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Master In Biotechnology Jobs in Elizabeth, NJ (NOW HIRING)

CRA 1, IQVIA Biotech

New York, NY ยท On-site

$71K - $145K/yr

Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ... Master File (TMF) and the Investigator Site File (ISF). A central part of this role involves ...

... master batch records, forms, etc. * This individual will be responsible for multiple work centers ... A minimum of 5 years of operations experience within a cGMP environment in the biotech/biopharma ...

... instructions, master batch records, forms, and support and manage change controls. * This ... A minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma ...

... instructions, master batch records, forms, and support and manage change controls. * This ... A minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma ...

... master batch records, forms, etc. * This individual will be responsible for multiple work centers ... A minimum of 5 years of operations experience within a cGMP environment in the biotech/biopharma ...

... master batch records, forms, and support and manage change controls. * Work closely with Operations ... A minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma ...

Showing results 41-60

Master In Biotechnology information

What is a master in biotechnology?

A Master in Biotechnology is a graduate-level degree program focused on the advanced study of biological processes and the use of technology to manipulate living organisms for applications in medicine, agriculture, and industry. Students learn about molecular biology, genetics, bioinformatics, and laboratory techniques, as well as how to apply these skills to develop new products and solutions. This degree prepares graduates for careers in research, pharmaceuticals, healthcare, environmental management, and biotechnology companies, or for further study at the doctoral level.

What are typical career paths for a master in biotechnology, and how can they progress within the industry?

Graduates with a Master in Biotechnology can pursue diverse career paths, such as research scientist, quality control analyst, regulatory affairs specialist, or roles in product development and project management. Advancement often involves taking on leadership responsibilities, such as managing teams or projects, or specializing further in areas like bioinformatics or clinical research. Many professionals also transition into roles in biotech startups, pharmaceuticals, or government agencies, and may further their expertise through certifications or a doctoral degree. Networking, continuous skill development, and staying updated with industry trends are key to progressing within the biotechnology sector.

What are the key skills and qualifications needed to thrive as a master in biotechnology, and why are they important?

To thrive as a Master in Biotechnology, you need advanced knowledge in molecular biology, genetics, and laboratory techniques, typically supported by a master's degree in biotechnology or a related field. Familiarity with bioinformatics tools, PCR, and laboratory information management systems (LIMS) is essential, and certifications in laboratory safety can be advantageous. Strong problem-solving, critical thinking, and teamwork skills distinguish top professionals in this field. These competencies enable effective research, innovation, and collaboration in the rapidly evolving biotech industry.

What is the difference between Master In Biotechnology vs Biotechnology Research Associate?

CriteriaMaster In BiotechnologyBiotechnology Research Associate
Required CredentialsMaster's degree in Biotechnology or related fieldBachelor's or Master's degree in Biotechnology or related field
Work EnvironmentLaboratories, research facilities, academic institutionsLaboratories, biotech companies, research organizations
Employer & Industry UsageAcademic, research, biotech industryBiotech companies, research labs, pharmaceutical firms
Common Search & ComparisonYesYes

The Master In Biotechnology typically prepares individuals for advanced roles in research, development, and academia, requiring a master's degree. A Biotechnology Research Associate usually holds a bachelor's or master's degree and works directly in research projects within biotech companies or labs. While both roles involve laboratory work and research, the Master's degree often leads to more senior or specialized positions.

Is a Master in Biotechnology a good career?

A Master in Biotechnology prepares individuals for careers in research, development, and quality control within biotech, pharmaceutical, and healthcare industries. It offers opportunities in laboratory work, product development, and regulatory roles, often requiring skills in molecular biology, data analysis, and laboratory techniques. The field is growing due to advances in medical research and biomanufacturing, making it a viable career path for those interested in science and innovation.

What can I do with a master in biotechnology?

A master in biotechnology prepares individuals for roles such as research scientist, bioprocess engineer, quality control analyst, or laboratory manager in industries like pharmaceuticals, healthcare, agriculture, and environmental science. Graduates often work with laboratory techniques, data analysis, and regulatory compliance, and may pursue certifications or further specialization to advance their careers.

What cities near Elizabeth, NJ are hiring for Master In Biotechnology jobs?

