Senior Laboratory Technician - Virus Production

Minaris Advanced Therapies • Philadelphia, PA

15d

About The Position

Be part of something bigger at Minaris Advanced Therapies—where every role contributes to creating hope for patients around the world. As a global leader in cell and gene therapy development, manufacturing, and testing, we turn breakthrough science into real-world treatments that change lives. Our team of over 1,000 experts across North America, Europe, and Asia has helped bring transformative therapies to market. At Minaris, you’ll join a purpose-driven community focused on innovation, collaboration, and patient impact. Whether you’re in the lab, in the cleanroom, or behind the scenes, your work will directly support life-saving therapies and make a lasting difference. If you're passionate about advancing cutting-edge science and believe in the potential of cell and gene therapies, we invite you to help shape the future of medicine—one patient at a time. Position Summary Supports Viral Clearance Virus Production Team in the performance of Virus Production and Purification techniques for the overall operations of the lab. Performs and directs assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Demonstrates strong oral and written communication skills and actively contributes to training, report generation and documentation. Demonstrates strong technical skills and contributes to the achievement of company and departmental goals and objectives.

Requirements

• Experience with aseptic technique, mammalian cell culture and has worked with various types of viruses.
• Knowledge of GDP, GLP and cGMP
• Effective multi-tasking skills and time management skills required
• Ability to evaluate technical data and record data accurately and legibly
• Ability to use judgement as dictated by complexity of situation.
• Ability to work under limited supervision and to handle problems of a more difficult nature.
• Ability to accomplish the described duties through the use of appropriate laboratory equipment (i.e. biosafety cabinet, centrifuge, incubator, autoclave, etc.)
• Ability to accurately and reproducibly perform arithmetic calculations including factions, decimals, and percentages and basic algebraic and geometric calculations.
• Ability to understand verbal and demonstrated instructions.
• Proficient in oral and written communication skills
• Need to be able to read, write and understand English
• Proficient in Microsoft (Excel, Word, Outlook)
• Bachelor (science preferred) degree with over 3 years of relevant or equivalent experience
• At least 2 years of relevant experience in downstream purification, chromatography, nanofiltration or a combination thereof.

Nice To Haves

• AKTA FPLC and Unicorn Software experience is a plus.

Responsibilities

• Conducts virus production assays and lab procedures as outlined in testing record and regulatory guidelines.
• Accurately completes testing records and other required documentation according to Good Documentation Practices.
• Reports observations of ongoing tests to Study Director/Technical Reviewer or Laboratory Supervisor/Manager.
• Accurately completes test methods and other required documentation according to and in compliance with GLP, cGMP, CFR, and/or PTC guidelines and SOPs.
• Communicates with Supervisor and other colleagues re: daily lab activities.
• Performs lab upkeep per GLP, cGMP, CFR and/or PTC guidelines and SOPs.
• Prepares reagents and restock labs with supplies.
• Maintains equipment, equipment logs, cleaning logs and initiate change controls.
• Aids in the training of new employees.
• Performs self and peer review of testing records to ensure documents are accurate and complete.
• Authors non-conforming events and laboratory investigations.
• Evaluates SOPs for accuracy and efficient operations and makes amendments as necessary.
• Understands the importance of the regulatory compliance and comprehension of the laboratory assays.
• Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required.
• Normally receives minimal instruction on routine work and detailed instructions on new assignments.
• Contributes to the overall operations and to the achievement of departmental goals.
• As assigned by Management, acts as Technical Reviewer for specific assay and assumes all associated responsibilities.
• Initiates, prepares and revises technical documents and reports.
• Effectively communicates and defends science through written and verbal communication.
• Provides training on areas of technical expertise and compliance issues relevant to the lab setting.
• Effectively interacts with clients, both internal and external, through written and verbal communication.
• Authors and contributes to deviations/investigations, corrective/preventative action initiatives, change control procedures, technical protocols and logistical planning
• Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required.
• Normally receives minimal instructions on routine work and detailed instructions on new assignments.
• Regular and reliable attendance on a full-time basis.
• Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
• Embodies Minaris Advanced Therapies values and aligns daily actions with department and company culture.

Benefits

• Minaris Advanced Therapies employees are eligible for a comprehensive benefits package, including medical insurance, vision insurance, dental insurance, 401(k), paid time off, tuition assistance, and more.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 251-500 employees