QC Associate Scientist I Job at Randstad (Basingstoke)

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

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

New

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

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

Scientist, LCMS PK Bioanalytical

An exciting opportunity is available for a Scientist to join the PK LCMS group i...

Location

United States , Andover

Salary:

79400.00 - 128500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MS with 4 to 6 years of relevant work experience, ideally mostly in industry (or BS/BA with 6 to 8 years of experience)
Expertise in development, characterization, and implementation of bioanalytical LCMS assays
Experience in the operation and troubleshooting of LCMS instrumentation and associated operating/data analysis software including Skyline, Analyst, Sciex OS and Xcalibur
Hands-on experience of biological sample preparation procedures for quantitative LCMS assays on biotherapeutics
Knowledge of writing scripts to set up methods for automated liquid handler system
Knowledge of protein biochemistry of therapeutic antibodies, fusion proteins or ADCs

Job Responsibility

Responsible for the development, qualification and implementation of PK/PD assays using mass spectrometry in support of discovery and preclinical projects
Works with group leads or other discovery and regulated bioanalytical team members and project team members to accomplish goals
Participates in technology development and implementation by exploring new workflows, including automation, high throughput sample preparation and instrumentation in protein quantitation, to expand the group’s PK LCMS bioanalytical capabilities
Participate in all phases of mass spectrometry laboratory operations including technology evaluations, the development of sample preparation and separation methods, data analysis, interpretation, reporting and follow up discussions with the project teams on utilizing the data in appropriate decision making
Ensure all tasks and responsibilities are carried out according to scientific and ethical standards e.g. responsible for electronic notebook record keeping
QC and peer review of data and reports

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
bonus target of 7.5% of the base salary
Relocation assistance may be available

Fulltime

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 06, 2026

Expiration:
April 27, 2026

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Randstad

Location:United Kingdom , Basingstoke

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 06, 2026

Expiration:April 27, 2026

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Job Posted:
March 06, 2026

Expiration:
April 27, 2026