680 Control Analyst jobs in the United Kingdom

Quality Control Analyst

Dewsbury, Yorkshire and the Humber Network Scientific Recruitment

Posted 1 day ago

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Job Description

Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?


A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.


Role Overview


  • Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
  • Analysis of Raw Materials and Finished Products to SOPs.
  • Utilise analytical equipment , predominantly HPLC & GC.
  • Interpretation and checking of Analytical Data.
  • Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
  • Preparation of all relevant documentation in line with applicable standards.


Requirements


  • Prior working experience in a cGMP environment using HPLC and GC is essential.
  • Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
  • Ability to work independently in time pressured environment.
  • Excellent communication skills and attention to detail.


In return


This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.


For more information, please contact Louis Williams


If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

This advertiser has chosen not to accept applicants from your region.

Inventory Control Analyst

Computacenter

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Job Description

Life on the team

The GTS (Group Technology Sourcing) vision is to continue to 'be the best' in executing our purpose of enabling the success of our customers by being a trusted, agile and innovative provider of technology around the world.

We will achieve this by delivering great experiences for our customers, working closely with our Technology Partners to create Powerful Partnerships and enhancing our capability to ensure our future relevance. We must do this whilst supporting our customers internationally, wherever they need us, and at all times ensuring that we work closely as a one GTS team to deliver the best possible outcomes in the most effective and efficient manner.

As an Inventory Controller you will be proactively managing and monitoring GTS Inventory across the Group (UK, France & Germany) reviewing in collaboration with GPM and Sales against Customer Contracts, forecasts and SLAs. You will be responsible for reporting and analysing aged inventory working alongside the Purchasing Teams to reduce aged inventory.

What you'l
l
do

  • Producing, distributing, and analysing BATnet and cube reporting for GTS Inventory
  • Reporting, analysing and management of customer forecasts in collaboration with Sales and the relevant GTS departments for DLM Customer Contracts
  • Monitor GTS IC inventory levels with Purchasing and Logistics and Technical Services against agreed targets
  • Analyse and model inventory data making recommendations to all GTS Purchasing Managers in relation to aged inventory which includes international and portfolio Customers
  • Identify continual process and ways of working improvements in relation to Inventory Management
  • Monitor and mitigate inventory risks during product transitions in line with Customer requirements
  • Processing and monitoring stock provision charges.

What you'll need

The ideal candidate will come from a Purchasing and/or Logistics Administration background with excellent analytical and communication skills. They must be self-motivated with a high attention to detail and are able to manage a wide and time sensitive workload, bringing together multiple pieces of information from varied sources.

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Quality Control Analyst

Liverpool, North West SRG

Posted 8 days ago

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Job Description

  • Job Title: QC Specialist – Biosafety
  • Location: Speke, Liverpool.
  • Contract: until end of July 2026 initially
  • Rate: £15.25 (inclusive of shift uplift)
  • Shift : 4 on 4 off, 7am-7pm


SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some experience to further their career.


Main responsibilities:

  • Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
  • Performing routine QC testing
  • Documenting laboratory results in an accurate and timely manner.
  • Complying with GMP regulatory requirements at all times.


Key requirements:

  • Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
  • Biological background either from university degree or relevant work in the field
  • Computer skills, excel, word, outlook



Preferrable

  • Experience within cell cultures and/or assay testing.
  • LIMS and SAP
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Service Control Analyst

