MSAT Specialist 2nd Shift

Iovance Biotherapeutics; Philadelphia (Philadelphia County); On-site; USD 90,000 - 120,000; Full time

Job summary

Iovance Biotherapeutics is seeking an MSAT Specialist to join our Manufacturing Operations team. You will serve as a subject matter expert for cell therapy processes, own parts of tech transfer, and contribute to deviation analysis while ensuring compliance with GMP and safety standards.

This role involves cross-functional collaboration, documenting protocols, training operations staff, and performing hands-on MSAT lab work in a fast-paced environment.

Qualifications

• Bachelor-level degree in life sciences or equivalent.
• 1 year of hands-on operations experience in clinical or commercial life sciences.
• Expertise in cell culture and aseptic technique.
• Knowledge of GMP systems in manufacturing.
• Strong written and oral communication skills.

Responsibilities

• Represent MSAT during cross-functional meetings as SME.
• Serve as MSAT POC for clinical manufacturing escalations and PIP at CMOs.
• Oversee manufacturing operations and quality documentation.
• Execute technology transfer and train manufacturing personnel.
• Translate development reports to batch records and SOPs.
• Analyze manufacturing process data to identify improvements.

Skills

Cell culture

Aseptic technique

GMP systems

Data analysis

Tech transfer

Technical writing

Cross-functional work

Project teamwork

Adaptability

Education

Bachelor's degree in life sciences

Job description

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.

Shift: Monday to Friday from 3pm to 11:30pm

Overview

The MSAT Specialist is a Manufacturing Operations cell therapy subject matter expert. The MSAT Specialist reports to the Senior Manager, MSAT and EM and is responsible for manufacturing data analysis, contributing to deviation root cause analysis, and owning steps of the manufacturing process tech transfer. The MSAT Specialist is also responsible for protocol and report authoring, oversight of manufacturing operations, and execution of MSAT laboratory activities.

Essential Functions and Responsibilities

• Serve as a manufacturing processes technical SME representing MSAT during cross functional meetings.
• Serve as MSAT POC for clinical manufacturing execution escalations for cell and gene therapy GMP Processes. Perform Person-In-Plant (PIP) responsibilities at CMOs observing production and providing real time feedback and support during execution cell therapy batches.
• Observe and provide feedback of manufacturing operations, ensure alignment of manufacturing practices across multiple manufacturing facilities.
• Provide MSAT oversight, training, and support within the manufacturing cleanroom environment.
• Execute Technology Transfer responsibilities related to new product introduction or process improvements to internal and external manufacturing facilities. Provide hands-on manufacturing process training to manufacturing personnel as part of process tech transfer, as needed.
• The MSAT Specialists may be responsible for the authoring and the ownership/management of the following documentation:
• Quality Systems (minor to complex) – Change Controls, Deviations, CAPAs, Action Items
• Minor Study or investigational protocols and corresponding reports
• Process Characterization, Validation, Qualification protocols and report amendments
• Product Impact and Risk Assessments, Failure Modes Risk Analysis
• SOPs, COPs, MSAT MBRs
• MSAT Specialists will be involved in execution of investigation activities which may include execution of studies, GEMBA, Kaizen, Risk Analysis etc.
• Translate process development reports into manufacturing batch records and SOPs as part of process tech transfer. Will assist manufacturing and quality when authoring Master Batch Records and implementing process improvements.
• Analyze and interpret manufacturing process data. Emphasize operational excellence and continuously identify process improvements, i.e. efficiencies, within the manufacturing operations environment.
• Execute hands on experiments in the MSAT lab (as applicable).
• Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
• Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.

Required Education, Skills, and Knowledge

• S degree in a relevant discipline or equivalent industry experience.
• A minimum of 1 year of relevant hands‑on operations experience for clinical or commercial production and/or process development experience in the life sciences industry.
• Expertise in cell culture and aseptic technique.
• Knowledge and understanding of GMP systems within a manufacturing facility.
• Ability to organize and analyze manufacturing process data.
• Knowledge of manufacturing process tech transfer.
• Excellent oral and written communication skills. Strong technical writing ability required.
• Ability to work cross functionally within the organization as part of a project team.
• Self‑motivated and willing to accept temporary responsibilities outside of initial job description.
• Must be comfortable in a fast‑paced small company environment and able to adjust workload based upon changing priorities.

Preferred Education, Skills, and Knowledge

• Prior cell therapy experience is highly preferred.
• Involvement in prior manufacturing process tech transfer is preferred.

The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation.

Physical Demands and Activities Required

• Must be able to move to and from the office to the lab located on separate floors and move about the office and lab as needed.
• Must be able to remain in a stationary position standing or sitting for prolonged periods of time.
• Must be able to grasp with both hands, perform repetitious actions such as pinch with thumb and forefinger, turn with hand/ arm, and reach above shoulder height.
• Must be able to use several types of laboratory equipment and pipettes for extended periods.
• Must be able to work on a tablet or computer typing for 50% of a typical working day.
• Must be able to move and lift 20 pounds multiple times daily.
• Must be able to use near vision to view samples at close range.
• Wear proper personal protective equipment when in a laboratory setting, i.e., safety glasses, lab coats, and closed‑toed shoes.

Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work‑related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines

This position will work in both an office and a laboratory setting. When in the lab, there may be a risk of exposure to hazardous or biological waste within the environment through receipt, transport, storage, preparation, dispensing, administration, cleaning, and/or disposal of contaminated areas and waste.

The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.

Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal‑opportunity employer, our employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact [e-mail] .