Manufacturing Specialist

Downstream Manufacturing Associate or Scientist

Downstream Processing Manufacturing Associate or Scientist to oversee the purification of 50L to 2000L volumes for engineering, clinical, and commercial batches in a cGMP environment. This role requires advanced technical expertise in downstream processes, including AKTA purification skids (or similar), tangential flow filtration (TFF), and comprehensive knowledge of batch records, protocols, investigations, and technical documentation.

Essential Duties & Responsibilities

• Conduct downstream purification processes at various scales (50L to 2000L) within a cGMP environment, including tasks such as column packing, troubleshooting, and data analysis.
• Lead the development and execution of downstream purification processes, providing technical guidance.
• Use software systems to gather, monitor, and assess operational data, making real-time adjustments to...

The Manufacturing Associate Scientist plays a key role in supporting the development, enhancement, and commercialization of new and existing products as well as assisting in the implementation of ISO 9001/17034 and other relevant standards or regulatory requirements. They support analytical and product development efforts by assisting in the execution of new products and testing services, which includes communication with clients and key stakeholders to ensure alignment and successful outcomes. This position performs laboratory experiments under the guidance of senior staff, including drafting and executing protocols, analyzing results, and identifying potential issues. They recommend and implement solutions, contribute to the development of innovative techniques, and collaborate with cross-functional teams to ensure project goals are met.
Responsibilities:

• Supports all activities associated with the development, enhancement, and execution of new...

The Manufacturing Quality Specialist is responsible for ensuring compliance with cGMP regulations, company policies, and customer expectations by supporting manufacturing operations through documentation review, quality event management, and process oversight. This role requires expertise in upstream and downstream biologics processes, quality systems, and regulatory requirements to ensure the highest standards of product quality and compliance.

Location: Piscataway, New Jersey

Shift: Mon-Fri, 9-5

Salary: $90,000 -$100,000 experience depending

Responsibilities:

• Perform inspection, sampling, and testing (where applicable) on incoming materials, packaging components, and returned goods following detailed written procedures.
• Ensure smooth flow of raw material and critical material testing through routine follow-up with internal and external laboratories.
• Perform...

The Manufacturing Quality Specialist is responsible for ensuring compliance with cGMP regulations, company policies, and customer expectations by supporting manufacturing operations through documentation review, quality event management, and process oversight. This role requires expertise in upstream and downstream biologics processes, quality systems, and regulatory requirements to ensure the highest standards of product quality and compliance.

Location: Piscataway, New Jersey

Shift: Mon-Fri, 9-5

Salary: $90,000 -$100,000 experience depending

Responsibilities:

• Perform inspection, sampling, and testing (where applicable) on incoming materials, packaging components, and returned goods following detailed written procedures.
• Ensure smooth flow of raw material and critical material testing through routine follow-up with internal and external laboratories.
• Perform...

The Manufacturing Quality Specialist is responsible for ensuring compliance with cGMP regulations, company policies, and customer expectations by supporting manufacturing operations through documentation review, quality event management, and process oversight. This role requires expertise in upstream and downstream biologics processes, quality systems, and regulatory requirements to ensure the highest standards of product quality and compliance.

Responsibilities:

• Perform inspection, sampling, and testing (where applicable) on incoming materials, packaging components, and returned goods following detailed written procedures.
• Ensure smooth flow of raw material and critical material testing through routine follow-up with internal and external laboratories.
• Perform cleaning and sanitization of ISO 7 areas and ISO 5 laminar flow hoods per written procedures.
• Assign and verify expiry dates and retest dates for all GMP raw...

Downstream Manufacturing Associate or Scientist

Downstream Processing Manufacturing Associate or Scientist to oversee the purification of 50L to 2000L volumes for engineering, clinical, and commercial batches in a cGMP environment. This role requires advanced technical expertise in downstream processes, including AKTA purification skids (or similar), tangential flow filtration (TFF), and comprehensive knowledge of batch records, protocols, investigations, and technical documentation.

Essential Duties & Responsibilities

• Conduct downstream purification processes at various scales (50L to 2000L) within a cGMP environment, including tasks such as column packing, troubleshooting, and data analysis.
• Lead the development and execution of downstream purification processes, providing technical guidance.
• Use software systems to gather, monitor, and assess operational data, making real-time adjustments to...

About TurnOnGreen Inc.:

TurnOnGreen Inc. and its subsidiary TOG Technologies, Inc. (also known as Digital Power Corporation) designs and manufactures innovative, feature-rich, and top-quality power products for mission-critical, lifesaving and sustaining applications spanning multiple sectors in the harshest environments. The diverse markets we serve include defense and aerospace, medical and healthcare, industrial, telecommunications and e-Mobility. With decades of experience, TurnOnGreen collaborates with clients to develop leading-edge products tailored to a wide range of needs. Our headquarters are located in Milpitas, CA; www.TurnOnGreen.com.

Position Summary:

We are seeking an experienced Procurement Specialist with extensive expertise in sourcing electronic components and materials. The ideal candidate will manage the procurement process, ensuring timely and cost-effective acquisition of high-quality parts essential...

At Tata Consumer Products Ltd, we stand #Forbetter – Planet, Sourcing, Nutrition, Communities. And #ForBetter Opportunities …. Here’s an exciting one!

Quality Assurance Specialist | Landover, MD | On-Site | Non-Exempt FTE

How does this Job align to our Strategy?

We are seeking a driven and talented individual to play a critical role in leading compliance and continuous improvement projects within the Quality function. This individual will directly be responsible for assuring and enabling the compliance and continuous improvement of all product materials, manufacturing processes and finished products including the supporting systems and processes and the operating environment. The person will be responsible to identify opportunities and lead improvement efforts working cross-functionally with Production, Maintenance, New Product Development, and Supply Chain teams with support from Quality Supervisor.

This...

Manufacturing QMS Specialist who will be responsible for writing and reviewing deviations, change controls, investigation reports, batch records, SOPs, CAPA etc. This position requires technical expertise in upstream and downstream process of biologics (Cytokines, monoclonal antibodies manufacturing).

Responsibilities:

• Responsible to support manufacturing team with all kinds of documentation.
• Documentation includes reviewing executed batch records (both Upstream department and Downstream batch record).
• Responsible for filing change controls, deviation, CAPA for manufacturing department.
• For all critical / major investigation, will have to use investigation tools like 5why or 6M method.
• Attend daily meetings with both upstream and downstream process to get all the documentation requirement for the day.
• Meet weekly with QA to avoid any delay in the QMS closure.
• Author batch records, SOPs and...

NOTICE: This is a remote role when not traveling in the field.

About Maneva
Maneva, a startup founded by an ex-Google Deepmind researcher, is an AI service provider revolutionizing manufacturing operations with cutting-edge AI solutions for autonomous factory operation and optimization. Our solution generates AI-powered actions and insights using off-the-shelf hardware or existing vision systems for real-impact manufacturing problems in products and equipment inspection, production efficiency, safety, and more.

Position Overview

The Continuous Improvement Specialist - Manufacturing role is designed to a leading role in supporting the founding and scaling of early customer acquisition in the local region.

We are seeking a dynamic and results-driven professional with extensive experience in the manufacturing sector. The ideal candidate will have experience engaging...