Bracknell, South East Fujitsu

Posted 9 days ago

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Job Description

Service Control Centre (SMSM10)
Bracknell (BRA01)
Are you someone who likes a challenge in your working environment as well as the role you are carrying out? Can you manage a varied workload and successfully deliver on all levels of Service Management? Do you want to shape your world and change the way the world works? Do you want to collaborate and achieve together with committed people to deliver a world class Service Management service? If this is your world, this is your opportunity to shape it for the better.
Reporting to the Service Team Lead, the primary objective of the Service Control Centre is to ensure adherence to Best Practice Incident handling within Resolver Groups through positive reinforcement and monitoring, therefore reducing impact to contractual Key Performance Indicators
**Role Description**
+ Ability to deputies for Service Control Team Lead, taking ownership in all aspects of the Team Lead role. Including Port Billing and Working Day 1 reporting.
+ Able to take ownership of all processes ensuring that all aspects of the SIAM model are followed across the team.
+ Follows, owns, and monitors established processes and implements improvements to these as appropriate to resolve routine customer/stakeholder enquiries, both via telephony and electronically
+ Owns relationships and engagement into the OSM and Customer as part of the SIAM model.
+ Follows and owns and ensures that service delivery is monitored effectively and that identified actions to maintain or improve levels of service are implemented and followed.
+ Owns, utilises, and inputs into standardised Policies, Processes and Procedures and ensures all documentation is up to date and valid.
+ Ensures the processes in place are aligned with the contractual requirements.
+ Acts as point of escalation for the Service Control Centre and owns management of the processes leading to successful resolution of escalated issues, in the absence of the Service Control Centre Team Lead.
+ Assists and being responsible for the implementation of any new processes resulting from account changes as well as ensuring full team engagement in the new developments.
+ Monitors delivery of service levels and meets or exceed customer expectations / SLA.
+ Monitors all aspects of Incident Management processes to ensure adherence to best practice.
+ Monitor resolution of incidents to agreed service levels.
+ Utilising statistical reporting and analysis, monitors performance across all groups.
+ Analyses and identifies areas of improvement to the service to ensure customer satisfaction.
+ Prevents negative trends by properly raising and reacting to performance and progress gaps.
+ Builds and enhances strong stakeholder relationships and acts as an escalation point.
+ Act as point of escalation in dispute or uncertainty over appropriate resolver group for an incident.
+ Ensures process, procedures and work instructions are adhered to by all relevant parties via Service Performance audits and provide regular feedback within the Service Operations environment.
+ Works with the Service Control Centre Team Lead and SLM Service Delivery Manager in developing and maintain the core SLM capabilities.
**Skills:**
+ Be able to gain SC level Security Clearance.
+ Must have good communication skills, via telephony and electronically
+ Ability to learn quickly and under pressure
+ Good teamwork skills
+ Good knowledge of Microsoft Office, including excel
**Desirable - Experience across technologies such as:**
+ Knowledge of Global Connectivity.
+ Knowledge of Port Billing
+ Knowledge of KPI's and calculation
+ Working knowledge of CASD toolsets
+ Service Request Management
**Your benefits:**
25 Days annual leave plus public holidays (3 flexible)
Pension - Double matching contributions of up to 10%
Life assurance
Companywide incentive plans
Your choices (Flexible benefits such as increased holidays/ travel/ dental critical illness and more)
Perks at work - employee discounts
Employee assistance programme/ virtual GP
**Recruitment process**
The recruitment process consists of one stage of interviews.
We are a Disability Confident Employer and will offer an interview to disabled applicants who meet the minimum/essential criteria for the role. Email if you would like to apply through the Disability Confident Interview Scheme.
**Achieve together**
**We are recognised as a responsible and inclusive employer:** Not only are we a certified Disability Confident Leader, a Times Top 50 employer for Gender Equality, a Top 75 employer for Social Mobility, accredited with the Living Wage Foundation and a signatory for the Race at Work Charter, but we are also committed to the United Nations standards for LGBTI+ and a Stonewall Top 100 Employer.
**We are people centric:** Our work environments enable you to **Be Completely You.** Our active people-led Inclusive Community networks are representative of all aspects of diversity and are instrumental in enabling and supporting our innovative approach to inclusion.
**#LifeAtFujitsu**
**Requisition ID** : 30812
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Quality Control Analyst

Dewsbury, Yorkshire and the Humber Network Scientific Recruitment

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?


