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Graduate In Usa Jobs in New Jersey (NOW HIRING)

Nishi Enterprise Inc

Be Seen First

Business Development Associate

South Plainfield, NJ · On-site

$46K - $63K/yr

Recent graduate or 0-2 years of experience in sales, business development, customer service, retail ... USA and Canada. We sell mainly thru our website and personal visit by business customers.

Nishi Enterprise Inc

Be Seen First

Business Development Associate

South Plainfield, NJ · On-site

$46K - $63K/yr

Recent graduate or 0-2 years of experience in sales, business development, customer service, retail ... USA and Canada. We sell mainly thru our website and personal visit by business customers.

Metals USA

ACCOUNTING CLERK

NJ · On-site

$25 - $30/hr

Metals USA is a leading metals processor/distributor in North America, providing a wide range of ... High School Graduate or Equivalent. * Ability to interface effectively with all departments to ...

Metals USA Holdings Corp.

ACCOUNTING CLERK

Union, NJ · On-site

$25 - $30/hr

Metals USA is a leading metals processor/distributor in North America, providing a wide range of ... High School Graduate or Equivalent. * Ability to interface effectively with all departments to ...

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Graduate In Usa information

What is a graduate in the USA?

Graduates in the USA are individuals who have successfully completed a degree program at a college or university, such as a bachelor's, master's, or doctoral degree. After graduation, they receive a diploma certifying their academic achievement. Graduates often seek employment, pursue further education, or engage in research or professional development. In the US, the term 'graduate' can also specifically refer to someone who has completed a postgraduate program (master's or doctorate), but it is commonly used for anyone who has finished a degree.

What are the key skills and qualifications needed to thrive as a graduate in the USA?

To thrive as a recent graduate in the USA, you typically need a relevant academic degree, foundational knowledge in your field, and internship or practical experience. Familiarity with productivity software, research tools, or industry-specific platforms is often expected depending on your chosen career path. Strong communication, adaptability, and problem-solving skills help set you apart during job searches and in the workplace. These skills and experiences are crucial for transitioning smoothly from academia to professional environments and for long-term career growth.

What are the common challenges recent graduates face when starting their first job in the USA?

Recent graduates in the USA often encounter challenges such as adjusting to workplace expectations, managing time effectively, and navigating professional communication. Transitioning from an academic environment to a corporate or professional setting can require adapting to new responsibilities, meeting deadlines, and collaborating within diverse teams. Many also find it helpful to seek mentorship and participate in training programs to accelerate their learning curve and successfully integrate into the organization.

What is the difference between Graduate In Usa vs Intern in Usa?

AspectGraduate In UsaIntern in Usa
Required CredentialsDegree or ongoing studiesUsually students or recent graduates
Work EnvironmentFull-time, professional settingPart-time or temporary, learning-focused
Employer & Industry UsageEmployers hiring graduates for entry-level rolesOrganizations offering training or experience
Search & Comparison IntentUnderstanding entry-level opportunities for graduatesSeeking internship opportunities or experience

In summary, a Graduate In Usa typically refers to individuals who have completed their degree and are seeking full-time entry-level positions, while an Intern in Usa is usually a student or recent graduate gaining practical experience through temporary or part-time roles. Both are important for career development but serve different purposes in the job market.

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Graduate In Usa jobs near you

Director, Global Sterility Assurance Team Lead

Novartis

Morris Plains, NJ • On-site

Full-time

Medical, Retirement, PTO

Re-posted 29 days ago

Key responsibilities

  • Lead and manage a team of 4-6 direct reports and 20-30 indirect reports across manufacturing sites to ensure aseptic processing and sterility assurance.

  • Oversee site readiness and support preparation for Health Authority inspections, including developing materials and ensuring compliance with GMP regulations.

  • Monitor and improve aseptic processes, including sterilization, microbiological monitoring, and contamination control, across the manufacturing network.

Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

Job Description Summary

As Director, Global Sterility Assurance Team Lead you will:
• Lead a team (4-6 direct reports, 20-30 indirect) of Key functional Expert for Aseptic processing within the Novartis manufacturing network (includes Large Molecules and Advance therapies and third parties producing for Novartis).
• Ensures and verifies that all actions related to FDA and other health authority inspections are understood and implemented by the sites in the platform, avoiding re-occurrence of 483’s and Warning Letters.
• Assure that key projects are implemented in the manufacturing sites as per committed plan to FDA and other health authorities
• Ensure implementation of changes to support GMP updates (i.e. Annex 1) within all the sites in scope in order to assure ongoing compliance for the upcoming years. In this regard supports the gap assessment process and respective remediation and action tracking.
• Liaise with TechOps to ensure implementation, follow up and completeness of all related Quality/ Compliance programs, documentation and Quality reporting of Aseptic related projects / metrics.
• Ensure adequate Health Authority Inspection preparation of the Sites in scope and successful inspection outcomes. Interactions with sites mainly require interpretation of complex information and persuasion both internally with other areas of the business and the site leadership team and externally.


Job Description

Major Accountabilities:

  • Overall team leader that has the responsibility of 4-6 individual contributors hosted in US, Spain and Austria, plus 20-30 indirect reports located within the manufacturing sites performing sterile operations.
  • Lead cross site/platform and network projects and harmonization initiatives as assigned
  • Provide expert advice and appropriate technical support to ensure site readiness for Health Authority and GGA inspections by supporting sites in their preparation, up to and including hands on preparation of materials (i.e. storyboards for complex cases, etc.)
  • Primary Responsible for optimization of aseptic processes (as e.g. cleaning and disinfection programs, microbiological monitoring and sterilization techniques) between sites and platforms within the Novartis manufacturing network
  • Support escalations for specific topics (i.e. Microbial contaminations, sterility issues, etc.) with the manufacturing sites if needed, and in collaboration with the other members of the platform (i.e. QA operations, QA compliance lead, QC/AS&T lead)
  • Own, Monitor and act as Primary contact for the sterility assurance from the sites and define improvement plans as appropriate.
  • Build fit for purpose aseptic governance and training program in collaboration with engineering and MS&T to support sites in development, training and understanding of aseptic topics
  • Provides input for the selection, training, people development and performance evaluation, development planning and participating in recruiting process of the Aseptic experts within the manufacturing sites / global functions.

Obligatory requirements:

  • Education: Graduate in Chemistry, Pharmacy, Microbiology or another related science; desirable: Ph.D. in science or related discipline
  • 12 - 15 years experience in management and leadership roles in the pharmaceutical industry, preferably in a FDA-regulated environment and in QA Operations & Compliance of a strategic Site or a global role. Pharma production experience indispensable. Quality Assurance / cGMP regulations in USA, EU (Self Inspections, Auditing of 3rd parties, Complaint/Deviation Handling, GMP-Training, SOP-Systems).
  • Deep understanding of microbiology and aseptic processes
  • Solid People Management / Communication skills (To explain difficult business processes and related GMP-requirements to a community of very diversely oriented and educated people from a multitude of different units.
  • Excellent Project Management skills, especially with crossfunctional projects.
  • Fluent English written and spoken.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

You will receive: Competitive salary, Annual bonus, Pension scheme, Share scheme, Health insurance, 27 days annual leave, Flexible working arrangements, subsidized dining facilities, Employee recognition scheme, learning and development opportunities.

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.


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