COE Quality Leader
Quality control technician job in Schenectady, NY
SummaryCOE Quality Leader leads the implementation of Built-In Quality eco-system and tools to support strategy. It implements a culture of Quality within production cell and defines and leads improvement initiatives to achieve business excellence. Leads PQE within COE and support the Plant Quality Leader on a daily basis. Presents business solutions to leaders in functional area. Communicates complex messages and negotiates mainly internally with others to adopt a different point of view. Influences peers to take action and may negotiate with external partners, vendors, or customers.Job Description
Roles & Responsibilities
Drives COE level Quality improvements, with emphasis on creating added value and business growth. Ensure that production cell follow same quality standards, harmonize documentation where applicable
Driving cell level Built-In Quality transformation based on BIQ workbook and QMS standards
Significantly minimizing manufacturing defects, internal and customer escapes; engages with key business stakeholders to lead initiatives to deliver improvement targets and engage them in the development of a Quality based culture.
Defines the technical path with strategic direction and tactical focus. Establishes solution options for complex issues affecting the organization to maximize Product Quality efficiency and customer satisfaction.
Ensures that harmonized Quality Management System requirements are effectively established and maintained, in compliance with all regulatory standards and agency authorities.
Coordinate third party, customer or GE internal audits, effectively interact with auditors
Develops internal (Cell level) audit plan, tracks quality audit findings and drives on-time closure
Leverages and adapts metrics to measure performance against Quality objectives, with clear accountability and ownership. Keep quality metrics up to date.
Qualifications/Requirements:
Bachelor's degree, preferably in Engineering or Quality from an accredited university or college with at least 6 years of experience as an Engineer.
Expertise in Six Sigma Quality concepts and tools (DFSS, DMAIC, Design and Process FMEA, MSA, SPC, etc.)
Competency in problem solving methods and processes such as 4D, 8D, Factor Tree Analysis, SPC, PFMEA, CP
Experience in leading Manufacturing, Quality, or highly cross-functional teams
Outstanding interpersonal and leadership skills, capable of influencing and driving a strategic change agenda across the organization.
Change agent, with strong credibility at all levels of the organization.
Strong communication skills, experience of working and leading across/within local cultures.
Desired Characteristics:
Previous leadership experience in implementing Built-In Quality
Experience with the value streams and processes used in manufacturing of Generator assembly and its components
Demonstrable experience in demanding Quality-focused industries, e.g. automotive, aviation, aerospace.
Experience in working with and communicating to Customers.
Strong analytical skills with ability to identify and explain critical and complex issues.
Six sigma/lean practitioner expertise is preferred, with experience of process simplification in a Quality context.
Capability to challenge, think differently, and influence the organization
Proven experience of auditing
Independent thinker; proven ability to lead across functions; data/fact driven decision maker; change agent; customer focus.
Pay Transparency
For U.S. based candidates only, for purposes of complying with U.S. pay transparency requirements, the base pay range for this position is $107,600.00 - 143,400.00 USD Annually. The specific pay offered may be influenced by a variety of factors, including the candidate's experience, education, and skill set. This position is also eligible for a 15% performance bonus/variable incentive compensation/equity. This posting is expected to close on or after November 10, 2025.
*The Company pays a geographic differential of 110%, 120% or 130% of salary in certain areas.
Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
General Electric Company, Ropcor, Inc., their successors, and in some cases their affiliates, each sponsor certain employee benefit plans or programs (i.e., is a “Sponsor”). Each Sponsor reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
Benefits Available to You
GE Vernova employees rise to the challenge of building a world that works. In order to meet this mission, we provide varied, competitive benefits to help support our workforce: Our Culture | GE Vernova (gecareers.com)
Our compensation & benefits are designed to reward high performers and help you manage your personal and family needs. We offer a robust benefits package depending on your employment status and your national requirements.
A healthy, balanced lifestyle can mean different things to different people. We've created programs that support the way you live and work today.
GE Vernova invests to provide opportunities to grow your career by providing a path for continued on-the-job learning and development.
Inclusion & Diversity
At GE Vernova, we believe in the value of your unique identity, background and experiences. We are committed to fostering an inclusive culture, where everyone feels empowered to do their best work because they feel accepted, respected and that they belong. Click here to learn more: **************************************************
About GE Vernova Gas Power
GE Vernova's Gas Power business engineers advanced, efficient natural gas-powered technologies and services, along with decarbonization solutions that aim to help electrify a lower carbon future. It is a global leader in gas turbines and power plant technologies and services with the industry's largest installed base.
GE Vernova offers a great work environment, professional development, challenging careers, and competitive compensation. GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Vernova will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
Relocation Assistance Provided: Yes
For candidates applying to a U.S. based position, the pay range for this position is between $107,600.00 and $179,200.00. The Company pays a geographic differential of 110%, 120% or 130% of salary in certain areas. The specific pay offered may be influenced by a variety of factors, including the candidate's experience, education, and skill set.Bonus eligibility: discretionary annual bonus.This posting is expected to remain open for at least seven days after it was posted on December 08, 2025.Available benefits include medical, dental, vision, and prescription drug coverage; access to Health Coach from GE Vernova, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Vernova Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and financial planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability benefits, life insurance, 12 paid holidays, and permissive time off.GE Vernova Inc. or its affiliates (collectively or individually, “GE Vernova”) sponsor certain employee benefit plans or programs GE Vernova reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a GE Vernova welfare benefit plan or program. This document does not create a contract of employment with any individual.
