Quality Control Specialist II, Sample Management Wednesday-Saturday shift 9am-7pm [Contract to Hire]

Iovance Biotherapeutics; Philadelphia (Philadelphia County); On-site; USD 45,000 - 85,000; Full time

Job summary

An established industry player is seeking a Quality Control Specialist II to oversee the logistics of quality control samples. This role involves managing sample inventory, ensuring compliance with regulatory standards, and facilitating the timely distribution of samples. The position requires a detail-oriented individual with strong communication and organizational skills, capable of thriving in a fast-paced environment. Join a team dedicated to maintaining high standards in a dynamic and inclusive workplace, where your contributions will directly impact the quality of innovative therapies. If you are passionate about quality control and thrive in a collaborative setting, this opportunity is perfect for you.

Qualifications

• Manage QC sample logistics for raw material and final product samples.
• Ensure compliance with cGMP for sample handling and distribution.

Responsibilities

• Maintain sample inventory and ensure timely distribution to testing vendors.
• Support audits and inspections while managing sample integrity.

Skills

Detail-oriented

Mathematical skills

Excellent written communication

Excellent verbal communication

Collaboration skills

Time management

Organizational skills

Problem-solving skills

Ability to work in a fast-paced environment

Education

Associate degree

3+ years of relevant GMP experience

Tools

LIMS

Temperature controlled dewars

Job description

Overview

The Quality Control Specialist II – Sample Management will ensure time-sensitive distribution of quality control samples in support of QC-related activities. They will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping under appropriate conditions, for all the iCTC cell therapy asset. The weekend position is either a Sunday to Wednesday or Wednesday to Saturday shift with a 9am - 7pm schedule.

Essential Functions and Responsibilities

• Manage all aspects of QC sample logistics for raw material, in-process, and final product samples including sample storage, sample inventory and reconciliation, scheduling, and shipping in LIMS based system.
• Maintain sample integrity by ensuring that all samples are managed (i.e., stored; handled; shipped) in compliance with procedures, specifications, and cGMP.
• Provide timely distribution of samples internally at the iCTC, and externally to testing vendors.
• Ensure that sample inventory records are maintained and accurate.
• Maintain current knowledge base of regulations, corporate policies, and industry best practices, trends, and standards to ensure that the logistics function remains in compliance with applicable requirements.
• Support audits and inspections as needed.
• Packaging of samples using temperature controlled dewars, cold packs, and dry ice.
• Support ramp up of Quality Control and other activities in a newly built facility.

Required Education, Skills, and Knowledge

• Associate degree or 3+ years of relevant GMP experience (sample management).
• Experience with inventory and/or logistics in the pharmaceutical industry.
• Detail-oriented with strong mathematical skills.
• Excellent written and verbal communication skills.
• Strong collaboration, time management, and organizational skills are required.
• Proven ability to effectively collaborate with a wide range of stakeholders.
• Excellent judgment and creative problem-solving skills.
• Ability to work in a fast-paced and dynamic environment.
• Hands-on laboratory experience with sample handling, inventory, and cryo-shipping.

Physical Demands and Activities Required:

• Must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE), i.e., scrubs, gowning coveralls, masks, gloves, etc.
• Able to stand and/or walk 90% (and sit 10%) of the scheduled workday, which may include climbing ladders or steps.
• Must be able to use near vision to view samples at close range.
• Able to crouch, bend, twist, reach, and perform activities with repetitive motions.
• Must be able to lift and carry objects weighing 45 pounds.

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.

Work Environment:

This position will work in both an office and a manufacturing setting. When in the lab, you may be exposed to various chemicals/biochemical, including latex and bleach. Additionally, there is potential for variable noise levels, equipment hazards, strong odors, and other detergents/sanitizers.

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 change the position’s responsibilities 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].

By voluntarily providing information and clicking “Submit Application”, you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice.

#LI-onsite