Remote Control Sample Jobs in Usa
789 positions found — Page 3
QC Analyst – Night Shift | Bethlehem, PA
$22–$24/hr. + 10% shift differential
7:00 PM – 7:30 AM | 2-2-3 schedule
6-month contract
Join a FAST growing Pharmaceutical Manufacturing site supporting the production of Critical Care drug products in a GMP lab environment.
Job Summary: Perform analytical testing of In-Process, Bulk, Stability and Finished Product to provide information about the quality, identity, purity, and safety of the material and provide decisions into the next steps in the manufacturing process.
Key Responsibilities:
- Perform sample preparation and GMP testing of raw materials, in-process, bulk, stability, and finished product
- Operate and maintain analytical instruments (HPLC, GC, UV, FTIR, KF, ICP/MS, or AA)
- Complete GMP documentation in compliance with SOPs and data integrity requirements
- Support OOS, deviations, and lab investigations
- Prepare standards, solutions, and calibration activities
- Maintain lab logbooks, inventory, and stability samples
- Review analytical data and production records, including peer review
- Follow all GMP, safety, and quality procedures in a 12-hour shift environment
Job Requirements:
- Must have at least 1 year of experience in a GMP laboratory setting.
- Familiar with GMP/GLP and FDA requirements a plus
- Strong documentation skills
- Familiar with SAP, OpenLab, Ensur, MS Office
Location: Frederick, MD,21704
Duration: 12 Months
Shift: Wednesday - Saturday, 7:00 AM - 6:00 PM
Position Summary
We are seeking a highly motivated QC Microbiology Technician to join our commercial cell therapy production center in Frederick, MD. The selected candidate will work with the Quality Control team to support microbiological testing activities related to clinical and commercial cell therapy products used in cancer immunotherapy.
This role is responsible for performing microbiological testing, environmental monitoring, water and utility testing, and supporting product release testing in a GMP-regulated manufacturing environment.
Key Responsibilities
- Perform environmental monitoring of cleanrooms.
- Collect water samples according to schedule and ensure timely testing.
- Perform and review microbiological assays including:
- Gram Stain
- Endotoxin
- Sterility testing
- Microbial identification
- Bioburden testing
- Plate reading
- Conduct utility monitoring for purified water systems and compressed gases.
- Perform data entry, trending analysis, and prepare reports or slides for management review.
- Assist with investigations related to Out-of-Specification (OOS) results and manage deviations related to microbiological procedures.
- Perform routine maintenance of laboratory equipment and lab areas.
- Review and approve final product release test results.
- Perform additional duties as assigned.
Basic Qualifications
- Associate Degree (AA) with 1+ year of experience in a Microbiology Lab or Environmental Monitoring, OR
- High School Diploma with 2+ years of experience in a Microbiology Lab or Environmental Monitoring.
Preferred Qualifications
- Experience with microbiological techniques, including:
- Environmental air monitoring
- Water testing
- Surface monitoring
- Experience with aseptic techniques and cleanroom operations.
- Ability to gown for entry into aseptic manufacturing areas and lift approximately 25 lbs.
- Knowledge of GMP, SOPs, and quality control processes in commercial manufacturing.
- Proficiency in MS Word, Excel, PowerPoint, and other computer applications.
- Strong interpersonal, verbal, and written communication skills.
- Ability to work in a fast-paced environment with minimal supervision and adapt to changing priorities.
- Flexibility to work overtime or adjust schedules as required.
Job Functions:
- Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
- Work cross functionally to coordinate testing schedules and communications in support of the weekly production activities and ensure QC testing and maintenance activities are completed per requirements.
- Perform testing as assigned.
- Schedule and ensure testing of production, raw materials, components, stability, validation, and support of protocol/experimental samples.
- Verify, review, and make appropriate changes if needed, to any controlled document(s) pertinent to area of responsibility.
- Ensure team compliance with all policies, procedures, and site/company regulations.
- Support investigations of process or product failures and customer complaints. Author, and/or review all area quality and safety exceptions and investigation reports.
