CrawlJobs Logo

QC Associate Scientist I

https://www.randstad.com Logo

Randstad

Location Icon

Location:
United Kingdom , Basingstoke

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

13.00 - 14.00 GBP / Hour

Job Description:

We are looking for a QC Associate Scientist I to join our Microbiology Division in Basingstoke. In this role, you will perform essential microbiological quality control testing to ensure our products meet the high safety and performance standards required to make the world healthier, cleaner, and safer. This is a full-time, onsite position with a 9-month duration.

Job Responsibility:

  • Carry out testing in accordance with specific methods, including Level 1-3 testing and media preparation
  • Record all test results within the SAP Quality Management module and maintain accurate training records
  • Complete Out of Specification (OOS) reports and assist with investigations into potential problems or failures
  • Perform equipment checks, audits, cleaning, waste management, and consumable replenishment
  • Use autoclaves and engage in continuous improvement using lean methodologies (PPI) to improve departmental processes

Requirements:

  • Level 6 equivalent qualification in Microbiology or a related subject (or equivalent experience)
  • Candidates currently studying toward this level will also be considered
  • Previous experience in a microbiological laboratory environment and basic lab skills (pipetting, swabbing, streaking, etc.)
  • High attention to detail, strong communication skills, and good numeracy
  • Proficiency in MS Office
  • experience with SAP is preferred

Additional Information:

Job Posted:
March 25, 2026

Expiration:
June 02, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for QC Associate Scientist I

Associate Scientist

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...
Location
Location
United States of America , South San Francisco
Salary
Salary:
110633.00 - 140020.00 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associate Degree or equivalent in Biological Science program with at least 3 years of histology laboratory experience
  • HT (ASCP) or HLT (ASCP) preferred
  • Experience in histopathology / pathobiology in an industry setting
  • Hands-on experience in a variety of histology-based methodologies and equipment
  • Experience in documentation, including laboratory information management systems usage
  • Comfortable working in a dynamic environment designed to promote frequent interaction and brainstorming
  • Ability to manage multiple projects simultaneously
  • Excellent communication skills
Job Responsibility
Job Responsibility
  • Perform workflows for histology preparation of specimens, including all documentation in required laboratory information systems and databases, as well as team communications
  • Perform basic and advanced histology procedures (fixation and processing of tissues, embedding, microtomy, H&E staining, special stains, coverslipping, slide scanning, slide QC)
  • Review work to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, and procedures
  • Ensure equipment is functional and maintained in good working order, and that lab safety protocols are adhered to
  • Perform all other related duties as assigned
What we offer
What we offer
  • Retirement and Savings Plan with generous company contributions
  • group medical, dental and vision coverage
  • life and disability insurance
  • flexible spending accounts
  • discretionary annual bonus program
  • stock-based long-term incentives
  • award-winning time-off plans
  • flexible work models where possible
  • Fulltime
Read More
Arrow Right

QC Associate II

As a QC Associate II, you will be responsible for inspecting raw materials, inte...
Location
Location
United States , Pleasanton
Salary
Salary:
31.78 - 43.03 USD / Hour
10xgenomics.com Logo
10x Genomics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. in Biological Engineering, Molecular Biology, Analytical Chemistry, Chemical Engineering, or related discipline
  • 3 years of relevant laboratory experience in manufacturing and QC of life science products (e.g., PCR, NGS, protein analysis, HPLC)
  • Willingness to rotate through various laboratory and administrative tasks and ability to prioritize workload, and adhere to deadlines
  • Proficiency in data entry using tools such as Excel, Oracle ERP and LIMS
  • Demonstrated ability to work both independently and as part of a team
  • Strong attention to detail, organization, and commitment to quality
  • Effective communication and observational skills
  • Excellent critical and logical thinking skills to analyze and troubleshoot issues
Job Responsibility
Job Responsibility
  • Conduct quality control testing on raw materials, intermediates, and finished products according to established procedures
  • Perform molecular biology techniques, including PCR, next-generation sequencing, microscopy, cell and tissue based assays, and HPLC
  • Participate in instrument QC workflows, including training to work with mechanical stages and read technical drawings and first article inspection report
  • Accurately follow work instructions and standard operating procedures, while proactively identifying and reporting discrepancies
  • Maintain comprehensive and accurate records, including QC batch files and Receiving Inspection Reports, in accordance with Good Documentation Practices
  • Efficiently communicate complications identified during QC testing and collaborate with engineers and scientists to resolve issues
  • Initiate non-conformance, deviation reports, engineering change orders (ECO) and follow up on necessary action items. Ensure that lab operations and workflow execution are compliant with ISO requirements. Drive completion of investigations and minimize disruptions to QC operations
  • Assist in root cause investigations for non-conforming lots and contribute to continual improvement efforts
  • Support process and product development activities, including process optimization, guard band and stability studies, and gauge R&R
What we offer
What we offer
  • Equity grants
  • Comprehensive health and retirement benefit programs
  • Annual bonus program or sales incentive program
  • Health Package
  • Easy-to-use Benefits
  • Family oriented policies like parental leave
  • Generous Time Off
  • Fulltime
Read More
Arrow Right

