Research Associate In Bioengineering Job at The University of Manchester (Manchester)

Research Associate, Sample Management

Location

United States , Boulder

Salary:

Not provided

Enveda

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry
Bachelor’s degree in Biochemistry
Bachelor’s degree in Pharmaceutical Sciences
Bachelor’s degree in Bioengineering
Industry experience related to compound or sample management, high-throughput screening (HTS), or analytical chemistry
Experience with handling and organization of sample collections, including maintaining accurate inventory and storage conditions
Proficiency with LIMS/ELN platforms such as Benchling or Mosaic/Cenovo

Fulltime

Research Associate, Sample Management

Join Enveda as a Research Associate, Sample Management in Boulder, CO, and help ...

Location

United States , Boulder

Salary:

80000.00 - 90000.00 USD / Year

Enveda

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Bioengineering, or related field
Proficiency with LIMS/ELN platforms, such as Benchling
Hands-on experience with liquid-handling robots and automated storage systems
Strong organizational skills and attention to detail
service-oriented mindset

Job Responsibility

Receive, organize, and maintain Enveda’s sample collection
Collaborate to enhance high-throughput processes for natural product plant materials, extracts and compound libraries
Ensure data integrity in LIMS/ELN systems and manage inventory across diverse storage conditions
Operate and program automated liquid-handling robots
engage in manual pipetting as required

What we offer

90% Medical, Dental, Vision
401k Match
Flexible PTO
Adoption Assistance

Fulltime

Associate Scientist, Display Technologies

BigHat Biosciences is seeking a curious and motivated Associate Scientist to joi...

Location

United States , San Mateo

Salary:

120000.00 - 135000.00 USD / Year

BigHat Biosciences

Expiration Date

Until further notice

Requirements

BS or MS in Biochemistry, Molecular Biology, Bioengineering, or a related field
4+ years of hands-on laboratory experience (academic or industry)
relevant internship or research experience welcome
Familiarity with general molecular biology techniques (PCR, molecular cloning, gel electrophoresis)
Exposure to antibody biology, display technologies (phage or yeast), and protein expression
Demonstrated ability to follow protocols carefully, troubleshoot experiments, and maintain detailed lab records
Effective time management and clear written and verbal communication skills
Collaborative, team-oriented mindset with an eagerness to learn in a fast-paced startup environment

Job Responsibility

Support R&D projects advancing display technologies at BigHat that expands BigHat's antibody discovery capabilities and feed its ML models
Lead in the construction and QC of phage and yeast display libraries across diverse antibody formats (VHH, scFv, Fab) using standard molecular biology techniques (PCR, molecular cloning, electroporation)
Execute phage and yeast display selections using naive and affinity and stability maturation libraries to discover and engineer antibodies with desired therapeutic properties
Express, purify, and characterize display-derived molecules using assays including ELISA, flow cytometry, BLI/SPR, CE-SDS, and others
Analyze selection results and contribute to discussions on next steps and future experimental design
Collaborate with BigHat's Data Science and Machine Learning teams to inform library design and interpret selection data for model training
Present experimental plans and results during regular meetings with manager and science teams
Maintain thorough records using LIMS and electronic notebooks

What we offer

Range of health insurance plan options through Anthem and Kaiser (monthly credit if benefit waived)
Dental and vision coverage through Guardian
Additional well-being benefits through Nayya, OneMedical, Wagmo, Rula, and more
401(k) with company match
DTO, two weeks of company-wide shutdown, and 12 company holidays
Paid parental leave
Bonus
Options

Fulltime

Process Development Sr Associate

Support the development, characterization and scale up of cell culture and prote...