A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.


Role Overview


  • Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
  • Analysis of Raw Materials and Finished Products to SOPs.
  • Utilise analytical equipment , predominantly HPLC & GC.
  • Interpretation and checking of Analytical Data.
  • Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
  • Preparation of all relevant documentation in line with applicable standards.


Requirements


  • Prior working experience in a cGMP environment using HPLC and GC is essential.
  • Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
  • Ability to work independently in time pressured environment.
  • Excellent communication skills and attention to detail.


In return


This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.


For more information, please contact Louis Williams


If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

This advertiser has chosen not to accept applicants from your region.

Senior Quality Control Analyst

Reading, South East Cranleigh STEM, Sustainability & SHEQ Recruitment

Posted 1 day ago

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Job Description

Quality Control Senior Laboratory Analyst (Level 1)

£30,000 + Overtime + Benefits

Full-time, On-site – Berkshire

Monday to Friday, 07:30–15:30 (37.5 hours/week) – Weekend rota supported via overtime

Must have full drivers licence and access to own transport


We’re supporting a leading life sciences organisation in their search for a Senior Quality Control Analyst to join their microbiology lab team based in Berkshire. This is a great opportunity for someone with a solid QC background to contribute to the quality and safety of biological products in a fast-paced, collaborative lab environment. The role offers hands-on testing responsibilities, with added exposure to quality systems and compliance support.


About the Role


As part of the Quality Control team, you’ll focus on microbiological analysis and support production through accurate sampling and timely testing. While your core focus will be lab-based, you’ll also have the opportunity to support QA-related activities such as documentation checks, deviation investigations, and maintaining audit readiness—ideal for someone seeking variety and development in a smaller, adaptable quality team.

You’ll also be part of a structured review process, with clear opportunities to progress to Senior Analyst Level 2 or 3 based on performance.


Key Responsibilities


  • Perform microbiological testing and environmental monitoring in line with QC protocols
  • Prepare labware, equipment, consumables, and bacterial strains for testing activities
  • Support production by initiating sampling routines and antigen preparation
  • Review and maintain accurate lab documentation, batch records, and test reports
  • Contribute to deviation investigations, change controls, and validations as required
  • Help maintain inspection readiness and support internal or external audits
  • Lead or support daily planning (PDR) meetings in the QC Supervisor’s absence
  • Train and support junior lab team members
  • Ensure lab cleanliness, stock control, and biohazard waste disposal


What We’re Looking For


  • Degree in Biological Sciences or equivalent lab-based experience
  • 1–2 years' experience in a microbiology or quality control laboratory
  • Solid understanding of GMP/ISO requirements in a lab environment
  • Hands-on lab skills and ability to support documentation and quality processes
  • Proactive, organised, and comfortable in a multi-tasking role
  • Team player with a flexible approach—especially in a small, dynamic QC/QA team
  • Vaccine or biological product experience is a bonus but not essential


Salary & Working Hours

  • Salary: £30,000 (with scope for quick progression through senior levels)
  • Hours: Monday – Friday, 07:30 – 15:30 (37.5 hours/week)
  • Weekend Rota: Occasional weekends with paid overtime


Looking to take the next step in a rewarding QC lab role with real career progression?

If you’re ready to contribute to a mission-driven team in a growing organisation, apply now or get in touch for a confidential chat.

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Governance and Control Analyst

Edinburgh, Scotland Royal London Group

Posted today

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Job Description

Job Title: Governance & Controls Analyst

Contract Type: Permanent

Location: Alderley Park or Edinburgh

Working style: Hybrid 50% home/office based

Closing date: 16th September 2025

Overview

We have an exciting opportunity for a Governance & Controls Analyst to join the Business Control Function at Royal London. You will work with the first line executive and management teams across functions to deliver the first line controls testing plan. You will work with the Governance and Controls Managers, playing an important role in assessing the effectiveness of control design and performance, identify weaknesses, driving improvements and reporting results.

