Manufacturing Associate

Global Life Science Hub is partnered with an incredible biopharmaceutical company specializing in difficult-to-formulate biologics. Recently, the company has achieved 2 FDA approvals and is transitioning from R&D to a full-scale commercial organization looking to build a new state-of-the-art facility in New Jersey as they ramp up production efforts from 50L to 2000L in Q4.

To support further expansion, we seek a Downstream Manufacturing Specialist responsible for purifying clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF, knowledge of initiating batch records, and experience packing chromatography columns.

Responsibilities:

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis.
• Provides technical direction in the execution and development of the purification...

Global Life Science Hub is partnered with an incredible biopharmaceutical company specializing in difficult-to-formulate biologics. Recently, the company has achieved 2 FDA approvals and is transitioning from R&D to a full-scale commercial organization looking to build a new state-of-the-art facility in New Jersey as they ramp up production efforts from 50L to 2000L in Q4.

We are searching for a passionate Upstream Manufacturing Associate with solid cell culture expertise to support the scale-up manufacturing efforts. The ideal candidate will have extensive experience working with CHO cells and perfusion-based bioreactor systems.

Responsibilities:

• Lead and execute upstream batches, including mammalian cell culture with a focus on CHO cell lines.
• Design, optimize, and troubleshoot cell culture processes in batch, fed-batch, and perfusion bioreactor systems.
• Maintain and scale up cell culture operations to support...

Global Life Science Hub is partnered with an incredible biopharmaceutical company specializing in difficult-to-formulate biologics. Recently, the company has achieved 2 FDA approvals and is transitioning from R&D to a full-scale commercial organization looking to build a new state-of-the-art facility in New Jersey as they ramp up production efforts from 50L to 2000L in Q4.

To support further expansion, we seek an on-site Downstream Manufacturing Associate in New Jersey who will be responsible for purifying clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF, knowledge of initiating batch records, and experience packing chromatography columns.

Responsibilities:

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis.
• Provides technical direction in the execution...

Global Life Science Hub is partnered with an incredible biopharmaceutical company specializing in difficult-to-formulate biologics. Recently, the company has achieved 2 FDA approvals and is transitioning from R&D to a full-scale commercial organization looking to build a new state-of-the-art facility in New Jersey as they ramp up production efforts from 50L to 2000L in Q4.

To support further expansion, we seek a Downstream Manufacturing Associate responsible for purifying clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF, knowledge of initiating batch records, and experience packing chromatography columns.

Responsibilities:

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis.
• Provides technical direction in the execution and development of the purification...

Global Life Science Hub is partnered with an innovative biopharmaceutical company specializing in difficult-to-formulate biologics. The company is building a brand-new state-of-the-art facility in New Jersey after recently gaining two FDA approvals.

Due to serious expansion plans, we seek an Upstream Biomanufacturing Associate responsible for executing purification on CHO cell culture processes and producing proteins for a wide range of mammalian-based biosimilars. The appointed candidate will require technical expertise in Cell Biology and Bioreactor Operations.

Responsibilities:

• Work with a collaborative team of manufacturing associates and engineers to execute upstream batches.
• Perform cell culture and bioreactor operations at multiple scales.
• Ensure that engineering and clinical batches are executed in a timely manner.
• Establishes operating equipment specifications and improves manufacturing techniques.
...

Global Life Science Hub are seeking a Downstream Manufacturing Associate to be on-site in New Jersey who will be responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian cells.

The appointed candidate will be responsible in the purification of 50L to 2000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents.

Essential Duties & Responsibilities

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis.
• Provides technical direction in the execution and development of the purification process.
• Uses programs to collect and evaluate operating data to conduct on- line...

Global Life Science Hub are seeking a Downstream Manufacturing Associate who will be responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian cells.

The appointed candidate will be responsible in the purification of 50L to 2000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents.

Essential Duties & Responsibilities

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis.
• Provides technical direction in the execution and development of the purification process.
• Uses programs to collect and evaluate operating data to conduct on- line adjustments to products,...

