Lab Technician – Medical Device Job at Network Scientific Recruitment (Cambridge)

Engineer Support Technician

Location

United States , Round Lake

Salary:

72000.00 - 99000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Associate’s degree in a technical, engineering, or scientific field (or equivalent experience)
Prior experience in a laboratory, technical support, documentation control, or similar environment preferred
Strong organizational skills with high attention to detail and ability to follow established procedures
Ability to work accurately and consistently in a regulated environment
experience in medical device, pharma, or biotech is a plus
Comfortable working with hand tools, basic lab equipment, and technical fixtures
Proficiency with Microsoft Office (Outlook, Word, Excel)
Effective communication skills and ability to collaborate with engineering, laboratory, and cross-functional teams
Ability to manage multiple routine tasks while maintaining reliability and quality

Job Responsibility

Coordinate sterilization, sample preparation, packaging, and shipping activities, including required documentation
Serve as liaison to internal and external laboratories for sample delivery, testing requests, and status tracking
Perform basic laboratory testing and hands-on engineering support tasks as trained (measurements, labeling, equipment checks, data entry)
Support prototype builds, simple assemblies, mockups, and sample preparation activities
Maintain and organize sample rooms and materials, including inventory, labeling, demos, and displays
Manage controlled documentation within the QMS, including uploads, routing, redlines, formatting updates, and revision control
Support product and project lifecycle activities, including DHFs, change controls, SNCs, obsolescence/EOL activities, and general technical administration

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Quality Assurance Technician (Night Shifts)

We are looking for a Complaints Investigator to join our Witney laboratory. You ...

Location

United Kingdom , Witney

Salary:

17.19 GBP / Hour

Randstad

Expiration Date

July 21, 2026

Requirements

Completed secondary education (Maths and English are essential)
Strong IT skills
Proficient in Microsoft Office (Word and Excel)
Analytical and methodical mindset
Documentation focused
Strong communicator
Experience in a lab or with Root Cause Analysis (RCA) is a plus but not required

Job Responsibility

Perform hands-on device testing
Use Excel to track quality trends
Collaborate with global teams to improve product design
Meticulously examine customer-returned devices
Use MS Excel and internal systems to log findings and identify emerging trends
Participate in Continuous Improvement projects
Share insights with local and international teams
Translate technical findings into clear reports for management

Fulltime

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Engineer Support Technician

Location

United States , Round Lake

Salary:

72000.00 - 99000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Associate’s degree in a technical, engineering, or scientific field (or equivalent experience)
Prior experience in a laboratory, technical support, documentation control, or similar environment preferred
Strong organizational skills with high attention to detail and ability to follow established procedures
Ability to work accurately and consistently in a regulated environment
experience in medical device, pharma, or biotech is a plus
Comfortable working with hand tools, basic lab equipment, and technical fixtures
Proficiency with Microsoft Office (Outlook, Word, Excel)
Effective communication skills and ability to collaborate with engineering, laboratory, and cross-functional teams
Ability to manage multiple routine tasks while maintaining reliability and quality
Applicants must be authorized to work for any employer in the U.S.

Job Responsibility

Coordinate sterilization, sample preparation, packaging, and shipping activities, including required documentation
Serve as liaison to internal and external laboratories for sample delivery, testing requests, and status tracking
Perform basic laboratory testing and hands-on engineering support tasks as trained (measurements, labeling, equipment checks, data entry)
Support prototype builds, simple assemblies, mockups, and sample preparation activities
Maintain and organize sample rooms and materials, including inventory, labeling, demos, and displays
Manage controlled documentation within the QMS, including uploads, routing, redlines, formatting updates, and revision control
Support product and project lifecycle activities, including DHFs, change controls, SNCs, obsolescence/EOL activities, and general technical administration

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

Pharmacist Ft Permanent - Specialty Setting

Are you an experienced Pharmacist in Edmonton looking to develop new skills in a...