Location

United States , Thousand Oaks

Salary:

96605.00 - 119055.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's Degree in Biotechnology, Bioengineering, Microbiology or related field and completion of a university-level course, research project, internship, thesis, or one year of experience in the following: Cell culture principles, cell metabolism profiles, protein chromatography, filtration and UF/DF operations to perform small scale bioprocess experiments that encompass both upstream (cell culture) and downstream (purification) operations
Experience with mammalian cell culture to maintain and scale up cell culture in shake flasks, culture bags and bench top bioreactors
Experience with purification operations to run bench-top chromatography columns to generate purified antibody product
Identify and solve problems by applying scientific and engineering principles
Design of experiments and statistical analysis of data and programming in JMP, R, or Python environments
Experience with automation efforts to enable high throughput technologies for accelerated process development

Job Responsibility

Support the development, characterization and scale up of cell culture and protein purification operations to enable commercial manufacturing advancement by conducting experiments, analyzing data, and documenting results
Work closely with senior scientists and engineers to implement process improvements
Support development of early phase cell culture, recovery and purification processes for Amgen's large molecule expansion through production bioreactor, harvest, clarification, chromatography, and/or filtration technologies as well as completing virus clearance studies
Identify, develop and implement solutions to practical problems through application of fundamental scientific and engineering principles

What we offer

stock
retirement
medical insurance
life insurance
disability insurance
eligibility for an annual bonus
health and welfare plans
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities

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

New

Senior ROV Pilot Technician

Make your mark as Senior ROV Pilot Technician at Boskalis Subsea Services in Abe...

Location

United Kingdom , Aberdeen

Salary:

Not provided

Boskalis

Expiration Date

Until further notice

Requirements

A minimum of 360 days offshore in the role of ROV Pilot Technician Grade I – CV with work history to date including at least 100 logged piloting hours demonstratable on IMCA ROV Logbook
Multi-discipline Project Experience: piloting observation or work-class ROVs, exposure to consoles, sonar, manipulator arms and common subsea tooling (preferred). In addition, previous involvement with fibre-optic, HV, or integrated ROV control and telemetry systems (preferred)
Valid and current IMCA Company Member Competence Certificate or completed and validated IMCA Competence Portfolio supporting completion of all ROV Pilot Technician Grade I (R03) competencies
Technical qualifications: recognized technical qualification in electrical, electronic, mechanical, or hydraulic discipline (e.g. NVQ Level 3, HNC, military trade, or equivalent)
ROV Introductory Training - successful completion of an IMCA-approved ROV Introductory Training course (IMCA R002 compliant), with valid certification
Technical Knowledge and Practical Skills - demonstrated competence in advanced fault finding, manipulator use, ROV piloting, and equipment maintenance across ROV systems
Communication and Leadership - proven ability to supervise and mentor junior team members, lead deck operations, and act as shift lead when required
Offshore availability and resilience - willingness to work rotational offshore shifts in physically demanding conditions
Strong communication - works collaboratively, follows instructions, and contributes to a positive, safety-focused team environment and contributes positively to team dynamics and maintains clear, respectful communication
Problem-solving and initiative - seeks feedback and engages in CPD activities to enhance technical and operational capabilities

Job Responsibility

Execute advanced ROV piloting operations in support of subsea tasks including construction, survey, inspection, intervention, and tooling deployment, ensuring precision, safety, and compliance with procedures
Lead the launch and recovery of ROV systems, coordinating deck crew, verifying safe working practices, and overseeing the use of LARS and TMS systems
Diagnose and resolve faults in ROV systems including electrical, electronic, fibre-optic, hydraulic, and mechanical components, using test equipment, circuit diagrams, and company maintenance procedures
Perform planned and corrective maintenance on ROV systems and sub-systems in accordance with manufacturer specifications and the company’s maintenance management system (MMS)
Monitor and interpret ROV telemetry, sonar, video feeds, sensor data, and vehicle diagnostics during live operations to support safe and accurate task execution
Operate and maintain manipulator systems, ensuring effective use for tasks such as valve operations, tool deployment, cutting, and recovery activities
Assist the ROV Supervisor in shift briefings, toolbox talks, risk assessments, and task planning, acting as operational lead in their absence (typically night shift or task-specific delegation)

What we offer

competitive salary
contributory pension scheme
private medical insurance
death in service benefit
career development opportunities through (online) courses at the Boskalis academy

Fulltime

New

Grad Pharmacist

You’ve invested a lot of time and energy in your education. Now you want the cha...

