Total 9 Others level Quality Assurance / Control job vacancies in Shirley, , B90 4AQ

Your new role

Hays are working with a small finance team in Bristol who are looking for a temporary Credit Controller. This role will last until the end of the year with a potential for extension in 2025. Pay for the role is dependent on experience. This role will allow an element of hybrid working. Duties of the role include:

• Chasing debt via post, email and over the phone
• Sending out monthly bills
• Resolving client queries
• Supporting the finance team with adhoc tasks

What you'll need to succeed

• Previous experience working in a similar role
• Proficiency with Excel
• Effective communication and people skills
• Happy to pivot within a small team

What you need to do now


If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

INDHAF

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

Your new role

Hays are working with an organisation in Bristol who are recruiting into their small finance team. They are looking for a temporary Credit Controller. This role will last until the end of the year with a potential for extension in 2025. Pay for the role is dependent on experience. This role will allow an element of hybrid working. Duties of the role include:

• Chasing debt via post, email and over the phone
• Sending out monthly bills
• Resolving client queries
• Supporting the finance team with adhoc tasks

What you'll need to succeed

• Previous experience working in a similar role
• Proficiency with Excel
• Effective communication and people skills
• Happy to pivot within a small team

What you need to do now


If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

INDHAF

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

MOT Tester / Vehicle Technician

Location: Stafford
Salary: £32,000 to £35,000 basic plus bonus
Hours: Monday to Friday 8.30-5, saturday morning on rota
OC15179

We are recruiting for an MOT Tester for our highly recognised client within the motor industry. You will be responsible for carrying out MOT tests in line with set standards and requirements, ensuring the highest levels of safety and quality are maintained for customers.
You will also be required to advise customers on the outcome of their tests and any remedial work that may be required to pass the test. You will also be required to do service work when required

MOT Tester Main responsibilities:
* Carrying out MOT tests to the highest of standards, ensuring accuracy and safety
* Advising customers on the outcome of their tests, and any remedial work that may be required
* Ensuring all paperwork is fully completed and up to date
* Maintaining a good working relationship with customers
* Maintaining a high level of customer service
* Following all Health & Safety regulations

MOT Tester Technical skills and qualifications:
* Relevant MOT testing qualification
* Proven experience working in a similar role
* Good working knowledge of vehicle diagnostics
* Good communication and customer service skills
* Ability to work under pressure, to tight deadlines
* Ability to work as part of a team
* Ability to work on own initiative
* Full UK driving licence

Benefits
* Childcare vouchers
* Long service recognition Generous holiday entitlement
* Staff events
* Access training
* Personal development programme
* Access to a financial advisor
* Pension plans
* Free eye tests

Consultant - William Olivier - Octane Recruitment
VTMDL

Octane Recruitment are a leading Recruitment agency specialising in Automotive, Motor trade, Engineering, OEM and various related industries.

We are recruiting across the UK for Vehicle Technician, Vehicle Mechanic, Commercial Vehicle Technician, Diagnostic Technician, Senior Technician, Master Technician, Mobile Vehicle Technician, PDI Technician, Prep Technician, MOT Tester, Fast Fit Technician, LCV Technician, Light Commercial Technician, HGV Technician, Bus Technician, LGV Technician, HGV Engineer, HGV Mechanic, HGV Fitter

Octane Recruitment cover a variety of different sectors including Technical, Mechanical, Engineering, Sales, Service, Aftersales, Bodyshop, Fleet & Rental Management, Accounts, Finance, Marketing, & Payroll, Managerial, Logistics, Parts, Administration, Call Centre / Contact Centre, Senior Appointments, Head Office Positions and Confidential Appointments.

Nature and Scope

This position in the Sterility Assurance Department will be primarily responsible for writing investigations/Excursions for Environmental and Personnel Monitoring with regards to assurance of sterility and being involved in technical projects from protocols to final reports.

Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

• Write technical protocols and reports for studies, trend reports, etc.

• Perform investigations for out-of-specification (OOS) or out-of-trend (OOT) when requested. 

• Plan daily workload to meet requirements.

• Report any issues with Aseptic Technique or cGMP compliance to Sterility Assurance Management.

• Work independently with minimal supervision.