Global Life Science Hub are seeking an Upstream Manufacturing Associate will be responsible for executing purification on CHO cell culture processes and producing proteins for a wide range of mammalian based biosimilars. The appointed candidate will require technical expertise in Cell Biology and Bioreactor Operations.

Responsibilities:

• Work with a collaborative team of manufacturing associates and engineers to execute upstream batches.
• Perform cell culture and bioreactor operations at multiple scales.
• Ensure that engineering and clinical batches are executed in a timely manner.
• Establishes operating equipment specifications and improves manufacturing techniques.
• Uses programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments or equipment.
• Ability to interpret and provide instructions furnished in written, oral, diagram, or schedule form.
• Should...

Global Life Science Hub is proud to partner with a specialised Biopharmaceutical company leading the charge of next-generation drug delivery technologies and oral//biosimilar drug development.

Having gathered 2 recent FDA approvals, they're in the process of gearing up for exponential growth. With brand new in-house Manufacturing capabilities set to triple production in 2025, this is an exciting time to join a rapidly expanding organization.

To support further expansion, the Upstream Manufacturing Associate will be responsible for executing mammalian cell culture processes and producing proteins for a wide range of mammalian based biosimilars. The appointed candidate will require technical expertise in Cell Biology and Bioreactor Operations.

Responsibilities:

• Collaborate with a dynamic team of manufacturing associates and engineers to carry out upstream production batches.
• Conduct cell culture and manage bioreactor operations...

The BioPharma Consulting JAD Group is currently seeking a highly motivated MCS Manufacturing Associate to join our team. This role offers the opportunity to support development, clinical, and launch activities in a dynamic production environment.

Key Responsibilities:

• Hands-On Operations:
• Set-up, clean, and sanitize various manufacturing equipment.
• Prepare buffers/media following Manufacturing Procedures (MPs) and SOPs.
• Perform and monitor critical processes, with the ability to execute basic troubleshooting.
• Perform in-process sampling and operate analytical equipment.
• Execute washroom activities, including cleaning small and large-scale equipment used in production.
• Compliance and Documentation:
• Adhere strictly to GMP documents (SOPs, MPs) with a focus on safety and compliance.
• Draft and revise routine documents, including...

Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do...

Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do...

The BioPharma Consulting JAD Group is seeking a highly motivated and dedicated MCS Manufacturing Associate to join our team in Thousand Oaks, CA. This role involves performing operations under general supervision in the manufacturing area, following Standard Operating Procedures (SOPs) and adhering to safety and compliance standards.
Responsibilities:

• Set-up, cleaning, and sanitization of various manufacturing equipment.
• Prepare buffers and media according to defined manufacturing procedures (MPs) and SOPs.
• Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance.
• Perform and monitor critical processes with basic troubleshooting abilities.

• Conduct in-process sampling and operate analytical equipment.
• Clean small and large-scale equipment used in production.
• Maintain an organized and clean workspace.
• Work in a clean room environment wearing full clean room...

Downstream Manufacturing Associate

We are recruiting a Downstream Manufacturing Associate for a hands-on role in the purification of mammalian cell-based cultures and production of recombinant proteins for biosimilars. This position involves handling purification volumes from 50L to 1000L for engineering, clinical, and commercial batches in a cGMP environment. Proficiency in operating AKTA purification skids, tangential flow filtration (TFF), and familiarity with batch records and technical documents is essential.

Essential Duties & Responsibilities:

• Execute downstream processes at various scales in a cGMP environment, including column packing, process troubleshooting, and data analysis.
• Operate and maintain downstream equipment, including AKTA skids and TFF systems.
• Perform in-process testing and data collection to ensure product quality and process consistency.
• Assist in preparing and...

Downstream Manufacturing Associate III

We are recruiting a Downstream Manufacturing Associate III for a hands-on role in the purification of mammalian cell-based cultures and production of recombinant proteins for biosimilars. This position involves handling purification volumes from 50L to 1000L for engineering, clinical, and commercial batches in a cGMP environment. Proficiency in operating AKTA purification skids, tangential flow filtration (TFF), and familiarity with batch records and technical documents is essential.

