Our client is a well-established MNC, market leader in the Water Treatment industry. They are looking for a QC Coordinator Engineer assist their Engineering team for the next phrase of their business. They are located in South – easily accessible.

Responsibilities:

• Conduct quality control audits.
• Organize pre-inspection meetings with clients.
• Create Project Inspection and Testing Plans.
• Draft Project Inspection and Testing Procedures.
• Address client feedback on QC documents.
• Coordinate and schedule QC activities, including inspection notices and factory acceptance tests.
• Manage coordination and scheduling of QC procedures, reports, and documents.

Requirements:

• Minimum of Bachelor Degree in Engineering or Quality Management
• Minimum of 5 years experience in Quality Control function.
• Experience in the Oil and Gas or offshore and marine industry
• Proficiency in metal welding inspection and piping system testing and inspection

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: tc1@recruitpedia.sg

Recruitpedia Pte. Ltd.
EA License No. 19C9682
EA Reg. No. R21101676 (Ng Zhi Qing Alethea)

Compliance Coordinator

Solihull

£13 per hour

Ongoing Contract

Our client are a market leading fleet management company, due to continued growth they are seeking a compliance coordinator to join their office in Solihull. The role will be responsible for booking MOT’s and Services for a range of HGV’s and LCV’s as well as handling all associated documentation. The role will be on an ongoing contract basis working 2 days at home and 3 in the office.

Key Responsibilities – Compliance Coordinator

• Proactively monitor all compliance schedules for all vehicle types
• Outbound chase all compliance bookings liaising with vendors, drivers and customers.
• Ensure all required job types are booked within the specified date or date range
• Ensure all data is updated in a timely and accurate manner
• Highlight any incorrect contact data to specified account contact
• Ensure any slippage is reported to fleet contact and account contact
• Confirm booking dates to all parties
• Act as point of contact for other departments for any changes in bookings or information needed
• Follow up all bookings to ensure completion and pass
• Assist with gathering any documents required as proof of completion

Qualifications & Experience – Compliance Coordinator

• A good general level of education is required
• Must be adept in the use of a PC, internet and email and able to grasp new software applications easily and quickly.
• Able to use Microsoft Word, Excel and Outlook to an intermediate level
• CPC or FTA training preferred, but not essential
• Experience of O’licence requirements- MOTs, PMIs, Laden Brake Tests, Tachograph Calibrations, Loler certification
• Ability to demonstrate experience and understanding of various inspection intervals and scheduling of events
• Experience of working in a transport team/ department with exposure to planning and service scheduling

For more information on this role, please contact Andrew Haddon on 01453 796617 or send a copy of your CV to Andrew.haddon@omegaresource.co.uk

Omega Resource Group is acting as an Employment Agency in relation to this vacancy.

Omega Resource Group is an employment agency specialising in opportunities at all levels within the Engineering, Aerospace, Automotive, Electronics, Defence, Scientific, Oil & Gas, Construction and Manufacturing sectors.

For details of other opportunities available within your chosen field please visit our website www.omegaresource.co.uk

Omega Resource Group is acting as an Employment Business in relation to this vacancy.

Responsibilities

• Develop and implement quality control processes and procedures for trackworkand railway projects.
• Conduct inspections and tests on trackwork components and railway systems to ensure compliance with quality standards.
• Monitor and analyze quality data to identify trends and areas for improvement.
• Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.Manage and maintain the company's quality management system for trackwork and railway projects.
• Develop and deliver training programs on quality control and assurance specific to trackwork and railway projects.
• Conduct internal audits to evaluate the effectiveness of quality systems.
• Support continuous improvement initiatives to enhance overall trackwork and railway quality and customer satisfaction.

Requirements

• Bachelor's Degree in any Mechanical/Electronic/Mechatronics Engineering
• Good understanding in ISO standard for ISO 9000, 14000, and1800
• Railway project experience is a plus.lus

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume to julie@talenttradersg.com

EA License No: 13C6305

Reg. No.: R1981808

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

NorthWest Arkansas Community College (NWACC) provides quality and affordable higher education to empower lives and strengthen communities within Northwest Arkansas and surrounding areas.

