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About LabCorp Drug Development:As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role:Our UK site in York, is currently recruiting for a QC Analyst to join the BioPharmCMC team. Within the York BioPharmCMC business unit; the Protein Chemistry and Bioassay departments provide dedicated release and stability testing of Small and Large Molecule pharmaceutical products from preclinical through to the commercial phase. The department provides method development, transfer and phase appropriate validation of analytical methods. We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Analyst role within the York BioPharmCMC department is a laboratory scientist position. Alongside a host of other duties, you will perform analytical testing using a wide range of techniques for clinical, pre-clinical and commercial studies. Job Responsibilities:Performing analytical testing on small molecules and large protein molecules using the following analytical techniques: HPLC, Capillary Electrophoresis, Compendial Techniques, ELISA and Cell Based Assays. Recording of data on the appropriate documentation with strict adherence to current Good Manufacturing Practice (cGMP). Quality Control review of GMP analytical data and associated documentation. Involvement with the Quality Management System (QMS) for deviation, change control, lab investigations and associated change actions (CAPA). Lab level oversight and organisation of client projects; including organising study files and study data throughout the data life cycle, performing stock checks and ordering consumables/reagents, assisting with writing and updating a variety of documents. Working with QC Scientists to perform a wide range of analytical techniques in accordance with GMP regulatory requirements to deliver client projects. Assisting with the maintenance of laboratory equipment. What Labcorp Drug Development can offer you:A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salary dependent on experience, and a comprehensive benefits package including contributory pension. Key Information:Position includes a 6-month onboarding & probationary period during which working hours are 8:45am – 5pm, based at our site in York. Prerequisites:Required: Scientific degree (Biochemistry, Chemistry, Biology, Molecular Biology, Biomedical Sciences etc) OR relevant scientific industry experience. Required: Ability to multitask and prioritise workload, with excellent attention to detail. Required: Exceptional communication skills. Required: Ability to integrate well within an established and fast growing team. Required: Computing skills, including word processing and use of spreadsheets (e. g. Microsoft Office packages and Microsoft Project). Desirable: Previous analytical experience using any of the following techniques: HPLC, ELISA, Cell Based Assays, Capillary Electrophoresis and compendial techniques. Desirable: An understanding of health and safety policies and of GMP/GLP/GCP. Labcorp is proud to be an Equal Opportunity Employer:As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicants race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement.

QC Analyst York

<ul><li> Rowlands Gill, Tyne and Wear, England, UK </li></ul>SRG are working with a pharmaceutical manufacturer with a rapidly expanding programme. They are currently looking for experienced QC analysts to join their Pharmaceutical QC team in supervising the analysis of liquid bulk and finished products. Set into the west of Newcastle, this position offers the opportunity to join a leading company who are have high values and an incredibly supportive culture.The role<ul><li>Testing of: Raw materials and finished products using HPLC in accordance with specifications and laboratory methods.</li><li>Quantitative and qualitative chemical analysis of various materials including method development analysis</li><li>Support troubleshooting of the analytical team and head OOS/OOT investigations</li><li>Interpret and collate analytical data into reports for customers</li><li>Maintaining Quality and coordinating NPI activities and business improvements.</li><li>To Provide support and mentoring to develop your team effectively</li><li>To coordinate GMP and compliance to meet MHRA and ISO standards.</li></ul>Skills<ul><li>Degree (or equivalent) in Chemistry or a related scientific field</li><li>experience carrying out HPLC and other analytical techniques</li><li>Experience working within a pharmaceutical or nutraceutical industry is very advantageous</li><li>Experience with a variety of analytical equipment including Auto Titration, Moisture Analyser, Fluorimeter, UV and Infra-Red Spectrometers.</li><li>Knowledge of QMS, cGMP, H&S and COSHH procedures</li><li>Strong documentation skills: writing technical reports and tabulating Date</li></ul>If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV For more information regarding this position or any others, please call Matthew on 0161 868 2205.SRG is the UKs number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, bio-tech, chemical and medical device sectors.As scientists ourselves, our specialist sector knowledge and our passion are second to none. Its this combination that makes us different. Were committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srg.co.uk to view our other vacanciesCarbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