- Work safely with radioactivity and ensure all direct reports maintain radiological exposure to levels As Low As Reasonably Achievable (ALARA).
- Provide leadership for employees through effective communication, coaching, training and development and provide solutions for the success of the team.
- Conduct daily board meetings to update employees and track employee progress.
- Measure and communicate team progress against individual, team and site goals and Key Performance Indicators (KPI’s).
- Maintain and promote proper maintenance and cleanliness of the department areas of responsibility.
- Assure compliance with department training and qualification.
- Bachelor Degree in Chemistry, Science or related field required. Work experience is considered in lieu of degree.
- 10 or more years of relevant experience required with previous supervisory experience preferred.
- Proficiency in cGMP laboratory testing and major laboratory instrumentation.
- Ability to interpret laboratory data and make sound compliance decisions based on such interpretations.
- Excellent communication and experience leading a team.
Estimated Min Rate: $85000.00
Estimated Max Rate: $92000.00
What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
- Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
- Health Savings Account (HSA) (for employees working 20+ hours per week)
- Life & Disability Insurance (for employees working 20+ hours per week)
- MetLife Voluntary Benefits
- Employee Assistance Program (EAP)
- 401K Retirement Savings Plan
- Direct Deposit & weekly epayroll
- Referral Bonus Programs
- Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, 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, disability, or status as a protected veteran.
Visit to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
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.
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Job Title: Quality Control Specialist
Location: Charleston, SC
Employment Type: Full-Time / Direct Hire
Salary: $43,680-$49,920 DOE
Position Summary
The Quality Control Specialist plays a critical role in supporting Environmental Health & Safety, Production, and Raw Material Quality functions. This position ensures that all products meet established specifications and regulatory standards while contributing to continuous improvement initiatives across the organization.
Key Responsibilities
Quality & Compliance
- Ensure full compliance with all applicable laws, regulations, and company policies related to job and departmental functions.
- Maintain adherence to quality management standards and internal procedures.
- Follow daily workload and priorities established by the QC Group Leader.
- Maintain equipment and instruments in accordance with policies/procedures, including calibration and documentation.
- Complete all measurement reports accurately and thoroughly.
Product Testing & Documentation
- Conduct proper chemical testing of products to verify conformance to defined specifications, including new material evaluations and recertification testing.
- Maintain QC cards, samples, and documentation.
- Support activities related to product service, maintenance, and formulation optimization.
- Ensure consideration of environmental and occupational safety requirements throughout all tasks.
Customer Complaint Resolution
- Provide immediate and effective support in investigating and resolving customer complaints.
- Coordinate closely with Sales, Production, QC global teams, and other relevant departments.
Communication & Collaboration
- Maintain professional communication with internal teams, management (local and global), and external partners including raw materials suppliers.
- Utilize internal systems and software (e.g., SAP) as required.
- Contribute to continuous improvement efforts in workflow, safety, and efficiency.
Lean Management / 5S
- Maintain a clean, organized, and efficient workspace.
- Report safety concerns, process inefficiencies, and improvement opportunities promptly.
- Participate in Lean/5S initiatives and support long-term operational excellence.
Additional Responsibilities
- Participate in special projects as assigned by leadership (local and global).
- Perform other duties as required to support the company’s mission and goals.
- Maintain compliance with all company policies and procedures.
Role Requirements
- High school diploma or GED required; Bachelor's degree in Chemistry or related field preferred.
- Ability to obtain hazardous waste training within 6 months of hire and annually thereafter, in accordance with SCHWMR R.61-79.262.17(a)(7).
- Strong verbal and written communication skills, with the ability to interact effectively with internal and external customers.
- SAP software experience preferred.
- Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).
- Ability to work under pressure, meet deadlines, and maintain a positive attitude while delivering excellent customer service.
- Ability to work independently and complete assignments within established guidelines.
- Willingness and ability to travel domestically and internationally, including to locations requiring proof of vaccination.
Physical Demands & Work Environment
- Ability to perform essential functions safely and successfully under ADA, FMLA, and applicable standards.