Sr. QC Associate I

10x Genomics is looking for a Sr. QC Associate I to join our Quality Control tea...
Location
Location
United States , Pleasanton
Salary
Salary:
37.64 - 50.91 USD / Hour
10xgenomics.com Logo
10x Genomics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. in Analytical Chemistry, Biochemistry, or a related field
  • 5+ years of laboratory experience specifically in a QC environment
  • Strong hands-on experience with NGS and tissue-based assays (including immunofluorescence and flow cytometry)
  • Proficiency in PCR, qPCR, spectrophotometry, spectrofluorometry, and HPLC
  • Experience collaborating with R&D and QA on risk-based QC strategy assessment including assay robustness, assay cost, and alignment of QC checkpoints to the manufacturing process
  • A solid understanding of New Product Introduction (NPI) and manufacturing processes
  • Ability to manage and track diversified QC assays and projects in a rapidly evolving environment
  • Strong critical thinking, logical problem-solving skills, and the ability to communicate effectively with stakeholders
Job Responsibility
Job Responsibility
  • Execute QC Testing: Perform quality control operations according to defined procedures to ensure the integrity and quality of raw materials, intermediates, and finished goods
  • Data Analysis & Disposition: Complete QC testing in a timely manner and disposition materials based on established acceptance criteria
  • Product Development and Sustaining Support: Serve as the primary QC point of contact to oversee project completion, providing expert guidance on assay setup and assisting in the introduction and optimization of new products and processes
  • Assay Cross-Training: Cross-train on various inspections, including first article inspection, metrology, microscopy, analytical assays, and NGS
  • Documentation: Maintain quality control batch records and ensure Good Documentation Practices (GDP) under ISO requirements. Accurately track QC test data, calibration records, and inventory. Draft Work Instructions in collaboration with the Manufacturing Systems & Engineering team
  • Quality Compliance: Initiate non-conformance, deviation reports, engineering change orders (ECO) and follow up on necessary action items. Ensure that lab operations and workflow execution are compliant with ISO requirements
  • Problem Solving: Effectively identify and communicate complications arising from QC testing with minimal supervision. Work closely with scientists to establish and maintain technical solutions. Drive completion of investigations and minimize disruptions to QC operations
What we offer
What we offer
  • Equity grants
  • Comprehensive health and retirement benefit programs
  • Annual bonus program or sales incentive program
  • Generous time off
  • Competitive and comprehensive health benefits package
  • Family friendly policies like parental leave
  • Fulltime
Read More
Arrow Right

Associate Scientist, Process Development (Process Validation & Business Strategy)

In this vital role you will be a part of the Process Development Drug Substance ...
Location
Location
United States , Holly Springs
Salary
Salary:
97377.00 - 118653.00 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree and 3 years of Process Development or Scientific experience
  • Master’s degree and 1 years of Process Development or Scientific experience
  • 2 – 4 years of experience in a Biotech/Pharma Process Development, MFG, QC, or laboratory role
  • Knowledge in broad aspects of biologics processing, for example cell culture, purification, analytical methods, or product quality attributes
  • Familiarity in operational aspects of process development lab or commercial biopharma manufacturing
  • Experienced with software such as Holistic Lab Execution Environment (HLEE), Tableau, MS PowerBI, spotfire, and/or databricks
  • Able to apply digital tool skills to solve business process issues and evaluate opportunities for process improvements
  • Excellent written and verbal communication
  • Be a self-starter with the ability to take on several projects at one time.
Job Responsibility
Job Responsibility
  • Lead and develop the Process Development safety, training, and compliance monitoring operation
  • Holistic Lab Execution Environment (HLEE) champion for the process development lab
  • Develop digital tools to improve business process efficiencies and identify bottlenecks within the process development operation
  • Develop digital tools to support process validation and process monitoring activities
  • Support and develop the Amgen North Carolina (ANC) PD DST knowledge management ecosystem, alignment of ANC PD business process to network practice, and optimizing the ANC PD business process
  • Provide process floor or lab support as required.
What we offer
What we offer
  • Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
  • Fulltime
Read More
Arrow Right