QC Analyst - new job in Rowlands Gill, UK

<ul><li> Kingston Upon Hull, East Riding of Yorkshire, England, UK </li></ul> Synergy are currently looking for a QC Analyst to join their team working with a global health and wellbeing company based in Hull. <ul><li>JOB TITLE: QC Analyst</li><li>LOCATION: Hull</li><li>CONTRACT - 12 months with potential extension/perm opportunities</li></ul>Synergy are currently looking for a QC Analyst to join their team working with a global health and wellbeing company based in Hull.The successful candidate will work as part of a dynamic and high performing team providing Quality Control and stability analysis services across a portfolio of health and wellbeing products and projects.Working closely with R&D, the role will focus mainly on the generation, analysis, and reporting of QC data in line with GMP/GLP standards, using analytical techniques including HPLC, GC, and a variety of other instrumental and wet chemistry techniques.You will also have opportunity to be involved in stability studies, method development, validation and transfer and QC/QA processes such as deviations, lab investigations, CAPA and audit support.<h3>PRINCIPAL ACCOUNTABILITIES:</h3><ul><li>Order and receive samples for QC testing</li><li>Perform sample assays on HPLCs and other instrumentation, following established protocols</li><li>Set up and label samples in accordance with SOPs</li><li>Analysis and trending of results</li><li>Contribute to protocol development for QC and stability trials</li><li>Identify and escalate any out of specification / out of trend / unexpected results</li><li>Ensure compliance with all relevant Health and Safety systems and legislation applicable to your working environment</li></ul>QUALIFICATIONS AND EXPERIENCE:<ul><li>Degree in a relevant scientific discipline such as Chemistry, Pharmaceutical or Biological Science, or equivalent professional experience</li><li>Previous hands-on experience of analytical test methods such as HPLC within a Healthcare / FMCG / Medical Device environment is desirable</li><li>Results orientated, self-motivated with an ability to evaluate and take risks</li><li>Ability to work under pressure without compromising quality and delivery</li><li>Strong intellectual curiosity ability to think out of the box</li></ul>If this role is of interest, please apply online today, or contact / 020 3910 9513 to discuss in more detail.Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

QC Analyst - new job in Kingston Upon Hull, UK

<div>QC Analyst 12 month contract £18.33 per hour Liverpool 4 days on, 4 off (11.5 hours) Cpl Life Sciences are partnering with a global pharmaceutical company that focusses on developing life changing vaccines recruiting for a QC Analyst to join one of the laboratories in Liverpool. The main purpose of the QC Analyst is to perform quality tests on in-process, intermediate and finished vaccine products. Key Responsibilities; <ul><li>Perform QC laboratory testing and communicate all findings</li><li>Investigate of any invalid, OOS/ OOT results within the GLIMS system</li><li>Support with technical and validation studies</li><li>Manage deviationsand communicate with QA</li><li>Manage CAPAs, Change Control</li><li>Update SOPs</li><li>Perform quality risk assessments</li><li>Perform laboratory administrations, archiving of documentation</li><li>Manage QC samples</li><li>Laboratory maintenance, including cleaning, ordering and ensuring stock required is available</li></ul>Experience; <ul><li>A degree within a scientific subject </li><li>Previous experience of QC testing techniques </li><li>Experience working within the pharmaceutical industry </li></ul>For more information please contact <a href="#">amy.goddard@cpl.com</a></div>

QC Analyst

<div> Job Title: QC ScientistLocation: West NewcastleEmployment Term: PermanentSalary: £23,000 - 28,000SRG are working with a pharmaceutical manufacturer with a rapidly expanding programme. They are currently looking for experienced QC analysts to join their Pharmaceutical QC team in supervising the analysis of liquid bulk and finished products. Set into the west of Newcastle, this position offers the opportunity to join a leading company who are have high values and an incredibly supportive culture.The role<ul><li>Testing of: Raw materials and finished products using HPLC in accordance with specifications and laboratory methods.</li><li>Quantitative and qualitative chemical analysis of various materials including method development analysis</li><li>Support troubleshooting of the analytical team and head OOS/OOT investigations</li><li>Interpret and collate analytical data into reports for customers</li><li>Maintaining Quality and coordinating NPI activities and business improvements.</li><li>To Provide support and mentoring to develop your team effectively</li><li>To coordinate GMP and compliance to meet MHRA and ISO standards.</li></ul>Skills<ul><li>Degree (or equivalent) in Chemistry or a related scientific field</li><li>experience carrying out HPLC and other analytical techniques</li><li>Experience working within a pharmaceutical or nutraceutical industry is very advantageous</li><li>Experience with a variety of analytical equipment including Auto Titration, Moisture Analyser, Fluorimeter, UV and Infra-Red Spectrometers.</li><li>Knowledge of QMS, cGMP, H&S and COSHH procedures</li><li>Excellent communication skills</li><li>Strong documentation skills: writing technical reports and tabulating Date</li></ul>If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV For more information regarding this position or any others, please call Matthew on 0161 868 2205.SRG is the UKs number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, bio-tech, chemical and medical device sectors.As scientists ourselves, our specialist sector knowledge and our passion are second to none. Its this combination that makes us different. Were committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srg.co.uk to view our other vacanciesCarbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.</div>