• Manage Corrective and Preventive Actions (CAPAs) and ensure closure in a timely manner.

• Initiate Change Controls to procedures requiring modifications.

• Completing gowning qualifications to enter the Aseptic Processing Areas (APA).

• Addresses any problems that arise and bring quality issues to Management attention.

• Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

• Bachelor’s Degree in Microbiology, Biology or related field required.

• Minimum one-year experience in QC Microbiology, Environmental Monitoring or Sterility Assurance within the pharmaceutical industry, food industry, cosmetics, medical devices, Laboratory Pathology or similar FDA regulated environment, required.

• Knowledge of Aseptic Technique / Clean Room Experience preferred.

• Technical writing skills required.

• Organized individual with strong attention to detail.

• Excellent communication skills (oral and written).

• Proficient in Microsoft Office.

• Proficient in Trackwise and MODA/LIMS or equivalent software or equivalent preferred.

• Good work ethic and highly motivated.

• Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals.

Physical Environment and Requirements

• Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves.  PPE and Respirators are essential for the health and safety of employees. 

• Specific vision requirements include 20/40 near vision (can be corrected with eyeglasses or contacts) and color vision.

• Job activities require long periods of sitting and/or standing per assign duties.

• Employee must be able to occasionally lift and/or move up to 25 pounds.

Expected salary range:

$68,500 - $72,000

The salary range displayed is the minimum and maximum salary range for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 email hrtalentacquisition@americanregent.com.

Nature and Scope

This position will provide a comprehensive Quality compliance review of Environmental Monitoring data in LIMS (Laboratory Information Management System) & logbooks, cGMP Microbiology Lab analytical data & results for raw materials, in-process and finished product release, stability program results and summaries data related to the Validation of pharmaceutical processes.  To facilitate corrections and clarifications to the reviewed data and provide a final approval of the records.

Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

• Provides quality assurance review of laboratory raw data and reports including environmental monitoring and microbiological worksheets, test summaries, and trending data (for microbiological related data).

• Communicates any audit comments/ observations/ findings during review to respective stakeholders and get them corrected

• Informs the supervisors/manager immediately of any critical data integrity issues or data irregularity.

• Participates in identifying quality process improvements to increase efficiency and performance of systems, operations and personnel relating to the QA Data Review process.

• Writes and revises SOP’s and other GMP (Good Manufacturing Practices) documentation as needed. Initiate and complete Change Request process.

• Ensures compliance with cGMP/cGLP and good documentation procedure during the review process

• Follow SOPs (Standard Operating Procedure) and Safety Guidelines to ensure compliance within a cGMP environment.

• Extend help in collecting EM/PM data for investigation and author Investigation.

• Ensures all work is performed and documented according to existing Company policies and procedures, cGMP, compendia, and all applicable FDA (Food and Drug Administration) Guidance document requirements.  Perform cGMP training for department.

• Participates in other Quality System activities with other team members as needed.

• Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

• Bachelor’s degree in the Biological, Physical Sciences, Mathematics, or related field, or Associate's Degree with 2 years experience in data review within a laboratory setting, required.

• Minimum 2 years of microbiological experience (i.e. gram stains, plate counts, manufacturing of media, environmental monitoring, and microbiological assays) or at least 1 year of data review experience within a laboratory setting.

• Demonstrates extreme attention to detail to achieve quality results.

• Ability to perform multiple activities at the same time and produce outstanding results to meet required deadlines.

• Exercises a willingness to learn and participate in added responsibilities as needed.

• Excellent organizational, interpersonal, and communication skills (oral and written) to work in a team environment.

• Ability to work overtime as needed.

Expected Hourly Rate:

$37.55-$39.50

The hourly rate displayed is the hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 email hrtalentacquisition@americanregent.com.

Nature and Scope

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 email hrtalentacquisition@americanregent.com.