Associate Scientist Pharmaceuticals

Join our Scientist GMP analytical team to develop, validate, and transfer using ...
Location
Location
Belgium , Beerse
Salary
Salary:
Not provided
amaris.com Logo
Amaris Consulting
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BSc/MSc in Chemistry, Analytical Chemistry, or related field
  • 2+ years’ hands-on experience with Karl Fischer titration in a GMP pharmaceutical environment
  • Proven track record in liquid-chromatography method development and validation (HPLC/UPLC)
  • Strong documentation skills in English
  • familiarity with ICH Q2(R1), USP <921>, and FDA/EMA guidelines
Job Responsibility
Job Responsibility
  • Karl Fischer Expertise: Design, validate, and execute KF titration methods (volumetric & coulometric) for APIs, excipients, and drug products
  • troubleshoot instrument drift, side reactions, and matrix effects
  • LC Method Development: Develop and validate U/HPLC assays for potency, impurities, and stability indicating methods
  • perform method transfers to QC and CMO partners
  • GMP Compliance: Author protocols, reports, and SOPs
  • review data for ALCOA+ principles
  • support regulatory inspections and deviations/CAPA
  • Cross-functional Collaboration: Partner with Process Chemistry, Formulation, and QA to align analytical strategies with project milestones
  • Continuous Improvement: Evaluate new KF reagents, columns, and LC technologies to increase throughput and reduce cost-of-goods
What we offer
What we offer
  • Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees
  • Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions
  • International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe
Read More
Arrow Right

Senior Associate Scientist

Proclinical is seeking a skilled Senior Associate Scientist to support laborator...
Location
Location
United States , Cambridge
Salary
Salary:
40.00 - 43.00 USD / Hour
proclinical.com Logo
Proclinical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Proficiency in cell culture techniques, including handling iPSCs and primary cells
  • Hands-on experience with qPCR and cell-based assays
  • Familiarity with RNA sequencing workflows, including library preparation and sequencing
  • Knowledge of liquid handling systems and automation tools is a plus
  • Ability to work independently and manage multiple tasks in a fast-paced environment
  • Strong communication and collaboration skills to effectively work within a team
  • A proactive and dependable approach to problem-solving and task execution
  • Bachelor's degree in biology or a related field
  • a Master's degree is preferred but not required
Job Responsibility
Job Responsibility
  • Perform cell culture using iPSCs, primary cells, and immortalized cell lines
  • Conduct qPCR and other cell-based assays to support research objectives
  • Maintain and optimize experimental protocols for RNA sequencing, including library preparation, QC, and sequencing
  • Operate and troubleshoot liquid handling systems and automation tools such as PerkinElmer JANUS and Beckman i7
  • Collaborate with team members to support NGS workflows and related tasks
  • Ensure accurate documentation of experimental results and maintain lab records
Read More
Arrow Right

Process Scientist I

This position is responsible for material processing, reagent formulation, techn...
Location
Location
United States , Stillwater, Minnesota
Salary
Salary:
61000.00 - 70000.00 USD / Year
int.diasorin.com Logo
Diasorin
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associates degree in Chemistry, Biology or Medical Technology required
  • 1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry
  • Basic understanding of immunology and immunoassay techniques
  • Ability to work in a regulated environment
  • Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
  • Working knowledge of MS Excel
  • familiarity with Google Suite
  • Basic understanding of statistical analysis
  • Advanced skills in: Math and calculations
  • Writing and documentation
Job Responsibility
Job Responsibility
  • Perform material processing and reagent for formulation bulk intermediates and components
  • Determine reprocessing need for calibrator, controls, and conjugates with assistance
  • Perform Good laboratory practices - maintain clean workspace in QC and Reagent Prep labs. Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
  • Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility
  • Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
  • Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family
  • Assign calibrator values to optimize kit performance
  • Assign kit control ranges per established procedures
  • Monitor internal control supplies and manufacture new controls as needed
  • Perform second-checking to ensure accurate records
What we offer
What we offer
  • comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks
  • may be eligible to participate in an annual incentive program
  • Fulltime
Read More
Arrow Right

Medical Laboratory Scientist II - Chemistry

Join a team that’s setting the standard for safety and quality. Every day as a Q...
Location
Location
United States , Royal Oak
Salary
Salary:
Not provided
questdiagnostics.com Logo
Quest Diagnostics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • One (1) year full-time experience or training (high complexity testing) in a clinical laboratory setting
  • BS/BA in Medical Technology, Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
  • Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
  • United States-educated candidates must provide a detailed original transcript
  • Proven leadership and problem-solving skills
  • Must be detail-oriented, have the ability to work independently, establish work priorities and to handle several tasks simultaneously for maximum department efficiency
  • Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients
  • Communication skills necessary to handle telephone inquiries from clients
  • Ability to deal with client information in a confidential manner
  • Proficiency in Microsoft Office (Word, Excel and Outlook) and Laboratory Information Systems
Job Responsibility
Job Responsibility
  • Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified
  • Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all applicable instruments/procedures in the department
  • Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned
  • Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
  • Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
  • Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
  • Ensure reagents/test kits have received dates, expiration dates and if applicable opened dates
  • Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test
  • Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures
  • Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same
What we offer
What we offer
  • Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
  • Best-in-class well-being programs
  • Annual, no-cost health assessment program Blueprint for Wellness®
  • healthyMINDS mental health program
  • Vacation and Health/Flex Time
  • 6 Holidays plus 1 "MyDay" off
  • FinFit financial coaching and services
  • 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
  • Employee stock purchase plan
  • Life and disability insurance, plus buy-up option
  • Fulltime
Read More
Arrow Right