About the role

As a key member of our Governance and Controls team, your primary focus will be on testing controls across the UK Business. You'll play a vital role in ensuring our risk and control management framework remains robust and effective.

Key Responsibilities:

  • Develop and document control testing procedures for both design and operational effectiveness, aligned with our established methodology.

  • Engage with risk and control owners to evaluate the practical operation of controls.

  • Identify and document findings, assessing them against Group RCSA (Risk and Control Self-Assessment) standards.

  • Gather and maintain appropriate evidence to support your conclusions.

  • Compile results into clear, actionable reports for local management, agreeing findings and remedial actions where necessary.

  • Record all testing procedures, outcomes, and findings within our risk management system.

  • Support risk and control owners in updating the system following the conclusion of control testing.

Additional Opportunities (Subject to Business Needs):

Depending on business requirements, the role may also offer opportunities to contribute to broader risk and control activities across the organisation:

  • Undertake agreed assignments, including reviewing risks and controls registers and gathering supporting evidence for control operation.

  • Maintain and enhance functional processes for risk and control management, such as risk acceptance, event reporting, and escalation procedures.

  • Provide support for functional risk committees, including contributing to discussions on risk and control activities, collation of papers, minute-taking, and action log maintenance.

  • Assist management in reporting and investigating risk events in line with the Risk Event & Escalation process.

  • Support Governance and Controls Managers in arranging and facilitating workshops, conducting walkthrough tests of controls, and reporting outcomes to local management with agreed actions.

About you:

  • Experience of using risk management systems such as Archer.

  • Understanding of the risk framework and procedures.

  • Experience in controls testing is preferred but not essential if you have strong exposure to risk and control management.

  • Data visualisation skills such a Power BI, are preferred.

  • Strong communication and influencing skills.

  • Good knowledge of relevant FCA/PRA regulations and applicable rules.

  • Excellent analytical ability.

  • Strong business report writing and presentation skills.

If you think you would be a great fit for our team at Royal London but don't meet all the requirements of the role, please get in touch as your application will still be considered.

About Royal London

We're the UK's largest mutual life, pensions and investment company, offering protection, long-term savings and asset management products and services.

Our People Promise to our colleagues is that we will all work somewhere inclusive, responsible, enjoyable and fulfilling. This is underpinned by our Spirit of Royal London values; Empowered, Trustworthy, Collaborate, Achieve.

We've always been proud to reward employees by offering great workplace benefits such as 28 days annual leave in addition to bank holidays, an up to 14% employer matching pension scheme and private medical insurance. You can see all our benefits here - Our Benefits

Inclusion, diversity and belonging

We're an Inclusive employer. We celebrate and value different backgrounds and cultures across Royal London. Our diverse people and perspectives give us a range of skills which are recognised and respected – whatever their background.

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Quality Control Analyst - Pharmaceutical

CV1 2GN Coventry, West Midlands £35000 Annually WhatJobs

Posted 13 days ago

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Job Description

full-time
Our client, a prominent pharmaceutical manufacturer, is seeking a meticulous and dedicated Quality Control Analyst to join their state-of-the-art facility in Coventry, West Midlands, UK . This crucial role involves performing a wide range of analytical tests to ensure the quality, safety, and efficacy of pharmaceutical products throughout the manufacturing process. The successful candidate will work with advanced analytical instrumentation and contribute to maintaining the highest standards of quality compliance. This is an excellent opportunity for an individual with a strong background in analytical chemistry and a commitment to pharmaceutical quality.