As the largest community college in Arkansas, NWACC is recognized as a leader in education. NWACC offers a full range of associate degrees, certificates and workforce training programs that prepare students for rewarding futures and careers.

NWACC employees are dedicated to fostering a diverse educational community and cultural learning environment that supports student success.

The Academic Coordinator supports the Dean and Department Chairs in implementing the academic assurance plan and academic processes for the division. This position will act as the BCIS Division representative, working with the Gen Ed Assessment committee, distance learning, and the Office of Institutional Effectiveness to create and keep records, including assessments of student learning, division outcomes, accreditation records, and state reviews of non-accredited programs. The coordinator helps the faculty leaders in keeping records required for the ACBSP Accreditation process, including outcomes measures, faculty credentials, curriculum records and other analysis required by the Accrediting body. The person in this position must have self-motivation and self-direction with the ability to prioritize work independently and meet deadlines. Strong analytical and computing skills are required. This is a full-time position with benefits.

Essential Duties

• Completes sections of accreditation self-study under direction of dean and department chairs.
• Coordinates and assists program coordinators in the completion of state program reviews.
• Under the direction of the dean and Department Chairs, develops scorecards and metrics to assure progress toward performance funding goals.
• Analyzes data from division program level assessments and updates assessment metrics.
• Provides support for Key Academic Initiatives in the division.  Measures results and reports to dean, department chairs and faculty.
• Provides student support as needed and backs up key functions of Academic advisor.
• Develops grant proposals and completes documentation for Academic Centers of Excellence or other initiatives.
• Performs any other related duties as required or assigned.
• Under the direction of the Distance Learning director, completes quality course checks at the beginning and mid semester.
• Coaches new faculty on effective Canvas usage.
• Coordinates with ACBSP and attends regional ACBSP conferences to inform the department of changing requirements.

Salary Range $48,000-$51,000, Commensurate with education and experience.

Knowledge, Skills, and Abilities

Knowledge of the organization and administration of various higher education academic and social programs.

Knowledge of campus and community resources.

Knowledge of state, federal, and campus rules, regulations, and requirements related to campus academic and social programs.

Ability to coordinate the activities of campus academic and/or social programs.

Ability to evaluate collected information and formulate into recommendations.

Ability to compile information into report form.

Physical Demands/Work Environment

The following physical activities described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and expectations.
While performing the functions of this job, the employee is:
Frequently:
• Manipulate items with fingers, including keyboarding
• Sitting
• Standing
• Walking
Constantly:
• Hearing
• Repetitive motion
• Talking

The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; and/or visual inspection at distances close to the eyes.

Environmental Conditions

The following work environment characteristics described here are representative of those an employee encounters while performing essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The noise level in the work environment is usually moderate.

Education and Experience

 Bachelor’s degree in business or education required plus 12 to 18 months related experience and/or training, and 12 to 18 months related management experience, or equivalent combination of education and experience (Master’s degree plus 12 months experience).   Proficiency in data analysis using database and / or excel software and outstanding writing skills are essential. Familiarity with course management software like Blackboard or Canvas.

NWACC is an Equal Opportunity Employer, please see our EEO policy.

Manpower UK Print & Packaging Division are excited to bring an opportunity to market for a Quality & Product Safety Coordinator based on our clients Sunderland site. This full-time permanent opportunity is working for one of our prestigious partners, a market-leading, global print business.

The successful candidate will support the QHSE Manager in maintaining the company's Quality and Hygiene Management System. The position involves working closely with the site management team daily. Focus is aimed at compliance with related policies and procedures and ensuring products supplied to customers are of a consistently safe and high standard of quality.

