QC Associate Scientist I Job at Randstad (Basingstoke)

QC Associate Scientist I

The main function of a QC Associate Scientist is to perform microbiological qual...

Location

United Kingdom , Basingstoke

Salary:

12.00 - 13.00 GBP / Hour

Randstad

Expiration Date

April 27, 2026

Requirements

Qualified educationally to a Level 6 equivalent in a Microbiology or related subject (or QBE)
Has good numeracy skills, and the ability to read and follow methods / SOPs precisely
Has at experience of QC testing within a microbiology laboratory environment and ideally has experience in using SAP and MS Office software packages
Has experience in basic laboratory skills and techniques (pipetting, swabbing, streaking, pouring plates etc)
Consistently demonstrates our 4i Values of Integrity, Intensity, Innovation & Involvement
Puts the Customer First
Owns Their Results
Finds a Better Way Every Day

Job Responsibility

Carry out Quality Control Testing in accordance with Oxoid test specifications and methods
Plan, track and control the progress of products under test, and provide accurate availability dates to planning and customer services
Alerting the QC Team Leader of potential problems/failures and assist with further investigation
Ensure all test results are recorded within the SAP Quality Management module
Equipment checks and audits
Cleaning
Waste management
Consumable replenishing
Use of autoclaves
Ensure processes and procedures are carried out in accordance with the laboratory and company Quality Systems

QC Associate II

As a QC Associate II, you will be responsible for inspecting raw materials, inte...

Location

United States , Pleasanton

Salary:

31.78 - 43.03 USD / Hour

10x Genomics

Expiration Date

Until further notice

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

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

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

Sr. QC Associate I

10x Genomics is looking for a Sr. QC Associate I to join our Quality Control tea...

Location

United States , Pleasanton

Salary:

37.64 - 50.91 USD / Hour

10x Genomics

Expiration Date

Until further notice

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

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

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

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

In this vital role you will be a part of the Process Development Drug Substance ...

Location

United States , Holly Springs

Salary:

97377.00 - 118653.00 USD / Year

Amgen

Expiration Date

Until further notice

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

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

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Fulltime

New

Associate Scientist Pharmaceuticals

Join our Scientist GMP analytical team to develop, validate, and transfer using ...

Location

Belgium , Beerse

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

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

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

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

Senior Associate Scientist

Proclinical is seeking a skilled Senior Associate Scientist to support laborator...

Location

United States , Cambridge

Salary:

40.00 - 43.00 USD / Hour

Proclinical

Expiration Date

Until further notice

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

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

Process Scientist I

This position is responsible for material processing, reagent formulation, techn...

Location

United States , Stillwater

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates degree in Chemistry, Biology or Medical Technology required
Bachelor's or Master's degree preferred in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience
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

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

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

Lab Analyst I

Lab Analyst I- Early Phase Clinical Research- ICON San Antonio TX. ICON plc is a...

Location

United States , Houston

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Associate or bachelor’s degree in medical laboratory science
MT/MLT/ASCP required (Clinical Lab Scientist license)
Minimum 2 years in a laboratory environment, preferably in a clinical pathology laboratory or related industry
Proficient in laboratory techniques
Good communication skills and the ability to work effectively in a team environment

Job Responsibility

Performs and reports routine and special laboratory tests on clinical trial specimens to aid in subject safety and in accordance to protocol requirements
Detect abnormalities as indicated in protocol
Performs specimen processing and testing independently to include waived and moderate complexity testing
Analyzes test results and assumes accountability for accuracy
Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary and knows when to notify lab management
Understands, performs, and practices quality control management to include running controls, evaluating data, documentation of data, and taking corrective action as required
Communicates any relevant QC information to Supervisor or Manager
Must cross-train to other laboratory sections as needed
Calculates, enters, and/or verifies results of laboratory procedures
Utilizes the Laboratory Information System and eSource system

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Parttime

QC Associate Scientist I

Randstad

Location:
United Kingdom , Basingstoke

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 25, 2026

Expiration:
June 02, 2026

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Location:United Kingdom , Basingstoke

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Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 25, 2026

Expiration:June 02, 2026

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