Location

Canada , Edmonton

Salary:

114000.00 - 120000.00 CAD / Year

Randstad

Expiration Date

July 25, 2026

Requirements

Successful completion of a B.Sc. Pharmacy degree (or higher) and current registration in good standing with the Alberta College of Pharmacy (ACP)
Additional Prescribing Authority is strongly preferred (competitive advantage) - if in process, we can consider your candidacy
Minimum 2 years of experience in retail, hospital, or specialty pharmacy (with demonstrated exceptional clinical and operational strength)
Must demonstrate the ability to independently perform clinical assessments, interpret labs, and document activities for audits
Strong working knowledge of Kroll and Microsoft Office (Outlook, Word, Excel)
Strong verbal and written communication skills - you must be comfortable counseling patients on complex therapies over the phone
While primarily day shifts, candidates must be open to a potential rotation of 10:00 AM – 6:00 PM or 12:00 PM – 8:00 PM (likely no more than once every 4 weeks) and occasional on-call availability if business needs change

Job Responsibility

Comprehensive Clinical Care: perform thorough patient assessments over the phone, including reviewing patient profiles, checking lab results, and monitoring for complex drug interactions
Full Scope of Practice: Actively utilize Alberta’s expanded scope to renew prescriptions, adapt dosages or devices, and perform initial prescribing (e.g., for out-of-province patients or immediate assessments) as appropriate and within scope
Specialty Workflow Management: Adjudicate and verify prescriptions in Kroll with high speed and accuracy, handling specialty medication issues and collaborating with Patient Programs, Nursing divisions, and Distribution teams
Documentation & Compliance: Maintain rigorous documentation standards to satisfy insurance audits, respond to fax audits, and report Adverse Events in accordance with provincial and internal regulations
Stakeholder Collaboration: Build and maintain relationships by liaising with physicians, caregivers, and other healthcare providers to resolve coverage or clinical issues
Operational Flexibility: While primarily a clinical pharmacist role, you must be willing to step in and perform technician or assistant duties from time-to-time to support the team workflow
Continuous Improvement: Assist in driving operational improvements

What we offer

Full-time, permanent career opportunity with strong career growth potential
Strong paid time off policy for Pharmacists
Comprehensive benefits program from day one
retirement program, paid license and insurance and more
Bonus Eligibility: You are eligible for annual performance-based bonus potential

Fulltime

Engineer Support Technician

Being an Engineer at Baxter means you play a critical role in helping us achieve...

Location

United States , Round Lake

Salary:

72000.00 - 99000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Associate’s degree in a technical, engineering, or scientific field (or equivalent experience)
Prior experience in a laboratory, technical support, documentation control, or similar environment preferred
Strong organizational skills with high attention to detail and ability to follow established procedures
Ability to work accurately and consistently in a regulated environment
experience in medical device, pharma, or biotech is a plus
Comfortable working with hand tools, basic lab equipment, and technical fixtures
Proficiency with Microsoft Office (Outlook, Word, Excel)
Effective communication skills and ability to collaborate with engineering, laboratory, and cross-functional teams
Ability to manage multiple routine tasks while maintaining reliability and quality

Job Responsibility

Coordinate sterilization, sample preparation, packaging, and shipping activities, including required documentation
Serve as liaison to internal and external laboratories for sample delivery, testing requests, and status tracking
Perform basic laboratory testing and hands-on engineering support tasks as trained (measurements, labeling, equipment checks, data entry)
Support prototype builds, simple assemblies, mockups, and sample preparation activities
Maintain and organize sample rooms and materials, including inventory, labeling, demos, and displays
Manage controlled documentation within the QMS, including uploads, routing, redlines, formatting updates, and revision control
Support product and project lifecycle activities, including DHFs, change controls, SNCs, obsolescence/EOL activities, and general technical administration

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Senior Technician, Instrumentation and Calibration

The Senior Facility Technician, Instrumentation and Calibration is a multi-disci...