Auto-ApplyASU Production Technician
Quality control technician job in Albany, NY
Responsible for Maintaining and Improving Plant performance. This is typically a non-shift work position although situations may require work outside normal shift. Production Technician will perform mechanical, instrument and electrical maintenance. See skill set listed below:
Essential Functions
Manipulates air separation controls to meet product specifications and production requirements
Adjust plant control variables, monitor and manage process equipment parameters to meet production goals.
Obtain knowledge base of the theory of air separation and related equipment associated with the process; understand the plant's water chemistry to assure proper cooling tower operations and equipment functioning.
Develop skills to trouble shoot, evaluate process upsets and take corrective actions.
Must maintain Qualified Electrical Worker certification
Performs maintenance on compressors, pumps, turbines, valves, motors, and other plant equipment, when required.
Reads and interprets technical drawings and manuals.
Develop ability to interpret Process & Instrument Drawings to understand process operations, equipment and aid in trouble shooting system anomalies.
Participate in the maintenance/updating of work instructions to assure accurate and current start-up and operational procedures.
Demonstrate mechanical aptitude, evaluate equipment performance, perform routine calibration and maintenance of analytical test equipment and maintain appropriate records.
Be safety conscious, i.e., meetings, work areas, eliminate hazards, etc.
Ability to prepare and maintain production operations and distribution records to meet the requirements of FDA, DPA, OSHA, ISO Quality Systems and other internal and external requirements.
Participate in the maintenance and updating of plant and equipment work instructions.
Prepare and maintain production operations and distribution records to meet internal and external requirements.
Prepare QA documents to certify product quality; transcribe/transfer data from process computer data bases and tables, etc. to prepare product loss and reports.
Good communication skills (inter departmental, team members, vendors, etc.
Responsible for reviewing and releasing medical grade product per FDA regulations.
Troubleshooting the causes of plant operational issues and alarms, either directly or in conjunction with the local team.
Assisting with starting / stopping the plants in a safe manner as dictated by operating conditions and business needs.
Optimizing plant performance by tracking performance data and implement the best operating plan for all plants.
Executing productivity ideas and Best Practices to keep plant costs down.
Interacting closely with all the supporting groups/personnel for performance optimization and troubleshooting.
Perform other projects and duties as assigned.
Performs other duties as assigned. Complies with all policies and standards
QUALIFICATIONS
Education
Associate's Degree High School diploma, Technical School or related industrial experience required
Work Experience
1-3 years Compressors, pumps, valves and expanders, also Instrument & electrical testing equipment preferred
Knowledge, Skills and Abilities
Basic Computer skills.
On call for plant needs of any kind, (Personnel, Equipment, Customer problems) Statistical and analytical skills.
Clean driving record.
Strong understanding of Safety Practices and policies for the Industrial Gas Industry
Strong understanding of Air Separation Principles
Strong understanding of compressors, pumps and expanders
Strong understanding of electrical motors, electrical power distribution and electrical safety.
Possess skills to utilize I&E test equipment, including DVM, megger, process calibrator, transmitter simulator.
Ability to utilize troubleshooting skills on Medium voltage panels, low voltage panels, Programmable Logic Controllers, field process measuring equipment and vibration equipment
Understanding of Analytical principles.
PHYSICAL DEMANDS/WORKING CONDITIONS
Stationary Position - FREQUENTLY
Move/Traverse - FREQUENTLY
Stationary Position/Seated - OCCASIONALLY
Transport/Lifting - OCCASIONALLY - 30lbs.
Transport/Carrying - OCCASIONALLY - 30lbs.
Exerting Force/Pushing - FREQUENTLY
Exerting Force/Pulling - FREQUENTLY
Ascend/Descend - FREQUENTLY
Balancing - RARELY
Position Self/Stooping - FREQUENTLY
Position Self/Kneeling - FREQUENTLY
Reaching - RARELY
Handling - OCCASIONALLY
Grasping OCCASIONALLY
Feeling - OCCASIONALLY
Communicate/Talking - FREQUENTLY
Communicate/Hearing - FREQUENTLY
Repetitive Motions - OCCASIONALLY
Coordination - OCCASIONALLY
Travel Requirements
10% Travel for scheduled Training where applicable.
The Company is an Equal Opportunity Employer that complies with the laws and regulations set forth under EEOC. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. EOE AA M/F/VET/Disability
Process Technician
Quality control technician job in Pittsfield, MA
The Process Technician, also known as an Injection Molding Process Technician/Operator, is responsible for setting up, monitoring, and optimizing plastic molding processes, including injection, extrusion, and blow molding. The role focuses on achieving daily production, safety, and quality goals by performing changeovers, verifying machine parameters, troubleshooting issues, and documenting results using standard work and scientific molding principles.
Responsibilities
* Perform setup and changeovers by installing and removing molds/dies, connecting auxiliaries, and verifying material, tooling, and downstream equipment for each job.
* Configure process parameters, such as temperature, pressure, shot size, and cycle time, according to the approved process sheet and maintain documentation.
* Start up jobs, monitor machines during production, and make adjustments to maintain throughput, first-pass yield, and cycle time targets.
* Apply troubleshooting techniques to address part defects, equipment alarms, and material inconsistencies.