Key Activities and Responsibilities

• Liaising with certification bodies; organising site audits; responding to non-conformance's and ensuring full compliance certification standards and accreditation systems.
• Working with the QHSE Manager to review and update policies & procedures to continually strengthen & improve quality management systems.
• Completion of customer questionnaires and preparation of technical specifications.
• Manage the company's internal audit and self-inspection programs.
• Help develop and implement a robust and efficient CAPA Program.
• Maintain up-to-date calibration records & arrange service and repair of laboratory equipment.
• Conduct and document forward and reverse traceability exercises and a product withdrawal.
• Assist in maintaining the company's HACCP's plan.
• Deliver short training programs and conduct information and awareness briefings.
• General quality assurance duties: process quality checks, compiling certificates of analysis, archiving samples, conducting laboratory tests including oxygen transmission rate, heat-seal / lamination bond strengths, coefficient of friction, solvent retention, and primary aromatic amines.

Other Requirements

Qualifications

• GCSE grades 3/C or above in Math's and English essential.

So, if you tick the above boxes, we encourage you to apply today, and a member of the team will review your details and book in a call at a time convenient to you!

Our client is a well-established MNC, market leader in the Water Treatment industry. They are looking for a QC Coordinator Engineer assist their Engineering team for the next phrase of their business. They are located in South – easily accessible.

Responsibilities:

• Conduct quality control audits.
• Organize pre-inspection meetings with clients.
• Create Project Inspection and Testing Plans.
• Draft Project Inspection and Testing Procedures.
• Address client feedback on QC documents.
• Coordinate and schedule QC activities, including inspection notices and factory acceptance tests.
• Manage coordination and scheduling of QC procedures, reports, and documents.

Requirements:

• Minimum of Bachelor Degree in Engineering or Quality Management
• Minimum of 5 years experience in Quality Control function.
• Experience in the Oil and Gas or offshore and marine industry
• Proficiency in metal welding inspection and piping system testing and inspection

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: tc1@recruitpedia.sg

Recruitpedia Pte. Ltd.
EA License No. 19C9682
EA Reg. No. R21101676 (Ng Zhi Qing Alethea)

Company :

Allegheny Health Network

Job Description : 

GENERAL OVERVIEW:

Responsible for supporting the QSV Division's need around technology maintenance and administration, quality data analysis and triage, regulatory survey/tracer coordination and related data management. Coordination of QSV division communication to Sate and Regulatory agencies. Coordination of clinical registry data and reporting. Coordination of medical staff quality data, reporting and related processes. Coordination of QSV committee meeting preparation and materials. This position is to be the "hub" of QSV support across the network

ESSENTIAL RESPONSIBILITIES:

• Responsible for QSV Technology Platform maintenance and administration. (15%)
• Responsible for coordinating Network quality, regulatory, patient safety, infection prevention and risk communication to State and Regulatory agencies. QSV data coordination and triage. Assimilating work done at the hospital level, trending and analyzing data and making recommendations for further focus and actions.(15%)
• Responsible for regulatory survey and tracer coordination, data management and plan implementation. (15%)
• Coordination and support clinical registry data, reporting and standardization processes. (10%)
• Coordination and support of medical staff quality data and processes and plan implementation. Coordinating work across the network and helping in efforts to standardize processes and increase efficiencies, etc.(15%)
• Support the preparation of data, materials and presentations for various QSV committees. (15%)
• QSV data coordination and triage activities. (15%)

QUALIFICATIONS:

Minimum

• Bachelor's degree in Business or Healthcare related field required OR 4 years of progressive and relevant experience in lieu of Bachelor’s degree.
• Minimum of 2 years’ experience in coordinating cross-functional activities/projects. Experience working with various software platforms/databases. Experience in analyzing data for trending purposes.

Preferred

• Lean/Six Sigma certification preferred

Disclaimer: The job description has been designed to indicate the general nature and essential duties and responsibilities of work performed by employees within this job title. It may not contain a comprehensive inventory of all duties, responsibilities, and qualifications required of employees to do this job.