Title: QC Scientist IV

Job Location: 5 Ramsey Road, Shirley, NY 11967

DESCRIPTION

Duties: Coordinate Chemistry Laboratory testing to ensure that all required samples (raw materials, in process, and finished products) are received and tested. Monitor laboratory activities and achieve a smooth and timely operation. Conduct quality control tests. Communicate and give guidance to chemists and technicians where required. Maintain an adequate supply of inventory levels. Order supplies based on workload requirements. Review of testing and documentation as required. Assist in the operation, calibration, preventive maintenance, and troubleshooting of laboratory instruments to ensure proper working order. Update and/or create monographs/SOPs to meet current compendial regulations/specifications. Oversee/perform investigations as required of SOP and cGMP deviations in the Chemistry Laboratory. Provide technical assistance on new and existing products to other departments. Assist and write events, technical protocols (laboratory instrument IQ/OQ/PQ) and initiate change controls when necessary. Undertake or oversee special projects (ex: validation of new equipment and software, and introduction of new tests or procedures in the laboratory). Advise management as to new employee's proficiency on various stages of training; train new employees. Assist in supervisory duties in the absence of management. Perform any other tasks/duties as assigned by management.

The position hours are for third shift (11:00PM – 7:30AM, Sunday – Thursday). Due to several types of tests that are conducted in the course of this position, individuals must possess 20/20 vision (corrective lenses allowed) and be able to make decisions on color. As such, upon hiring, individuals will be required to provide evidence of possessing 20/20 vision (corrective lenses allowed) and must undergo Color Blindness Screening (D15).

Salary: $113,318 - $125,000

QUALIFICATIONS

Master’s Degree in Chemistry or related science, or foreign equivalent, and minimum of five (5) years of pharmaceutical laboratory experience. In addition, five (5) years of experience in the following is required:

• Analytical Instrumentation and wet chemistry techniques
• Analytical Instruments such as HPLC, GC, AA, UV-VIS, and ICP
• Empower, MS Word, Excel, and Outlook

Alternatively, the employer will accept a Bachelor’s degree or foreign equivalent in Chemistry or related science plus eight (8) years of pharmaceutical laboratory experience, as well as in the skills outlined above.

Please apply at https://www.americanregent.com/Careers

using Req. ID R-102170.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees.  We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 John Rossini, Talent Acquisition Director at at jrossini@americanregent.com.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 email hrtalentacquisition@americanregent.com.

Nature and Scope

The primary responsibilities of the Manufacturing Quality Engineer is to assure timely and accurate completion of investigations and CAPAs.  This position will organize and communicate events between Manufacturing, the Process Investigations Team, and Deviations Management as well as bring visibility to open investigations as they relate to priority for review and disposition of materials.  This individual will take a scientific and risk-based approach to exemplify unwavering commitment to product quality and patient safety.

Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

• Initiate and complete or assign investigations and CAPAs related to Manufacturing departments (Formulation, Equipment Prep, Sterile Filling, Autoclave, Inspection, Packaging, Facilities and Engineering).
• Technical writing to support manufacturing operations including but not limited to, Standard Operating Procedures (SOPs), CAPAs, change controls, risk assessments, protocols, batch records and white papers.
• Review of product support documentation (e.g., batch records, process validation, work orders and logbooks).
• Perform root-cause analysis for events utilizing investigation tools (e.g., 5 whys, 6M, Fishbone Diagrams)
• Initiate and complete or assign corrective action or preventive actions (CAPAs) to resolve and prevent recurrence of events.
• Utilize project management tools to drive critical CAPAs and their associated work to effective and timely completion.
• Utilize risk management tools for recommendation on disposition of materials.
• Act as liaison between Manufacturing and Quality including Deviations Management for the acceptability and timeliness of investigations.
• Act as liaison between Manufacturing and Quality including CAPA Management for the acceptability and timeliness of CAPAs.
• Present completed investigations to Deviations Management for review, reconciling the investigations against feedback to facilitate final approval.
• Facilitate, track, and trend all assigned Manufacturing investigations, CAPAs, protocols, and change controls.
• Support Manufacturing and Quality departments to assist in data collection activities and prepare necessary documentation, as needed. 
• Assist Manufacturing personnel as needed to assure investigations and CAPAs are conducted according to established standards and remain compliant.
• Support data tracking and metrics for Manufacturing investigations and CAPAs.
• Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

