Bioprocess Associate I (Inoculum) - Days (Orange)

We are LOTTE BIOLOGICS! Delivering Therapies That Enable a Healthier World. 

A new company, built on 80 years of tradition. We embody our core values of being Inspired by Science, Embracing Diversity, Fostering Talent, and Connecting Lives. Our mission is to be the most trusted partner in the industry, with high standards of quality and continuous innovation, to reliably deliver benefits for patients worldwide. 

Position Summary

The primary role of the Bioprocess Associate I is working on assignments that train for proficiency in the operation of production equipment within Manufacturing Operations (Inoculum, Cell Culture, and Purification) according to detailed procedures and batch records while ensuring compliance with cGMP and safety requirements. Work is performed in a medium-scale production facility with classified areas requiring appropriate personal protective equipment (PPE), specified gowning, and clean hygiene to maintain established environmental specifications.

Duties & Responsibilities

• Train for proficiency in the set-up, operation, and cleaning of production and support equipment within assigned functional area(s).


• Prepare buffers, media, and reagents.


• Work as a dependable member of a team demonstrating commitment to safety, quality, and compliance.


• Recognize and report safety, quality, and maintenance events to area management.


• Maintain accurate documentation.


• Monitor process parameters and escalate abnormal conditions.


• Sustain a clean and orderly work environment. 


• Achieve and maintain proficiency through training.

Education & Experience

• High school diploma or equivalent is required. Knowledge of science generally attained through studies resulting in a B.S. in science, engineering, biochemistry, or related discipline or its equivalent is desired.


• Experience in aseptic technique and mammalian cell culture is desired.


• Preferred experience:
  
  
  
  • Familiarity with general chemistry, microbiology, or clean room operations
  
  
  • Prior manufacturing experience
  
  
  • Prior experience with cGMP operations or aseptic technique
  
  
  • Mechanical aptitude
  
  
  
  

Knowledge, Skills, Abilities

• Ability to adhere to written instruction, verify data, and accurately document results.


• Ability to collaborate with teammates to execute scheduled work safely and compliantly.


• Familiarity with common computer tools, such as web-based applications.


• Possess a continuous improvement mindset and a desire to learn and contribute to a culture of excellence.

Physical Demands

This position is located in a medium-scale manufacturing facility with classified areas requiring appropriate personal protective equipment (PPE). This role will require contact with hazardous materials such as caustic, acids and steam. Frequent bending, twisting, squatting, kneeling, climbing and reaching is required. Role also requires infrequent unassisted lifting (not to exceed 50 lbs). Repetitive use of arms/hand/wrists, grasping is also required. This position is a team-based position that requires shift work, weekends, holidays, and overtime. Shift hours are 6am-6pm on a rotating 48/36 hour rotating schedule. 

Work Environment

The work environment involves activities in a medium scale manufacturing facility, lab space, and office space. The environment includes limited exposure to noise (> 85 dBA), hazardous chemicals and equipment temperature extremes.

Shift Differential

5%

Target Bonus

5%

Work Location:

East Syracuse, NY 

We are an Equal Employment Opportunity (“EEO”) Employer. 

We believe that women, people of color, veterans and LGBTQ communities must participate in the work we do, so we strongly encourage applications from people with these identities or who are members of underrepresented communities!  If this is the work that you want to do, in a culture of inclusion and excellence with the goal of making our world to be a healthier place, then please apply today!