Compliance Requirement: This job adheres to the ethical and legal standards and behavioral expectations as set forth in the code of business conduct and company policies.

As a component of job responsibilities, employees may have access to covered information, cardholder data, or other confidential customer information that must be protected at all times.  In connection with this, all employees must comply with both the Health Insurance Portability Accountability Act of 1996 (HIPAA) as described in the Notice of Privacy Practices and Privacy Policies and Procedures as well as all data security guidelines established within the Company’s Handbook of Privacy Policies and Practices and Information Security Policy. 

Furthermore, it is every employee’s responsibility to comply with the company’s Code of Business Conduct. This includes but is not limited to adherence to applicable federal and state laws, rules, and regulations as well as company policies and training requirements.

Highmark Health and its affiliates prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, age, religion, sex, national origin, sexual orientation/gender identity or any other category protected by applicable federal, state or local law. Highmark Health and its affiliates take affirmative action to employ and advance in employment individuals without regard to race, color, age, religion, sex, national origin, sexual orientation/gender identity, protected veteran status or disability. 

EEO is The Law

Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation/Gender Identity (https://www.eeoc.gov/sites/default/files/migrated_files/employers/poster_screen_reader_optimized.pdf)

We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact number below.

For accommodation requests, please contact HR Services Online at HRServices@highmarkhealth.org

California Consumer Privacy Act Employees, Contractors, and Applicants Notice

Become a part of our caring community and help us put health first
 

The Quality Improvement Coordinator participates in quality improvement (QI) activities for the South Carolina Humana Healthy Horizons Medicaid Market to comply with state requirements. This includes, but is not limited to, outbound calls to members to support various quality improvement activities/campaigns, medical record review and committee preparations.

               

The Quality Improvement Coordinator performs member and provider outreach calls, medical record audits and assists with QI project documentation.   Decisions typically focus on methods, tactics and processes for completing administrative tasks/projects. Regularly exercises discretion and judgment in prioritizing requests and interpreting and adapting procedures, processes and techniques, and works under limited guidance due to previous experience/breadth and depth of knowledge of administrative processes and organizational knowledge.  The Quality Improvement Coordinator performs advanced customer support/administrative/operational duties that require independent initiative and judgment. May apply intermediate mathematical skills.

Use your skills to make an impact
 

Required Qualifications

• Practicing LPN, LCSW license in the state of South Carolina
• 4+ years clinical/quality management or healthcare related experience.
• 2+ years’ experience in a fast-paced insurance or health care setting reviewing HEDIS supplemental or hybrid data.
• Understanding of Medicaid healthcare quality measures such as HEDIS etc.
• Comprehensive knowledge of Microsoft Office Word, Excel and PowerPoint
• Excellent communication skills, both oral and written
• Strong relationship building skills
• Must be passionate about contributing to an organization focused on continuously improving quality of care and consumer experiences

Preferred Qualifications

• Project Management, Lean Project experience
• Knowledge of Humana's internal policies, procedures, and systems
• Experience participating in and coordinating quality improvement projects and other quality improvement activities.

Additional Information

Humana is an organization with careers that change lives – including yours.  As an innovator in the fast-paced industry of healthcare, we offer our associates careers that challenge, support and inspire them to use their passion for helping others and to lead their best lives.  If you’re ready to help people achieve lifelong well-being and be a part of an organization that is growing and posed to make an impact on the future of healthcare, Humana has the right opportunity for you.

Scheduled Weekly Hours

40

About us
 

Humana Inc. (NYSE: HUM) is committed to putting health first – for our teammates, our customers and our company. Through our Humana insurance services and CenterWell healthcare services, we make it easier for the millions of people we serve to achieve their best health – delivering the care and service they need, when they need it. These efforts are leading to a better quality of life for people with Medicare, Medicaid, families, individuals, military service personnel, and communities at large.