Location

United States , Durham

Salary:

50.00 - 70.00 USD / Hour

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Post-secondary degree, certification(s), or equivalent experience in a technical discipline related to MEP, construction, utilities, or trades
Supervisory experience with technicians &/or vendors preferred
8-10 years’ experience in calibration and maintenance with a preference for biotech, pharma, or medical device manufacturing
Working knowledge of process equipment, utility systems, and lab equipment
Computer systems literacy, with Siemens BAS, DeltaV, and CMMS experience required
Ability to manage competing priorities and timelines and adapt quickly to changing circumstances
Flexible and results oriented, with a focus on excellent customer service and demonstrated collaboration in a team environment
Must be able to work onsite daily and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed

Job Responsibility

Extensive experience with performing calibrations on Utility, Lab, and Process Equipment
Experience with the management of instrument standards
Drive change and champion continuous improvements by improving calibration procedures
Execute planned and demand maintenance activities for plant utilities (HVAC, Electrical, Chilled/Heating Hot Water, Compressed Air), gene therapy manufacturing equipment, and QC laboratory instrumentation
Support CapEx and Process Improvement project initiatives as required
Coordinate and schedule vendors for maintenance and calibration tasks
Respond and remediate alarms from the Building Automation and Process Control systems and site equipment
Create individual work and review vendor work within the site CMMS system
Ensure compliant operations in accordance with site cGMP, environmental, and government requirements
Ability to participate in on-call rotation with members of the Facility Maintenance team

Fulltime

Senior Engineering Group Leader - Process Engineering

Reporting to the Functional Manager, responsible for assigning and overseeing th...

Location

United States , Bedford

Salary:

160000.00 - 190000.00 USD / Year

werfen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in ME/EE/System Engineering (or equivalent) with a minimum of 15 years of product development experience, or a BS and MS in Engineering discipline with at least 10 years of experience
Collaborate with Product Design & Analytical Groups
Ensure designs incorporate DFM (Design For Manufacturability) techniques
Risk Assessment
Create and maintain pFMECA’s & Process Impact Analysis (PIA)
Contribute to the dFMECA as required (for new product introduction) and supplement determination of critical to quality (CTQ) components. Develop control plans and inspection routings
Develop or Select Test Automation & Equipment
Lead proof of concept demonstration of robust and novel test & automation solutions, and identify/develop equipment required for product manufacture
Process Development
Develop new manufacturing processes employing Six Sigma methodologies to ensure processes meet capacity and capability requirements. QA assurance methods result in reduce error and decreased Time-to-Market

Job Responsibility

Oversees the shared application of technology across programs in area of expertise
Performs design reviews to ensure that designs are reliable and meet cost targets, product requirements and all safety standards
Presents findings and implements solutions
Performs all required engineering analysis of characteristics of the system being designed
Ensures the proper access and availability of required development tools
Oversees the proper implementation of required documentation and archiving as defined by corporate compliance agreements
Manages and supervises team consisting of engineers and technicians as required
Produces realistic schedules that are consistent with phased delivery requirements of the PLC
Ensures availability of relevant resources to programs and anticipate future needs
Coordinates and integrates development efforts with other technical groups

What we offer

medical insurance
dental insurance
vision insurance
401k plan retirement benefits with an employer match
paid vacation
sick leave

Fulltime

Engineer II / Scientist II

Primary focus of this position is to support in developing, optimizing, implemen...

Location

United States , Tempe

Salary:

Not provided

BD

Expiration Date

Until further notice

Requirements

Bachelors degree in Engineering or Science plus 1 year of experience

Job Responsibility

Design components of a medical device, translating intangible design inputs into tangible engineering specifications and drawings
Select appropriate materials, processes and vendors to achieve the design, and challenge these designs against design specifications, clinical use scenarios and international standards
Build test parts for engineering evaluation, pre-clinical studies and clinical studies
assists in the development and optimization of processes to understand key process inputs and outputs, using statistic methods such as DOE as appropriate
Supports new process equipment and tooling development, including specification development, vendor selection and negotiation
prepare work instructions and standard operating procedures (SOP), write technical documents and reports
Prepare raw material specifications and drawings
Assist in preparing verification and validation protocols and reports
develop new engineering test methods and clinically relevant simulated use test methods in conjunction with R&D technicians
prepare and assist in the validation of test methods

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Lab Technician – Medical Device

Job Description

Job Responsibility

Requirements

What we offer

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