- Maintain regular and punctual attendance.
- Frequent walking, standing, lifting (up to 50 lbs), carrying, stooping, bending, kneeling, and reaching.
- Exposure to fumes and hazardous chemicals.
- Ability to wear a respirator and pass annual fit-testing.
- Ability to stand for an 8‑hour shift.
- Ability to communicate clearly in person and by phone.
WHO WE ARE
RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.
THE ROSLINCT WAY
Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.
ACCELERATING YOUR FUTURE
· Author, review, approval, and final authorization of microbiology methods (test results and records, test methods, equipment records) and ensuring adherence to regulatory agency requirements, Client standards, policies, SOPs for cell therapy products and experience with EU Annex requirements.
· Execute procedures for microbiology methods in support of method lifecycle activities including method transfer, qualification, validation, compendial verification, and performance monitoring.
· Support microbiology equipment installation and qualification, ensuring 21 CFR Part 11 compliance.
· Participate as microbiology method subject matter expert (SME) in investigations, OOS, deviation, change controls, and CAPAs to support cGMP operations.
· Provide support to QC Operations as method SME: develop training approach, training documents and provide training for new methods.
· Perform non-routine/routine QC testing for in process samples, product testing, stability testing, or raw material testing as needed.
· Work collaboratively with cross functional departments including but not limited to QC Technical Services, Quality Assurance, and Program Management.
· Ability to prepare technical data and present to senior leadership.
WHAT YOU WILL BRING
· Bachelor’s degree in Biology (Microbiology)
· 4+ years of microbiology laboratory experience with rapid microbiological methods is a plus (rapid sterility, endotoxin, gram stain).
· Experience in a cGMP QC laboratory environment performing environmental monitoring, contamination control and investigation writing.
· Excellent/Effective written and verbal communications skills.
· Prepare technical data and present to senior leadership.
· Escalate issues professionally and on a timely basis.
OUR COMMITMENT
All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.
RoslinCT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.
Kodak is looking for a Material Control Coordinator to join our Specialty Chemicals and Inks Manufacturing team in Rochester, NY.
We are seeking a motivated and detail-oriented individual to join our team as a Material Control Coordinator. In this role, you will be in the front line of communication with our customers, coordinating with operations, ensuring accurate order processing and supporting our business development team. This position requires the ability to multi-task, as well as organize and manage all forms of requests while providing excellent service to our customers.
Responsibilities:
• Maintain records (data entry) for all deliveries and shipments. File hardcopy documents per standard work.
• Create purchase requisitions for incoming materials and perform goods receipt once materials are delivered.
• Point of contact for product orders.
• Create orders for sales of solvents and invoices for incoming materials.
• Collect necessary documents after raw material receipt and product sales and send to customers.
• Collect necessary records from generator/broker for proper documentation to receive initial load/trial of material (manifest template, Land Disposal Restriction Forms, etc.)
• Create hazardous waste manifest documents for customers.
• Set up new customers, vendors, raw material items, and products items.
• Order internal production materials.
• Create purchase requisitions and manage purchase orders for railcar leases, subscriptions, contractors, and trade group memberships.
• Manage sample and small package shipments.
• Flexibility to learn operations work and assist as necessary.
• Hazardous waste receipt data entry into regulatory websites.
• Support Logistics Coordinator job functions.
• Monday – Friday, 40 hours/week with potential for overtime as needed.
• On location role with no remote work flexibility.
Job Skills:
• Excellent communication and teamwork skills, able to interface with sales, operations, engineering, transportation, transportation, management, logistics staff, etc.
• Good computer skills – SAP, MS Office (Outlook, Word, Excel, PowerPoint), familiarity with customer billing portals (Ariba).
• Initiative-taking - able to work independently.
• Problem solving – able to adapt and improve work processes.
• Willingness to learn and make positive contributions.
• Positive attitude.
• Flexibility - able to adjust to changing demands.
Job Summary
Provide analytical support and data generation for daily chemistry testing activities related to raw materials, in- process and finish products. Perform all testing in a timely and accurate manner in accordance with approved GMP documents (test methods, Specifications, SOPs).