If you are looking for a company where you can personally advance healthcare and make a difference in peoples lives with your bold ideas and unique point of view, consider working at Labcorp Drug Development as a Quality Control Analyst - Molecular Biology. Within the CMC (Chemistry, Manufacturing and Controls) business unit at our site in Harrogate, North Yorkshire , the Molecular BioA department is dedicated to the development, validation and execution of molecular techniques, such as qPCR, RTqPCR, Droplet Digital PCR and DNA/RNA Extractions to support Cell Therapies, Gene Therapies and Vaccines. In addition, the department also provides method development, transfer, phase appropriate validation of analytical methods. We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. Alongside a host of other duties, you will perform analytical testing using a wide range of techniques for clinical, pre-clinical and commercial studies. Alternative terminologies for QC Analyst include Research Associate, Laboratory Analyst, Analytical Scientist. Y our responsibilities will include <ul><li>Working as part of a team alongside other QC Analysts and QC Scientists to perform analytical testing on small molecules and large protein molecules using the following analytical techniques: DNA/RNA Extraction, qPCR, RTqPCR, Droplet Digital PCR</li><li>Data processing and analysis, using the appropriate documentation, with strict adherence to current Good Laboratory Practice (GLP) and/or Good Clinical Practice (GCP)</li><li>Quality Control review of GLP/GCP analytical data and associated documentation</li><li>Involvement with the Quality Management System (QMS) for deviation, change control, lab investigations and associated change actions (CAPA)</li><li>Study supervision and oversight of client projects at lab level; including organising study files and study data throughout the data life cycle, performing stock checks and ordering consumables/reagents, assisting with writing and updating a variety of documents</li><li>Working with QC Scientists to perform a wide range of analytical techniques in accordance with GLP/GCP regulatory requirements, to undertake data processing, and to deliver client projects</li><li>Assisting with the maintenance of laboratory equipment and process improvements</li></ul> Thrive personally and professionally at Labcorp Drug Development Working at Labcorp Drug Development, youll continue to grow in our learning-based culture so youll know how to expertly respond and adapt as the industry continues to evolve. Here, youll put your education to work as you play a meaningful role in advancing healthcare and making a difference in peoples life. In addition, Labcorp Drug Development offers great benefits, global experience and the opportunity to work independently within a team-oriented environment. Key Information <ul><li>The position includes a 6-month onboarding & probationary period with working hours of 8:45am - 5pm, based at our site in Harrogate.</li><li>Following the initial training period, you will move onto a shift pattern of 6:00am - 2:15pm.</li><li>The role requires fully on-site working, with both laboratory and office-based activities.</li></ul> What were looking for Quality Control Analysts are the most successful at Labcorp with: <ul><li>Scientific degree (Biochemistry, Chemistry, Biology, Molecular Biology, Biomedical Sciences etc) OR relevant scientific industry experience.</li><li>Ability to multitask and prioritize workload, with excellent attention to detail.</li><li>Exceptional communication skills.</li><li>Ability to integrate well within an established and fast growing team.</li><li>Computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages).</li><li>An understanding of GLP and GCP guidelines (desirable).</li><li>Previous analytical experience using any of the following techniques: qPCR and DNA/RNA Extractions (desirable).</li><li>An understanding of health and safety policies (desirable).</li></ul> Get to know Labcorp Drug Development At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 75,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on peoples lives. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement . Create a job alert and receive personalised job recommendations straight to your inbox.

