{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/lottebiologicsusallc/jobs/5233991008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4481367008,"location":{"name":"Syracuse, NY"},"metadata":null,"id":5233991008,"updated_at":"2026-06-01T10:46:01-04:00","requisition_id":"182","title":"Bioprocess Associate I (Inoculum) - Days (Orange)","company_name":"LOTTE BIOLOGICS USA, LLC","first_published":"2026-06-01T09:41:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;We are\u0026amp;nbsp;\u0026lt;span style=\u0026quot;color: rgb(224, 62, 45);\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;LOTTE BIOLOGICS\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;! \u0026lt;strong\u0026gt;Delivering Therapies That Enable a Healthier World\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A new company, built on 80 years of tradition. We embody our core values of being \u0026lt;strong\u0026gt;Inspired by Science\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Embracing Diversity\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Fostering Talent\u0026lt;/strong\u0026gt;, and \u0026lt;strong\u0026gt;Connecting Lives\u0026lt;/strong\u0026gt;. 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.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Position Summary\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Duties \u0026amp;amp; Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Train for proficiency in the set-up, operation, and cleaning of production and support equipment within assigned functional area(s).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare buffers, media, and reagents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work as a dependable member of a team demonstrating commitment to safety, quality, and compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recognize and report safety, quality, and maintenance events to area management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor process parameters and escalate abnormal conditions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sustain a clean and orderly work environment. \u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Achieve and maintain proficiency through training.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Education \u0026amp;amp; Experience\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;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.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in aseptic technique and mammalian cell culture is desired.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preferred experience:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with general chemistry, microbiology, or clean room operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior manufacturing experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with cGMP operations or aseptic technique\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mechanical aptitude\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills, Abilities\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to adhere to written instruction, verify data, and accurately document results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to collaborate with teammates to execute scheduled work safely and compliantly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with common computer tools, such as web-based applications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possess a continuous improvement mindset and a desire to learn and contribute to a culture of excellence.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Physical Demands\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;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.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Environment\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The work environment involves activities in a medium scale manufacturing facility, lab space, and office space. The environment includes limited exposure to noise (\u0026amp;gt; 85 dBA), hazardous chemicals and equipment temperature extremes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Shift Differential\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;5%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Target Bonus\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;5%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;East Syracuse, NY\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;New York Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$22.87\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$22.87 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;We are an Equal Employment Opportunity (“EEO”) Employer.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;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!\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017716008,"name":"Biologics Manufacturing","child_ids":[],"parent_id":4016256008}],"offices":[{"id":4012978008,"name":"Syracuse Bio Campus","location":"Syracuse, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/lottebiologicsusallc/jobs/5160917008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4447108008,"location":{"name":"Syracuse, NY"},"metadata":null,"id":5160917008,"updated_at":"2026-04-09T13:46:57-04:00","requisition_id":"169","title":"Senior Engineer, ADC Manufacturing","company_name":"LOTTE BIOLOGICS USA, LLC","first_published":"2026-03-27T12:05:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;We are\u0026amp;nbsp;\u0026lt;span style=\u0026quot;color: rgb(224, 62, 45);\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;LOTTE BIOLOGICS\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;! \u0026lt;strong\u0026gt;Delivering Therapies That Enable a Healthier World\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A new company, built on 80 years of tradition. We embody our core values of being \u0026lt;strong\u0026gt;Inspired by Science\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Embracing Diversity\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Fostering Talent\u0026lt;/strong\u0026gt;, and \u0026lt;strong\u0026gt;Connecting Lives\u0026lt;/strong\u0026gt;. 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.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Position Summary\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Engineer, ADC Manufacturing is an individual contributor that serves as a technical SME for antibody drug conjugate (ADC) manufacturing processes across clinical and commercial programs. This role provides subject matter expertise in conjugation chemistry, purification, scaleup, and technology transfer. The Senior Engineer drives process robustness, investigates deviations, implements process improvements, and ensures that manufacturing operations comply with cGMP standards. The ideal candidate combines hands-on technical skills with strategic influence across cross-functional teams, will identify best practices and provide technical trainings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Duties \u0026amp;amp; Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Technical Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serves as the primary technical authority for ADC conjugation, formulation, and purification processes across multiple development stages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads technical transfers of ADC processes for First in Human, scale up, late-stage, Validation activities and design of Critical Process Parameter readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports a high-performing technical team through effective communication and mentoring of junior engineers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and maintains process descriptions, process flow diagrams, and process models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a liaison between Manufacturing and HSE team for the handling of High toxicity compounds and oversees safety of manufacturing activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and improve key unit operations (e.g., TFF, chromatography, conjugation reactions, solvent handling and Buffer Preparations).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with partners and customers, such as Automation, MSAT, HSE and Facilities to achieve site manufacturing deliverables for manufacturing production.