Column Chromatography jobs

Specialist, Operations (Night Shift)

MSD · Posted Nov 9, 2026

Open

Durham, North Carolina, United States
On-site
$79K–$125K per year
5+ years

Specialist, Operations (Night Shift)

MSD · Posted Nov 9, 2026

Open

Durham, North Carolina, United States
On-site
$79K–$125K per year
5+ years

Specialist, Operations (Night Shift)

Merck · Posted Nov 9, 2026

Open

Durham, North Carolina, United States
On-site
Full-time · Mid
$79K–$125K per year
1+ years

Apply with RefersoAI Apply on careers page

An energetic individual responsible for supporting shop floor execution, batch closeout, and general troubleshooting.

Compensation

$79,200.00 - $124,700.00

Responsibilities

Partnering with the Operations management team to create and execute strategies that support design, development, delivery and evaluation of projects related to steady-state production and/or continual process improvement.
Authoring and reviewing documents and SOPs
Batch Record Review
eLog Review
Lead safety investigations

Requirements

High School Diploma
Bachelor’s degree in a technical field
Nice to have: Understanding of MPS methodologies
Nice to have: Experience with shop-floor cGMP manufacturing and related systems (i.e. SAP)
Nice to have: Familiarity with pharmaceutical regulatory requirements

Skills

Adaptability Batch Record Review CAPA Management cGMP Compliance Column Chromatography

Specialist, Operations (Project Management)

MSD · Posted Nov 9, 2026

Open

Durham, North Carolina, United States
Full-time · Associate
$79K–$125K per year
2+ years

Apply with RefersoAI Apply on careers page

The role supports the Durham manufacturing site by coordinating project activities, maintaining accurate project information, supporting change controls and incident writing, and helping teams complete actions to support PAI and filing.

Compensation

$79,200 - $124,700

Responsibilities

Support Pre-Approval Inspection (PAI) and filing-readiness plans by tracking deliverables, owners, due dates, dependencies, and open actions
Update readiness trackers and dashboards so milestones, risks, gaps, and recovery actions are visible and current
Coordinate meetings, prepare materials, document decisions, and follow up with owners on assigned actions
Help organize inspection evidence, procedures, training records, and filing-related documents for review by subject matter experts
Maintain project and portfolio records, including project status, priorities, milestones, risks, resource needs, and dependencies

Requirements

Bachelor's degree in Engineering
Science
Business
Project Management
Nice to have: pharmaceutical

Skills

Adaptability cGMP Compliance Coaching

Research Associate - Synthetic Chemistry

Centrillion Technologies, Inc. · Posted Nov 9, 2026

Open

Palo Alto, California, United States
On-site
Full-time · Associate
$50K–$75K per year
3+ years

Apply with RefersoAI Apply on careers page

Centrillion Technologies is seeking a highly motivated and skilled Research Associate - Synthetic Chemistry to join their chemistry team to design and synthesize complex organic molecules.

Compensation

The expected salary range for this position is between $50,000 to $75,000. Actual pay may be more or less than the posted range.

Responsibilities

Design of multi-step syntheses of intermediates, building blocks and final products.
The use of solid-phase and solution chemistry techniques
The thorough purification of the compounds and characterization of synthetic products.
Execution of new synthetic routes
Troubleshooting problematic routes

Requirements

BS in Organic Chemistry
MS in Organic Chemistry

Skills

organic chemistry synthesis purification characterization NMR infrared spectrometry mass spectrometry

3rd Shift Supervisor, cGMP Biomanufacturing Downstream

The Fountain Group LLC · Posted Nov 2, 2026

Open

Madison, Wisconsin, United States
Contract · Senior
$45–$53 per hour
3–10 years

Apply with RefersoAI Apply on careers page

Senior Supervisor overseeing downstream biologics manufacturing in a clinical and commercial cGMP environment.

Compensation

Pay: $45-53/hr.

Responsibilities

Supervise and lead a team of 5–15 employees overseeing downstream biologics manufacturing in a clinical and commercial cGMP environment.
Oversee execution of downstream manufacturing processes, including column chromatography, normal flow filtration, tangential flow filtration (TFF), viral reduction/filtration, and bulk drug substance filling.
Provide hands‑on floor support to ensure manufacturing activities are performed in compliance with SOPs, GMP guidelines, and safety standards.
Manage shift activities, production schedules, batch readiness, and manufacturing deliverables while coordinating with other shift Supervisors.
Coach, train, and develop employees while promoting a culture of accountability, continuous improvement, and right‑first‑time execution.

Requirements

PhD in a scientific, engineering, or biomanufacturing discipline
Master's in a scientific, engineering, or biomanufacturing discipline
Bachelor's in a scientific, engineering, or biomanufacturing discipline
Associate's in a scientific, engineering, or biomanufacturing discipline
High School Diploma in a scientific, engineering, or biomanufacturing discipline

Core Technician I

Tailored Management · Posted Nov 4, 2026

Open

Houston, Texas, United States
Contract · Entry
$25–$25 per hour

Apply with RefersoAI Apply on careers page

Support GMP production of viral products and mammalian cell culture.

