quality control scientist

United Pharma Technologies Inc

<div>
 
 
 Job Title: QC Scientist
 
 
 
 
 Location: North Carolina (Onsite)
 
 
 
 
 
 
 
 Job Description:
 
 
 
 Seeking a
 
 QC Scientist
 
 with 2&ndash;5 years of experience in a regulated medical or pharmaceutical environment. The role involves routine quality control testing, GMP documentation, and support of laboratory investigations to ensure product quality and compliance.
 
 
 
 
 
 
 Responsibilities:
 
 
 <ul>
 <li>
 Perform QC testing using techniques such as HPLC, GC, UV, FTIR, and wet chemistry
 </li>
 <li>
 Document and review results per GMP/FDA requirements
 </li>
 <li>
 Support OOS/OOT, deviations, CAPA, and method validation activities
 </li>
 <li>
 Maintain SOPs, lab records, and instrument documentation
 </li>
 </ul>
 
 
 
 
 
 Requirements:
 
 
 <ul>
 <li>
 BS/MS in Chemistry, Biology, or related field
 </li>
 <li>
 2&ndash;5 years QC lab experience in medical/pharma industry
 </li>
 <li>
 Strong knowledge of GMP and regulatory guidelines
 </li>
 </ul>
 
 
</div>

Quality Control Scientist

Adecco

Quality Control Associate Scientist (Temporary - until February 2026) Basingstoke, UK Full-time, Temporary Contract Are you an experienced Quality Control professional looking to make an impact in a leading life sciences organisation? We have an exciting opportunity for a Quality Control Associate Scientist to join our team in Basingstoke on a temporary basis until February 2026. About the Role As a Quality Control Associate Scientist, you will play a key role in ensuring our products meet the highest standards of quality and compliance. You will carry out a range of QC testing activities in accordance with Oxoid test specifications and methods, supporting the timely and accurate release of products. Key Responsibilities <ul> <li> Perform Quality Control testing in line with Oxoid test specifications, including Level 1, 2, and 3 testing methods. </li><li> Prepare media and manage the use of autoclaves. </li><li> Complete Out of Specification (OOS) reports and assist with investigations. </li><li> Maintain accurate and up-to-date training records. </li><li> Plan, track, and control the progress of products under test, providing reliable availability dates to Planning and Customer Services. </li><li> Proactively alert the QC Team Leader to any potential issues or failures and support follow-up investigations. </li><li> Record all test results within the SAP Quality Management module. </li><li> Conduct equipment checks, cleaning, and audits to ensure compliance with quality standards. </li><li> Manage waste disposal and replenish consumables as required. </li></ul> About You We're looking for someone with: <ul> <li> Previous experience in a Quality Control or laboratory environment (ideally within life sciences, microbiology, or pharmaceuticals). </li><li> Strong attention to detail and a proactive approach to problem-solving. </li><li> Familiarity with SAP Quality Management or similar systems (desirable). </li><li> Excellent organisational and communication skills. </li><li> The ability to work effectively in a fast-paced, team-oriented environment. </li></ul> Contract Details <ul> <li> Location: Basingstoke </li><li> Contract type: Temporary (until February 2026) </li><li> Hours: Full-time </li></ul> Join a team dedicated to maintaining the highest standards of product quality and safety - and help us deliver excellence every day. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

QC Associate Scientist

Thermo Fisher Scientific

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact?
 
You'll perform sophisticated analyses to ensure product quality and safety in our laboratories. As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll work with analytical instruments and technologies while making a meaningful impact on patient health through precise quality control testing. 
 
