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ES
Warehouse Order Picker - $19.50/hr
E.A. Sween Company
Lewisville, TX
- $19.5 USD / hour
$19.50/HR | 4-DAY WORKWEEK | DAY SHIFT | OVERTIME AVAILABLE · Day shift only — no overnight shifts
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Production Assembler
NEW LEADER MANUFACTURING
Cedar Rapids, IA
The Production Assembler position proficiently produces product by assembling parts in one (1) of the following work areas including multipliers or bottoms.
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Application Developer Intern - Summer 2027
Hunt
Dallas, TX
…work with experienced developers, get hands-on exposure to production systems, and build skills in modern, AI-enabled software…
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Purchasing Manager
at Marriott
Detroit, MI
Communicates with kitchen, restaurant management and vendors to ensure timing of deliveries satisfies advanced food production needs.
Added 1 min ago
Assistant Plant Manager - Evening Shift
PACCAR
Louisville, KY
…components, subassemblies, and specialized services. Dynacraft has production facilities in Louisville, KY and McKinney,…
Added 1 min ago
Fleet Mechanic
Acme Barricades
MIdway, FL
Must have own tools · Must have electrical and welding experience
Added 1 min ago
BM
Machine Operator
Burton Mill Solutions
Hampden, ME
- $19 to $21 USD / hour
…industry. You will play a key role in meeting customer demands and production targets by ensuring high-quality, precision-ground…
Added 1 min ago
SD
Assembler – Light Production – First Shift – $17.00/hr
Seko Dosing Systems Corporation
Tullytown, PA
- $17 USD / hour
SEKO Dosing Systems Corp. is hiring full-time Assemblers for our production team in Tullytown, PA. Entry-level candidates are encouraged to apply - paid training is provided. This is a…
Added 1 min ago
ZA
Lean Practitioner - AMT
Zenix Aerospace Inc
Arlington, WA
- $104,000 to $129,000 USD / year
…manufacture high quality complex parts through cost effective…
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Robotics and Automation Engineer
GE Gas Turbines (Greenville) L.L.C.
United States
…them to life in GE Vernova factories. Your work helps make production safer, faster, and more…
Added 1 min ago
Lead Industrialization Engineer – Process Qualifications & Industrialization
GE Gas Turbines (Greenville) L.L.C.
United States
…right tools, documentation, and processes in place to meet our production goals safely and efficiently. From participating in early process development reviews to overseeing the successful…
Added 1 min ago
General Assembler - 2nd Shift
GE Renewables Grid LLC
United States
Discusses errors in diagrams or production order with supervisor or engineer to clarify assembly problems.
Added 1 min ago
GN
Flexible FCO Operator
Global Nuclear Fuel-Americas, LLC
United States
- $32.31 to $35.3 USD / hour
Analyze and interpret UT and EC charts for flaw characterization and process control.
Added 2 mins ago
Construction Project Executive
ESI Electrical Contractors
Haskell, TX
Valid driver’s license required
Added 2 mins ago
Senior Manager Planning
Leonardo DRS, Inc.
Menomonee Falls, WI
The Leonardo DRS Naval Power Systems business is a trusted provider of innovative naval gas and hybrid power systems, control technology and support solutions for the U.S. Navy and navies…
Added 3 mins ago
T
Business Analyst Consultant
TEKsystems
Tacoma, WA
- $68 to $77 USD / hour
Apply governed application lifecycle management practices, including managed solutions, source control where applicable, environment strategy, deployment pipelines, release planning,…
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Data Engineer II
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Hanover, MD
- $78,400 to $117,600 USD / year
Builds all data management/analytics solutions following applicable Info-sec, quality control, and governance/maintenance standard
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P
Production Supervisor
PeopleReady
Fresno, CA
- $31 USD / hour
Must have excellent communication skills and an aptitude for detailed work requiring high accuracy · Must have good PC skills, including Microsoft office software knowledge
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APPAREL/CLERK
The Kroger Co.
Fairbanks, AK
Maintain workload to guarantee that production deadlines are met.
Added 4 mins ago
AT
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Los Angeles, CA
- $240,000 to $300,000 USD / year
…Design Engineers on each Vehicle Director’s team - and with production to take spacecraft hardware from concept through qualification, flight, and rate production. This is a role for a…
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Audio Artist
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The Audio Artist role reports to the Head of Production and, as a part of the Sphere Studios audio team, works across the entire audio pipeline, from recording concepts and techniques to…
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Sr Manufacturing Engineer - Onsite
TE Connectivity
FAIRVIEW, NC
…(collectively "items") subject to U.S. and non-U.S. export control laws and regulations. Under these regulations, it may be necessary for TE to verify a candidate's national origin and/or…
Added 4 mins ago
Global AI Development Lead
ELECTRICAL COMPONENTS INTERNATIONALHOLDINGS COMPANY
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…world’s leading suppliers of electrical distribution systems, control box assemblies, and other critical engineered components for diversified markets. With approximately 17,000 employees…
Added 4 mins ago
MM
Industrial Electrician / Controls Technician (CNC & PLC)
Manufacturing Maintenance Solutions (MMS)
Pekin, IL
- $35 to $45 USD / hour
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Heat Treat/ Controls- AWS Night Shift Senior Maintenance Technician
Manufacturing Maintenance Solutions (MMS)
East Peoria, IL
- $30 to $42 USD / hour
Schedule: AWS Night Shift | 6:00 PM – 6:00 AM | 12-Hour Shifts