Chemist I
Essential Functions:
- Inspects components, products and/or processes to ensure conformance with standards.
- Executes laboratory procedures for sample preparation
- Performs materials analysis of substantial variety & complexity using ARx test methods, compendia methods, specifications with minimal supervision.
- Ensure all analytical operations comply with cGMPs & ARx procedures and all laboratory experiments are properly documented in notebook and are in accord with regulatory requirements.
- Provide support to routine USP water and environmental testing.
- Works with minimal supervision/direction in expediting completion of laboratory assignments.
- Abide by the ARx Laboratory Chemical Hygiene Plan and other safety policies. Maintains a safe and clean work environment, notifying the supervisor of unsafe practices, conditions, or acts; L-II takes on increasing responsibility for surfacing and implementing improved safety practices.
- Responsible for following all applicable waste handling procedures.
Additional Responsibilities:
- Completes required paperwork / documentation accurately, neatly and in a timely manner.
- Responsible for the proper disposal of hazardous waste into the proper labeled containers and drums.
- Performs other duties and responsibilities as assigned.
- Make identifiable and substantial contributions to continuous improvement. Performs all duties consistent with established ARx guideline consistent with all regulatory requirements. Actively complies with and endorses Department and Company objectives.
Job Specifications:
- BS (or higher) degree in Chemistry, Microbiology, or closely related discipline and 0-2 years lab experience (preferably pharmaceutical GMP) or requires high school education and 5 years minimum lab experience (preferably pharmaceutical GMP).
- Knowledgeable in the application of various analytical techniques such as chromatography and spectroscopy; thermal analysis and wet chemistry techniques desired.
- Basic knowledge and understanding of scientific principles involved in the performance of analytical test methods.
- Ability to efficiently utilize time (coordinate several assignments concurrently).
- Ability to read and interpret documents such as test methods and procedure manuals.
- Knowledge of requirements for maintaining proper laboratory otebook documentation
- Must have above average computer skills and knowledge; specially in the operational use of analytical equipment have a computer interface.
- Ability to perform basic mathematical functions and apply basic concepts such as mean and standard deviation.
- Good communication skills (verbal and written).
- Excellent interpersonal skills.
- Requires common physical characteristics and abilities, such as above average agility and dexterity; physical exertion such as long periods of standing, recurring bending, crouching, stooping, stretching, reaching or similar activities should be expected.
- Work environment involves moderate risks or discomforts requiring special safety precautions, will be required to use personal protective equipment.
Physical Demands:
Sitting: 67-100%/day
Standing: 67-100%/day
Walking: 67-100%/day
Kneeling: 1-33%/day
Reaching: 1-33%/day
Overhead Reaching: 1-33%/day
Crawling: Never
Twist/Pivot at Waist: 1-33%/day
Bending: 1-33%/day
Upward Gaze: 1-33%/day
Downward Gaze: 1-33%/day
Squat: 1-33%/day
Balance: Rarely
Light Grasping: 1-33%/day
Heavy Grasping: Rarely
Fine Motor: 1-33%/day
Foot Pedal: Rarely
Hand Controls: 34-66%/day
Title: QC Analyst
Location : Boulder, CO
Duration : 12-18 Months contract
First shift hours: Mon-Friday, 8 am - 4 pm
- Conduct routine preparations for stability, raw materials, in-process, microbiology/ cleaning validation program and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements
- Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements
- Ability to exercise judgment and appropriately raises issues to QC management
- Key focus will be preparing solutions (mobile phase, diluent, etc) and standard/sample preparations
- Outstanding interpersonal skills, both written and oral, and will be encouraged to collaborate with other analysts and management
- Ensures equipment is performing well and communicates and takes appropriate action as necessary
- Required to follow good documentation practices
- Works cross-functionally to complete projects and testing
- Job Posting Qualifications
Job Posting Qualifications
- Bachelor’s or equivalent
- Generally, requires minimal to no prior relevant work experience
- Demonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpful
- Proven skills in coordinating and leading day to day tasks and working in collaboration to accomplish deadlines and objectives
Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess’ patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world.