Compensation

$25.00/hr. W2 + Weekly Pay & Benefits

Responsibilities

Support GMP production of viral products and mammalian cell culture.
Perform cell culture, column chromatography, and aseptic processing.
Prepare buffers and operate steam autoclaves.
Assist with product filling, cell banking, and cleanroom setup.
Maintain batch records, SOPs, and other manufacturing documentation.

Requirements

Associate or Bachelor's degree required.
Nice to have: Aseptic technique and cell culture experience preferred.

Skills

cell culture column chromatography aseptic processing steam autoclaves product filling cell banking cleanroom setup

Manufacturing Technician II

VetJobs · Posted Nov 5, 2026

Open

Waco, Texas, United States
On-site
$21–$38
2+ years

Apply with RefersoAI Apply on careers page

Perform cGMP manufacturing operations in a biologics production facility, including setup, calibration, rework, quality testing, and process development.

Compensation

$ 21 - 37.8 USD

Responsibilities

Shipping finished materials
Maintaining inventory levels
Sampling of in process and raw materials
Running glass washer / autoclave
Buffer / media preparation

Requirements

Associates degree in science
BS in science
BS in Engineering

Skills

LIMS SAP automated control systems CIP SIP glass washer autoclave cell culture column chromatography

Manufacturing Associate II

Catalent Pharma Solutions · Posted Nov 4, 2026

Open

Harmans, Maryland, United States
On-site
Full-time · Associate
$34–$38 per hour
1+ years

Apply with RefersoAI Apply on careers page

Support GMP upstream or downstream manufacturing processes for bulk biologics from microbial and cell culture systems.

Compensation

The anticipated hourly rate for this position in MD is $33.65 – $38.46 Plus Bonus.

Responsibilities

Complete Batch Production Records under current Good Manufacturing Practices and document processes using Standard Operating Procedures and Batch Production Records
Generate operational protocols and internal or external documents including Standard Operating Procedures, Batch Production Records, deviations, and summary reports
Collaborate with Process Development and Manufacturing Sciences and Technology teams to transfer new projects into GMP
Generate and revise internal and external documents such as Standard Operating Procedures and Batch Records
Support initiation and closure of deviations; may lead departmental investigations and close deviations and Corrective and Preventive Actions

Requirements

High School diploma or General Education Diploma
Associate’s degree in a Scientific, Engineering, or Biotech field
Bachelor’s degree in a Scientific, Engineering, or Biotech field

Skills

GMP compliance Batch Production Records

Process and Synthetic Chemist, Mining & Metals

Ohr · Posted Nov 3, 2026

Open

Boulder, Colorado, United States +1 more
On-site
Full-time · Senior
$125K–$180K per year
3–8 years

Apply with RefersoAI Apply on careers page

As a Process and Synthetic Chemist in Ohr's mining and metals vertical, you will design and build mineral processing, hydrometallurgical refining, and metal finishing molecules.

Locations (2)

Boulder, Colorado, United States
Lafayette, Colorado, United States

Compensation

The annual base salary range for this position is $125,000 – $180,000, commensurate with experience, plus equity.

Responsibilities

Run synthesis campaigns that carry the portfolio through its decision year, sized to deliver 100 g of characterized material, across heterocyclic, aromatic, chelating-ligand, and phenolic condensation chemistry.
Select routes on delivered cost per kilogram based on step count, step type, yield, and reagent choice.
Own the hazard case for routes, including reaction calorimetry, thermal characterization, quench design, and handling of hazardous reagents.
Propose and triage new candidates on Ohr's platform chemistries.
Judge which duties the binding chemistry can reach (gallium, zinc, alumina, manganese, magnesium, nickel, cobalt).

Manufacturing Technician II

Mindlance · Posted Nov 3, 2026

Open

North Chicago, Illinois, United States
3–5 years

Apply with RefersoAI Apply on careers page

Manufacturing Technician II responsible for maintaining fibroblast cell cultures and supporting production processes in a biologics facility.

Responsibilities

Maintain human fibroblast cell culture in a clean room environment
Assist in the manufacture of solutions used in production and processing of raw materials
Sample by-products using standard methodologies
Complete all relevant documentation compliant with cGMP and GDP guidelines
Maintain the cell culture complex and surrounding environment

Requirements

Bachelor’s degree preferably in a Natural Science, Cell Biology, Biology, Biochemistry, Chemical Engineering or a related field
Associate degree from an accredited two-year program with relevant work experience will be considered
Nice to have: experience working with mammalian cell cultures in a cleanroom environment
Nice to have: strong understanding of biology, including animal organisms, their tissues, cells and cell-cell interactions and function
Nice to have: intermediate problem-solving attitude

Skills

cGMP manufacturing operations GDP guidelines LIMS