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicates and work with internal teams and clients to resolve on the floor issues, document revisions for successful process execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports real time-on-the-floor support to manufacturing teams during batch execution as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead investigations, root cause analysis, and CAPA development for OOS, OOT, and deviations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess process performance trends using statistical tools and identify process improvement opportunities for manufacturing robustness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as SME during audits, including regulatory inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and implement new technologies, raw materials, equipment, and methods to enhance process performance and safety.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Quality Assurance, Quality Control, Supply Chain, Process Development, and Facilities to support seamless operations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Documentation \u0026amp;amp; Technical Writing\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Author and review technology transfer documents, equipment fit gap assessments, and batch records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review master batch records (MBRs), SOPs, technical protocols and reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Regulatory agency responses for continued regulatory compliance and filing content (IND/IMPDs, BLAs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical justification for changes using risk-based methodologies (FMEA, QbD principles).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Education \u0026amp;amp; Experience\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Chemical Engineering, Chemistry, Biology or related field required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (MS/PhD) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years of experience in biopharmaceutical MSAT, Process Engineering, or Manufacturing Sciences is required; 2–4 years of experience specifically in ADCs or complex bioconjugation processes is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands on experience with cGMP clinical or commercial manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven success in working in teams within a matrixed environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success in with tech transfers, and process scale up.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills, Abilities\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Technical Abilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Technical understanding of:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Conjugation chemistries (e.g., maleimide thiol, enzymatic, site specific)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Purification technologies (TFF, chromatography)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience handling highly potency drug linkers, highly potent active pharmaceutical ingredients (HPAPIs) and knowledge of Occupational Health Category (OHC) classifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;cGMP and regulatory expectations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competency with Data analysis tools (e.g., JMP), DOE and multivariate analysis for process performance evaluations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity of regulatory issues pertaining to the manufacture of ADCs, large scale biopharmaceutical unit operations and process validations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret engineering drawings, P\u0026amp;amp;IDs, and equipment manuals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to perform risk assessments and apply QbD principles to technical decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to lead cross functional technical investigations to closure.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Interpersonal/Leadership Abilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong verbal communication, technical writing skills and problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Meeting facilitation, technical discussions and alignment across teams and clients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate effectively in a fast-paced, cross-functional team environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with and mentor junior engineers and manufacturing personnel.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Physical Demands\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lift up to 50 lbs unassisted and perform physical activities such as crouching, kneeling, crawling, climbing stairs and ladders, and walking on level surfaces.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform visual inspections of installations and equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;On the floor monitoring (if necessary) while using appropriate personal protective equipment (PPE) or Powdered Air Purifying Respirator (PAPR), If necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in classified clean-room environments (e.g., ISO8), requiring gowning procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work around hazardous chemicals, solvents, and high potency compounds while following appropriate control strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to move equipment or materials using carts or similar devices (if applicable).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Environment\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work is performed in office and supporting on the floor monitoring (if necessary) while in the controlled manufacturing areas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May involve exposure to chemical odors, solvents, and high potency materials under controlled conditions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work may involve proximity to moving mechanical equipment and standard manufacturing utilities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Supervisory Responsibilities\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a senior individual contributor role with technical leadership responsibilities but no direct people management.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Travel\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;lt;5% travel required for this role.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Target Bonus\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;16%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;East Syracuse, NY\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;New York Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$91,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$142,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;We are an Equal Employment Opportunity (“EEO”) Employer.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;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!\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4016256008,"name":"Manufacturing","child_ids":[4017718008,4017716008,4017717008],"parent_id":null}],"offices":[{"id":4012978008,"name":"Syracuse Bio Campus","location":"Syracuse, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/lottebiologicsusallc/jobs/5195072008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4462665008,"location":{"name":"Syracuse, NY"},"metadata":null,"id":5195072008,"updated_at":"2026-04-23T18:36:43-04:00","requisition_id":"174","title":"Senior Specialist, Computer System Validation","company_name":"LOTTE BIOLOGICS USA, LLC","first_published":"2026-04-23T18:36:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;We are\u0026amp;nbsp;\u0026lt;span style=\u0026quot;color: rgb(224, 62, 45);\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;LOTTE BIOLOGICS\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;! \u0026lt;strong\u0026gt;Delivering Therapies That Enable a Healthier World\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A new company, built on 80 years of tradition. We embody our core values of being \u0026lt;strong\u0026gt;Inspired by Science\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Embracing Diversity\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Fostering Talent\u0026lt;/strong\u0026gt;, and \u0026lt;strong\u0026gt;Connecting Lives\u0026lt;/strong\u0026gt;. 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.