Manufacturing Specialist

PackGene Biotech, Inc.; Houston, Northern (TX, KY); On-site; USD 70,000 - 90,000; Full time

Job summary

PackGene Biotech seeks a Manufacturing Specialist to join our Houston team, focusing on AAV-based gene therapy manufacturing. The role starts with lab startup activities, planning, and executing development studies and technology transfers in a fast-paced, regulated environment.

You will perform solution prep, cell culture, purification, fill finish, and related tasks while adhering to SOPs and safety standards; collaborate across QC, QA, and MFG teams and assist with training and new processes.

Qualifications

• AS/BS in biology, biotech, chemistry, engineering or related field.
• GMP environment experience required.
• Aseptic techniques and lab competency expected.

Responsibilities

• Execute startup activities for lab and equipment, coordinating installations with vendors.
• Perform manufacturing processes (solution prep, assembly prep, cell culture, purification, fill finish, area cleaning) following SOPs and batch records.
• Document activities and ensure regulatory compliance; collect samples for QC testing.
• Maintain and calibrate manufacturing equipment; troubleshoot issues.
• Assist training of new staff and organize daily tasks.
• Support qualification of new equipment and technology transfers; assist with product introductions; CAPAs and deviations investigations.

Skills

GMP experience

Aseptic techniques

Cell culture

Purification

Fill finish

Teamwork

Communication

Problem solving

Education

AS or BS in biology/biotech/chemistry/engineering

Job description

Description

Mission Statement

The mission of PackGene Biotech is to accelerate gene therapy product development by providing an integrated one-stop shop solution to the gene therapy industry. We strive to make gene therapy accessible to more patients in needs.

Gene therapy is believed to revolutionize the healthcare field in upcoming years. PackGene is well positioned to play a big role in this transformation.

Company Background

PackGene Biotech was founded in 2014 and headquartered in Guangzhou, China. It is a leading gene therapy CRO/CDMO service provider in Asia and is planning to start up its operations in Houston, TX.

PackGene is looking for a highly motivated hands-on individual to join our fast-growing Houston site. A fantastic opportunity to join a dynamic team and make a great impact!

Requirements

Manufacturing Specialist

We are currently looking for a highly motivated Manufacturing Specialist, specializing in AAV-based gene therapy to join our Manufacturing team.Initially, the Manufacturing Specialist is involved in Houston lab startup activities, planning and executing development studies, technology transfers, new project implementation and execution in a timeline driven manner.

Responsibilities as a Manufacturing Specialist

• Execution of initial manufacturing lab startup activities, including new equipment acquisition, coordinating with various vendors for equipment installation, and testing of new equipment.
• Perform manufacturing processes (solution prep, assembly prep, cell culture, purification, fill finish, and area cleaning) while following SOPs, batch records, and safety guidelines.
• Execute and document activities in compliance with regulatory requirements.
• Aseptically manipulate samples and submit samples to QC testing.
• Support inventory and supply coordination and tracking.
• Maintain manufacturing equipment by performing routine maintenance, calibrations, and troubleshooting of problems.
• Maintain cleanroom area organization.
• Author/Revise manufacturing documents including SOPs and Batch Records.
• Assist with training of new staff.
• Assist with organization of daily tasks.
• Support qualification of new equipment.
• Support new product introductions.
• Write deviations & support deviation investigations.
• Support change management and implementing corrective and preventive actions (CAPAs).
• Collaborate closely with other team members such in QC, QA, PAD, MFG, Logistics, external and internal stakeholders.
• Perform other duties as assigned.
• Maintain high level of accountability, integrity, teamwork, and communication.
• Build strong & cohesive working relationships with colleagues across the company to accomplish goals.

Qualifications

• A.S. (B.S. or higher preferred) in biology, biotechnology, chemistry, engineering, or other gene therapy related field.
• With A.S.: 2~4+ years of related experience in biologics manufacturing (AAV viral vector experience is a plus).
• Advanced understanding of laboratory equipment and aseptic techniques.
• Prior experience working in a GMP environment is required.
• Experience in Cell culture, Purification, or Fill Finish is required.
• Proficient in MS Office suite of products.
• Demonstrated ability to work with a team.
• Excited to learn new things and open to new ideas.
• Passion for helping others.
• Excellent communication skills.
• Ability to work under pressure while maintaining professionalism.

Working Conditions:

• Manufacturing Lab Cleanroom

Physical Qualifications:

• Reaching: Extending hand(s) and arm(s) in any direction.
• Standing: Remaining upright on the feet, particularly for sustained periods of time.
• Walking: Moving about on foot to accomplish tasks, particularly for long distances or moving from one work site to another
• Sitting: sitting for a period of time
• Pushing: Using upper extremities to press against something with steady force in order to thrust forward, downward or outward.
• Pulling: Using upper extremities to exert force in order to draw, drag, haul or tug objects in a sustained motion.
• Lifting: Raising objects from a lower to a higher position or moving objects horizontally from position to-position. This factor is important if it occurs to a considerable degree and requires the substantial use of the upper extremities and back muscles.
• Talking: Expressing or exchanging ideas by means of the spoken word; those activities where detailed or important spoken instructions must be conveyed to other workers accurately, loudly, or quickly.
• Hearing: Perceiving the nature of sounds at normal speaking levels with or without correction, and having the ability to receive detailed information through oral communication, and making fine discriminations in sound.
• Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers.
• The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication of parts at distances close to the eyes.