Essential Duties & Responsibilities:

• Execute downstream processes at various scales in a cGMP environment, including column packing, process troubleshooting, and data analysis.
• Operate and maintain downstream equipment, including AKTA skids and TFF systems.
• Perform in-process testing and data collection to ensure product quality and process consistency.
• Assist in preparing and...

Downstream Manufacturing Associate

We are recruiting a Downstream Manufacturing Associate for a hands-on role in the purification of mammalian cell-based cultures and production of recombinant proteins for biosimilars. This position involves handling purification volumes from 50L to 1000L for engineering, clinical, and commercial batches in a cGMP environment. Proficiency in operating AKTA purification skids, tangential flow filtration (TFF), and familiarity with batch records and technical documents is essential.

Essential Duties & Responsibilities:

• Execute downstream processes at various scales in a cGMP environment, including column packing, process troubleshooting, and data analysis.
• Operate and maintain downstream equipment, including AKTA skids and TFF systems.
• Perform in-process testing and data collection to ensure product quality and process consistency.
• Assist in preparing and...

Summary: At BioPharma Consulting JAD Group, we are seeking a motivated MCS Manufacturing Sr. Associate to join our Team. As a Senior Associate, you will be responsible for supporting manufacturing operations and leading continuous improvement initiatives. You will collaborate with cross-functional teams to ensure quality, safety, and compliance in all manufacturing processes.

Responsibilities:

• Under minimal supervision, performs manufacturing according to Standard Operating Procedure
• Understand process parameters and can identify process anomalies
• Operate critical processing equipment
• Assist in ensuring operations are completed per manufacturing schedule
• Resource related to processing operations on the mfg. floor
• Responsible for identifying and communicating problems during operations
• Review, revise, and audit documents
• Ability to perform computer operations (MES,...

BioPharma Consulting JAD Group is seeking a MCS Manufacturing Associate to join our team. This role works in a dynamic production environment supporting development, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs).

Responsibilities:

• Set-up, cleaning, and sanitization of manufacturing equipment.
• Preparing buffers and media following defined manufacturing procedures (MPs) and SOPs.
• Performing in-process sampling of equipment and operating analytical equipment.
• Conducting washroom activities: cleaning small and large-scale equipment used in production activities.
• Initiating quality reports and maintaining an organized and clean workspace.
• Drafting and revising SOPs and MPs.
• Performing and monitoring critical processes, including basic...

Parallel Employment is assisting a local Manufacturer located in Lakewood, NY, with their search for Production associates. Positions available are in Assembly, Fabrication and Paint. Qualified employees will be part of a team manufacturing high end specialty Tool Boxes. If you have experience in manufacturing and are looking for a position where you can make competitive wages while growing your skills this could be a great opportunity for you. 1st and 2nd shifts available, work week Monday through Friday with overtime. Starting pay rates of $17.50 to $19.50

Requirements

• Manufacturing experience
• High attention detail
• Ability to lift up to 45lbs
• Must be willing to cross-train and assist in any area of production to drive results
• Must remain flexible with regard to shift hours and responsibilities

Apply with us at:

Website:...

R2Net is a diamond bridal jewelry company with a technology soul. R2Net Inc. is an innovative technology company that provides e-commerce and supply chain platforms to connect the entire span of the diamond industry ecosystem, including manufacturers, retailers, and consumers.

We are seeking a Manufacturing Operations Associates who will be responsible for a range of tasks including data entry, order processing, and shipping. As part of this role, the Manufacturing Operations Associate will handle order issues, provide support with administrative tasks, oversee inventory, and ensure accuracy in the ERP system. Additionally, managing quality control and vendor invoices are integral parts of the position. The ideal candidate for this role will possess strong organizational skills, meticulous attention to detail, and the ability to thrive in a fast-paced environment.

Responsibilities:

• Perform data entry and order verification.
...

Global Life Science Hub is proud to partner with a specialised Biopharmaceutical company leading the charge of next-generation drug delivery technologies and oral//biosimilar drug development.