* Perform in-process inspections using calipers, gauges, and check fixtures, and stop production to correct quality issues.
* Record inspection data and maintain ISO/compliance forms.
* Conduct routine cleaning and checks on hydraulic, electrical, and auxiliary systems, and coordinate repairs with maintenance.
* Keep work areas organized and compliant with 5S/LEAN principles.
* Follow OSHA/site safety procedures, resin handling protocols, and company policies.
* Collaborate with operators during ramp-up, coach on standard work, and provide feedback to engineering on mold design and processing improvements.
Essential Skills
* 3-5 years of experience in plastics processing with a focus on injection molding, including setups, startups, and troubleshooting.
* Ability to read and interpret process sheets, work instructions, and basic drawings.
* Familiarity with scientific molding concepts, such as process windows, shot size, hold pressure, and cooling.
* Proficiency with calipers, gauges, basic hand tools, and comfort with HMI screens and auxiliary equipment like loaders, dryers, vision systems, and grinders.
* Physical capability to stand/walk most of the shift, lift up to approximately 50 lbs, and work safely around hot equipment and moving machinery.
* High school diploma or equivalent is required.
Additional Skills & Qualifications
* Associates or bachelor's degree in science is preferred.
* RJG/Paulson certifications or similar are advantageous.
* Some managerial experience is desirable.
Work Environment
This position is based in a manufacturing/lab setting with a schedule of Monday to Friday from 7 AM to 4 PM. There are no weekend shifts. The work environment requires adherence to safety protocols and the use of PPE
.
Job Type & Location
This is a Contract to Hire position based out of Pittsfield, MA.
Pay and Benefits
The pay range for this position is $28.00 - $35.00/hr.
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)
Workplace Type
This is a fully onsite position in Pittsfield,MA.
Application Deadline
This position is anticipated to close on Dec 26, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Production Technician
Quality control technician job in Rensselaer, NY
Production Technician in Rensselaer, NY - 12 Hour Nights
We provide global contract research and manufacturing services to the pharmaceutical and biotechnology industries.
The Production Technician is an integral part of the team, contributing to our success by weighing out chemicals and preparing various types of solutions for use in process.
Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients' lives with the pharmaceuticals we develop and manufacture.
We proudly offer
Generous benefit options
Paid training, vacation and holidays
Career advancement opportunities
Education reimbursement
401k program
And more!
In this role, you will:
Complete training's; Building specific safety, Document training on SOP review, Production Technician Core Competency in the Learning Management System, Site safety and emergency notification and response procedures.
Learn and understand common chemical terminology; Reflux, Distillation, Azeptrope, Separations, pH, ML's, Filtration, Melting Point, Flash point, Vapor Pressure, Density, Boiling Point, Filter Press and Filtrate.
Read, understand and interpret Material Safety Data Sheets.
Understand and maintain plant documentation; Batch Records, Cleaning Protocols, Equipment Use Logs, Equipment Status Tags and Labeling systems/Label generation.
Learn how to; properly weigh and scale operations, review batch records, inspect equipment, drum and package material, understand purging, follow labeling procedures, Read and understand sampling and analytical report forms, Use, clean and reset Niagara ceramic and Furan box filters, calibrate ph meters, set up and charge reactors, understand the scrubber operation and recharging, exercise proper grounding practices, control intermediates, accept raw materials, control finished products, use HHT's and bar code system, conduct pressure filter operation, set up rectors for reflux, distillation and azeotrope, use and understand pumps, use TCM's, use manual jacket services for reactor heating and cooling, proficiently document
Follow our dress code and personal protective equipment SOP
Perform all duties safely in accordance with; Rensselaer Safety Program, guidelines outlined by Good Manufacturing Practices for active pharmaceutical intermediates, Rensselaer Environmental Program.
Learn the buildings process and recommend and implement methods to increase the quality of products and/or service.
Participate in self-development activities.
Perform other related duties as may be reasonably assigned in the course of business.
Qualifications and background to be successful in this role:
Required
Willingness to work a 7 PM -7 AM or a 7 AM - 7 PM shift-this position is for the 7 PM - 7 AM shift.
Willingness to train on Days or nights
High School diploma or equivalent
Must be able to lift maximum of 50 lbs
Advanced math skills
Ability to follow FDA manufacturing guidelines
Communication skills
Preferred
Knowledge and understanding of plant documentation such as batch records, cleaning protocols, equipment use logs, equipment status tags, and labeling systems/label generation
Associates or Bachelor's degree
Prior chemical experience
Pay Range: $27.70/hour
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
LI-DR1
Auto-ApplyProduction Technician II
Quality control technician job in Ravena, NY
Job Description
At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands-including Curaleaf, Select, and Grassroots-offer premium products and services in both medical and adult-use markets.
Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our
Rooted in Good
initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.
Production Technician
Job Type: Full-Time; Non-Exempt
Shift:7am- 3:30pm M-F
Hourly Rate: $19.50/hr.
Location: Ravena, NY
Who You Are:
As a Production Technician, you will be responsible for the packaging and labeling of the finished goods at our cultivation and manufacturing centers. You will be responsible for the production of a variety of finished products including packaged, dried flower, pre-rolls, vape cartridges and vape pens, and infused products. Our production team is expected to maintain quality control measures to ensure high-quality products and will carry out day-to-day tasks including prepping, packaging, and labeling per standard operating procedures set by Curaleaf and our production management.
