Entry Level Manufacturing Production Associate Job at Mohawk Industries (Rome)

Production associate - cleaning machine operator - swing shift

Cintas Corporation is a leading provider of products and services designed to he...

Location

United States , Compton

Salary:

17.05 - 21.33 USD / Hour

OysterLink

Expiration Date

Until further notice

Requirements

Must be authorized to work in the US
must be 18 years of age or older
must adhere to attendance policy
willing to work near others for extended periods
able to work in a fast-paced, schedule-driven environment
willing to handle soiled materials with protective equipment
able to stand for most of the shift
able to perform repetitive motions including bending, stretching, turning, and reaching
High school diploma or equivalent
prior experience in production or manufacturing preferred

Job Responsibility

Inspect mats for quality
feed mats into cleaning machine
sort cleaned mats to staging areas
perform machine checks
clean machine filters
maintain cleanliness of work area
meet or exceed quantity and quality standards

What we offer

competitive pay
401(k) with Company Match
Profit sharing
Employee stock ownership plan
Disability insurance
Life insurance
Paid Time Off
Holidays
skills development
Training

Fulltime

Production Associate

Production Associate for a Medical Device Company. A Shift 6am – 6pm. Duration: ...

Location

United States , Columbus

Salary:

17.00 - 20.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

High school diploma or equivalent
Ability to read, write, interpret and comprehend specifications written in English and perform basic math calculations
Must be able to work flexible and/or extended hours and report to work on a regular, punctual basis
Ability to get along with people and be able to work in a team environment
Willingness to rotate into different tasks and responsibilities
Develops skills in basic tasks, techniques and procedures within one skill area / process / method
Applies basic knowledge and skills to complete routine tasks consisting of prescribed steps
Effective communication skills at a level co-workers and Team Lead/Supervisor can understand

Job Responsibility

Performs routine production functions including filling, utility operations, packing, packaging, assembling, labeling and inspecting under general supervision
Maintains accurate records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization)
Effectively works in a team setting, supporting team goals and objectives
Makes effective decisions relative to position requirements
Must follow instructions and work within routine, standard practices, making decisions as required
Works under direct supervision, following standard operating procedures

Fulltime

Production Associate

Production Associate position at a Medical Device Company. 3rd Shift (8PM - 8AM)...

Location

United States , Sumter

Salary:

6.00 - 12.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Zero (0) to one (1) year of manufacturing assembly experience
Effective communication skills at a level co-workers and Team Lead/Supervisor can understand
Ability to read, write, interpret and comprehend specifications written in English and perform basic math calculations
Ability to use basic tools of measurement, such as microscopes
Must be able to work flexible and/or extended hours and report to work on a regular, punctual basis
Has good attention to detail
Ability to get along with people and be able to work in a team environment
Willingness to rotate into different tasks and responsibilities
High school diploma or equivalent

Job Responsibility

Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices
Setting up, operating, performing maintenance on and troubleshooting equipment
May conduct quality inspections on processing line in accordance with quality specifications
Works within clearly defined SOPs and / or scientific methods and adheres to quality guidelines

Fulltime

Drug Product Manufacturing Associate II

The Manufacturing Associate II is responsible for executing GMP production of in...

Location

United States , San Diego

Salary:

27.09 - 31.60 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

High school diploma required
Minimum of two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions
Ability to work with cross functional teams
Detail oriented with strong written and verbal communication skills
Ability to work independently, within prescribed guidelines, or as a team member
Demonstrated ability to follow detailed directions in a manufacturing GMP environment
Familiarity with cGMP, manufacturing, machine operations, and data entry
Must be familiar with Microsoft Office applications
Ability to constantly perform duties while donning aseptic gowning
Ability to constantly sit and reach to use computers and other office equipment

Job Responsibility

Execute GMP production of injectable pharmaceuticals by following all applicable SOP's
Prepare equipment and materials for GMP aseptic production
Operate equipment such as glasswashers, autoclaves, depyrogenation ovens and automated filling machines
Participate in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility
Assist technical personnel with troubleshooting mechanical issues that arise with manufacturing equipment
Perform various semi-routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations
Troubleshoot manufacturing processes that are semi-complex in level under cGMP guidelines and under the supervision of management
Assist in the research and implementation of new methods and technologies to enhance operations
Prepare components, media, buffers, and other solutions as needed
Accurately document data and write/review batch records under cGMP guidelines

What we offer

Eligibility for an annual performance bonus
Paid time off
Health insurance coverage (including dental and vision)
Flexible spending account
401(k) plan

Fulltime

Records Management Specialist

This position is responsible for responding to inquiries and processing applicat...