Location

United States , Middletown

Salary:

21.75 - 42.00 USD / Hour

CVS Health

Expiration Date

September 30, 2026

Requirements

PharmD graduate of a U.S. accredited program prior to beginning the Post-Graduate Training Program at CVS Health
Ability to obtain required pharmacist licensure within the required timeframe, per state guidelines. Failure to obtain required Pharmacist licensure within 120 days of graduation will result in separation of employment
Must possess, or be in the process of obtaining, valid intern and/or technician licensure as required

Job Responsibility

Living our purpose by following all company SOPs at each workstation to help our Pharmacists and Technicians manage and improve patient health
Following pharmacy workflow procedures at each pharmacy workstation (i.e., production, pick-up, drive-thru, and drop-off) for safe and accurate prescription fulfillment
Contributing to positive patient experiences by showing empathy and genuine care: creating heartfelt and personalized moments while serving patients at pick-up, drive-thru, and over the phone
keeping patients healthy by offering immunizations and other services at the register and over the phone
and demonstrating compassionate care by solving or escalating patient problems
Offering to counsel, fielding medical questions, and soliciting information on a patient’s medical history to provide optimal care, when appropriate under the direct supervision of a licensed pharmacist
Taking telephonic prescriptions from the prescriber, and calling the prescriber to clarify prescriptions or facilitate medication changes, where allowed by state regulation
Maintaining the highest level of self-awareness and providing in-the-moment coaching, training, and mentoring to pharmacy team members while sharing best practices
Completing basic inventory activities, as permitted by law, and as directed by the pharmacy leadership team, such as accurately putting away medication deliveries and completing cycle counts, returns-to-stocks, waiting bin inventories, etc.
Contributing to a high-performing team, embracing a growth mindset, and being receptive to feedback

What we offer

dental
vision
wellness resources
employee discounts
access to certain voluntary benefits
other programs

Parttime

New

Grad Pharmacist

You’ve invested a lot of time and energy in your education. Now you want the cha...

Location

United States , Arroyo Grande

Salary:

23.10 - 28.10 USD / Hour

CVS Health

Expiration Date

Until further notice

Requirements

PharmD graduate of a U.S. accredited program prior to beginning the Post-Graduate Training Program at CVS Health
Ability to obtain required pharmacist licensure within the required timeframe, per state guidelines. Failure to obtain required Pharmacist licensure within 120 days of graduation will result in separation of employment.
Must possess, or be in the process of obtaining, valid intern and/or technician licensure as required

Job Responsibility

Living our purpose by following all company SOPs at each workstation to help our Pharmacists and Technicians manage and improve patient health
Following pharmacy workflow procedures at each pharmacy workstation (i.e., production, pick-up, drive-thru, and drop-off) for safe and accurate prescription fulfillment
Contributing to positive patient experiences by showing empathy and genuine care: creating heartfelt and personalized moments while serving patients at pick-up, drive-thru, and over the phone
keeping patients healthy by offering immunizations and other services at the register and over the phone
and demonstrating compassionate care by solving or escalating patient problems
Offering to counsel, fielding medical questions, and soliciting information on a patient’s medical history to provide optimal care, when appropriate under the direct supervision of a licensed pharmacist
Taking telephonic prescriptions from the prescriber, and calling the prescriber to clarify prescriptions or facilitate medication changes, where allowed by state regulation
Maintaining the highest level of self-awareness and providing in-the-moment coaching, training, and mentoring to pharmacy team members while sharing best practices
Completing basic inventory activities, as permitted by law, and as directed by the pharmacy leadership team, such as accurately putting away medication deliveries and completing cycle counts, returns-to-stocks, waiting bin inventories, etc.
Contributing to a high-performing team, embracing a growth mindset, and being receptive to feedback

What we offer

dental
vision
wellness resources
employee discounts
access to certain voluntary benefits
other programs

Parttime

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Research Associate In Bioengineering

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