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Position Summary\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;The Computer System Validation (CSV) role is responsible for developing, executing, and maintaining validation documentation to ensure IT systems comply with local and global regulatory requirements, quality standards, and Lotte Biologics internal policies. This position partners closely with IT, Quality, Manufacturing, and Engineering teams to support system lifecycle activities, ensure timely completion of quality management system (QMS) actions, and maintain ongoing system compliance within the Information Technology organization.\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Duties \u0026amp;amp; Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Create Computer System Validation (CSV) Plans, requirement specifications, and test scripts and coordinate associated activities following Lotte Biologics CSV program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other IT teams’ execution of CSV deliverables such as architecture diagrams, configuration specifications and executing test scripts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of routine compliance tasks such as periodic review, user access review, and disaster recovery plans to ensure timely completion of activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with other IT functional areas to document robust impact assessments for change controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independently work with complex issues related to day-to-day activities and escalate issues when necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actively participate within IT and others to analyze and address process deficiencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively with others in the Validation, Manufacturing, Manufacturing Engineering, Quality Assurance and Quality Control groups.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Education \u0026amp;amp; Experience\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Engineering, Computer Science, Information Systems, or a related technical discipline preferred,\u0026lt;strong\u0026gt; OR\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Associate degree with 1–3 years of hands‐on experience in computer/software validation within a pharmaceutical, biotech, or other GMP‐regulated environment, \u0026lt;strong\u0026gt;OR\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Equivalent combination of education and relevant CSV experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience and understanding of 21 CFR Part 11, GAMP compliance for computer system (hardware, application software and operating system).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Knowledge, Skills, Abilities\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proactive, self-starter with good decision-making skills and capable of working alone or in a team environment to develop CSV documentation and to propose mitigations to problems and gaps identified.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience and knowledge in Computer/Software validation (creating validation plans, URS/FRS documents, IQ/OQ/PQ, and validation summary reports)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in written and verbal communication skills with ability to effectively collaborate with technical and senior management staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in data governance, data integrity (DI) assessment, audit trail review, security, user access review, trace matrices, etc. is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively under pressure, handle multiple projects, and meet deadlines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to develop and apply new and innovative approaches to projects and processes; a working understanding of lean principles and establishment of effective process metrics is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An understanding of deviation and change management for plant manufacturing equipment software is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to policies and procedures (SOPs), training materials and tools to ensure quality standards and regulatory requirements are met.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Physical Demands\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This is primarily an office‑based position; however, appropriate personal protective equipment (PPE) is required when performing field‑based work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Frequent, repetitive motions such as keyboarding are required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Environment\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position is based indoors, and the employee will primarily be working with others, but also independently. This position requires personnel presence on site, 50-100% of the time. This position is a team and project-based position that may require occasional shift work, weekends, and holidays.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Target Bonus\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;8%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;East Syracuse, NY\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;New York Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$60,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$88,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;We are an Equal Employment Opportunity (“EEO”) Employer.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;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!\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017747008,"name":"IT Quality","child_ids":[],"parent_id":4017739008}],"offices":[{"id":4012978008,"name":"Syracuse Bio Campus","location":"Syracuse, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/lottebiologicsusallc/jobs/4985286008","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4367738008,"location":{"name":"Syracuse, NY"},"metadata":null,"id":4985286008,"updated_at":"2026-04-09T13:46:57-04:00","requisition_id":"155","title":"Sr Project Manager, Project Management Office (PMO)","company_name":"LOTTE BIOLOGICS USA, LLC","first_published":"2025-11-12T16:21:13-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;We are\u0026amp;nbsp;\u0026lt;span style=\u0026quot;color: rgb(224, 62, 45);\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;LOTTE BIOLOGICS\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;! \u0026lt;strong\u0026gt;Delivering Therapies That Enable a Healthier World\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A new company, built on 80 years of tradition. We embody our core values of being \u0026lt;strong\u0026gt;Inspired by Science\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Embracing Diversity\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;Fostering Talent\u0026lt;/strong\u0026gt;, and \u0026lt;strong\u0026gt;Connecting Lives\u0026lt;/strong\u0026gt;. 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.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Position Summary\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Sr. Project Manager, Site PMO, leads cross-functional client‑facing and internal initiatives and influences how the site executes strategic and operational priorities. This role drives project delivery excellence and establishes and embeds project management best practices. The Sr. Project Manager maintains project governance tools including metrics, dashboards, and performance reports., and uses these insights to influence decision‑making at governance meetings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Sr. Project Manager ensures alignment across Manufacturing Operations, Development (MS\u0026amp;amp;T, PD, AS\u0026amp;amp;T), Quality, Supply Chain, and Business Development. The individual anticipates organizational needs, identifies interdependencies, and proactively guides teams toward solutions that support long‑term site objectives. As a trusted liaison for clients, the Sr. Project Manager fosters strong relationships, ensures transparency, and upholds accountability throughout the project lifecycle.