• Bachelor’s Degree in a science discipline, required.
• Minimum of 2-5 years’ experience with sterile manufacturing and/or Quality Systems, required.
• Superior technical writing, critical thinking, and problem-solving skills, required.
• In-depth knowledge of deviation documentation procedures and requirements, required.
• Strong oral, written, communication, presentation, and interpersonal skills. Capable of interfacing with multiple levels of people within the organization, including corporate management, third party customers, and plant personnel, required.
• Must be capable of organizing data from multiple sources, extracting key information and documenting events in a timely manner, required.
• Experience with word-processing, spreadsheet and presentation software (e.g. MS Word, Excel, PowerPoint, Outlook, etc.), required.
• Experience working in a cross-functional, matrix environment to drive projects to completion.
• Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals
• Experience in a pharmaceutical industry, preferred.
• Experience in TrackWise, preferred.
• Working knowledge of environmental monitoring and aseptic manufacturing, preferred.
• Lean Six Sigma Green Belt Experience, preferred.

Physical Environment and Requirements

• Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves.  PPE is essential for the health and safety of employees. 
• Employee must be able to occasionally lift and/or move up to 15 pounds.

Expected Salary Range:

$89,100-$95,000

The salary range displayed is the  minimum and maximum annual salary range of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide

range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 email hrtalentacquisition@americanregent.com.

Nature and Scope
This position is responsible for providing Quality oversight in manufacturing areas including, but not limited to Formulation, Filling, Inspection, Equipment Prep and Packaging through the execution of site policies and procedures, programs, and work instructions. This position ensures all processes and products meet specifications and that products are produced in accordance with cGMP requirements. The QA Inspector maintains compliance with quality programs.

Essential Duties and Responsibilities

• All inspections are conducted in compliance with the Code of Federal Regulations (CFR 211.134) Drug product inspection.

• Achieve and maintain Aseptic Processing Area (APA) gown qualification.

• Adhere to all SOP related to working in an aseptic environment, including volume/weight checks of product filled in vials and ampoules; s well as the monitoring of personnel Aseptic Technique.

• Checks product lot number information, documents in the batch record where applicable, and reviews Master Batch Records for accuracy at all stages in the manufacturing process - Formulation, Filling, Inspection, and Packaging.

• Conducts product in-process inspections at designated intervals.

• Determines the Acceptable Quality Limits (AQL) by using the (American Nation Standards Institute) ANSI Z1.4 Standard Inspectors Rule, the ruler assists with the calculation of sample size and Accept/Reject (A/R) numbers.

• Conducts inspection of formulation equipment (e.g. tanks) for cleanliness, imperfections, and acceptable operating condition.

• Documents verification of task performed (where applicable).

• Conducts visual inspection of filled vials and ampoules after manual or automated inspection for defined critical major and minor defects, as well as particulate matter.

• Conducts inspection of printed materials (e.g. labels), inserts, finished units, unit packs, and shipping containers for critical major and minor defects.

• Perform monthly inspection of the retentions samples to ensure quality of finished products until expiration.

• Assist in the management of the sample retention room (removing samples for monthly inspections, putting away samples from monthly inspections, adding new samples to the room, and removing samples from the room that have expired).

• Reports all non-conformances to supervision.

Education Requirements and Qualifications

• High School Diploma or GED equivalent, required.

• 1 year of related experience in Quality Assurance and/or manufacturing within a cGMP environment, preferred.

• Experience in a pharmaceutical, biotech, food, or related manufacturing environment, preferred.

• Working knowledge of good manufacturing systems, familiarity with regulatory and manufacturing SOPs and cGMPs, preferred.

• Ability to perform accurate mathematical calculations, required.

• Basic computer skills including Microsoft Outlook, Word, Excel, required.

• Strong attention to detail, adherence to SOPs, and a desire for ensuring a high-quality product.

• Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals.

• Ability to meet and maintain sterile gowning requirements.

• Ability to work overtime as needed, including weekends when required.

Physical Environment and Requirements

• Employee must be able to occasionally lift and/or move up to 25 pounds.

• Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees.

• Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision.

Expected Hourly Rate:

$23.10-$25.00

The hourly rate displayed is the  minimum and maximum hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide

range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

American Regent Inc. endeavors to make https://americanregent.com/Careers 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 email hrtalentacquisition@americanregent.com.