Cities near Elizabeth, NJ with the most Master In Biotechnology job openings:

Sr. Manager Supply Chain Planning

Legend Biotech US

Raritan, NJ โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago


Job description

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTIยฎ (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.
Legend Biotech is seeking a Sr. Manager, Supply Chain Planning as part of the Manufacturing & Supply team based in Raritan, NJ.
Role Overview
The Senior Manager, Supply Chain Planning & MRP will lead the Raritan CAR-T site Materials Planning and MRP function in support of commercial CAR-T manufacturing. This position is accountable for the creation, execution, and continuous improvement of the site Supply Plan and Material Requirements Planning (MRP) processes to ensure uninterrupted manufacturing execution and patient supply.
This role serves as the site leader for material planning and inventory management activities and is responsible for translating demand, production schedules, inventory strategies, and supplier commitments into executable material and inventory plans that support current manufacturing requirements and future site growth.
The individual will partner closely with Capacity Planning, Production Scheduling, Manufacturing Operations, Warehouse & Logistics, Procurement, Quality, MS&T, Finance, and Enterprise Supply Chain teams to proactively identify and mitigate supply risks, maintain inventory health, and ensure material readiness across short-, medium-, and long-term planning horizons.
The position will lead a team of MRP planners and inventory professionals while driving planning excellence through standardized processes, KPI management, SAP S/4HANA optimization, inventory governance, digital planning adoption, and continuous improvement initiatives.
Success in this role requires strong technical supply chain expertise, advanced analytical capabilities, the ability to lead through influence, and the potential to develop into a strong people leader within a highly regulated cell and gene therapy manufacturing environment.
Key Responsibilities
  • Own the end-to-end Material Requirements Planning (MRP) process supporting CAR-T manufacturing operations at the Raritan site.
  • Lead creation, execution, and governance of material supply plans ensuring alignment to manufacturing demand, inventory strategy, and capacity plans.
  • Own inventory management strategy and execution for planning-controlled materials, including coverage analysis, safety stock, inventory targets, shelf-life risk, scrap/obsolescence risk, and inventory health governance.
  • Establish and maintain planning master data including planning parameters, lead-times, lot sizing, safety stock strategies, reorder points, and inventory policies.
  • Drive accurate material coverage analysis and proactively identify future supply constraints, shortages, inventory exposure, and material readiness risks.
  • Serve as the site subject matter expert (SME) for SAP S/4HANA planning processes and associated planning systems.
  • Lead the Site Critical Materials Review process including supply risk identification, escalation, mitigation planning, and executive communication.
  • Establish proactive inventory and supplier risk monitoring processes to minimize manufacturing disruptions and support uninterrupted patient supply.
  • Partner with Procurement, Supplier Quality, Manufacturing, Warehouse, and Quality organizations to resolve supply disruptions and drive root-cause elimination.
  • Develop contingency plans and alternative supply strategies for critical materials and suppliers.
  • Support Anaplan implementation, process design, adoption, governance, and sustainability as a planning business lead or key process SME.
  • Drive continuous improvement of SAP S/4HANA planning capabilities, master data governance, reporting tools, and system utilization.
  • Partner with enterprise planning, digital, and business systems teams to improve data visibility and planning performance.
  • Support development and deployment of planning dashboards and KPI reporting utilizing SAP, Anaplan, Power BI, and related tools.
  • Lead, coach, develop, and manage a team of MRP Planners and Inventory Management Specialists supporting CART manufacturing operations.
  • Establish clear performance expectations, succession plans, cross-training strategies, and standard work processes to ensure organizational effectiveness and business continuity.
  • Build a high-performing, engaged planning organization capable of supporting continued site growth, increasing manufacturing volumes, and future-state operational requirements.
  • Demonstrate strong technical leadership and coaching mindset; prior people-leadership experience is preferred but not required.
  • Represent Site Supply Chain Planning in Vein-to-Vein, Site Supply Chain, Capacity Review, CRR/S&OP, Operational Readiness, and Enterprise Planning governance forums.
  • Provide planning recommendations, risk assessments, inventory insights, and scenario analyses to support operational and executive decision making.
  • Develop and maintain inventory strategies that balance supply assurance, inventory investment, shelf-life constraints, and manufacturing flexibility.
  • Drive inventory optimization initiatives while minimizing scrap, obsolescence, expired inventory, and stockouts.
  • Own inventory health metrics and ensure adherence to approved inventory targets,
  • Own planning and inventory performance management through development and maintenance of KPIs including Material Availability, OTIF, Inventory Health, Inventory Turns, Safety Stock Compliance, Material Shortages, MRP Exceptions, Supplier Performance, Planning Parameter Accuracy, Scrap and Obsolescence.
  • Utilize KPI trends to identify improvement opportunities and drive corrective actions.
  • Lead or support investigations, root cause analyses, CAPAs, and corrective actions related to supply disruptions, inventory discrepancies, planning failures, and material shortages.
  • Ensure planning and inventory processes remain compliant with applicable GMP, regulatory, and internal quality requirements.
  • Own and continuously improve planning- and inventory-related SOPs, work instructions, training curricula, change controls, and planning governance processes.
  • Interpret, analyze, and translate demand into supply requirements, ensuring material requirements are delivered within supplier lead times and in alignment with OTIF expectations.
  • Lead the monthly supply planning cycle, including creation and updating of supply plans and identification of key supply decisions with relevant stakeholders covering both material and capacity.
  • Monitor execution of daily MRP activities in alignment with the published manufacturing plan and facilitate ERP troubleshooting related to purchase orders, process orders, code conversions, and stock transfers.
  • Collaborate with Quality, QC, Incoming QA, and Warehouse teams to prioritize incoming inspection, release, and availability of raw materials and components.
  • Support Quality, Regulatory, Finance, and operational audits as the planning and inventory process owner or supply chain SME.
  • Provide timely responses to business unit representatives, internal stakeholders, and supplier inquiries.
  • Establish strong working relationships with site, enterprise, and external stakeholders including Manufacturing Operations, Production Scheduling, Warehouse & Logistics, Procurement, Supplier Quality, QA/QC, MS&T, Finance, Enterprise Supply Chain, Digital/Business Systems Teams, and external suppliers.
  • Ability to effectively influence and communicate with stakeholders ranging from operational personnel through executive leadership.