Equal Opportunity Employer

It is the policy of  Humana not to discriminate against any employee or applicant for employment because of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or because he or she is a protected veteran. It is also the policy of  Humana to take affirmative action to employ and to advance in employment, all persons regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or protected veteran status, and to base all employment decisions only on valid job requirements. This policy shall apply to all employment actions, including but not limited to recruitment, hiring, upgrading, promotion, transfer, demotion, layoff, recall, termination, rates of pay or other forms of compensation and selection for training, including apprenticeship, at all levels of employment.

Our client is a well-established MNC, market leader in the Water Treatment industry. They are looking for a QC Coordinator Engineer assist their Engineering team for the next phrase of their business. They are located in South – easily accessible.

Responsibilities:

• Conduct quality control audits.
• Organize pre-inspection meetings with clients.
• Create Project Inspection and Testing Plans.
• Draft Project Inspection and Testing Procedures.
• Address client feedback on QC documents.
• Coordinate and schedule QC activities, including inspection notices and factory acceptance tests.
• Manage coordination and scheduling of QC procedures, reports, and documents.

Requirements:

• Minimum of Bachelor Degree in Engineering or Quality Management
• Minimum of 5 years experience in Quality Control function.
• Experience in the Oil and Gas or offshore and marine industry
• Proficiency in metal welding inspection and piping system testing and inspection

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: tc1@recruitpedia.sg

Recruitpedia Pte. Ltd.
EA License No. 19C9682
EA Reg. No. R21101676 (Ng Zhi Qing Alethea)

Our client is a well-established MNC, market leader in the Water Treatment industry. They are looking for a QC Coordinator Engineer assist their Engineering team for the next phrase of their business. They are located in South – easily accessible.

Responsibilities:

• Conduct quality control audits.
• Organize pre-inspection meetings with clients.
• Create Project Inspection and Testing Plans.
• Draft Project Inspection and Testing Procedures.
• Address client feedback on QC documents.
• Coordinate and schedule QC activities, including inspection notices and factory acceptance tests.
• Manage coordination and scheduling of QC procedures, reports, and documents.

Requirements:

• Minimum of Bachelor Degree in Engineering or Quality Management
• Minimum of 5 years experience in Quality Control function.
• Experience in the Oil and Gas or offshore and marine industry
• Proficiency in metal welding inspection and piping system testing and inspection

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: tc1@recruitpedia.sg

Recruitpedia Pte. Ltd.
EA License No. 19C9682
EA Reg. No. R21101676 (Ng Zhi Qing Alethea)

Our client is a well-established MNC, market leader in the Water Treatment industry. They are looking for a QC Coordinator Engineer assist their Engineering team for the next phrase of their business. They are located in South – easily accessible.

Responsibilities:

• Conduct quality control audits.
• Organize pre-inspection meetings with clients.
• Create Project Inspection and Testing Plans.
• Draft Project Inspection and Testing Procedures.
• Address client feedback on QC documents.
• Coordinate and schedule QC activities, including inspection notices and factory acceptance tests.
• Manage coordination and scheduling of QC procedures, reports, and documents.

Requirements:

• Minimum of Bachelor Degree in Engineering or Quality Management
• Minimum of 5 years experience in Quality Control function.
• Experience in the Oil and Gas or offshore and marine industry
• Proficiency in metal welding inspection and piping system testing and inspection

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: tc1@recruitpedia.sg

Recruitpedia Pte. Ltd.
EA License No. 19C9682
EA Reg. No. R21101676 (Ng Zhi Qing Alethea)

 

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

For our Quality Assurance team in Bioconjugates we are currently looking for a dedicated person who would like to work as a Senior QA Specialist, Project Manager (f/m/d) in a fast growing and innovative environment. The person will support clinical phase manufacturing and will interact with internal and external stakeholders to represent Quality.

