Laboratory Support Co-ordinator Job at Proclinical (London)

Project Quality Engineer

We are seeking a Project Quality Engineer to join the team based at Pembridge, o...

Location

United Kingdom , Pembridge

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Degree level education in a technical or quality related discipline
Six Sigma Green Belt qualification
Experience within a similar Quality role
Understanding of Quality tools such as FMEA, Control Charts, GR&R, SPC, Capability Analysis, 8D etc
Ability to interpret analyse and present data
Good communication skills
Experience of statistical software techniques such as MINITAB
Attention to detail
Ability to manage projects
Risk based thinking skills

Job Responsibility

Support the Head of Quality / Director to establish a framework to deliver quality related deliverables in CMEX
Suggest, test, implement and maintain any software used to support the co-ordination of qualification activities
Devise procedures outlining APQP Principles
Facilitate Design Failure Modes Effects Analysis (DFMEA) and Process Failure Modes and Effects Analysis (PFMEA) sessions and raise significant risks for appropriate mitigation
Support the design and execution of test plans for new and existing process changes
Calculate and monitor process capability, using a representative sample
Support the commission of any new laboratory equipment (purchased specifically to support a new project), including but not limited to calibration, service, master samples, SSW’s and G R&R’s
Support the CMEX Team to deliver projects and changes in line with expected milestones
Present regular status updates at CMEX Meetings
Compile handover packs and facilitate gate review and project hand overs

What we offer

Competitive salary range
25-days annual leave plus bank holidays
Contributory pension scheme
Employee Assistance Programme
Discounted health care

Fulltime

Tech, Metrology & Qualification

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Well versed with GxP and National Standards, NABL requirements, Regulatory requirements in terms of Calibration & Maintenance
Strong interpersonal skills and demonstrated ability to work in team environment
Strong technical skills in terms of Calibration, Maintenance, Qualifications, Vendor Management, Quality Systems
Strong skills in terms of writing, reviewing & approving GMP documents such as protocols, tests, SOP's
Strong team player, interpersonal, soft skills, communication & organizational skills
Knowledge & experienced in MS-Office tools
Fluency in English - communication, Speaking & writing
Bachelor's degree in Instrumentation & electronics or Equivalent
Minimum 2-6 years’ experience in Calibration/Maintenance/Qualifications for Pharma or Medical device industry

Job Responsibility

Part of R&D Tech, Metrology & Qualification team
Responsible for end-to-end Calibration Asset lifecycle management through BMRAM tool
Supporting the users/instrument owners for Qualification & Validations for new installation of laboratory instruments & existing re-qualifications
Participating in the external/Internal audits for M&Q
SOP Management for M&Q
Complying to the Quality as per the QMS requirements for M&Q activities
Supporting CFT team for CSV for user privileges in application software’s
End-to-end vendor management for Calibration/Maintenance/Qualification services
Responsible for the following in BMRAM tool: Registration of new equipment's, Scheduling of Calibration & Maintenance, Execution of Calibrations (by vendors), Review & approval of Calibration/Maintenance documents, Retirement of equipment's, Initiating OOTs/UOOTs
Preparing and maintaining Validation Master Plan for periodic re-qualification of equipment's

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

R&D Technologist / Lab Assistant

To develop & deliver formulations and samples to support the EU Business in the ...

Location

United Kingdom , Salford

Salary:

Not provided

Morson Talent

Expiration Date

Until further notice

Requirements

Lab experience (ideally in a similar FMCG company)
Excellent organisational skills allowing role holder to plan and organise own workload, typically planning a week ahead, ensuring delivery of agreed objectives in line with commercial requirements
Excellent attention to detail and ability to work accurately. Clear and accurate recording of experimental data. Data storage according to agreed ways of working and is easily retrievable
Strong communication skills with ability to effectively communicate technical results and recommendations within and outside the technical team
Understanding of personal wash formulations and raw materials. Knowledge of formulating performance and stability testing. Good understanding of scale up of Personal Wash products
Excellent collaborator across the technical team and NPD team

Job Responsibility

Responsible for the development of new NPD and EPD formulations within cost parameters to deliver samples to consumer research supporting brand plans
Assist R&D Manager to deliver larger projects ensuring delivery of project outputs in line with specified objectives
Manage technical data required to support production (BOMs, Production Batch Cards, Inspection Plans, DIRs. Support seal process)
Accountable for project and laboratory data and record keeping
Responsible for running experiments, recording data and accurately report results. May be responsible for protocol design
Responsible for sample preparation for sensory evaluation tests and product evaluation tests. Prepare test reports and recommend conclusions
Maintain practical knowledge of raw material, formulation and manufacturing methods. Able to make recommendations for product improvement or margin improvement
Partner cross-functional NPD teams and Brand teams to deliver NPD
Comply with all laboratory H&S requirements and lab standards. May co-ordinate some areas as defined in objectives

Project Quality Engineer

We are seeking a Project Quality Engineer to join the team based at Pembridge, H...

