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Manufacturing Operations Associate Jobs in New York

Legend Biotech US

Operations Associate

Raritan, NJ · On-site

Be part of the manufacturing operations team responsible for production of autologous CAR-T ... OR // Associates Degree required in Life Sciences or Manufacturing with 2 - 3 years of related ...

Legend Biotech US

Operations Associate

Raritan, NJ · On-site

Be part of the manufacturing operations team responsible for production of autologous CAR-T ... OR // Associates Degree required in Life Sciences or Manufacturing with 2 - 3 years of related ...

Naturalvert

Operations associate

Hawthorne, NJ · On-site

Are you looking to learn more about what goes into running a food manufacturer? This individual ... A successful operations associate should be highly organized and have a versatile skill set to ...

Legend Biotech USA

Operations Supervisor

Raritan, NJ · On-site

... to manufacturing of cell-based products, and cleanroom behaviors. * Must exhibit strong Leadership skills and ability to effectively communicate and influence Operations associate and convey ...

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Manufacturing Operations Associate information

What is the difference between Manufacturing Operations Associate vs Manufacturing Technician?

AspectManufacturing Operations AssociateManufacturing Technician
CredentialsHigh school diploma or equivalent; some roles may require technical certificationsHigh school diploma; technical certifications or associate degree often preferred
Work EnvironmentFactory floor, production lines, assembly areasFactory floor, equipment maintenance, quality control stations
Employer & Industry UsageManufacturing plants across various industriesManufacturing plants, especially in electronics, automotive, and machinery sectors
Common Search & ComparisonOften compared for entry-level manufacturing rolesCompared for technical and hands-on manufacturing roles

The Manufacturing Operations Associate typically handles production support, quality checks, and process documentation, often requiring minimal technical certifications. Manufacturing Technicians focus more on equipment maintenance, troubleshooting, and technical tasks. Both roles are essential in manufacturing environments, but the Technician usually requires more technical skills and certifications.

What do you do as a manufacturing operations associate?

A manufacturing operations associate is responsible for supporting production processes, monitoring equipment, and ensuring quality standards are met. They often operate machinery, follow safety protocols, and document production data to maintain efficient manufacturing workflows.

What is the role of a manufacturing operations associate?

A manufacturing operations associate is responsible for supporting production processes, ensuring quality standards, and maintaining safety protocols on the manufacturing floor. They often operate machinery, monitor workflows, and assist with inventory management to ensure efficient production. Strong attention to detail and familiarity with manufacturing tools or software are beneficial for this role.

What are the most commonly searched types of Manufacturing Operations jobs in New York?

The most popular types of Manufacturing Operations jobs in New York are:

What cities in New York are hiring for Manufacturing Operations Associate jobs?

Cities in New York with the most Manufacturing Operations Associate job openings:

Infographic showing various Manufacturing Operations Associate job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Associate Director Manufacturing Operations

Saddle Brook, NJ

Lynkx Staffing LLC
Recruiting and Staffing Services • 1 - 10 employees
Learn more about Lynkx Staffing LLCexternal

Full-time

Re-posted 26 days ago

Key responsibilities

  • Manage all Operations scheduling, training, and compliance activities to ensure smooth and efficient daily operations.

  • Oversee capacity planning and resource availability for clinical manufacture looking 3-6 months ahead.

  • Create, enforce, and measure Operator training schedules and personnel assignments to meet production needs.

Job description

Associate Director, Manufacturing OperationsAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The Associate Director, Manufacturing Operations is responsible for efficient utilization of Operations resources to meet customer demand. This role will be responsible for maintaining and overseeing the site Operations scheduling and training capacities for a time period looking ahead to the next 3-6 months. The Associate Director, Manufacturing Operations will understand upcoming needs and constraints and help drive strategy accordingly. This includes the management of all Operations scheduling, training and compliance resources. The Associate Director, Manufacturing Operations is also responsible for assessing the needs of the company to contribute to the big picture by ensuring daily operations run smoothly and as efficiently as possible. This role will also drive individual and team development to ensure a prepared and empowered workforce to become the provider of choice for the industry.
  • Meeting client process demands through planning, scheduling, manufacture and delivery of clinical cell therapy products according to established procedures, regulations and contracts
  • Looking out 3-6 months to ensure capacity and availability of resources (room/equipment/staff) to perform clinical manufacture for processing needs
  • Manages all training and compliance activities in the Operations organization
  • Responsible for creating, enforcing and measuring Operator training schedules in order to ensure that all production schedules can be carried out
  • Creates and maintains a process to ensure that personnel schedules are being accurately and fairly assigned to all Associates
  • Supporting and driving special long-term projects and identified and assigned by the PPU Head
  • Responsible for creating maintaining and communicating all Operations based KPI’s
  • Ensuring department staff compliance with corporate and site-specific HR policies, safety, and business policies and practices
  • Approving job specific curriculum for the training and professional development of department staff
  • Responsible for streamlining the batch record review process
  • Responsible to understand the profit and loss for the PPU’s as well as all related documentation, and how these items impact Operations
  • Driving continuous improvement
  • Liaison with support groups for short- and medium-term needs – Supply Chain, Training, Quality Systems, Quality Assurance, Quality Control, and others
  • Set team expectations and goals and assists in delivering the business direction for the PPU
  • Aligning departmental goals, processes and resource allocation with the organizational strategy
  • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
  • Direct reports: Associate Manager Training, Associate Manager, Compliance, Scheduling Associate, Quality Engineer Associates. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.
REQUIREMENTS
  • Bachelor's degree (i.e. Biology, Biotechnology, Bioengineering, Chemical Engineering).
  • 5-10 years of cGMP environment, aseptic processing, mammalian cell culture, monoclonal antibody, cell processing, cryopreservation or similar experience.
  • 5-10 years of leadership experience or equivalent combination of experience.
  • Deep Understanding of cGMP and cGLP
  • Working knowledge of financial operations and budget development
  • Relevant IT skills (able to work with Microsoft Office and corporate scheduling system)
  • Competencies/Candidate Profile
  • Strong collaborative and influencing skills and ability to work well in a cross-functional, matrixed environment
  • Flexible and able to adapt to company growth and evolving responsibilities
  • Accountability, integrity, and strong dedication to regulatory compliance
  • Strong business and personnel management acumen
  • Strong emotional intelligence
  • Ability to think strategically and tactically (detail-oriented)
  • Strong analytical and problem-solving skills
  • Strong written and verbal communication skills
  • Drive to create and maintain order in a fluid, technically complex environment
  • Continuous improvement mindset
  • Ability to multi-task is essential
  • Must have the ability to work in a team-oriented environment and with clients
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen.
Environment requires gowning, hair net, safety glasses, gloves, and foot coverings.Must be capable of moving, sitting, stretching, stooping, using hands and fingers, reaching with hands and arms, talking and exchanging information, and vision sufficient to read materials.Duties, responsibilities, and activities may change at any time with or without notice