Quality Control Analyst II - 2nd Shift

Immatics•Houston, TX

1d•Onsite

About The Position

Join Immatics and shape the future of cancer immunotherapy; one patient at a time! Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics. 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. FLSA Classification: Non-Exempt/Hourly Schedule: Monday to Friday; (Second Shift 12:00pm – 8:30pm) Department: Quality Control Reports to: Associate Quality Control Manager Supervisory responsibilities: No Locations: 13203 Murphy Road Stafford TX 77477; UTH -1941 East Rd. Houston TX 77030 Position Summary/objective: The main role of the Quality Control Analyst is to execute bio-analytical, cell-based, and/or molecular methods for product release in the Quality Control laboratory.

Requirements

BA or BS in any science-related field
Minimum two (2) years' experience in a regulated laboratory environment
Cell Culture experience
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
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 - Exerting force upon an object so that the object moves away from the object.
Pulling - Exerting force upon an object so that the object moves toward the force.
Sitting – remaining in a sitting position for at least 50% of the time.
Standing/Walking - remain on one's feet in an upright position at a workstation.
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.
Manual Pipetting – using one’s dominant hand, wrist, and thumb to dispense small amounts of liquids using micropipettes.
Biosafety Cabinet work – holding both arms out extended from the body for the duration of performing aseptic techniques.
Less than 10%, minimal
Must have dependable transportation to travel between sites.
Legal eligibility to work in the United States is required.

Nice To Haves

BA or BS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering
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
Cell Based Potency Assays
Microsoft Applications Word Excel Power Point

Responsibilities

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, immunoassays, 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.
Travel from QC laboratory to manufacturing facility to perform visual inspections.
Transport controlled documents between OQS office and QC laboratory.
Transport QA-released QC materials between QC laboratories.
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.
Perform routine equipment maintenance and troubleshooting.
Maintain data integrity and logs for equipment.
Assist with 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
Training junior analysts.
Assist with equipment and assay qualifications and validations.