Requirements
  • Bachelor's degree in Supply Chain, Engineering, Business, Operations, Life Sciences, or related field required. Advanced degree or relevant professional certification preferred.
  • Minimum 6 years of experience in Supply Chain, Materials Planning, MRP, Manufacturing Planning, Inventory Management, Procurement Planning, or related disciplines.
  • Experience working within GMP-regulated manufacturing environments.
  • Experience supporting complex manufacturing operations with significant supply chain interdependencies.
  • Strong SAP S/4HANA or equivalent ERP/MRP experience, including material master / planning parameter maintenance, MRP exception management, purchase requisition / purchase order flow, process order support, stock transfer processes, and inventory planning analytics.
  • Demonstrated ability to lead planning and inventory processes and develop high-performing teams.
  • Strong understanding of end-to-end supply chain processes including procurement, inventory management, production planning, warehouse operations, quality systems, and supplier management.
  • Advanced analytical skills including scenario modeling, supply risk analysis, inventory optimization, and data-driven decision making.
  • Strong SAP S/4HANA planning knowledge including MRP execution, planning parameters, material master governance, purchase requisitions, process orders, and inventory transactions.
  • Proven ability to influence across matrix organizations and drive cross-functional alignment.
  • Strong presentation and executive communication skills.
  • Ability to balance tactical operational execution with long-term strategic planning.
  • Ability to promote a mindset of continuous improvement, problem solving, and prevention.
    Technologically savvy with the ability to quickly adopt new systems and processes. Proficient in Excel, Word, PowerPoint, and planning/reporting tools.
  • Language: English

Preferred
  • Cell & Gene Therapy, CAR-T, Biologics, or Personalized Medicine manufacturing experience.
  • People-leadership experience preferred; strong technical leadership, coaching mindset, and demonstrated potential to develop into a people leader will be considered.
  • Experience with Anaplan, SAP APO, SAP IBP, OMP, Kinaxis, or related planning platforms.
  • APICS CPIM, CSCP, Lean Six Sigma Green Belt or Black Belt certification.
  • Experience supporting audits, change controls, deviations, CAPAs, SOPs, and planning-related GMP documentation.

#Li-BZ1
#Li-Onsite
The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.
Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.
Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
Pay Range (Base Pay):
$146,410-$192,164 USD
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
Work Authorization & Employment Eligibility
Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates.
EEO Statement
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.