Jobs in the United States

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Added 6 mins ago
ER Registered Nurse RN Highlands Ranch PRN Nights
AdventHealth
Highlands Ranch, CO
…achieve positive outcomes. Ensure compliance with infection control protocols, safety standards, and regulatory requirements to maintain a safe healthcare environment. Provide emotional…
Added 6 mins ago
RN Registered Nurse Regional Float Pool ED PRN Nights
AdventHealth
Greenwood Village, CO
…achieve positive outcomes. * Ensure compliance with infection control protocols, safety standards, and regulatory requirements to maintain a safe healthcare…
Added 6 mins ago
RN Registered Nurse Regional Float Pool LDRP PRN Nights
AdventHealth
Greenwood Village, CO
Ensure compliance with infection control protocols, safety standards, and regulatory requirements to maintain a safe healthcare environment.
Added 28 mins ago
Clinical Laboratory Technician - Hematology
Labcorp
Birmingham, AL
Perform and document preventative maintenance and quality control procedures
Added 28 mins ago
Diagnostic Radiologic Technologist - Computerized Tomography
Veterans Affairs, Veterans Health Administration
Montgomery, AL
Added 33 mins ago
UO
Senior Assistant Director of Slate
University of Colorado Denver
Boulder, CO
- $82,000 to $83,000 USD / year
…Senior Assistant Director of Slate! This position reports to the Associate Director of Systems and Technology and maintains the undergraduate instance of the Technolutions Slate system for…
Added 33 mins ago
UO
Director of Primary Care Faculty Practice
University of Colorado Denver
Aurora, CO
- $103,750 to $115,278 USD / year
This position reports to the Associate Dean for Clinical and Community Affairs and includes a balanced workload of 1.0 FTE, comprised of:
Added 33 mins ago
UO
Open Rank Assistant/Associate Professor Neuroscience
University of Colorado Denver
Aurora, CO
- $120,000 to $145,000 USD / year
Job Title: Open Rank Assistant/Associate Professor Neuroscience
Added 1 hour ago
Office Assistant
Management Business Solutions
Grand Rapids, MI
…and compile data for reports and documentation. - Establish document control procedures for proper handling, storage, and retention of records in accordance with applicable laws. - Provide…
Added 2 hours ago
Histopathology Technician (Advanced)
Veterans Affairs, Veterans Health Administration
Charleston, SC
Added 2 hours ago
Quality Technician (Temporary) (2)
AMBAC International
Elgin, SC
Document and analyze quality data, reporting findings to relevant personnel.
Added 2 hours ago
Senior Risk Manager - AI Risk & Governance
Edward Jones
Saint Louis, MO
The Senior Risk and Control Associate - AI Risk & Governance will effectively control the risks associated with business activities via the execution of firm's Enterprise Risk Management…
Added 2 hours ago
GA
Sr Staff Applications Operations Engineer - Engineering Tools Automation & AI Ops
GE Aerospace
Saint Louis, MO
- $131,000 to $174,000 USD / year
+ Partner with cybersecurity and compliance teams to meet security, export control, and regulatory requirements (e.g., CMMC / NIST SP 800-171).
Added 2 hours ago
GA
Sr Staff Applications Operations Engineer - Engineering Tools Automation & AI Ops
GE Aerospace
Kansas City, MO
- $131,000 to $174,000 USD / year
+ Partner with cybersecurity and compliance teams to meet security, export control, and regulatory requirements (e.g., CMMC / NIST SP 800-171).
Added 3 hours ago
PT
Inspector
PDS Tech Commercial
Kinston, NC
- $42.85 USD / hour
Identify, document, and process non-conforming materials, parts, and assemblies according to established procedures.
Added 3 hours ago
CAD Manager
OHIO TRANSMISSION CORPORATION
Fairfield, OH
…- Manage the SOLIDWORKS PDM (Vault) environment, including document control, revision management, engineering change processes, workflow administration, and data governance. - Review and…
Added 3 hours ago
RI
Quality Inspector-2nd shift
REXNORD INDUSTRIES LLC
Cleveland, OH
- $20 to $30 USD / hour
…inspection layouts. - Create and maintain inspection plans, control plans, and related quality documentation. - Document inspection results and maintain accurate quality records. -…
Added 3 hours ago
AH
CT Scan Technologist - Per Diem
Atria Health and Research Institute
NY · New York, NY
- $80 to $82 USD / hour
Document all procedures and patient interactions accurately in the medical record.
Added 3 hours ago
Per-diem CT Technologist
Atria Health and Research Institute
Palm Beach, FL
Document all procedures and patient interactions accurately in the medical record.
Added 4 hours ago
Clinical Care Nurse (RN)
CenterWell
Grand Prairie, TX
Document all outreach efforts, clinical interactions, and outcomes accurately and in compliance with organizational and CMS regulatory standards.
Added 4 hours ago
Clinical Care Nurse (RN)
CenterWell
Richardson, TX
Document all outreach efforts, clinical interactions, and outcomes accurately and in compliance with organizational and CMS regulatory standards.
Added 4 hours ago
MA
Administrative Coordinator -Radiation Therapeutic Administration
MD Anderson Cancer Center
Houston, TX
- $25.48 to $37.98 USD / hour
The ideal candidate will possess an Associate's degree or Bachelor's degree and administrative experience in a healthcare, business, or related environment. Successful candidates…
Added 4 hours ago
Clinical Histology Technician- Day Shift
MD Anderson Cancer Center
Houston, TX
…blocks and slides, and use laboratory information systems to document workflows and track specimens. Your work will help maintain specimen integrity and support the teams responsible for…
Added 4 hours ago
Clinical Histology Technician- Night Shift
MD Anderson Cancer Center
Houston, TX
…blocks and slides, and use laboratory information systems to document workflows and track specimens. Your work will help maintain specimen integrity and support the teams responsible for…
Added 4 hours ago
Quality Control Inspector
The Dixon Group
Houston, TX
The Dixon Group is looking for a Quality Control Inspector to join our team! In this role, you will perform in-process and final inspections of machined metal components using precision…