Key Responsibilities:
  • Conduct routine and non-routine analytical testing on raw materials, in-process samples, and finished products.
  • Perform tests using various laboratory techniques, including HPLC, GC, UV-Vis spectroscopy, and titrations.
  • Prepare reagents, standards, and samples for analysis.
  • Operate and maintain analytical instruments, ensuring calibration and performance.
  • Accurately record test results and maintain laboratory documentation in compliance with GMP.
  • Investigate out-of-specification (OOS) results and participate in root cause analysis.
  • Prepare certificates of analysis and analytical reports.
  • Ensure laboratory safety procedures are followed at all times.
  • Participate in method validation and transfer activities.
  • Collaborate with production, quality assurance, and R&D teams.
  • Stay updated with current Good Manufacturing Practices (GMP) and relevant pharmacopoeial standards.
Qualifications:
  • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related science discipline.
  • Minimum of 2-3 years of experience in a Quality Control laboratory, preferably within the pharmaceutical industry.
  • Hands-on experience with HPLC and other common analytical techniques.
  • Knowledge of GMP principles and regulatory requirements.
  • Proficiency in laboratory data recording and documentation.
  • Strong attention to detail and accuracy.
  • Good organisational and time management skills.
  • Ability to work effectively both independently and as part of a team.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills.
This on-site role offers a competitive salary, comprehensive benefits, and opportunities for professional development within a leading pharmaceutical organisation. Contribute to the quality and safety of essential medicines.
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Pharmaceutical Quality Control Analyst

EH1 2HB Edinburgh, Scotland £40000 Annually WhatJobs

Posted 16 days ago

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Job Description

full-time
Our client, a prominent pharmaceutical company in **Edinburgh**, is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their vital laboratory team. This role is critical in ensuring the safety, efficacy, and quality of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment such as HPLC, GC, and UV-Vis spectrophotometers. Adherence to strict Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) guidelines is paramount. The ideal candidate will possess a strong scientific background, ideally in chemistry, biochemistry, or a related field, with a Bachelor's degree or higher. Proven experience in a pharmaceutical QC laboratory setting is essential. You will be skilled in method validation, instrument calibration, and data interpretation. Accurate record-keeping and detailed report writing are integral to this position. The ability to work independently and as part of a team, managing multiple tasks efficiently and meeting deadlines, is crucial. This role demands exceptional attention to detail, a commitment to scientific integrity, and a proactive approach to problem-solving. You will contribute to the continuous improvement of quality control processes and participate in regulatory audits. The successful applicant will be dedicated to upholding the highest standards of quality and compliance within the pharmaceutical industry. This is an excellent opportunity to advance your career in pharmaceutical quality assurance.Location: This role is based at our client's facility in **Edinburgh**, Scotland, UK.
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Pharmaceutical Quality Control Analyst

MK9 2EU Milton Keynes, South East £30000 Annually WhatJobs

Posted 16 days ago

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full-time
Our client, a reputable pharmaceutical company in Milton Keynes, Buckinghamshire, UK , is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst. This role is crucial in ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. The successful candidate will perform a variety of laboratory tests and analyses on raw materials, in-process samples, and finished products using sophisticated analytical instrumentation. Responsibilities include executing validated analytical methods, meticulously documenting all experimental procedures and results, and adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be responsible for operating and maintaining laboratory equipment, troubleshooting analytical issues, and participating in method validation and transfer activities. A key aspect of this role involves contributing to deviation investigations and ensuring that any quality issues are addressed promptly and effectively. A Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline is required. Prior experience in a pharmaceutical QC laboratory setting, with hands-on experience in techniques such as HPLC, GC, spectroscopy (UV-Vis, IR), and wet chemistry, is highly desirable. Strong understanding of pharmacopoeial standards (e.g., USP, EP) and regulatory guidelines (e.g., MHRA, FDA) is essential. Excellent organisational skills, attention to detail, and the ability to manage multiple tasks in a fast-paced environment are critical. This role offers a hybrid working arrangement, allowing for a balance between on-site laboratory work and remote administrative tasks. Our client provides a supportive work environment with opportunities for continuous learning and professional development in the pharmaceutical quality assurance field.
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