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Downstream Manufacturing Lead Jobs (NOW HIRING)

CIRCOR Aerospace

Manufacturing Supervisor

Corona, CA · On-site

$100 - $125/hr

This role directly supervises one Manufacturing Lead and a team of production employees while ... Interface with upstream and downstream operations to address manufacturing issues affecting ...

Woodhaven Furniture

Hardwood Mill Manager

Cairo, GA · On-site

What You'll Own As the Hardwood Mill Manager, you'll lead all aspects of the Hardwood Mill, ensuring rough lumber is transformed into precision components that support downstream manufacturing ...

Woodhaven Furniture

Hardwood Mill Manager

Cairo, GA · On-site

What You'll Own As the Hardwood Mill Manager, you'll lead all aspects of the Hardwood Mill, ensuring rough lumber is transformed into precision components that support downstream manufacturing ...

Ichor Systems

Manufacturing Supervisor

Fremont, CA · On-site

$99K - $169K/yr

Oversee saw operations to ensure materials are processed and delivered on schedule to downstream ... Lead continuous improvement projects focused on safety, quality, throughput, and cost reduction.

Woodhaven Furniture

Hardwood Mill Manager

Cairo, GA · On-site

What You'll OwnAs the Hardwood Mill Manager, you'll lead all aspects of the Hardwood Mill, ensuring rough lumber is transformed into precision components that support downstream manufacturing ...

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Downstream Manufacturing Lead information

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How much do downstream manufacturing lead jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for downstream manufacturing lead in the United States is $26.85, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $29.81 per hour, depending on experience, location, and employer.

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Infographic showing various Downstream Manufacturing Lead job openings in the United States as of September 2026, with employment types broken down into 88% Full Time, 10% Part Time, and 2% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $55,858 per year, or $26.9 per hour.

Manufacturing Associate

West Chester, PA • On-site

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Integrated Resources INCexternal

Full-time

Re-posted 7 days ago

Job description

Company Description

IRI believes in commitment, Integrity and strategic workforce solutions.



Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.

Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success

Job Description

The Manufacturing Associate will contribute to the Downstream Manufacturing group within the brand new state-of-the art biologics manufacturing facility.

We are seeking a highly self-motivated person willing to contribute to the development, qualification, and eventual operation and overall success of downstream operations.

This includes but is not limited to column packing, column chromatography and tangential flow filtration (TFF) and aseptic filling operations for proprietary and biosimilar biologics pipeline.

Assist in developing procedures (SOP's & Master Batch Records) for the Manufacturing Downstream group.

Complete assigned tasks associated with Purification operations and assist in execution of operations such as column chromatography, TFF, CIP, column packing.

Ability to work independently to develop and write documentation associated with Purification.

Assist in troubleshooting equipment or process issues.

Initiate and complete deviations, change controls, investigations, as assigned using TrackWise or any similar software system.

Compliance to safety guidelines and current Good Manufacturing Practices (cGMP).

Ability to train other associates and willing to be involved in cross-training in other groups, as required.

Follow standard operating procedures.

Ability to lead the purification operations.

Assist in Factory Acceptance Test (FAT), Site Acceptance Test (SAT) and other validation needs such as IOQ and PQ.

Ability to multi-task and work well with the team.

Completes all training documentation within a defined time-frame.

Analyze in process samples generated from purification activities by using pH/conductivity meters, scales, spectrophotometers etc.

Performs review of the manufacturing documentation of the associated area.

Other duties as assigned.

Practice a continuous improvement mindset by making suggestions on process improvements.

Qualifications

At minimum, an Assoc. degree in biology, chemistry or a related scientific or technical area.

2 to 4 years of experience within cGMP manufacturing.

Ability to work in fast paced, dynamic environment.

3-5 years hands on experience with Purification equipment such as columns, TFF, filling.

Experience with buffer solution preparations within a cGMP environment.

Experience with TrackWise for performing change controls, deviations.

Strong background in aseptic technique and microbial controls.

Experience with process development, tech transfer and optimization a plus.

Strong understanding of cGMP's as applicable to biologic operations.

Good analytical skills to interpret and understand purification equipment and data.

Excellent oral and written communication skills.

Ability to stand, walk, bend and reach for long periods of time.

Ability to work flexible working hours.

Effectively manages time and must pay attention to detail.

Ability to lift and push up to 30 pounds or more.

Must be able to read, interpret, and follow SOP's, batch documents and other procedures.

Additional Information

Christie Mathew 

christie @irionline.com

7328448739

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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