QC Analyst III

<h3>Location</h3>Ebbw Vale<h3>Job Reference</h3>BBBH4057M<h3>Job Type</h3>Permanent<h3>Posted Date</h3>28/12/2022Senior QC analyst required to join an expanding and growing company that is a leading name in their industry. You will receive a salary of up to £35,000 plus a potential annual bonus, pension, etc. The role will involve working a 2 shift rota involving 1 week of days (6am-2pm) and afternoons (1:30pm-9:30pm). The company is part of a larger global group of companies that produces profits of close to £500million and employs 10,000+ staff around the world. The South Wales site is one of the leading companies in Europe in their field and prides itself on the innovation it can provide its clients. You will work closely with the QC team leader and take on a senior role in the team being pivotal in the efficient running of the laboratory. Senior QC analyst duties will include:<ul><li> Taking responsibility for the operations of the QC shift, particularly outside of office hours where you will be the most senior point of contact within the laboratory </li><li> Performing a range of complex analysis on samples received into the laboratory against defined lead times </li><li> Calibration of laboratory instrumentation </li><li> Ensuring the integrity of data generated within the laboratory </li><li> Accurately perform checks of analytical data/results in line with company procedures </li><li> Participating in the resolution of operational issues </li><li> Consulting with the quality management team to ensure laboratory resources and testing performance meet regulatory expectations for compliance </li><li> Achieving set targets for laboratory sample throughput </li><li> Ensuring effective communication with the other shift to ensure cohesion </li></ul>To apply for the Senior QC analyst role, you will need:<ul><li> Experience in working in a quality control laboratory in a manufacturing, scientific or technical environment </li><li> To be skilled in the use of analytical techniques such as HPLC, GC and ICP-OES </li><li> A good understanding of GMP </li><li> Previous experience in a supervisory / team leading capacity is desirable </li></ul>In return, the Senior QC analyst will receive a salary of £31,000-£35,000 (dependent on experience) + pension, potential annual bonus, 24 days holiday plus Bank Holidays, etc. The working hours will be a rotating shift pattern of days (6am-2pm) and afternoons (1:30pm-9:30pm). If you are a QC analyst, quality control analyst, senior QC analyst, QC team leader, QC technician, quality control technician, lab analyst, laboratory analyst, lab technician, laboratory technician, etc. and you wish to be considered for the Senior QC analyst role, please click on the apply button. By clicking "apply", youre accepting our privacy policy and giving consent for Sigma Recruitment to contact you via email, phone & SMS regarding this job, general recruitment services and other vacancies were recruiting for. Privacy Policy https://sigmarecruitment.co.uk/privacy-policy/ If you opt out but then opt in again by applying for positions/being active on job boards, we will contact you again until you opt out again. Job Skills: QC analyst, quality control analyst, senior QC analyst, QC team leader, QC technician, quality control technician, lab analyst, laboratory analyst, lab technician, laboratory technician, engineering recruitment agencies, ads@sigmarecruitment.co.uk

Senior QC Analyst

<div>Reference Number: JO-2302-511168 
QC Analyst 
Rate: Negotiable 
Job Type: Contract 
Location: LiverpoolQC Analyst12 month contract£18.33 per hourLiverpool4 days on, 4 off (11.5 hours)Cpl Life Sciences are partnering with a global pharmaceutical company that focusses on developing life changing vaccines recruiting for a QC Analyst to join one of the laboratories in Liverpool. The main purpose of the QC Analyst is to perform quality tests on in-process, intermediate and finished vaccine products.Key Responsibilities;<ul><li>Perform QC laboratory testing and communicate all findings</li><li>Investigate of any invalid, OOS/ OOT results within the GLIMS system</li><li>Support with technical and validation studies</li><li>Manage deviations and communicate with QA</li><li>Manage CAPAs, Change Control</li><li>Update SOPs</li><li>Perform quality risk assessments</li><li>Perform laboratory administrations, archiving of documentation</li><li>Manage QC samples</li><li>Laboratory maintenance, including cleaning, ordering and ensuring stock required is available</li></ul>Experience;<ul><li>A degree within a scientific subject</li><li>Previous experience of QC testing techniques</li><li>Experience working within the pharmaceutical industry</li></ul>For more information please contact <a href="#">amy.goddard@cpl.com</a></div>

