Qc Associate Scientist I Job at Randstad (Basingstoke)

QC Associate Scientist

Are you looking to kickstart or advance your career within a world-class laborat...

Location

United Kingdom , Basingstoke

Salary:

14.14 GBP / Hour

Randstad

Expiration Date

June 10, 2026

Requirements

Degree qualified (Level 6) in Microbiology or a related science subject (or currently studying towards one)
Candidates with equivalent industry experience (QBE) are also encouraged to apply
Experience in basic lab techniques such as pipetting, swabbing, streaking, and pouring plates
Proficiency in MS Office
experience with SAP is highly desirable
High attention to detail
strong numeracy skills
ability to follow complex methods precisely
Candidates must be eligible to live and work in the UK

Job Responsibility

Carry out Quality Control testing in accordance with strict specifications and methods
Microbiological Testing: Conducting AST (Antibiotic Susceptibility Testing) and media preparation
Laboratory Maintenance: Operating autoclaves, managing waste, replenishing consumables, and ensuring a clinical level of cleanliness
Data Integrity: Recording all test results accurately within the SAP Quality Management module
Compliance: Following Standard Operating Procedures (SOPs) and assisting with Out of Specification (OOS) investigations
Collaboration: Participating in Daily Tier Board meetings and providing availability dates to planning and customer service teams

What we offer

Early finish on Friday (14:30)

Fulltime

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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

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States of America , South San Francisco

Salary:

110633.00 - 140020.00 USD / Year

Amgen

Expiration Date

Until further notice

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

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

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

Process Scientist I

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

Location

United States , Stillwater, Minnesota

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

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

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

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

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

Senior Scientist I, Quality Control

This position is within the Quality Control structure, under the Quality Organiz...

Location

United States , Verona

Salary:

90000.00 - 108000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

Requirements

M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience
B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience
Fully knowledgeable of cGMP and ICH laboratory requirements and operations
Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices

Job Responsibility

Fully knowledgeable of cGMP requirements and ICH guidelines
Works independently to meet project timelines and deliverables with minimal supervision to no supervision
Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols
Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures
Proficient with various analytical instrumentation theory and practice
Executes training requirements for assigned SOPs and participates in department specific training modules
Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples
Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation
Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization
Performs analyses in a timely and efficient manner to support ongoing prioritized studies

What we offer

competitive salaries and an excellent benefit package

Fulltime

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Qc Associate Scientist I

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