Working with cross-functional teams, you'll execute validated test methods, participate in method development and validation activities, investigate out-of-specification results, and maintain detailed documentation of analyses. You'll contribute to continuous improvement initiatives and help establish robust analytical processes while adhering to cGMP requirements and safety standards.
We have 2 positions available.
A Day in the Life:<ul><li>
Perform testing on In-Process, DS release, DP release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects</li><li>
Participate in analytical method validation/transfer, method establishment/qualification routine and stability analysis.</li><li>
Conduct GMP testing in an analytical laboratory environment using Separation Techniques, BioAssay Analysis and Compendia test methods (i.e. Reverse Phase, SEC, Titer concentration, iCE, pH, Osmolarity, Residual DNA, Appearance)</li><li>
Compiles data for documentation of test procedures, prepares reports. Ensures all testing processes, monitoring, and departmental documentation meet SOPs and cGMP regulatory standards.</li><li>
Participate in the development of new concepts, techniques, and standards. Involved with assisting in the preparation of CoAs.</li><li>
Recognize and report out-of-specification/ out-of-trend results to laboratory management; recommend solutions.</li><li>
Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines</li><li>
Partake in laboratory activities, including safety inspections and client audits in a timely matter.</li></ul><div>
Keys to Success: 
<ul><li>Advanced degree with no prior experience, or Bachelor's degree with 2 years of experience in a GMP regulated laboratory environment performing analytical testing</li><li>Preferred Fields of Study: Chemistry, Biology, Biochemistry, or related scientific field</li><li>Expertise in analytical techniques such as HPLC, GC, CE, ELISA, PCR, and other bioanalytical methods</li><li>Proficient in aseptic techniques and environmental monitoring procedures</li><li>Strong knowledge of cGMP regulations and quality control requirements</li><li>Experience with laboratory information management systems (LIMS) and quality management systems</li><li>Excellent documentation practices and attention to detail</li><li>Strong problem-solving and analytical skills</li><li>Ability to work both independently and collaboratively</li><li>Proficiency with Microsoft Office applications</li><li>Strong written and verbal communication skills</li><li>Ability to lift up to 30 pounds and stand for extended periods</li><li>Willingness to wear required PPE including lab coat, safety glasses, and gloves</li><li>May require flexible scheduling including occasional weekend work</li><li>Experience with method validation and transfer activities preferred</li><li>Knowledge of data integrity requirements and good documentation practices</li><li>Demonstrated ability to investigate out-of-specification results and author technical reports</li></ul></div>
Excellent Benefits<ul><li>
Benefits &amp; Total Rewards | Thermo Fisher Scientific</li><li>
Medical, Dental, &amp; Vision benefits-effective Day 1</li><li>
Paid Time Off &amp; Designated Paid Holidays</li><li>
Retirement Savings Plan</li><li>
Tuition Reimbursement</li></ul>
OTHER<ul><li>
Relocation assistance is NOT provided</li><li>
Must be legally authorized to work in the United States now or in the future, without sponsorship.</li><li>
Must be able to pass a comprehensive background check, which includes a drug screening</li></ul></div>

QC Scientist II

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact? 
Join our collaborative team at Thermo Fisher Scientific, where you'll contribute to our mission of making the world healthier, cleaner, and safer. As a QC Scientist III, you'll perform sophisticated analytical testing and provide quality oversight for biopharmaceutical products. You'll work with advanced technology and collaborate with cross-functional teams to ensure product safety and compliance with regulatory requirements. This role offers significant opportunities to grow your expertise while supporting the development and manufacturing of life-changing therapeutics. 
 
You'll conduct complex analytical testing, lead method validations, perform data review, and troubleshoot technical issues. Key responsibilities include executing and reviewing tests for product release, stability, and in-process samples; authoring and reviewing technical documentation; participating in investigations; and interfacing with clients and regulatory authorities. Your work will directly impact patient safety and product quality while advancing scientific innovation.
A Day in the Life:<ul><li>
Conduct GMP testing in an analytical laboratory environment using Separation Techniques, BioAssay Analysis and Compendia test methods (i.e.,Reverse Phase, SEC, Titer concentration, iCE, pH, Osmolarity, Residual DNA, Appearance)</li><li>
Help develop and build the foundation of a liquid chromatography technical team by implementing standard practices and policies.</li><li>
Perform testing on In-Process, DS release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects</li><li>
Recognize and report out-of-specification/ out-of-trend results to laboratory management; recommend solutions</li><li>
Participate in analytical method validation/transfer, method establishment/qualification routine and stability analysis.</li><li>
Compiles data for documentation of test procedures, prepares reports. Ensures all testing processes, monitoring, and departmental documentation meet SOPs and cGMP regulatory standards.</li><li>
Participate in the development of new concepts, techniques, and standards. Involved with assisting in the preparation of CoAs.</li><li>
Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines</li><li>
Participating in laboratory activities, including safety inspections and client audits</li><li>
Communicate findings and discuss relevance of your data to a multi-discipline team consisting of upstream and downstream process development scientists, quality control, quality assurance, process engineers and our customers.</li></ul>
Keys to Success:<ul><li>Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in GMP pharmaceutical/biopharmaceutical quality control</li><li>Preferred Fields of Study: Chemistry, Biology, Biochemistry, or related scientific field</li><li>Expertise in analytical techniques such as HPLC, UPLC, CE-SDS, cIEF/ICE, ELISA, and cell-based assays</li><li>Strong knowledge of FDA, EMA, ICH, and GxP regulations</li><li>Experience with method validation, transfer, and qualification</li><li>Proficiency in data analysis and laboratory information management systems</li><li>Advanced technical writing and documentation skills</li><li>Strong project management and organizational abilities</li><li>Excellent interpersonal and communication skills</li><li>Ability to work independently and lead cross-functional teams</li><li>Experience with quality investigations and CAPAs</li><li>Proficiency with Microsoft Office Suite and relevant analytical software</li><li>Ability to wear PPE and work in laboratory environments</li><li>May require weekend/flexible scheduling based on business needs</li><li>Physical requirements include standing, lifting up to 25 lbs, and manual dexterity</li><li>Strong attention to detail and problem-solving skills</li><li>Experience mentoring team members preferred</li></ul>
Excellent Benefits<ul><li>
Benefits &amp; Total Rewards | Thermo Fisher Scientific</li><li>
Medical, Dental, &amp; Vision benefits-effective Day 1</li><li>
Paid Time Off &amp; Designated Paid Holidays</li><li>
Retirement Savings Plan</li><li>
Tuition Reimbursement</li></ul>
OTHER<ul><li>
Relocation assistance is NOT provided.</li><li>
Must be legally authorized to work in the United States now and in the future, without sponsorship.</li><li>
Must be able to pass a comprehensive background check, which includes a drug screening.</li></ul></div>