Key responsibilities:

• As a member of the quality assurance team (Bioconjugates), you will be responsible to ensure production of API`s is in accordance with Good Manufacturing Practice (GMP)

• Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP

• Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results

• In addition, you will be the quality contact for our clients, and will present during their GMP audits

Key requirements:

• A degree in Life Science (microbiology, biotechnology, chemistry)

• Relevant experience in the biopharmaceutical industry, ideally in GMP area

• Strong communication skills, experience in working with stakeholders from different departments

• Experience with TrackWise, SAP, LIMS and DMS is a plus

• Fluency in English (writing and speaking) is required for stakeholder communication, German skills on B1 level are required to interact with colleagues on a daily bases

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

 

Associate Director, Compliance and Project Support, Automation Biologics

Location – Visp, Switzerland

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

The site in Visp, Switzerland is growing and for our Biologics organization, we are seeking a senior Manager Automation who can manage our Compliance and Project Support team with significant experience in DeltaV and MES and a passion for Biotechnology to join our Lonza talent community. Become part of this exciting opportunity and apply now for the position as senior Manager Automation Ops Readiness.

Key Responsibilities:

• Managing a team of Senior automation experts and specialists with full responsibility for all aspects of human resource management such as development, coaching, hiring, pay decisions and discipline issues;
• Managing a local Center of Excellence for Operations Automation (Delta V, Syncade) of bioprocesses;
• Working with the team in Capital investment projects and strengthening the respective automation teams with expert knowledge on process automation;
• Working with the global Center of Excellence to standardize automation approaches in biopharma manufacturing;
• Providing high-level troubleshooting support with the team;
• Collaborating with the Operations to provide resource plans for automation set-up;
• Driving the ambition level for automation in the design of the facilities by incorporating innovation, operational improvements, and other aspects influencing the manufacturing costs;
• Contributing automation expertise to design development teams;
• Managing the automation teams during the initial engineering phases and providing leadership to cross-functional teams of experts;
• Supporting LONZA culture via openness for change and new ideas, cooperative teamwork and continuous improvement even outside specific area of responsibility.

Key requirements:

• Recognized expert in the area of Bioprocess Automation (OT, Delta V, MES Syncade)
• Deep understanding of bioprocesses, GMP and biopharma production
• Strong leadership skills
• Ability to communicate internally and externally at higher levels; strong business understanding, strong team orientation
• Structured and proactive working attitude
• Open-minded for new ideas

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

#LI-SG

A Vacancy at Barking Havering and Redbridge Univ Hospitals NHS Trust.


An exciting opportunity has arisen within Pathology, for a suitably qualified Quality and Safety Coordinator. We are looking for an individual with expert knowledge of the Quality, Governance and Safety agenda and its constituent components and be able to identify working plans to address these. Experience of using Q-Pulse or any other similar quality management Systems will be an advantage. The post holder will be expected to work with multidisciplinary teams to identify work streams proactively to promote clinical governance and learning within Pathology; review information on the strands of clinical governance producing reports and highlighting areas for actions.

To develop and maintain positive and constructive working relationships with peers and colleagues.

BHRUT Pathology is currently managed across laboratories based at Queens Hospital Romford and King George Hospital Goodmayes. All staff are expected to be able to work on either site as required; this post will be expected to cover the quality requirements at both sites. Pathology plays a pivotal role in the provision of 26 million diagnostic tests annually for the Trust and primary care services.

The successful candidate will join an excellent team providing an efficient and effective Quality and Training service to 2 busy district general hospitals. The ideal candidate should be highly motivated with good interpersonal, and organisational skills.

The post holder will provide co-ordination and management of Quality, Governance & safety across Pathology for the Cancer and Clinical Support Division. The post holder will be expected to prioritise and manage their own workload.

The post holder will be expected to have expert knowledge of the Quality, Governance and Safety agenda and its constituent components and be able to identify working plans to address these. The post holder will be expected to work with multidisciplinary teams to identify work streams proactively to promote clinical governance and learning within Pathology; review information on the strands of clinical governance producing reports and highlighting areas for actions.

To develop and maintain positive and constructive working relationships with peers and colleagues.