Location

United Kingdom , Pembridge

Salary:

30000.00 - 35000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Degree level education in a technical or quality related discipline
Six Sigma Green Belt qualification
Experience within a similar Quality role
Understanding of Quality tools such as FMEA, Control Charts, GR&R, SPC, Capability Analysis, Poka Yoke 8D etc
Ability to interpret analyse and present data
Good communication skills
Experience of statistical software techniques such as MINITAB
Attention to detail
Ability to manage projects
Risk based thinking skills

Job Responsibility

Support the Head of Quality / Director to establish a framework to deliver quality related deliverables in CMEX, based on Advanced Product Quality Planning (APQP) principles
Suggest, test, implement and maintain any software used to support the co-ordination of APQP activities
Devise procedures outlining APQP Principles
Facilitate Design Failure Modes Effects Analysis (DFMEA) and Process Failure Modes and Effects Analysis (PFMEA) sessions and raise significant risks for appropriate mitigation
Ensure Research and Development (R&D) have access to FMEA’s, serving as a source of lessons learnt for next generation products
Highlight any undesirable risks, so they can either be designed out or mitigated with poka yoke or improved detection (Sensors, Statical Process Control (SPC), Gauges etc)
Support the design and execution of test plans for new and existing process changes
Calculate and monitor process capability, using a representative sample
Support the commission of any new laboratory equipment (purchased specifically to support a new project), including but not limited to calibration, service, master samples, SSW’s and G R&R’s
Where inline sensors are used to detect errors within the process itself, consideration shall be given to the testing and maintenance of these

What we offer

Competitive salary range
25-days annual leave plus bank holidays
Contributory pension scheme
Employee Assistance Programme
Discounted health care

Fulltime

Principal Physician, Patient Safety

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Expertise in drug safety and the drug development process
Demonstrated success in technical proficiency and scientific creativity
Ability to work on complex problems requiring in-depth evaluation
Ability to exercise judgment within broadly defined practices and policies
Good presentation and verbal/written communication skills
Good interpersonal skills
Client focused approach to work
Demonstrated ability to balance technical expert responsibilities with people management duties when assigned
Computer proficiency, ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Communicating and discussing issues related to review process with Line Manager/Project Leader/Designee
Interacting with internal and external stakeholders for resolving issues
Attending and/or presenting at client/cross functional meetings along with other stakeholders
Working as Subject Matter Experts (SMEs)
Assisting the Project Lead/Functional Lead for audits and inspections, Act as a Subject Matter Expert during Audits/inspections
Provides inputs for process improvements
Works closely with Project Lead/Functional Lead for process co-ordination and to ensure meeting all Key Performance Indicators (KPIs) for the process
Function as pharmacovigilance representative/safety scientist

Fulltime

Laboratory Manager

As Laboratory Manager, you’ll lead the day-to-day running of our embryology serv...

Location

United Kingdom , Royal Tunbridge Wells

Salary:

78000.00 GBP / Year

CARE Fertility

Expiration Date

Until further notice

Requirements

A senior HCPC-registered embryologist, ideally with Laboratory Manager experience
A strong leader with proven experience managing and developing high-performing teams
A clear, confident communicator who builds trust and collaboration
Strong knowledge of quality management, regulatory compliance, and laboratory governance
Excellent attention to detail and commitment to best practice
A proactive mindset with a passion for continuous improvement and innovation

Job Responsibility

Lead the day-to-day running of our embryology service
Manage and co-ordinate workloads
Develop your team
Ensure the highest standards of quality and compliance
Take ownership of regulatory requirements, quality management systems, and laboratory governance
Support audits, inspections, and continuous improvement initiatives
Contribute to performance, service development, and strategic direction
Support complex clinical cases
Work collaboratively with the multidisciplinary team

What we offer

Salary up to £78,000
33 days’ annual leave (including public holidays)
Pension scheme
Life assurance
Additional benefits including retail discounts, wellbeing hub, and holiday trading

Fulltime

Microbiologist

This is where you make a difference in our patients’ safety. As a member of the ...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Detail Oriented
Continuous Learner
Courageous
Collaborative
Critical Thinker
Influential

Job Responsibility

To ensure the implementation and maintenance of Current Good Manufacturing Practice (cGMP) standards
To enumerate and report the tubes and plates and to supervise the discarding method of the same
To perform periodic microbiological tests, as per Standard Operating Procedure (SOP)
To perform the Bacterial Endotoxin Test
To test the material for their pre-sterile bio-burden and to test Raw Material (RM)/ Packing Material (PM) for bio-burden test
To co-ordinate with Technical department for any kind of machine related abnormality, which might be affecting the quality of the product, and its microbiological content
To take the samples for sterility test and to carry out the sterility testing
Document contemporaneously all the activities performed
To test water samples for physicochemical tests, Biochemical and chemical tests and to document the activities
To maintain and update stock record of Limulus Amoebocyte Lysate (LAL) reagents

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Technical Placement Student

Avara Foods Technical Placement Programme 2026 – 2027. Do you have a passion for...

Location

United Kingdom , Hereford

Salary:

12.21 GBP / Hour

Avara Foods

Expiration Date

Until further notice

Requirements

A team player with the ability to work effectively independently
Adaptable to varied situations
An excellent communicator with a range of stakeholders and colleagues
Comfortable taking a hands-on approach
Driven to achieve results and find solutions
On course to achieve a minimum of a 2:2 degree, ideally with a focus on Food Science

Job Responsibility

Assisting the Product Specifications Co-ordinator and Production team with both new and existing products (QAS & Specifications)
Supporting the control and accurate maintenance of the Quality Management System, including document control and revision of procedures and forms
Co-ordinating GMP audits, ensuring all areas are regularly assessed to maintain compliance
Submitting laboratory sample data
Planning, organising and communicating trials
Co-ordinating sampling activities
Completing technical information and supporting project work

What we offer

Structured one-year development programme to support you in your day-to-day placement and build skills for your future career
Structured training, mentoring and support from peers and managers throughout the programme
Real responsibilities from Day 1, providing challenge and genuine opportunity to enhance your skills

Fulltime

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Laboratory Support Co-ordinator

Job Responsibility

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