QC Scientist III

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact: 
Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you'll conduct testing of raw materials, in-process samples, finished products, and stability samples. Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients.
We have 3 positions available.
A Day in the Life:<ul><li>
Perform testing on In-Process, DS release, DP release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects</li><li>
Conduct GMP testing in an analytical laboratory environment using Separation Techniques, BioAssay Analysis and Compendia test methods (i.e.,Reverse Phase, SEC, Titer concentration, iCE, pH, Osmolarity, Residual DNA, Appearance)</li><li>
Compiles data for documentation of test procedures, prepares reports. Collaborate with team members and other departments such as quality assurance and data reviewers.</li><li>
Contributes to the development of new concepts, techniques, and standards.</li><li>
Recognize and report invalid/ lab incident/ out-of-specification/ out-of-trend results to laboratory management; recommend solutions.</li><li>
Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines.</li><li>
Participate in laboratory activities, performing safety inspections and ordering supplies.</li></ul><div> 
Keys to Success: 
<ul><li>Bachelor's degree required, no prior experience required</li><li>Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field</li><li>Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods</li><li>Experience with microbiological testing, environmental monitoring, and aseptic techniques</li><li>Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards</li><li>Strong attention to detail with ability to follow standard procedures and maintain data integrity</li><li>Excellent problem-solving skills and logical approach to scientific challenges</li><li>Proficient computer skills including Microsoft Office and laboratory information systems</li><li>Strong written and verbal communication abilities</li><li>Ability to work both independently and collaboratively in a dynamic environment</li><li>Physical requirements include standing/walking for extended periods, lifting up to 50 lbs, and manual dexterity</li><li>Must be able to work in cleanroom environments wearing required PPE</li><li>Ability to work various shifts including nights, weekends, and holidays as needed</li><li>Experience in pharmaceutical/regulated environment preferred but not required</li></ul></div>
Excellent Benefits<ul><li>
Benefits &amp; Total Rewards | Thermo Fisher Scientific</li><li>
Medical, Dental, &amp; Vision benefits-effective Day 1</li><li>
Paid Time Off &amp; Designated Paid Holidays</li><li>
Retirement Savings Plan</li><li>
Tuition Reimbursement</li></ul>
OTHER<ul><li>
Relocation assistance is NOT provided</li><li>
Must be legally authorized to work in the United States now or in the future, without sponsorship.</li><li>
Must be able to pass a comprehensive background check, which includes a drug screening</li></ul></div>

QC Scientist I

Rawabi Integrated Gas Company

Job Description<ul><li>Responsible for both gas and bulk products quality analysis and certification.</li><li>Incoming inspection of raw materials and outsourced products.</li><li>In-process inspection in the gas plants.</li><li>Carry out Final product analysis of all gas products.</li><li>Report failure rate to the concerned immediately and support for the necessary action.</li><li>Maintaining all QC documents relevant to ISO 9001 QMS & ISO 17025</li><li>Responsible for maintaining all analytical equipments and instruments.</li><li>Responsible for housekeeping and safety in Q.C laboratory and premises.</li><li>Carryout in process product quality inspection in coordination with plant operators.</li><li>Inform QC manager about failure rate of products.</li><li>Ensure all equipments (Gas analyzers / G.C's) are being calibrated at regular interval and intact.</li><li>Maintain analysis reports.</li><li>Follow-up quality standards set by the company.</li><li>Measure / monitor KPI's</li><li>Any other tasks assigned by Quality control Manager</li></ul>Skills<li>University degree in Chemistry (Bachelor / Master)</li><li>Minimum 5 years' experience in Quality control functions at manufacturing industries, industrial gas,field experience is an added advantage.</li><li>Professional knowledge of Laboratory analytical equipments, instruments and chemicals</li><li>Technical / analytical ability to execute.</li><li>Self-motivated</li><li>Good computer skills such as MS office and other software knowledge and experience</li><li>Fluent in English and local language</li>EducationBachelor in ChemistryApply Now

Quality Control (QC) Chemist

Prof Compounding Centers of America

<div>Position Summary

The Quality Control Microbiologist performs quality review activities supporting both sterile and non-sterile microbiological testing. This role is responsible for reviewing routine microbiology data, documentation, and quality investigations to ensure compliance with cGMP, cGLP, ISO 17025, A2LA, and USP requirements, as well as Eagle Analytical&rsquo;s Quality Management System. The position works closely with laboratory operations to maintain data integrity, regulatory compliance, and continuous improvement across microbiology testing functions.