Regularly has contact with Senior Managers / Clinicians / Directors / Executive members of Trusts and CCGs/ Chief Executives/ Department of Health and Strategic Support Units (SSU) officials.

Liaises with other staff and colleagues within all BHRUT Trusts at all levels.



We provide care for the residents of three diverse London boroughs. Most of our 7,800 permanent staff live in Barking and Dagenham, Havering and Redbridge and the majority are from black, Asian and minority ethnic groups. We also provide healthcare services to people in south west Essex, and specialist neurosciences services to the whole of the county.

Our services include all the major specialties of large acute hospitals and we operate from two main sites - King George Hospital in Goodmayes and Queen’s Hospital in Romford. We have two of the busiest emergency departments in London – more than 300,000 people visited our A&Es in 2023. We also provide outpatient services at Brentwood Community Hospital, Barking Community Hospital, Loxford Polyclinic, and Harold Wood Polyclinic.

We’re pleased to be leading the way inreducing the time our patientswait to get the treatment they need. The Elective Surgical Hub at King George Hospital is one of eight to beaccredited as part of a national scheme; the Care Quality Commission has raised the ratings for urgent and emergency care at Queen’s and King George hospitals; and data released by NHS England showed that the Trust was the most improved in 2023 for reducing waits for emergency care.

We are particularly proud of our regional Neurosciences Centre; Radiotherapy Centre; Hyper Acute Stroke Unit; and dedicated breast care service at King George Hospital. We’re also part of theNorth East London Cancer Alliance.

We operate a 24/7 service on both sites, and registered, experienced staff are expected to participate in the out of hours rotas as required once fully competent. The Trust is currently exploring an alternative system to accommodate increasing demand for routine testing 24/7

This busy speciality is undergoing a major modernisation and the post holder will play a key role in helping to implement these changes. The Trust's services include a large maternity unit, regional neurosurgical unit, hyper acute stroke unit, clinical haematology, haemoglobinopathy and oncology and busy accident and emergency services.

For further information on this role, please see the attached detailed Job Description and Person Specification.

The person specification listed below is not the full specification requirements for the role. Please ensure you review the full specification on the job description prior to submitting your application.

Applicants are advised to read all the information on the advert and the supporting information before completing and submitting an application. As you complete your application please ensure you clearly demonstrate how you meet the criteria in the person specification for this post by adequately completing the supporting information section of the application form.

All new staff appointed at the Trust are subject to a probationary period.

Applications should be made online, however, queries regarding the application process, assistance with completion of the application form or if you require any adjustments (for applicants with a disability) please contact Amanda Vickers, Recruitment Advisor, on 01708 435000 ext. 5926. Further details regarding the post may be obtained by contacting the manager as per the contact details above.


This advert closes on Friday 22 Mar 2024

Proud member of the Disability Confident employer scheme

Job Type:

Seasonal (Fixed Term) (Seasonal)

Agropur Dairy Cooperative is currently accepting resumes from students to work for the summer work term, May6 to August 30, 2024 as a Quality Control Student Coordinator at our plant located in Bedford, Nova Scotia. 

We are seeking individuals who are:

• Highly motivated and have the ability to work independently
• Demonstrate consistency, quality, and accuracy in their work performance
• Educational background in food sciences or microbiology

As a Quality Control Coordinator, you will:

• Support the production team and assist in the development and maintenance of the following programs
  • Standard Operating Procedures (SOP’s)
  • Product Specification Sheets
  • Hazard Analysis and Critical Control Points Documentation
  • Training Records

Hourly wage ranges between $19.00 and $20.65 per hour depending on qualifications required for position.

We thank all applicants for their interest; however only candidates being interview will be contacted.

Agropur welcomes people from all backgrounds and walks of life. We are proud to be an employer with a diverse community and are committed to providing a respectful and inclusive experience for all employees and applicants. We will therefore work with candidates who request accommodation. Please note that an adequate knowledge of French is required for positions in Quebec.