Having gathered 2 recent FDA approvals, they're in the process of gearing up for exponential growth. With brand new in-house Manufacturing capabilities set to triple production in 2025, this is an exciting time to join a rapidly expanding organization.

To support further expansion, the Upstream Manufacturing Associate/Scientist will be responsible for executing mammalian cell culture processes and producing proteins for a wide range of mammalian based biosimilars. The appointed candidate will require technical expertise in Cell Biology and Bioreactor Operations.

Responsibilities:

• Collaborate with a dynamic team of manufacturing associates and engineers to carry out upstream production batches.
• Conduct cell culture and manage bioreactor...

The Manufacturing Associate collaborates directly with the team coordinator and department manager to produce quality processes that meets or exceeds IPC standards. This position is key to company quality standards.

Vanguard EMS, Inc. is in the service business. Even with Vanguard's state of the art technology, vast manufacturing capability, and leading-edge information tools, we wake up every day thinking about how best to serve our customers, suppliers, and the communities in which we live.

What you’ll do:

• Prepare circuit boards for the coating process
• Manually apply conformal coating to circuit boards with an HVLP spray gun.
• Apply adhesives to circuit boards
• Able to work with chemicals
• Inspect and quality check work to ensure that products meet all customer and regulatory requirements
• Communicate quality issues to the appropriate team and manager as...

Summary:
At BioPharma Consulting JAD Group, we are seeking a motivated MCS Manufacturing Sr. Associate to join our Team. As a Senior Associate, you will be supporting New Product Introduction (NPI) initiatives within the clinical and commercial manufacturing facility. If you have a strong background in project management, change control, and continuous improvement, and are dedicated to delivering operational excellence with a focus on quality, safety, and compliance, then this role is for you!

Responsibilities:

• Manage Change Control processes, ensuring comprehensive and compliant records in accordance with GMP regulations.
• Lead diverse projects with strong project management skills, ensuring timely closure of change control records.
• Act as the primary contact for incoming Technology Transfers and New Product Introductions into Building 20 Manufacturing.
• Using project management tools and...

The Manufacturing Associate collaborates directly with the team coordinator and department manager to produce quality processes that meets or exceeds IPC standards. This position is key to company quality standards.

Vanguard EMS, Inc. is in the service business. Even with Vanguard's state of the art technology, vast manufacturing capability, and leading-edge information tools, we wake up every day thinking about how best to serve our customers, suppliers, and the communities in which we live.

What you’ll do:

• Prepare circuit boards for the coating process
• Manually apply conformal coating to circuit boards with an HVLP spray gun.
• Apply adhesives to circuit boards
• Able to work with chemicals
• Inspect and quality check work to ensure that products meet all customer and regulatory requirements
• Communicate quality issues to the appropriate team and manager as...

Summary:
As a Senior Associate Manufacturing, you will be part of the New Product Introduction Team at Thousand Oaks, supporting clinical and commercial manufacturing operations. This role encompasses program and project management, change control ownership, and continuous improvement initiatives. You will work cross-functionally to ensure timely delivery of new products and operational excellence, with a focus on quality, safety, and compliance.

Responsibilities:

• Change Control and Project Management:
• Own and manage change controls for new product introductions (NPI).
• Ensure records are comprehensive and compliant per GMP regulatory procedures with a Right the First-Time approach.
• Lead projects of diverse subjects and complexity, ensuring timely closure of change control records.
• Represent Manufacturing as the receiving site for incoming Technology Transfers/New...

Description: As a Manufacturing Associate at Amgen's Thousand Oaks Site, you will play a crucial role in supporting development, clinical, and launch activities within a dynamic production environment. Operating under general supervision, you will execute various manufacturing operations according to Standard Operating Procedures (SOPs), ensuring strict adherence to safety and compliance standards. The ideal candidate will demonstrate the ability to troubleshoot, maintain cleanliness, and contribute to continuous improvement initiatives.

Functions:

• Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment

• Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
• Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
• Performing and monitoring critical processes with the ability to...