
FLSA Classification: Salary , Non-Exempt
Schedule: 8:00 AM – 5:00 PM; Monday to Friday; On-site
Reports to: Associate Director - GMP Quality Control
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477
What You’ll Do:
As an Sr. Quality Control Analyst, you will play a key role in:
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Conduct Tests and Analyze Results: Perform routine and non-routine testing on products and materials to verify compliance with established standards.
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Collaboration: Manage, in collaboration with other team members, purchasing, receiving, formulating, testing, release of materials and reagents, equipment and assay qualifications and validation.
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Quality Records: Lead quality documents and processes such as GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc.
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Documentation:
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Author and conduct periodic review of procedures.
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Conduct and document all activities consistent with cGMP/GxP, regulatory filings, and written procedures.
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Maintain data integrity and logs for equipment.
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Data Analysis: Ability to analyze complex data sets and interpret results accurately. Able to identity trend and deviations, and take initiative to troubleshoot issues
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Manage Laboratory Equipment: Perform and oversee the maintenance and calibration of laboratory equipment
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Ensure Compliance: Involved in the creation of systems used in quality control to maintain compliance with regulations.
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Safety: Always demonstrate good safety practices and promote safety awareness
Secondary Functions:
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Train and support junior analysts.
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Transport controlled documents, QA-released QC materials and human biological samples.
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Assist with group tasks scheduling
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Maintain knowledge of internal procedures and current regulatory requirements.
Required Experience and Education:
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BA or BS in any science-related field
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Minimum five (5) years experience in a regulated laboratory environment
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MS degree or specialized skill set may substitute for 3 years
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Experience as a QC personnel in a related field.
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Experience in aseptic technique, cell culture and either flow cytometry or cell-based assays.
Preferred Experience and Education:
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MS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering
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Minimum five (5) years experience in a regulated laboratory environment
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Laboratory skills include a few of the following: visual inspection, flow cytometry, molecular and cell-based assays.
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Demonstrate technical competence and knowledge in method transfer and assay qualification/validation activities
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Excellent technical writing and troubleshooting/investigational skills.
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Demonstrate knowledge of cGMP/ICH/EU regulations and requirements.
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Experience writing GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc.
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Experience with LIMS and statistical software is a plus
Competencies:
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Initiative
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Problem Solving
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Very detail oriented
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Strong analytical, technical writing, verbal communication, and interpersonal skills
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Ability to work independently and manage multiple projects with aggressive timelines
Work Environment:
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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.
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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. The employee can be occasionally exposed to wet and/or humid conditions, risk of electrical shock, sharps, or cuts, while performing tests. 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:
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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.
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Hearing – the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds.
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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.
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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.
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Near Visual Acuity – clarity of vision at approximately 20 inches or less (working with small objects, reading small print, including the use of computers).
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Pushing - Exerting force upon an object so that the object moves away from the object.
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Pulling - Exerting force upon an object so that the object moves toward the force.
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Sitting – remaining in a sitting position for at least 50% of the time.
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Standing/Walking - remain on one's feet in an upright position at a workstation.
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Stooping – occasional bending the body downward and forward by bending the spine at the waist - requiring full use of the lower extremities and back muscles.
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Biosafety Cabinet work – holding both arms out extended from the body for the duration of performing aseptic techniques.
Work authorization/security clearance requirements :
Legal eligibility to work in the United States is required. Immatics participates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment
Affirmative Action/EEO statement:
Immatics is an equal opportunity employer. All employment decisions including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs.
Why Join Us?
At Immatics, we believe in investing in our team’s health, safety and well-being. Here’s what you can expect if you join Immatics
Comprehensive Benefits:
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Competitive rates for Health, Dental, and Vision Insurance
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4 weeks of Paid Time off, granted up front each year and prorated for first and last year of employment.
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Sick Time Off – 56 hours
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12 Paid Holidays
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100% Employer-Paid Life Insurance up to at 1x annual salary, up to 100K ( club together)
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100% Employer Paid Short- and Long-Term Disability Coverage
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401(k) with Immediate Eligibility & company match…
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You are eligible for 401(k) plan participation as of your first paycheck.
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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.
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Partially paid Parental Leave for eligible employees. (3 weeks)
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Additional voluntary employee paid coverages including Accident, Hospital Indemnity, and Critical Illness Employee Paid Identity Theft Protection and Pet Insurance.
Professional Growth:
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Opportunities to work with leading experts in the field of T-cell immunotherapy.
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Company provided learning and development opportunities
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Fast paced, high demand collaborative and dynamic environment.
What We Do
Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. We are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer.
Read more about Immatics on our homepage: https://immatics.com/
Find us also on:
Twitter: https://twitter.com/immatics
Instagram: https://www.instagram.com/immatics/
YouTube: https://www.youtube.com/channel/UCv7uTpsGXvSNzwSX_xOtYSA
Legal notice: https://immatics.com/imprint/