Senior Laboratory Support Associate Job at Beautiful Recruitment (Oxford)

Senior/ Principal Laboratory Support Technologist, Optical/ Electrical Characterizations

We are seeking an R&D Laboratory Support Technologist to join our team in conduc...

Location

United States , Albuquerque

Salary:

74700.00 - 144400.00 USD / Year

Sandia National Laboratories

Expiration Date

Until further notice

Requirements

Associates degree in relevant field, or 4 years of equivalent demonstrated experience
Experience with optical characterization techniques, particularly photoluminescence
Experience with electrical characterization methods for semiconductor devices
Ability to obtain and maintain a DOE L clearance

Job Responsibility

Collaborate with technical staff to perform optical characterization using photoluminescence and other methods
Conduct electrical characterization of semiconductor devices
Maintain and update safety documentation to ensure compliance with laboratory standards
Develop and refine standard operating procedures for characterization techniques
Support general lab operation tasks (e.g., keeping supplies stocked and maintaining test capabilities)
Analyze data and present findings in reports and at technical meetings

What we offer

Challenging work with amazing impact
Extraordinary co-workers
Some of the best tools, equipment, and research facilities in the world
Career advancement and enrichment opportunities
Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home)
Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance

Fulltime

Senior Associate Quality Control - Microbiology

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

Location

United States , Thousand Oaks

Salary:

78724.45 - 106509.55 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 4 years of Quality experience OR Associate's + 2 years of Quality experience OR Bachelor's degree and 6 months of Quality, Microbiology or Operations experience
Master's degree

Job Responsibility

Perform microbial assessments and other GMP documentation as required (reports, assessments, SOP revisions)
Support microbial and other QC laboratory investigations
Perform Microbiological testing to support GMP operations across ATO
Perform Microbiological sample and method qualifications including bioburden, microbial identification, sterility, and other microbiological assays as assigned
Perform testing and data review for compendia, non-compendia methods, and routine laboratory procedures
Generate complete, accurate, and concise laboratory documentation using electronic systems, such as LMES, LIMS, and laboratory notebooks
Operate and maintain specialized laboratory equipment and instrumentation
Perform general laboratory housekeeping activities and safety inspections
Maintain training compliance and proficiency
At all times, comply with safety guidelines, cGMPs and other applicable regulatory requirements

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Senior Associate Medical Data Reviewer

In this vital role, the Senior Associate - Medical Data Reviewer is responsible ...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

MBBS, MD, PharmD, BDS, BAMS, BHMS, or other relevant medical/healthcare degree with clinical research experience
Master’s degree in Life Sciences, Pharmacy, Public Health, or related field with 5+ years of clinical research experience
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related discipline with 7+ years of clinical research experience

Job Responsibility

Conduct ongoing medical review of clinical trial data to ensure accuracy, consistency, and clinical relevance
Evaluate adverse events, laboratory data, vital signs, ECGs, imaging, and other key safety and efficacy endpoints
Identify trends, outliers, protocol deviations, and emerging safety signals across studies
Apply medical judgment to distinguish clinically meaningful findings from normal variability
Provide medical input into study start-up activities, including risk assessments and data review strategy
Partner cross-functionally with Clinical Operations, Data Management, Safety, Biostatistics, and vendors to resolve data issues
Contribute to the development and refinement of medical review tools, visualizations, and dashboards (e.g., Spotfire)
Lead or contribute to data review meetings, governance discussions, and issue escalation processes
Author and maintain clear, defensible medical documentation to support inspection readiness
Drive continuous improvement by identifying systemic data quality trends and strengthening review standards and workflows

Process Development Senior Associate - Pivotal Attribute Sciences

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

Location

United States , Thousand Oaks

Salary:

80044.50 - 108295.50 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's degree
OR Bachelor's degree and 2 years of Scientific experience
OR Associate's degree and 4 years of Scientific experience
OR High school diploma / GED and 6 years of Scientific experience
Preferred: Scientific background in method development and product characterization for therapeutic proteins
Preferred Degree in Biochemistry, Analytical Chemistry, Protein Chemistry or related subject area
Excellent written and verbal communication skills, ability to multitask, efficiently plan and follow through on complex projects
A self-starter, and someone who values working in teams

Job Responsibility

Participate in protein characterization studies to support regulatory filings using HPLC/UPLC and mass spectrometry (MS)
Develop, qualify, and transfer analytical methods to Quality Control
Optimize and troubleshoot existing methods
Collaborate with other process development departments to support commercial process development and process characterization studies
Perform method development and qualification studies using HPLC, UPLC, and Capillary Electrophoresis platforms
Perform chromatographic fractionation, peptide mapping, intact mass, and other LC-MS studies
Author results in laboratory notebooks and method development reports
Participate in maintenance of Attribute Sciences instruments
Coordinate and perform attribute identification and characterization studies
Conduct and coordinate accelerated stability studies

What we offer

Comprehensive employee benefits package
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

Fulltime

Senior Associate (In Vivo Pharmacokinetics and Drug Metabolism)

We are seeking a highly motivated, detail-oriented, and collaborative Senior Ass...