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Duties \u0026amp;amp; Responsibilities\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead strategic client‑facing projects from initiation through closeout, ensuring delivery on time, within scope, and within budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Align site PMO objectives with global governance standards, reporting expectations, and best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a trusted liaison for clients, internal leadership, and project sponsors, fostering transparency and strong working relationships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage detailed project plans, identifying critical path activities, key milestones, and strategic intent; ensure stakeholder alignment on expectations and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define project team structure, communicate resource needs, and secure appropriate cross‑functional support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead all project meetings, including client kickoff, technical transfer, routine team meetings, and vendor coordination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute project communication strategies, including stakeholder updates and governance reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the primary point of contact for client communication, scope management, change orders, and performance reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify and resolve project risks and issues; escalate to senior leadership when needed to ensure timely resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Manufacturing Operations, Development (MS\u0026amp;amp;T, PD, AS\u0026amp;amp;T), Quality, Supply Chain, and Business Development to support technical transfers, change controls, and business growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Business Development on financial tracking, invoicing, and identifying new opportunities; develop and execute change orders for out‑of‑scope work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage portfolio‑level resource requirements and coordinate communication across all stakeholder groups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply PMO frameworks to maintain project metrics, dashboards, timelines, documentation repositories, risk logs, and KPI reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support client visits, audits, and Person‑in‑Plant (PIP) activities at the Syracuse site.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster continuous improvement of project management tools, templates, and processes with a focus on safety, quality, schedule, and budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support non‑client project activities as needed to advance site initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster diverse, inclusive, high‑performance teams and maintain strong relationships with functional leaders and client representatives.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Education \u0026amp;amp; Experience\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Engineering, Life Sciences, or a related technical field required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5–10 years of project management experience with demonstrated success influencing and aligning cross‑functional teams within a matrixed organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3–5 years of experience in the CDMO industry, including leadership of complex cGMP or technical transfer projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PMP or equivalent project management certification preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing strategic client relationships preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Knowledge, Skills, \u0026amp;amp; Abilities\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of biopharma project management methodologies, risk management practices, and stage‑gate governance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of biologics manufacturing processes, analytical and process technical transfer, and regulatory requirements in a GMP environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong financial acumen, including purchase order and invoicing processes, cost estimation for scope changes, and accurate tracking of development and manufacturing expenditures (materials, consumables, labor) to support client billing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong negotiation and stakeholder management skills with the ability to influence across a matrixed organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with Microsoft Project, Smartsheet, Power BI, and other project management and data visualization tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance strategic thinking with hands‑on project oversight and execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written, verbal, and presentation skills, with the ability to communicate complex information clearly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical skills, including data aggregation, interpretation, and presentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently with a high level of accountability and sound judgment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interact effectively with all levels of management and cross‑functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to manage competing priorities and drive results in a fast‑paced, matrixed environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent customer service skills for servicing as the primary point of contact to customers and representing the entire LOTTE Biologics organization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Physical Demands\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prolonged periods of sitting or standing at a desk, participating in meetings, and working on a computer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Frequent use of standard office equipment (computers, monitors, telephones, printers, projectors).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasional movement throughout the site to attend meetings, observe project activities, or interface with operations teams in manufacturing or laboratory areas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to wear required personal protective equipment (PPE) when entering controlled manufacturing or lab environments (e.g., safety glasses, lab coats, shoe covers).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Visual acuity to review project data, timelines, and technical documentation in both electronic and printed formats.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasional lifting or carrying of materials (up to 15 lbs.), such as binders, laptops, or presentation materials.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Work Environment\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Onsite role based at the Syracuse Bio Campus (cGMP manufacturing facility), requiring regular presence and engagement with cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with global counterparts in Korea and other regions, balancing multiple time zones to maintain clear communication and alignment across projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work is primarily performed in an open or shared office environment, requiring a high degree of collaboration, communication, and adaptability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Frequent interaction with internal departments (Manufacturing, Development, Quality, Supply Chain, Finance, Business Development) and external clients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasional entry into GMP manufacturing and laboratory spaces, which requires adherence to gowning and safety procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May involve extended hours or flexibility during critical project phases, client audits, or leadership meetings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Travel\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimal travel required (less than 5%), primarily for corporate meetings, training, or client visits.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Target Bonus\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;16%\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Work Location:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;East Syracuse, NY\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;New York Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$91,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$142,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;We are an Equal Employment Opportunity (“EEO”) Employer.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;text-align: center;\u0026quot;\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;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!\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4018480008,"name":"Project Management Office (PMO)","child_ids":[],"parent_id":4048313008}],"offices":[{"id":4012978008,"name":"Syracuse Bio Campus","location":"Syracuse, New York, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":4}}