Lyophilization Technology, Inc. (LTI), established in 1992, is a
unique Contract Development and Manufacturing Organization enjoying
a leadership position in the health care and related industries. The
company conducts applied research, provides scientific services and
technical support, and manufactures clinical supplies for freeze
dried pharmaceuticals, biologics, diagnostics, biopharmaceuticals
and fine chemicals. LTI is located in Ivyland, Bucks County, Pennsylvania.
We have a position opening for a Manufacturing
Technician. An opportunity for a detail oriented,
self-motivated, creative and energetic individual to join a dynamic,
technology oriented organization. As a member of the scientific
team, you will participate in the preparation of parenteral
preparations for clients conducting toxicological and clinical trial
studies. This unique aseptic processing operation that includes
containment capabilities focuses on preparing sterile lyophilized
products for toxicology and clinical studies of critical freeze
dried products. Collaborating with client project teams, you will be
able to apply your skills and knowledge to the preparation of new
and novel lyophilized health care products ranging from antibiotics
* Day-to-day operations in the GMP Manufacturing Area, including
development and sterile product preparation.
o Procure, and maintain inventory of materials and supplies
o Maintain and support an aseptic operation, including cleaning,
sanitization and environmental monitoring activities.
* Preparation of sterile toxicology and clinical supply materials.
o Be engaged in preparing sterile product, collaborating with
other Manufacturing Technicians, supervisor and Project Director,
o Participate in batch preparation, fill, lyophilization,
inspection and packaging activities,
o Execute procedures for preparation and processing, completing
* Process development and manufacturing techniques for
processing, including sterile products that include cytotoxic,
highly potent compounds and biologicals using isolators.
o Work with the supervisor and Safety Officer for sustaining
proper conditions for containment,
o Compose and review Standard Operating Procedures,
o Maintain containment equipment and execute proper procedures.
* Equipment Qualification and Process Validation.
o Execute validation studies, compile and evaluate data,
o Compose validation reports.
* Follow all aspects of cGMP compliance for the Clinical
Manufacturing Area including all its related elements such as
facilities, equipment and documentation, training, reports and records.
* Work with the Quality Assurance staff on procedures and
documentation associated with production of GLP and cGMP supplies.
Applying your background, knowledge, and experience in a unique
technology with an internationally recognized organization will
afford you an excellent salary and comprehensive benefits that
include tuition reimbursement, as well as opportunities for
professional development and career growth.