What You Will Do
<ul>
<li>Ensure compliance with Eagle Analytical policies, Standard Operating Procedures (SOPs), and the Quality Management System.</li>
<li>Interpret and apply regulatory and accreditation standards, including ISO 17025, cGMP, cGLP, USP, and A2LA requirements.</li>
<li>Support regulatory inspections, client audits, and accreditation assessments as required.</li>
<li>Review microbiological test data and documentation related to sterility, endotoxin, bioburden, microbial limits, environmental monitoring, and particulate matter testing.</li>
<li>Verify data integrity, accuracy, completeness, and traceability for laboratory worksheets, logbooks, and reports.</li>
<li>Maintain accurate and compliant quality records and documentation.</li>
<li>Review and approve quality investigations, including Out-of-Specification (OOS), Nonconformance Reports (NCR), Deviations (DV), Corrective and Preventive Actions (CAPA), change controls, and customer complaints.</li>
<li>Evaluate root cause analyses and corrective action plans for laboratory and process-related issues.</li>
<li>Prepare audit finding reports and determine appropriate corrective and preventive actions.</li>
<li>Support and conduct internal audits of quality systems and microbiology laboratories.</li>
<li>Perform routine compliance walk-through audits to ensure ongoing adherence to regulatory and quality requirements.</li>
<li>Manage auditing, storage, retention, and control of quality documentation and quarantined materials.</li>
<li>Write, review, and approve SOPs, work instructions, forms, and quality records to ensure regulatory compliance and operational consistency.</li>
<li>Assist in creating and maintaining quality manuals, procedures, and controlled documentation.</li>
<li>Prepare and maintain quality-related training materials as assigned.</li>
<li>Communicate findings, trends, and risks with laboratory management and quality leadership.</li>
<li>Support continuous improvement initiatives related to quality systems, documentation, and laboratory compliance.</li>
<li>Perform additional duties and special projects as assigned to support quality and regulatory objectives.</li>
</ul>
Who You Are
<ul>
<li>Bachelor&rsquo;s degree in Microbiology, Biology, or a related life science required.</li>
<li>Experience in sterile and/or non-sterile microbiology testing preferred.</li>
<li>Knowledge of cleanroom practices and microbiological testing principles.</li>
<li>Experience working in a regulated laboratory environment (ISO 17025, cGMP, cGLP) preferred.</li>
<li>Experience reviewing GMP/GLP documentation and quality investigations preferred.</li>
<li>Strong attention to detail with a demonstrated commitment to data integrity and regulatory compliance.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to work independently while collaborating effectively with cross-functional teams.</li>
<li>Proficiency in Microsoft Office applications and electronic document management systems.</li>
<li>ASQ certification or related quality credentials preferred.</li>
</ul>
Who We Are

Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility, bacterial endotoxins, microbial detection, beyond-use dating (BUD) determination and active ingredient potency. State-of-the-art equipment, combined with the experience and knowledge of our team, makes Eagle the best choice for all testing needs. The Eagle team is committed not only to performing the best quality control testing, but also working relentlessly with our customers on solutions if tests receive unexpected results. Learn more at www.eagleanalytical.com.<h4 class="jobSectionHeader">
Education</h4>
Preferred<ul><li>
Bachelors or better in Microbiology and Molecular Cell Sciences or related field</li><li>
Bachelors or better in Microbiology or related field</li><li>
Bachelors or better in Biology or related field</li><li>
Bachelors or better in Biochemistry or related field</li></ul><h4 class="jobSectionHeader">
Behaviors</h4>
Preferred<ul><li>
Team Player: Works well as a member of a group</li><li>
Dedicated: Devoted to a task or purpose with loyalty or integrity</li><li>
Detail Oriented: Capable of carrying out a given task with all details necessary to get the task done well</li></ul><h4 class="jobSectionHeader">
Motivations</h4>
Preferred<ul><li>
Goal Completion: Inspired to perform well by the completion of tasks</li><li>
Self-Starter: Inspired to perform without outside help</li></ul>
Equal Opportunity Employer 
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.</div>

Quality Control Microbiologist

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