What You Will Do:
Stage product and packaging supplies across various production lines to meet daily production schedule
Perform quality assurance protocols as designated by Curaleaf's procedures
Increase operational efficiency and reduce waste through ownership, teamwork, communication and collaboration
Perform in-process and post-process quality assurance, testing and conducting visual inspections to ensure all product meets or exceed Curaleaf's specifications and patient's expectations
Ensure 100% compliance involving proper weighing, data recording, product tracking and security throughout the entire packaging process
Operate in an efficient manner that also complies with all OSHA regulations, Curaleaf SOP's and all applicable required procedures
Ensure each product is properly labeled in compliance with state regulations
Work in a quick and efficient manner and strive to consistently increase productivity
Maintain the organization and cleanliness of the extraction room while performing all duties
What You Will Bring:
High School Diploma or G.E.D minimum
Effective communication skills working in a team-based environment
Strong attention to detail skills working in a high-volume production environment
Strong work ethic and the ability to be punctual, reliable, and contribute to a positive, professional work environment
Ability to be trained on various production equipment, SOPs, and consistently meet performance expectations set by leadership
Ability to perform repetitive tasks for long periods of time
Even Better If:
You have one year of manufacturing and packaging experience with a focus on ensuring product safety, consumer safety and satisfaction, and high product quality is strongly preferred
Physical Requirements:
Allergen warnings, potential exposure to dust, pollen, and plant pathogens.
Exposure to cleaning solvents, such as high volumes of isopropyl alcohol.
Daily use of provided PPE, such as masks, hair nets, beard covers, respirators, boot covers, scrubs, non-slip shoes, and Tyvek suits as necessary.
Ability to work in confined spaces
Exposure to loud noises, including but not limited to air compressors, packaging equipment, and alarms.
Exposure to CO2 manufacturing procedures at OSHA approved CO2 levels.
High-stress tolerance, adaptable, flexible ability to work in an ever-changing environment
New York Hiring Range$19.50-$19.50 USD
What We Offer:
Career Growth Opportunities
Competitive Pay and Benefits
Generous PTO and Parental Leave
401(K) Retirement Plan
Life/ Disability Insurance
Community Involvement
Referral Bonuses and Product Discounts
Benefits vary by state, role type, and eligibility.
Follow us on Social Media:
Instagram: @curaleaf.usa
Twitter: @Curaleaf_Inc
LinkedIn: Curaleaf LinkedIn
Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis.
Our Values:
Lead and Inspire.
Commit to Win.
ONE Curaleaf.
Driven to Deliver Excellence.
Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Individuals adversely impacted by the war on drugs are encouraged to apply.
Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.
FIB/SEM Process Technician
Quality control technician job in Albany, NY
Responsibilities: Perform technical tests and experiments for process engineering, including the set up and operation of process equipment. Prepare records, charts, and graphs of test results. Operate metrology tools, (including particle counter, film thickness measurement, and others as needed), to qualify process equipment and optimize processes.
Monitors, audits and provides guidance to engineering staff.
Processes test runs and prepares records, charts, and graphs of results for presentation to engineering to identify tool/process problems.
Provides technical assistance to process development and engineering personnel.
Adjust hardware/software parameters to correct issues or execute experiments.
Work closely with cross-functional engineering teams to troubleshoot process/integration problems.
Perform minor electrical or mechanical troubleshooting on equipment.
Perform preventative and unscheduled maintenance on process equipment
We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form (****************************************** Og4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (*********************************************************************************************** .
To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: *************************************************** .
Skills and Requirements
Qualifications:
- Willing to work night shift is a MUST (6pm-6am)***
- Minimum of 3-4 years of semiconductor processing experience in thin film deposition, lithography or etch, preferably in a high-volume manufacturing facility.
- 1 year of experience with SEM tools in a lab environment
- Associate's degree or equivalent
- Experience with troubleshooting and maintaining vacuum-based processing equipment.
- Skilled in the use of Microsoft Office applications (Outlook, Word, Excel, and PowerPoint).
Must be legally authorized to work in US without sponsorship
Quality Control Lab Technician Weekday Nights
Quality control technician job in Schenectady, NY
Overview: Responsible for conducting qualitative and quantitative testing of raw materials and finished goods.
Responsibilities:
Safely perform laboratory tests on beverages to ensure product is produced within established parameters and make adjustments where necessary.
Conduct qualitative and quantitative testing of beverages, syrups, and raw materials throughout the entire production process.
Analyze syrup beverage and/or water attributes
Audit container rinsers, air blowers, filters, and coders to ensure proper operations.
Conduct package quality inspection and quality audits and isolate product that does not meet standards.
Maintain highest possible housekeeping standards to prevent microbial contamination
Monitoring package appearance, integrity and correct package codes.
Requires working with other lab technicians, line foreman, line operators, fork truck drivers, and other production personnel.
Responsible for Food Safety and Food Quality
Requirements:
Demonstrated attention to detail and accuracy
Strong analytical skills
Ability to read, write and keep records
Good computer skills including literacy with Excel and Word
Ability to “be on your feet” from beginning to end of shift.
