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$76k–$113k/yr
Full-time
bachelor degree, professional certificate
10% Target bonus
Posted 22d ago
~40 hrs/week
Responsibilities
The Manager, Process Safety leads the site's Process Safety Management, Electrical Safety, and Energy Control programs to ensure regulatory compliance and operational risk mitigation. They partner with cross-functional teams to integrate safety principles into manufacturing operations and drive continuous improvement initiatives.
Requirements
Candidates must hold a bachelor's degree in a relevant field and possess at least 7 years of experience in process safety or HSE leadership within regulated manufacturing environments. Strong knowledge of OSHA PSM, EPA RMP, and ISO 45001 standards is required, along with demonstrated success in risk assessment and incident investigation.
Full job description
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 Manager, Process Safety is responsible for leading and continuously improving the site's Process Safety Management (PSM), Electrical Safety, and Energy Control programs. This position serves as the site Subject Matter Expert (SME) for process safety and operational risk management, ensuring compliance with applicable federal, state, and local regulations, industry standards, and company policies while supporting safe, reliable, and compliant manufacturing operations. Additionally, this position will be the lead HSE contributor for maintenance of LOTTE’s International Organization for Standardization (ISO) 45001 certification.
The position partners closely with Operations, Engineering, Facilities, Maintenance, Quality, Validation, and Corporate HSE to identify, assess, and mitigate risks associated with manufacturing processes, utilities, equipment, and facility operations. This position drives a proactive safety culture through technical expertise, risk-based decision-making, regulatory compliance, and continuous improvement initiatives.
This position must comply with all Security requirements, Health, Safety, and Environment (HSE) regulations, and current Good Manufacturing Practices (cGMPs) applicable to the job function.
Duties & Responsibilities
Serve as the site Subject Matter Expert (SME) for Process Safety Management (PSM), Electrical Safety, and Energy Control (LOTO) programs.
Lead the implementation, maintenance, and continuous improvement of site Process Safety Management programs to ensure compliance with OSHA PSM, EPA Risk Management Program (RMP), NFPA requirements, and company standards.
Facilitate Process Hazard Analyses (PHA), HAZOP studies, risk assessments, and other structured hazard evaluation processes to identify, assess, and mitigate operational risks.
Manage the site's Management of Change (MOC) program, ensuring health, safety, environmental, quality, and operational risks are appropriately evaluated and controlled prior to implementation.
Partner with Operations, Engineering, Facilities, Maintenance, and Quality teams to integrate process safety principles into manufacturing operations and business processes.
Support the design, installation, startup, qualification, and modification of manufacturing equipment, utility systems, facilities, and processes to ensure safety and regulatory requirements are met.
Administer and continuously improve Electrical Safety and Energy Control programs, including Arc Flash assessments, Lockout/Tagout compliance, training programs, and risk mitigation activities.
Lead process safety reviews associated with new technologies, capital projects, process modifications, and equipment installations.\
Coordinate internal and external ISO45001 audits with third-party consultants and internal resources. Contribute to other ISO certifications as assigned.
Execute industrial hygiene exposure monitoring in coordination with the site’s Industrial Hygienist.
Act as the HSE representative for client projects as assigned.
Conduct compliance audits, inspections, program assessments, and field observations to evaluate effectiveness of safety controls and identify opportunities for improvement.
Lead or facilitate incident investigations, root cause analyses, and development of corrective and preventive actions (CAPAs) related to safety, process safety, and operational events.
Monitor, analyze, and report process safety and HSE metrics, key performance indicators (KPIs), and leading indicators to drive continuous improvement.
Maintain regulatory records, compliance documentation, and required reports for internal and external stakeholders.
Support contractor safety and qualification programs to ensure adherence to company safety requirements and industry best practices.
Serve as a site representative during regulatory inspections, customer audits, and corporate assessments related to process safety and HSE compliance.
Deliver technical training, coaching, and guidance on process safety, hazard recognition, risk mitigation, and regulatory requirements.
Participate in emergency response planning and provide technical support during emergency events and operational incidents.
Stay current with emerging process safety technologies, regulatory developments, and industry best practices to enhance site performance.
Support the Senior Manager, HSE with departmental objectives, strategic initiatives, budgeting activities, and continuous improvement efforts.
Participate on cross-functional teams, committees, and corporate initiatives as required.
Perform other duties as assigned.
Education & Experience
Bachelor's degree in Environmental Health & Safety, Engineering, Industrial Hygiene, Chemistry, Biology, Occupational Health, or a related discipline required.
7+ years of experience in Process Safety, Health, Safety & Environment (HSE), Operational Risk Management, or HSE program leadership within pharmaceutical, biologics, biotechnology, chemical, or other highly regulated manufacturing environments.
Demonstrated success leading risk assessments, process safety initiatives, incident investigations, and regulatory compliance programs.
Experience supporting enterprise-wide process safety and operational risk initiatives across complex manufacturing operations.