PSC Biotech

Validation Engineer II

York, PA, United States

Apply on biotech.zohorecruit.com About employer

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Job details

Experience: 3–5 years of validation/CQV experience within pharmaceutical, biotechnology, biologics, or other regulated life-sciences manufacturing.
Posting language: English
Posted: Nov 10, 2026

Original job description

BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill-finish services. From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team’s expertise to create a process design for our clients’ products that best suits their needs.

The Experience

With operations spanning the globe and featuring a multi-cultural team, BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered a compensation and benefits structure that rewards you but also be provided with the tools that will help you grow and learn.

At BioTechnique, it’s about more than just a job - it’s about your career and your future.

Your Role

BioTechnique is seeking a Validation Engineer II, with experience supporting validation and qualification activities in pharmaceutical, biotechnology, or sterile manufacturing environments.

The ideal candidate will have hands-on experience with facility and equipment qualification, cleanroom/airflow visualization studies, and autoclave validation. This role will work cross-functionally with Engineering, Facilities, Manufacturing, Microbiology, and Quality to execute validation activities in a fast-paced GMP manufacturing environment.

Author and execute IQ/OQ/PQ protocols, validation plans, and summary reports.
Support qualification and requalification of GMP facilities, utilities, manufacturing equipment, and cleanrooms.
Support airflow visualization/smoke studies, including static and dynamic studies in aseptic environments.
Perform autoclave qualification, including temperature mapping, heat penetration, leak testing, Bowie-Dick testing, biological indicators, and load qualification.
Analyze validation and thermal mapping data and identify appropriate worst-case locations.
Support equipment commissioning and qualification activities.
Investigate validation discrepancies and support deviations, CAPAs, change controls, and impact assessments.
Collaborate with Engineering, Facilities, Manufacturing, Quality, and Microbiology to ensure compliant and timely execution of validation activities.
Maintain documentation in accordance with cGMP and Good Documentation Practices (GDP).

Requirements

Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related technical discipline.
3–5 years of validation/CQV experience within pharmaceutical, biotechnology, biologics, or other regulated life-sciences manufacturing.
Hands-on experience executing IQ/OQ/PQ protocols.
Experience with facility, utility, and equipment qualification.
Strong technical writing, troubleshooting, and data-analysis skills.
Working knowledge of cGMP, GDP, deviations, CAPA, change control, and risk-based validation.
Preferred Experience
Airflow visualization/smoke studies in aseptic or ISO-classified environments.
Steam sterilization/autoclave qualification and temperature mapping.
Experience with thermocouples, biological indicators, Kaye, or similar validation systems.
Cleanroom qualification and ISO 14644 experience.
Experience with electronic validation/documentation systems such as Kneat or similar platforms.

Benefits

Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.

Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
401(k) and 401(k) matching
PTO, Sick Time, and Paid Holidays
Education Assistance
Pet Insurance
Fitness Benefits (Membership discounts and other perks/services at qualifying gyms like Anytime Fitness, 24-Hour Fitness, and more)
Financial Perks and Discounts

Equal Opportunity Employment Statement

PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

Apply on biotech.zohorecruit.com About employer

More about this job

Skills

Design process
Biotechnology
Good manufacturing practices
Documentation
SAP IQ
Technical writing
Troubleshooting
Data analysis
Apache Airflow

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Work requirements

Jobs in the United States