Actalent

Purification Technician III Day Shift

Morrisville, NC, United States

$38 to $43 USD / hour

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Job details

Pay: $38 to $43 USD / hour
Posting language: English
Posted: Nov 2, 2026

Original job description

Job Title: Purification Technician III Day ShiftJob DescriptionThe Purification Technician III Day Shift supports downstream biologics manufacturing operations in a cGMP-regulated environment. This role focuses on purification processes, including chromatography and filtration, and requires hands-on operation of manufacturing equipment, execution of batch activities, and meticulous GMP documentation. The technician ensures safe, compliant, and efficient commercial production while collaborating with cross-functional teams and contributing to continuous improvement initiatives.Responsibilities

Execute purification manufacturing operations in accordance with current Good Manufacturing Practices (cGMP), standard operating procedures, and batch record requirements.
Perform downstream processing activities such as chromatography, filtration, buffer preparation, equipment setup, and process monitoring.
Conduct in-process sampling and testing, including pH and conductivity measurements and visual inspections, to ensure process control and product quality.
Execute validation protocols following approved procedures and GMP requirements to support qualified and compliant manufacturing processes.
Utilize manufacturing systems and process control platforms, including Distributed Control Systems (DCS) and Manufacturing Execution Systems (MES), to manage production activities.
Perform takeouts, identity checks, material transactions, and production-related entries within electronic manufacturing systems.
Execute cleaning and sanitization activities, including Clean-in-Place (CIP) and Steam-in-Place (SIP) processes, to maintain equipment and facility readiness.
Maintain accurate, complete, and timely GMP documentation for all manufacturing operations and related activities.
Support manufacturing investigations and deviation management by identifying issues, documenting observations, and contributing to root cause analysis and corrective actions.
Participate in continuous improvement initiatives aimed at enhancing safety, quality, and operational efficiency within the manufacturing area.
Collaborate with cross-functional teams to ensure safe, compliant, and efficient production operations and effective communication across functions.
Participate in shift turnover activities, clearly communicating process status, issues, and priorities to incoming teams.
Identify and document deviations and initiate maintenance work orders when necessary to address equipment or process concerns.
Support production schedules and meet operational timelines in a fast-paced biologics manufacturing environment.
Perform other duties as assigned to support overall manufacturing objectives.