Location

United States , Landover, MD

Salary:

Not provided

PN Automation, Inc

Expiration Date

Until further notice

Requirements

High School Diploma
BS degree preferred
Three (3) years related experience with two (2) years direct experience processing documents and at least one (1) year of office, records, or computer experience
Technical background with knowledge of folder structure systems for electronic documents
Proficient with office automation tools such as Microsoft Office and other common desktop applications
Must have a combination of excellent analytical skills and attention to detail
Possess excellent verbal and written communication skills
Ability to lift and move standard boxes (35 lbs.)
Must be able to work in a fast-paced paper and electronic production environment
Requires ability to bend and stretch to reach files, and push a fully loaded mail cart

Job Responsibility

Process paper and electronic documents in accordance with current SOP's
Selection of appropriate method from a wide variety of procedures or simple interpretations of a limited number of SOP's
Understanding multiple data entry systems
Selection and identification of relevant data, labeling, jackets, logging, assignments and all associated data entry with a high level of accuracy
Perform data entry functions, as needed
Redact patient and/or manufacturer data

Fulltime

Drug Product Manufacturing Associate II

The Manufacturing Associate II is responsible for executing GMP production of in...

Location

United States , San Diego

Salary:

27.09 - 31.60 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

High school diploma required
Minimum of two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions
Ability to work with cross functional teams
Detail oriented with strong written and verbal communication skills
Ability to work independently, within prescribed guidelines, or as a team member
Demonstrated ability to follow detailed directions in a manufacturing GMP environment
Familiarity with cGMP, manufacturing, machine operations, and data entry
Must be familiar with Microsoft Office applications
Constantly perform duties while donning aseptic gowning
Constantly required to sit, and to reach to use computers and other office equipment

Job Responsibility

Participate in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility
Assists technical personnel with troubleshooting mechanical issues that arise with manufacturing equipment
Performs various semi-routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations
Troubleshoots manufacturing processes that are semi-complex in level under cGMP guidelines and under the supervision of management
Assists in the research and implementation of new methods and technologies to enhance operations
Prepares components, media, buffers, and other solutions as needed
Accurately documents data and writes/reviews batch records under cGMP guidelines
Prepares material components for production
Regular and reliable attendance on a full time basis [or in accordance with posted schedule]
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices

What we offer

Eligibility for an annual performance bonus
Paid time off
Health insurance coverage (including dental and vision)
A flexible spending account
A 401(k) plan

Fulltime

Specialist Contract Development & Manufacturing

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States , Thousand Oaks

Salary:

111577.00 - 150507.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED and 10 years of Manufacturing experience
Associate’s degree and 8 years of Manufacturing experience
Bachelor’s degree and 4 years of Manufacturing experience
Master’s degree and 2 years of Manufacturing experience
Doctorate degree
Bachelor’s in Business Administration, Engineering, or Science-related field
5+ years of experience in protein, API, DS, DP, or packaging manufacturing environment
5+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles
2+ years of project management experience leading multi-functional and/or multi-location team
1+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products

Job Responsibility

Provide information insight and data analysis, drive execution of transactional/tactical tasks to ensure performance execution across the external manufacturing network
Ensure accuracy and completion of data entries and/or tasks for budget development, monitoring, and reporting
inputs to contracts, confidentiality disclosure agreement(s), scope of work agreement(s), request for pricing/information, supply agreement(s) etc
Own NC Class II/III records, CAPA, CAPA EV, and more complex change control records
Report contract site performance metrics to site lead
identify improvement opportunities for site performance
daily duties will include coordination, issuance, and review of meeting minutes, conclusions from analysis of data and metrics, continuous improvement and standardization of performance tools used by the Work Center Teams (WCT), oversight and reporting of procurement/payment of invoices, and active participation in WCT meetings with the contract site as well as internal site team
Follow-up and track activities in a department-wide project from conception to implementation and close-out
Manage timeline and highlight risks of transfer team activities
coordinate risk management activities as part of transfer

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Material Handler

Accountable for development, planning, execution, and management of various acti...

Location

United States , Chippewa Falls

Salary:

15.82 - 33.65 USD / Hour

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

Associate degree preferred or equivalent experience
Typically 2-4 years of experience in materials and/or distribution
Strong knowledge of warehouse management applications and Microsoft Office suite
Strong written and verbal skills
Fluency in English and local language
Strong technical knowledge specific to business function
Strong multi-tasking ability
Demonstrates basic- to complex level functional process self-thinking (inventory control, conducting cycle counts) and seeks guidance for resolution
Understanding of and able to work within a team-based work environment, able to perform clear and concise communication, and understands the urgency to keep production orders flowing
Computer data entry, inventory variance analysis, root cause analysis, knowledge of SAP ERP

Job Responsibility

Performs varied and general tasks involved in controlling inventory
shipping, receiving, storing and distributing materials, parts, supplies, and equipment (e.g. movement of materials through the use of pallet jacks, daily collection of appropriate statistics, routine maintenance)
Supports intermediate-level transactional processes that require independent judgment
Follows detailed documentation and instructions to execute a variety of process- oriented tasks to support inventory control and materials management activities (e.g. works externally to expedite routine shipment and deliveries
clearing of Shipment Delay Advisories)
Identifies basic- to complex level functional process anomalies (e.g. inventory control, shipping and receiving, conducting cycle counts) and seeks guidance for resolution
Supports the training of new hires

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Entry Level Manufacturing Production Associate

Mohawk Industries

Location:
United States , Rome

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Requirements:

Additional Information:

Job Posted:
December 10, 2025

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