Professional certification such as: Certified Safety Professional (CSP), Certified Industrial Hygienist (CIH), Certified Process Safety Professional (CCPSC), or an equivalent credential preferred.
Knowledge of Arc Flash hazards, electrical safety, and NFPA 70E compliance programs preferred.
Knowledge, Skills, Abilities
Strong knowledge of OSHA Process Safety Management (PSM), EPA Risk Management Program (RMP), NFPA standards, Electrical Safety, and Energy Control (LOTO) requirements.
Experience conducting Process Hazard Analyses (PHA), HAZOPs, risk assessments, incident investigations, and Management of Change (MOC) reviews.
Experience with the ISO45001 standard and maintaining a certified occupational health and safety management system.
Familiarity with standard industrial hygiene monitoring techniques including noise dosimetry, air sampling, and real-time monitoring instruments.
Working knowledge of cGMP requirements and pharmaceutical, biologics, biotechnology, or regulated manufacturing environments.
Strong understanding of risk management methodologies and operational excellence principles.
Ability to analyze complex technical issues and develop practical risk-based solutions.
Strong leadership, project management, organizational, and influencing skills.
Excellent written, verbal, and presentation communication skills.
Proficiency with Microsoft Office applications and HSE management systems.
Experience utilizing data analytics, performance metrics, and reporting tools to drive continuous improvement.
Ability to work independently and effectively within cross-functional teams.
Korean language proficiency is beneficial but not required.
Physical Demands
Ability to sit, stand, walk, climb stairs and ladders, and traverse manufacturing, utility, warehouse, and office areas for extended periods.
Ability to conduct field inspections, audits, risk assessments, and incident investigations in operating manufacturing environments.
Ability to wear required personal protective equipment (PPE) and comply with site safety requirements.
Ability to lift, carry, push, and pull up to 25 pounds occasionally.
Ability to access confined or restricted industrial spaces, elevated work areas, and outdoor locations when required and in accordance with site safety procedures.
Ability to respond to emergencies, incidents, and business-critical situations, including occasional after-hours support for a 24/7 manufacturing operation.
Ability to travel between facilities and vendor or contractor locations as business needs require.
Work Environment
This position operates in both office and manufacturing environments.
Routine exposure to active production, utility, laboratory, warehouse, and construction areas should be expected.
Position is based on a manufacturing campus and requires frequent presence in operational areas to support risk assessments, inspections, audits, investigations, and safety initiatives.
Work may involve exposure to noise, moving mechanical equipment, chemicals, temperature variations, and other industrial conditions typical of pharmaceutical and biotechnology manufacturing facilities.
Access to GMP and classified manufacturing areas is required and may necessitate the use of appropriate PPE, including safety glasses, hearing protection, safety footwear, hard hats, respirators, and other site-required protective equipment.
Occasional work outside of normal business hours may be required to support incident response, project activities, shutdowns, or a 24/7 manufacturing operation.
Travel
Less than 5% travel is required for this position.
Target Bonus
10%
Work Location:
East Syracuse, NY
New York Pay Range
$76,000—$113,000 USD
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!
Related keywords
Process Safety ManagementPSMOSHAEPARMPNFPAISO 45001cGMPHAZOPPHAMOCLOTOArc FlashIndustrial HygieneRoot Cause AnalysisCAPA
LOTTE Biologics is a global CDMO providing integrated development and manufacturing solutions across the United States and South Korea.
Through its Dual Hub Service model, LOTTE Biologics supports clients across the biopharmaceutical lifecycle—from early-stage development and clinical supply through commercial manufacturing—while enhancing supply security, manufacturing flexibility, and consistent quality across regions.
At the Syracuse Bio Campus in New York, LOTTE Biologics provides established GMP manufacturing capabilities backed by more than 62 global regulatory approvals. The campus offers 40,000 L of capacity across eight 5,000 L stainless steel bioreactors, along with analytical and warehouse infrastructure. Integrated bioconjugation capabilities, including antibody-drug conjugates (ADCs), enable a streamlined pathway from biologic drug substance manufacturing through bioconjugation within a single campus.
In South Korea, the Songdo Bio Campus is designed as a next-generation, large-scale biologics manufacturing hub, with 120,000 L of manufacturing capacity across eight 15,000 L stainless steel bioreactors, complemented by a flexible 3,000 L bioreactor configuration to support diverse manufacturing needs.
With capabilities spanning monoclonal antibodies, fusion proteins, multispecific modalities, and bioconjugation, LOTTE Biologics combines scientific expertise, advanced technologies, scalable manufacturing, and a partnership-driven approach to deliver flexible solutions tailored to the needs of each client and program.
Guided by the vision “Possibilities Beyond Limits,” LOTTE Biologics is committed to being a trusted long-term partner in advancing innovative biologics for patients worldwide.
Offices: 300, Olympic-ro, Songpa-gu, Seoul, KR · 6000 Thompson Rd, East Syracuse, New York 13057, US · 418, Songdo-dong, Yeonsu-gu, Incheon, 406840, KR · 1 Broadway, Cambridge, Massachusetts 02142, US