Essential Skills

Strong written and verbal communication skills to document activities and interact effectively with team members.
Knowledge of cGMP regulations and safety requirements applicable to biopharmaceutical manufacturing operations.
Ability to work effectively in a team environment and collaborate with cross-functional groups.
Strong time management skills and attention to detail to execute complex manufacturing processes accurately.
Ability to identify and document deviations and initiate maintenance work orders when necessary.
Ability to exercise sound judgment, work independently, and solve problems in a manufacturing environment.
Ability to support production schedules in a fast-paced biologics manufacturing facility.
Hands-on experience with purification, chromatography, and filtration processes in a manufacturing setting.
Comfort using manufacturing systems and process control platforms such as DCS and MES.
Capability to perform cleaning and sanitization activities, including CIP and SIP processes.

Additional Skills & Qualifications

High School Diploma or GED with 4+ years of experience in a cGMP manufacturing environment; OR Associate degree in Life Sciences, Engineering, or a related technical discipline with 2+ years of cGMP manufacturing experience; OR Bachelors degree in Life Sciences, Engineering, or a related technical discipline; OR equivalent military training or experience.
Experience supporting purification, chromatography, filtration, recovery, or other downstream manufacturing operations.
Experience working within a GMP-regulated biologics, biotechnology, or pharmaceutical manufacturing environment.
Familiarity with automated manufacturing control systems and electronic batch records.
Experience operating AKTA systems, chromatography skids, tangential flow filtration (TFF) systems, depth filtration equipment, or other downstream processing equipment.
BioWork certification.
Ability to stand for extended periods while performing manufacturing tasks.
Ability to perform repetitive tasks using hands, wrists, and fingers for equipment operation and documentation.
Ability to bend, push, pull, reach, and lift materials up to 33 pounds as part of routine manufacturing activities.
Ability to ascend and descend ladders and access manufacturing equipment safely.
Ability to work in manufacturing environments requiring personal protective equipment, including respiratory protection when necessary.
Ability to work in temperature-variable manufacturing environments.

Work EnvironmentThis position is based in an onsite biologics manufacturing facility operating under cGMP regulations. The role is assigned to the day shift on a 2-2-3 rotation schedule, supporting commercial downstream purification operations. The environment includes regular use of purification equipment such as chromatography systems, filtration units, and automated manufacturing control platforms including DCS and MES. Work is performed in production areas that may have variable temperatures and require the use of personal protective equipment, including respiratory protection when needed. The role involves standing for extended periods, performing repetitive manual tasks, lifting materials up to 33 pounds, and accessing equipment via ladders. The facility emphasizes safety, quality, and teamwork, with structured shift turnover practices and a focus on continuous improvement to maintain efficient and compliant operations. Job Type & LocationThis is a Contract position based out of Morrisville, NC. Pay and BenefitsThe pay range for this position is $38.00 - $43.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of Morrisville, NC. Application DeadlineThis position is anticipated to close on Nov 16, 2026. Workplace TypeThis is a fully onsite position in Morrisville,NC.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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More about this job

Skills

Good manufacturing practices
Inspection
Control engineering
Manufacturing processes
Control systems
DCS
MES
Control production
Cleaning
Sanitation
SIP
Maintain equipment
Documentation
Root cause analysis
Process improvement
Communication skills
Time management
Attention to detail
Work independently
Military drill
Biotechnology
Pharmaceutical processes
Personal protective equipment
Teamwork

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