Able to lift materials up to 50 pounds
Ability to pass pre-employment math test
Monday - Thursday 10 hour shifts
Auto-ApplyTravel Cath Lab Tech - $2,059 per week in Albany, NY
Quality control technician job in Albany, NY
Cath Lab Tech Location: Albany, NY Agency: Triage Staffing LLC Pay: $2,059 per week Shift Information: Days - 5 days x 11 hours Contract Duration: 13 Weeks Start Date: ASAP
AlliedTravelCareers is working with Triage Staffing LLC to find a qualified Cath Lab Tech in Albany, New York, 12201!
Travel Radiology: Cath Lab Tech Albany, NY
Location: Albany, NY
Start Date: 9/29/2025
Shift Details: 11H Days (7:00 AM-6:00 PM)
36 hours per week
Length: 13 WEEKS 13 weeks
Apply for specific facility details.Cath Lab Tech
About Triage Staffing LLC
At Triage, we prefer to be real. Real about expectations--both ours and yours. Real about how a decision you make today could affect your tomorrows. Real about how compensation actually works. Real about how great-- or grating--your next supervisor may be.
Being real allows everyone at Triage to be ready. Ready to serve you with real honesty. So if that gig near the ocean is really no day at the beach, or that third shift comes with a second-class rate, we tell you. So you can be ready, too.
We staff all four major divisions of acute care - nursing, lab, radiology, and rehab therapy
One point of contact for both travelers and facilities (per division)
In-house compliance and accounting specialists
On-staff clinical liaisons
Mentoring program that is run and managed by actual clinicians - yeah, you read that right
And more (because of course there's more)
Are we the biggest? No. Are we the best? That's rather subjective, but we're trying to be. Will we work like hell to get you as close to your idea of heaven as possible? Yes. Yes, we will.
In 2021, Triage and TaleMed merged to become better together under the Triage name.
10672795EXPPLAT
Process Tech
Quality control technician job in Schenectady, NY
Process Technicians are responsible for operating machines in support of TSS Albany. We believe that potential matters more than experience. We're looking for motivated individuals who are ready to take the first step into the world of manufacturing. Grow and learn with Trelleborg Albany
Who are we?
As a world class manufacturer, Trelleborg Sealing Solutions is a forward-thinking company offering our customers solutions to their challenging applications. Seize this rare opportunity to be part of an industry leading organization that has been in business for over 100 years.
About the Job
You will have the opportunity to work in a growing, fast paced environment that provides hi-tech composite structures to critical applications. Your responsibilities will include operating articulated arm and gantry robots, support equipment (extractor, crane, fork truck) and basic power tools.
About the Ideal Candidate
Were you in a robotics club, do you like to tinker on equipment or your car? All good skills to bring to this job.
Ideal candidates will have the ability to operate basic machinery and have basic computer skills with familiarity of Microsoft Windows software. We provide on the job training so don't be afraid to apply.
Tasks and Responsibilities also include
Operate articulated arm and gantry robots
Machinery Preventive Maintenance (including basic mechanical, electronic and pneumatic skills)
Operate basic power tools to include saws, drills and other tools
Operate support equipment (extractor, crane, fork truck)
Basic programming
Knowledge, Skills, and Abilities
Mechanical aptitude
Good math skills
Knowledge and understanding of operational data, machine set-up, blueprints, and work instructions
Ability to use and read measuring instruments including but not limited to; tape measures, micrometers, pi tapes, thermometers, scales
Ideal candidates should have strong interpersonal skills with the ability to work cohesively in a diverse work environment. Strong organizational skills, the ability to multi-task and adjust to changing priorities quickly a plus.
Education and Experience
High School Diploma or equivalent
Experience in a manufacturing environment
ð Your Future Starts Now
This is more than just a job - it's a launchpad for a skilled trade career that can take you anywhere. If you're ready to learn, grow, and make things that matter, apply today and let's build your future together.
ð Apply now and take the first step toward a career you can be proud of.
Compensation starting rate is $20 - 25/hr depending on experience
QC Sample Management Technician - 2nd Shift (Wed-Sat)
Quality control technician job in Rensselaer, NY
At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits.
Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled.
Job Description
Verification of sample submissions to Quality Control
Handling, storage, and organization of samples
Delivering samples to QC laboratories for testing as required
Interacting with outside customers and functional peer groups
Compliance with all pertinent regulatory agency requirements
Conducting temperature, environmental, and/or CO2 monitoring.
Qualifications
Bachelor's degree (life sciences major required)
cGMP experience preferred
Authorization to work in the United States indefinitely without restriction or sponsorship
Candidates located within a commutable distance of Rensselaer, NY are encouraged to apply.
Additional Information
Position is full-time, schedule is 2nd shift Wednesday-Saturday | 1pm-11:30pm .
Base pay is between $21.50-22.50/hr. 2nd shift has a 10% shift differential.
A $50 flat-rate weekend shift differential will also be included for Saturday shifts.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
QC Sample Management Technician - 3rd Shift (Wed-Sat)
Quality control technician job in Rensselaer, NY
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you're looking for a rewarding career, apply with us today!
Job Description
Verification of sample submissions to Quality Control
Handling, storage, and organization of samples
Delivering samples to QC laboratories for testing as required
Interacting with outside customers and functional peer groups
Compliance with all pertinent regulatory agency requirements
Conducting temperature, environmental, and/or CO2 monitoring.
Qualifications
Bachelor's Degree required - life sciences major preferred
cGMP experience preferred
Candidates living within a commutable distance of Rensselaer, NY are encouraged to apply
Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Position is full-time.