The Role
We are seeking a motivated and detail-oriented Research Associate with strong hands-on experience in chromatographic analysis to support QC release and stability testing. The successful candidate will perform routine cGMP QC testing using HPLC methods (RP-HPLC, SEC, IEX), Agilent HPLC systems, and additional supporting assays in a fast-paced, collaborative environment. This is a unique opportunity to be part of an emerging early-phase clinical company bringing innovative technology to the global market.
Key Responsibilities
- Perform routine QC release and stability testing using HPLC methods including RP-HPLC, SEC, and IEX.
- Prepare samples, operate Agilent HPLC systems, verify system suitability, and ensure analyses meet method and specification requirements.
- Execute complementary analytical assays such as UV-Vis, pH, surface tension, and mechanical tests.
- Maintain complete, accurate documentation in compliance with cGMP, ALCOA+, and data integrity requirements.
- Conduct routine instrument care (solvent flushes, column care, daily checks) and assist troubleshooting under supervision.
- Process and review chromatographic data in Agilent OpenLab CDS.
- Support method qualification, validation, and transfer activities by executing protocols and recording observations.
- Maintain calibration, maintenance, and service records for analytical instrumentation.
- Independently author method SOPs, analytical protocols, technical reports, and contribute to regulatory submissions.
- Collaborate cross-functionally with QC, Analytical Development, Process Development, Manufacturing, and Regulatory teams to enable program success.
- Maintain rigorous laboratory documentation and complete, audit-ready analytical records.
- Thrive in a fast-paced, cross-functional environment with excellent communication and organizational skills.
Qualifications
- Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or related field with 1–3 years of experience; or a master’s degree with relevant laboratory experience.
- Hands-on experience operating HPLC systems; Agilent systems and OpenLab CDS experience strongly preferred.
- Practical experience with chromatographic techniques including RP-HPLC, SEC, and IEX.
- Experience supporting QC release or stability testing in a GMP/GLP environment.
- Strong attention to detail and ability to follow SOPs precisely.
- Excellent documentation practices and understanding of data integrity.
- Strong organizational skills with the ability to manage multiple workflows and prioritize effectively in a fast-paced environment.
- Excellent verbal and written communication skills and comfort working within interdisciplinary teams.
- Commitment to collaborative work within interdisciplinary project teams.
At Vaxess, we’re bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to
Step into a role where precision meets purpose-become a Materials Technician supporting essential pharma and respiratory operations
Proclinical is seeking a Materials Technician to support operations in the respiratory and pharmaceutical industry.
Primary Responsibilities:
The successful candidate will focus on material handling, shipping and receiving, inventory control, and adherence to quality and safety standards. You will play a key part in ensuring smooth workflows and compliance with cGMP procedures.
Skills & Requirements:
- High school diploma or equivalent education.
- Experience in material handling, inventory control, and shipping/receiving processes.
- Familiarity with SAP systems and cGMP procedures.
- Ability to operate forklifts and other material handling equipment.
- Knowledge of DOT requirements for material transport.
- Strong attention to detail and commitment to quality and safety standards.
The Materials Technican's responsibilities will be:
- Operate material handling equipment such as forklifts, pallet jacks, or hand trucks to move and organize materials.
- Utilize computerized or automated systems to complete tasks efficiently.
- Lead on-the-job training for new team members.
- Participate in departmental inspections as a trained L1 Auditor.
- Perform receipt and quarantine of incoming cGMP raw materials in SAP, adhering to quality and safety requirements.
- Conduct raw material control sampling and consumable inspections following material specifications and input data into sample tracking systems.
- Assist with shipping bulk drug products per cGMP procedures to ensure quality, integrity, and timely delivery.
- Follow DOT requirements for material transport.
- Maintain accurate inventory levels in SAP and conduct periodic inventory checks.
- Dispense controlled raw materials in clean room environments for cGMP use.
- Perform bulk drug freeze-down procedures using controlled rate freezing equipment.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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