We are LOTTE Biologics! 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.

We deliver therapies that make a Healthier World!

To help us meet our mission LOTTE BIOLOGICS is in need of a Scientist, Manufacturing Technology to support upstream cell culture and downstream purification commercial manufacture of biopharmaceutical drug substance produced at the LOTTE BIOLOGICS Syracuse facility. The Manufacturing Technology group supports a large-scale, cell culture, and purification facility. The is role reports into the Manufacturing Science and Technology (MSAT) organization.

This position provides resolution of complex problems associated with manufacturing of biopharmaceutical drug substance and/or newer modalities and will contribute to a dynamic and highly collaborative team environment. 

• Troubleshoot process-related manufacturing issues on the floor by leveraging strong upstream and/or downstream process knowledge to ensure quality of the product and compliance according to regulations
• Proactively identify and make formal recommendations for opportunities to improve process performance, productivity, robustness, quality, business process, and safety through on-floor observation and through active collection, routine process and data monitoring/review, and statistical analysis of process performance data/trends
• Drive improvements to completion and provide regular data updates to management to track process performance
• Use different data trending and statistical analysis tools to complete process review, modeling, principal component analysis, and multivariate analysis
• Author process-related Change Controls and applicable effectiveness checks
• Author Quality Events (QEs) with a view toward providing thorough root cause analysis, making a product impact assessment, and provide recommendations for effective Corrective Action and Preventive Action (CAPA)
• Support continued process verification program activities including authoring process monitoring plans, leading statistical alert event investigations, out-of-tolerance events, and support data lifecycle activities for internal and client needs, as applicable
• Support authoring, review, and approval of manufacturing retrospective reports for inclusion in Annual Product Review(s) and Annual Quality Product Review(s)
• Perform process facility fit, lead process technical transfers of new molecules and lead implementation of product/process transfers, including support of engineering and process validation (PV) studies, as appropriate
• Author technical documents and whitepapers, risk and impact assessments, Process Performance Qualification (PPQ) protocols and reports, provide floor coverage support for critical operations, and ensure that PV samples are collected and submitted
• Support and lead process development, process characterization, and process technical transfer activities from laboratory to manufacturing scales, including author/review of study protocols and final reports for studies required in Manufacturing, as applicable
• Support and lead implementation of new technologies and procedures from Development into Manufacturing, as applicable
• Support regulatory changes and filings through change control authorship and management, filing authoring and review, and data collection and analysis, as applicable
• Review cGMP documentation including Standard Operating Procedures (SOPs) and Manufacturing Batch Records (MBRs), as required
• Serve as designee for Manager as directed when training and qualifications are appropriate

Education/Experience:

• Degree in Biology, Chemistry, Biochemical or Chemical Engineering, or related industry experience:
  • Minimum of a B.Sc/B.Eng with 6+ years, M.Sc./M.Eng degree with 4+ years, or Ph.D degree with no experience (0 years)
• Prior experience with technical support of cGMP/Biologics manufacturing facility and/or cGMP investigations (R&D, technology transfer, manufacturing) is preferred
• Prior experience in or knowledge of cell culture, recovery, and/or purification of biopharmaceutical drug substance in a manufacturing environment is preferred
• Experience should include technical support of a cGMP biologics manufacturing facility, including strong knowledge and engineering leadership for drug substance processing equipment, manufacturing support, and technology transfer
• Prior experience in/knowledge of cell culture, recovery, and/or purification of biopharmaceutical drug substance in a manufacturing environment is required
• Technical writing and data presentation abilities are requirements
• Demonstrated leadership skills, and the ability to interact with diverse groups and teams is preferred
• Prior experience in leading cGMP investigations using formal Root Cause Analysis tools is preferred
• Prior experience with SOPs, cGMPs, and the know-how to work within a regulatory environment is required
• Prior experience facilitating/participating in Risk Assessments is preferred

Knowledge, Skills & Abilities:

• The candidate must have demonstrated verbal, written, and communication skills including ability to present complex information clearly and concisely, with a successful proved history of working with technical teams
• Project management skills (organization, collaboration, multi-tasking and communication), attention to detail, and the ability to perform well in a team-based environment is preferred
• This role will work independently, with minimal supervision, to develop and deliver on appropriate objectives and priorities, overcome obstacles, and deliver results within established timelines.
• This position is a team-based position that may require work on evenings, weekends, and holidays.

Physical Demands:

• Position requires repetitive use of hands and wrist (computer work), and infrequent lifting of items not to exceed 50 lbs
• Occasional bending, twisting and stooping to allow for gowning into classified environment is required

Work Environment:

• Position is primarily office based with occasional work in a classified GMP manufacturing environment
• Position is a team & project-based position that will require occasional shift work, weekends, and holidays

Travel:

This position requires up to 5% of domestic and/or international travel.

Work Location: 
East Syracuse, NY

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! 

http://www.lottebiologics.com/

LOTTE BIOLOGICS was established in 2022, and is headquartered in Seoul, South Korea. LOTTE BIOLOGICS entered the biologics CDMO business after acquiring Bristol Myers Squibb’s Syracuse biologics drug substance manufacturing site, as of January 1, 2023!

The newly established organization aims to become a Global Top 10 CDMO company in the biopharmaceutical industry.  With initial operations in 1948 in Japan, LOTTE has grown to become the fifth-largest conglomerate corporation in South Korea. LOTTE has various business units, including petro/fine chemicals, food, retail, hotels, electronics, construction, and IT. LOTTE has 30+ global locations across the US, Europe, and Asia.

An Equal Opportunity Employer

We do not discriminate based on race, color, religion, national origin, sex, age, disability, genetic information, or any other status protected by law or regulation. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.