Schedule: Wednesday-Saturday, 10:00 PM - 8:30 AM.
Base pay is between $21.50-22.50/hr. 3rd shift includes a 15% shift differential. A $50 flat-rate weekend shift differential will also be included for weekend shifts.
#LI-EB1
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
QC Supervisor
Quality control technician job in Albany, NY
Please, review and apply for this position through the QCI system following the link below (Copy and Paste): http://jobs.qcitech.com/jobseeker/QC_Supervisor_J02157409.aspx *You can apply through Indeed using mobile devices with this link.
Additional Information
QC Supervisor
Quality control technician job in Albany, NY
Please, review and apply for this position through the QCI system following the link below (Copy and Paste):
http://jobs.qcitech.com/jobseeker/QC_Supervisor_J02157409.aspx
*You can apply through Indeed using mobile devices with this link.
Additional Information
Quality Control Lab Technician Weekday Nights
Quality control technician job in Schenectady, NY
Overview: Responsible for conducting qualitative and quantitative testing of raw materials and finished goods.
Responsibilities:
Safely perform laboratory tests on beverages to ensure product is produced within established parameters and make adjustments where necessary.
Conduct qualitative and quantitative testing of beverages, syrups, and raw materials throughout the entire production process.
Analyze syrup beverage and/or water attributes
Audit container rinsers, air blowers, filters, and coders to ensure proper operations.
Conduct package quality inspection and quality audits and isolate product that does not meet standards.
Maintain highest possible housekeeping standards to prevent microbial contamination
Monitoring package appearance, integrity and correct package codes.
Requires working with other lab technicians, line foreman, line operators, fork truck drivers, and other production personnel.
Responsible for Food Safety and Food Quality
Requirements:
Demonstrated attention to detail and accuracy
Strong analytical skills
Ability to read, write and keep records
Good computer skills including literacy with Excel and Word
Ability to “be on your feet” from beginning to end of shift.
Able to lift materials up to 50 pounds
Ability to pass pre-employment math test
Auto-ApplyProduction Technician
Quality control technician job in Johnstown, NY
Who we are:
At Vireo Health, we're not just another cannabis company-we're a movement. Founded by physicians and driven by innovation, we blend science, technology, and passion to create top-tier cannabis products and experiences. Our team of 500+ bold creators and trailblazers are shaping the future of the industry, and we want you to be part of it.
We take pride in being one of the most diverse and inclusive workplaces in cannabis, fostering a culture where everyone belongs. Through employee engagement, community events, and non-profit partnerships, we're building more than a business-we're building a community.
As we rapidly expand nationwide, we're looking for talented, driven, and passionate people to join us. If you're ready to turn your passion into a career, let's grow the future together.
What the role is about
In this role The Production Technician is responsible for preparing flower for sale, including bucking, trimming, and packaging of cannabis flower products. This position reports to the Production Manager.
Starting union pay is $20
What impact you'll make:
Assist with bucking and de-stemming harvests.
Trim flower for sale, and process into final packaging.
Production of pre-roll cannabis products (If legalized by the NY DOH).
Assemble secondary packaging, and package cannabis products into secondary packaging.
Print and apply labels to various types of finish packaged product.
Can read instruments (balances, calipers, etc.)
Carry out quality control checks on finished products.
Maintain a clean and safe working environment including cleaning equipment.
Manage parallel workflows.
Keeps a detailed production log, dating and recording all tasks performed and relevant.
Comfortable performing in a goal driven work environment.
Interacts with electronic record keeping.
Perform other functions as necessary to provide an adequate supply of product to meet patient demand.
Provide feedback to improve process quality.
Some machine maintenance will be required.
What you've accomplished
High School Diploma.
At least 2 years relevant experience working in a manufacturing environment.
Must be at least 21 years of age.
Why Choose Vireo
Life's too short to work somewhere that doesn't ignite your passion. The cannabis industry is fast-paced, innovative, and full of opportunity-where science meets creativity, and wellness meets culture.
At Vireo Health, we're pioneering the future of cannabis with a team that's as dynamic as the industry itself. Here, you'll find a workplace that's collaborative, inclusive, and driven by HEART and purpose, where your work has a real impact on people's lives.
Whether you're cultivating the highest-quality plants, crafting cutting-edge products, or shaping unforgettable customer experiences, you'll be part of something bigger. If you're looking for a career that's exciting, meaningful, and full of growth, let's build the future of cannabis together.
✅ A Growing Industry: Work at the leading tech company in the cannabis industry and help shape the future
✅ Passionate Culture: Join a team that truly cares about the plant, the people, and the purpose behind what we do
✅ Employee Perks: Enjoy competitive pay and benefits, paid time off and employee discounts
✅ Making an Impact: We're committed to education, sustainability, and giving back to the communities we serve.
EEO Statement
Vireo Health, Inc. is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. *******************
Auto-ApplyTravel Cardiac Cath Lab Technologist - $2,490 per week
Quality control technician job in Albany, NY
Medical Solutions is seeking a travel Cath Lab Technologist for a travel job in Albany, New York.
Job Description & Requirements
Specialty: Cath Lab Technologist
Discipline: Allied Health Professional
Duration: 13 weeks
40 hours per week
Shift: 10 hours, days
Employment Type: Travel
We're seeking talented healthcare professionals whose adventure game is as strong as their clinical game. Those that want flexibility and high pay, we have the positions for you!