Location

United States , Thousand Oaks

Salary:

79424.85 - 107457.15 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's degree
Bachelor's degree with a minimum of 2 years of rodent laboratory animal research experience
Associate's degree with a minimum of 4 years of rodent laboratory animal research experience
High school diploma / GED with a minimum of 6 years of rodent laboratory animal research experience

Job Responsibility

Support senior team members in the execution of preclinical in vivo PKDM-BA studies using mouse and rat models
Assist with routine handling, restraint, husbandry support, and dosing of mice and rats through multiple administration routes including intravenous (IV), oral gavage (PO), subcutaneous (SC), and intraperitoneal (IP)
Perform biological sample collection from rodents including blood, plasma, serum, urine, feces, and tissue specimens under the guidance of experienced scientists and study leads
Conduct clinical observations, monitor rodent health and welfare, and accurately document findings in accordance with study protocols and institutional guidelines
Support rodent necropsy procedures, tissue collection and processing, and basic surgical manipulations as directed by senior staff
Prepare study materials, dosing formulations, laboratory supplies, and associated documentation to facilitate efficient study execution
Maintain accurate, organized, and compliant experimental records and laboratory documentation
Assist with laboratory organization, equipment readiness, and inventory management of research consumables and animal study supplies
Adhere to institutional animal care and use guidelines, SOPs, and laboratory safety procedures
Collaborate effectively with scientists, veterinarians, and laboratory staff to support research timelines and study objectives

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Process Development Senior Associate

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , Cambridge

Salary:

85306.00 - 103484.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree or (foreign equivalent) in Chemical Engineering, Bioengineering, Analytical Chemistry, Biochemistry or a related field & completion of a university-level course, research project, internship, thesis, or one year of experience in the following: 1. Analytical chemistry experience for small molecules, and completion of project deliverables including: designing and conducting targeted metabolomics experiments, extracting and analyzing results via dedicated software: ChemStation, MassHunter, or MassAnalyzer
2. Analytical method development (chromatography and mass spectrometry), related technologies and instrumentation including: U/HPLC, GC, or LC-MS
3. Method qualification and transfer for analytical instruments, along with data analysis and statistical evaluation of experimental results
4. Application analytical instrument troubleshooting across different platforms: Waters, Agilent, or Sciex, and problem solving of such technologies
5. Implementing Standard Operating Procedures in a laboratory environment in accordance with GLP standards
and 6. Maintaining a laboratory notebook.

Job Responsibility

Conduct experiments, analyze results, and implement process improvements to enhance efficiency and product quality
Design, develop, and optimize manufacturing processes
Collaborate closely with a team of analysts and scientists
Responsible for the technical aspects of developing analytical tools to gain understanding of quality attributes in product and process for late phase synthetic small molecule, synthetic peptide, and siRNA programs
Utilize platform and in-depth product attribute knowledge to advance Amgen products and ensure success through pivotal clinical phases to marketing authorization application
Develop, optimize, and execute analytical methods for synthetic small molecules, synthetic peptide, and SiRNA release testing and process characterization
Collaborate closely with drug substance process development team to achieve project objectives and provide analytical data to support drug substance product development.

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
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

Fulltime

Senior Associate - QC Technical Services

Supporting the technical services team, the Senior Associate is responsible for ...

Location

Ireland , Dun Laoghaire

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a Science related field is required
Minimum of 5 + years of laboratory experience in a cGXP laboratory environment including exposure to analytical instrument validation
Detailed knowledge of the methodology and instrumentation and analytical techniques used for biopharmaceutical testing
Understanding of current regulatory requirements for cGXP laboratory equipment validation and electronic record integrity
Demonstrated success in managing an equipment qualification or maintenance program advantageous

Job Responsibility

Supporting the Quality Control Laboratories, the System Owner is responsible for the complete life cycle of QC equipment
Select and procure laboratory equipment in accordance with Amgen requirements
Owns and project manages change controls and adhere to Change Control metrics
Planning, executing and documenting the qualification of new laboratory equipment in a cGxP regulated environment
Developing and maintaining an equipment qualification project plan, requirements, qualification protocols and summary reports as part of the commissioning of new laboratory equipment
Generation and resolution of protocol deviations as required
Writing/contributing to equipment operating procedures and manuals
Designing and conducting training for QC staff, and other department staff as applicable
Developing and maintaining Data Integrity Assessments for QC laboratory systems
Conduct periodic reviews of instrument validation as part of validation life cycle

Fulltime

Senior Associate Quality Assurance

The Incoming Quality Assurance (IQA) Associate position will provide support for...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Masters Degree OR Bachelor's Degree and 2 years of directly related experience OR Associate's Degree and 6 years of directly related experience OR High School Diploma / GED and 8 years of directly related experience
5 years of experience in regulated environment
Experience and basic troubleshooting skills with laboratory and process equipment
Experience with LIMS, SAP, TrackWise, Veeva
Ability to understand, apply and evaluate basic chemistry
Ability to adhere to regulatory requirements, written procedures and safety guidelines
Ability to evaluate documentation/data according to company and regulatory guidelines
Ability to interact with inspectors (internal and external)
Ability to interpret and apply Good Manufacturing Practice (GMP) knowledge
Ability to organize work, handle multiple priorities and meet deadlines

Job Responsibility

Comply with safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
Complete required assigned training prior to execution of required tasks
Perform raw material inspection, sampling and rapid ID testing in accordance to written SOPs and Methods.
Generate complete and accurate documentation using electronic or handwritten systems.
Review records to ensure raw materials are tested and inspected according to specification and SOPs
Perform business operations related to inspection/sampling/testing (i.e updating dashboards, relevant metrics, housekeeping, inventory management, audit support)
Support site/network Continual Improvement initiatives
Ensures facilities, equipment, materials and procedures comply with cGMP practices and other applicable regulations
Alert management of quality, compliance, supply and safety risks in a timely manner
Participate in raw material issues or deviations

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Select Country

Senior Laboratory Support Associate

Job Description

Job Responsibility

Requirements

Looking for more opportunities?