Some of the industry-leading benefits enjoyed by Medical Solutions travel nurses and travel allied healthcare professionals include:
Day One Medical, Dental, and Vision with low premiums
Day One 401(k) with Company Contribution
Personalized Compensation Packages
Paid, Private, Fully Furnished, Pet-Friendly Housing
Dedicated Recruiter and 24/7 Customer Care Line
Per Diem Allowance and Paid Travel
Licensure and Certification Reimbursement
Free Liability Coverage
Voluntary Benefits: Critical Illness, Hospital Indemnity, Accident, and Pet Insurance
Equal Employment Opportunity
And More!
Estimated pay package based on bill rate at time job was posted. Bill rates can change frequently and without notice. Exact pay package may vary based on guaranteed hours, distance being traveled, and customizations available for travelers.
Medical Solutions Job ID #960639. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cardiac Cath Lab
About Medical Solutions
At Medical Solutions, we're people who care, helping people who care. No matter how you look at it, there's a whole lot of care going on in our world and that's just the way we like it. What do we do? Medical Solutions is one of the nation's largest providers of total workforce solutions in the healthcare industry, connecting nurses and allied health clinicians with hospitals and healthcare systems across the country and around the corner. Through our family of brands, we also serve a segment of clients outside of the healthcare space. And we're the very best at what we do. You'll love our culture that's filled with heart and soul. As a company and employer, we're sincerely and unabashedly us. We lead as humans first and believe the unique qualities of each team member make us better together. We share a purpose for helping others and the drive to make a difference. And we offer endless opportunities for personal and professional growth, throughout your career. At Medical Solutions, you'll find a great place to work and a career home. We've received Best Places to Work awards, landed top industry awards, and received accolades for the impact we've made in business and within our community. But the only way to really get to know us, is to join us. We think you'll fit right in.
Benefits
Weekly pay
Holiday Pay
Guaranteed Hours
Continuing Education
401k retirement plan
Pet insurance
Company provided housing options
Cancelation protection
Wellness and fitness programs
Mileage reimbursement
Referral bonus
Employee assistance programs
Medical benefits
Dental benefits
Vision benefits
Benefits start day 1
License and certification reimbursement
Life insurance
Discount program
Advanced Engineering Technicians
Quality control technician job in Pittsfield, MA
Basic Qualifications
Associate's degree in related discipline or equivalent is required plus a minimum of 3 years of relevant experience. CLEARANCE REQUIREMENTS: Department of Defense Secret security clearance is obtainable within a reasonable amount of time after hire. Applicants selected will be subject to a U.S. Government security investigation and must meet eligibility requirements for access to classified information. Due to the nature of work performed within our facilities, U.S. citizenship is required.
Responsibilities for this Position
ROLE AND POSITION OBJECTIVES:
Representative Duties and Tasks
Teardowns, builds and tests electromechanical devices that utilize precision optics.
Assists engineering team with development and maintenance of written work procedures.
Operate test equipment and prepare test reports
Follow written work instructions
Un-pack and pack sensitive instruments for shipment to vendors
Work independently and with manufacturing teams
Knowledge, Skills and Abilities
Proficient use of hand tools
Comfortable working under a microscope
Cleanroom experience / working cleanroom assembly
Ability to follow work instructions
Experience in micro/precision assembly (medical devices, watchmaking, etc)
Familiarity with ESD safe procedures
Some experience in mechanical troubleshooting
Ability to work independently and with cross functional teams
What You Bring to the Table:
Associate's degree in electrical engineering (or related field) or equivalent field experience
Proficiency in electrical engineering concepts and design tools
Strong written and verbal communication skills
Ability to multi-task and think creatively
U.S. citizenship required; security clearance preferred
What sets you apart:
Prior experience in optics / mirrors / cameras
Ability to work comfortably under a microscope
Demonstrated skill in use of hand tools and mechanical assembly
Familiarity with cleanroom work / cleanroom procedures
Familiarity with wiring diagrams / schematics
Ability to run / operate Interferometer / Complex test equipment
Interpretation of Interferometer Test results
Familiarity with theodolites / optical surveying
Familiarity with vacuum systems / leak checking systems
Our Commitment to You:
An exciting career path with opportunities for continuous learning and development.
Research oriented work, alongside award winning teams developing practical solutions for our nation's security
Flexible schedules with every other Friday off work, if desired (9/80 schedule)
Competitive benefits, including 401k matching, flex time off, paid parental leave, healthcare benefits, health & wellness programs, employee resource and social groups, and more
See more at gdmissionsystems.com/careers/why-work-for-us/benefits
Workplace Options:
This position is fully on site.
While on-site, you will be a part of the Pittsfield Campus.
Salary Note This estimate represents the typical salary range for this position based on experience and other factors (geographic location, etc.). Actual pay may vary. This job posting will remain open until the position is filled. Combined Salary Range USD $30.36 - USD $32.56 /Hr. Company Overview
General Dynamics Mission Systems (GDMS) engineers a diverse portfolio of high technology solutions, products and services that enable customers to successfully execute missions across all domains of operation. With a global team of 12,000+ top professionals, we partner with the best in industry to expand the bounds of innovation in the defense and scientific arenas. Given the nature of our work and who we are, we value trust, honesty, alignment and transparency. We offer highly competitive benefits and pride ourselves in being a great place to work with a shared sense of purpose. You will also enjoy a flexible work environment where contributions are recognized and rewarded. If who we are and what we do resonates with you, we invite you to join our high-performance team!
Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans
Auto-ApplyQuality Control Analyst II
Quality control technician job in Rensselaer, NY
QC Analyst II in Rensselaer, NY The Quality Control Analyst II is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients' lives with the pharmaceuticals we develop and manufacture.
We proudly offer
* Generous benefit options
* Paid training, vacation and holidays
* Career advancement opportunities
* Education reimbursement
* 401k program
* And more!
Essential job duties
In this role, you will:
* Perform complex testing and data evaluation such as TGA
* Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues
* Participate in or assist with test method validations
* Evaluate data for trends and review data
* Support supervisors in OOS Investigations and complete CAPA requirements
* Interact with outside departments including attending meetings, providing updates, etc.
* Coordinate testing performed at outside testing labs, raw materials, etc.
* Maintain a detailed and accurate recording of activities and results on paperwork
* Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools
* Train upon and understand methods, equipment and standard operating procedures
* Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures
* Support equipment upkeep
* Prepare and order supplies, as necessary
* Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management
* Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry
* Interact with other departments within the company for testing needs and scheduling
* May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams
* May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results
Education, experience, certification and licensures Required
* Bachelor's degree in Chemistry or related field
* Minimum 3-5 year's pharmaceutical experience or equivalent combination of education and experience
Preferred
* Experience working in cGMP or GLP pharmaceutical industry environment
Knowledge, skills and abilities
* Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
* Ability to meet deadlines and work under pressure with limited supervision
* Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently
* Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
* Ability to write reports, business correspondence, and procedure manuals
* Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
* Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
* Ability to define problems, collect data, establish facts, and draw valid conclusions
* Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
* Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems
* Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus
Physical requirements
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; or sit; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Work environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; risk of electrical shock; explosives; risk of radiation and vibration. The noise level in the work environment is usually moderate.
Pay Range: $63,000 - $79,000
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-DR1
Quality Control Analyst II
Quality control technician job in Rensselaer, NY
QC Analyst II in Rensselaer, NY The Quality Control Analyst II is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients' lives with the pharmaceuticals we develop and manufacture.
We proudly offer
* Generous benefit options
* Paid training, vacation and holidays
* Career advancement opportunities
* Education reimbursement
* 401k program
* And more!
Essential job duties
In this role, you will:
* Perform complex testing and data evaluation such as TGA
* Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues
* Participate in or assist with test method validations
* Evaluate data for trends and review data
* Support supervisors in OOS Investigations and complete CAPA requirements
* Interact with outside departments including attending meetings, providing updates, etc.
* Coordinate testing performed at outside testing labs, raw materials, etc.
* Maintain a detailed and accurate recording of activities and results on paperwork
* Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools
* Train upon and understand methods, equipment and standard operating procedures
* Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures
* Support equipment upkeep
* Prepare and order supplies, as necessary
* Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management
* Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry
* Interact with other departments within the company for testing needs and scheduling
* May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams
* May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results
Education, experience, certification and licensures Required
* Bachelor's degree in Chemistry or related field
* Minimum 3-5 year's pharmaceutical experience or equivalent combination of education and experience
Preferred
* Experience working in cGMP or GLP pharmaceutical industry environment
Knowledge, skills and abilities
* Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
* Ability to meet deadlines and work under pressure with limited supervision
* Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently
* Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
* Ability to write reports, business correspondence, and procedure manuals
* Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
* Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
* Ability to define problems, collect data, establish facts, and draw valid conclusions
* Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
* Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems
* Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus
Physical requirements
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; or sit; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Work environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; risk of electrical shock; explosives; risk of radiation and vibration. The noise level in the work environment is usually moderate.
Pay Range: $63,000 - $79,000
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-DR1
Auto-ApplyProfessional, Credentialing QC Analyst
Quality control technician job in Schenectady, NY
Qualifications you'll bring: Associate's or Bachelor's degree in a related field (e.g., healthcare administration, business, or HR) preferred. 2+ years of experience in credentialing, compliance, or quality assurance. Experience in healthcare or insurance credentialing preferred.
Strong attention to detail and analytical skills.
Familiarity with credentialing software and databases.
Knowledge of regulatory standards (e.g., NCQA, URAC, Joint Commission) is a plus.
Excellent communication and organizational skills.
Ability to work independently and collaboratively in a fast-paced environment.
Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
Understanding of data privacy and confidentiality standards.
Curiosity to foster innovation and pave the way for growth
Humility to play as a team
Commitment to being the difference for our customers in every interaction
Your key responsibilities:
Conduct thorough quality control reviews of credentialing/recredentialing files and documentation.
Verify credentials, licenses, certifications, and other required documentation for accuracy and compliance.
Collaborate with credentialing specialists to resolve discrepancies and ensure timely updates.
Maintain detailed records of QC findings and corrective actions.
Assist in developing and refining QC procedures and checklists.
Monitor compliance with internal policies, accreditation standards, and regulatory requirements.
Provide feedback and training to credentialing staff on quality standards and best practices.
Support audits and reporting requirements related to credentialing activities.
Stay current with industry standards, regulations, and credentialing best practices.
Contribute to our humble pursuit of excellence by performing various responsibilities that may arise, reflecting our collective goal of enhancing healthcare delivery and being the difference for the customer.
Where you'll be:
Hybrid