<div>KYC QC Analyst Northampton As a Barclays KYC QC Analyst, you will have an exciting opportunity to take real ownership of performance reviews of KYC files, from corporate banking and investment bank clients, and independently assess whether client due diligence policy and regulatory requirements have been adhered to. You will work in partnership with other Barclays teams, as well as our wider business functions to deliver a ‘One Barclays’ client experience. Barclays is one of the worlds largest and most respected financial institutions, with 329 years of success, quality and innovation behind us. We offer careers that provide endless opportunity – helping millions of individuals and businesses thrive, and creating financial and digital solutions that the world now takes for granted. Working FlexiblyWe’re committed to providing a supportive and inclusive culture and environment for you to work in. This environment recognises and supports ways to balance your personal needs, alongside the professional needs of our business. Providing the opportunity for all our employees, globally to work flexibly empowers each of us to work in a way that suits our lives as well as enabling us to better service our customers’ and clients’ needs. Whether you have family commitments or you’re a carer, or whether you need study time or wish to pursue personal interests, our approach to working flexibly is designed to help you balance your life.  If you would like some flexibility then please discuss this with the hiring manager, and your request will be reviewed subject to business needs.We are currently in the early stages of implementing a hybrid working environment, which means that many colleagues spend part of their working hours at home and part in the office, depending on the nature of the role they are in. We’re flexible on how this works and it may continue to change and evolve. Depending on your team, typically this means that colleagues spend a minimum of between 20% to 60% of their time in the office, which could be over a week, a month or a quarter. However, some colleagues may choose to spend more time in the office over a typical period than their role type requires. We also have a flexible working process where, subject to business needs, all colleagues globally are able to request work patterns to reflect their personal circumstances. Please discuss the detail of the working pattern options for the role with the hiring manager. What will you be doing?• Analysing client data and documentation stored in the KYC Files in order to determine whether procedures, policy and regulatory requirements are met • Assisting assignment team leader in the preparation of executive summaries, reports and management information • Documenting all testing to a standard that allows re-performance of the work by an independent third party • Supporting the embedding of all relevant policies and regulatory requirements • Facilitating and sharing knowledge and best practices • Using excellent problem solving and team working skills to resolve complex cases, ensuring the bank’s policy and regulatory requirements are always met • Supporting the testing and the implementation of new controls and checks for KYC Operation teams  • Championing the delivery of what the Customer/Client & the Business want to become the Go-To-Bank What we’re looking for: • Previous experience of AML/KYC gained within investment or corporate banking • Communication skills allowing you to interact professionally with stakeholders at face-to-face meetings or via phone/ email • Excellent time management skills ensuring that you manage workloads effectively to complete complex and high-priority tasks within target timescales  • A high level of accuracy and attention to detail to undertake KYC analysis Skills that will help you in the role: • Good command of one of the following languages: German, French, Arabic, Italian, Spanish, Dutch, Portuguese • Basic legal knowledge in terms of corporate law and structure • Understanding of KYC rules and regulations  • Knowledge of High risk indicators and revision of complex structures and entity types, as well as experience of reviewing complex structures, PEPs and/or Sanctions screening Where will you be working: Northampton was the birthplace of Barclaycard in 1966 and weve been based in Pavilion Drive since the building opened in 1997. This state-of-the art energy efficient building holds up to 2,500 staff. The office location is perfect for travel from the midlands and London alike as we are based just off the A45, it is easily accessible by both car and bus routes. #LI-Hybrid</div>

KYC QC Analyst

<div>19.99 Shift 5 on 3 off (hours 8-5 , 5 on 3 off The purpose of the QC Analyst role is to compliantly perform QC laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs). Analysis is performed on in-process, intermediate and finished vaccine products, raw materials, components and utilities samples. QC Analysts are also required to participate in technical and validation studies in support of both departmental and site objectives. The primary responsibility of a QC Analyst is to compliantly perform laboratory testing, data review and data interpretation in accordance with approved SOPs. It is expected that analysts consistently work to the highest standards of cGMP (as defined in the EU GMP Annexes and FDA CFRs) and in accordance with the uppermost standards of HSE. In addition to testing, Analysts will be required to perform raw material and components inspection (quality receipt) and sampling. It is the responsibility of QC Analysts to communicate their findings as a result of testing promptly, to the QC Analytical leadership team (Team Coordinators and Manager). Specifically, it is expected that deviations (either out of specification results or compliance gaps) are highlighted to a leadership team member immediately as they are recognised It is the responsibility of QC Analyst, when assigned, to complete critical tasks such as: <ol> <li>It is the responsibility of QC Analyst, when assigned, to complete critical tasks such as:</li> </ol> <ul> <li>Instrument Maintenance and Calibration</li> <li>Sampling booth cleaning and monitoring</li> <li>Reagent and Standard Qualification</li> <li>Initiation of deviations</li> <li>Initiation, and completion, of CAPAs</li> <li>Completion of Change Control actions</li> <li>Updates and reviews of SOPs</li> <li>Participation in quality risk assessments</li> </ul> QC Analysts must be fluent in English as the primary operating and reporting language used within the industry, in addition they must: <ul> <li>Have experience in QC testing techniques appropriate to their role</li> <li>Have experience in cGMP application</li> <li>Have an awareness of the requirements for equipment and method validation</li> <li>Have awareness of root cause analysis</li> <li>Be computer literate and be able to demonstrate an understanding of electronic systems</li> </ul> <table> <tbody> <tr> <td> <table> <tbody> <tr> <td> QC Analysts must be fluent in English as the primary operating and reporting language used within the industry, in addition they must: Have experience in QC testing techniques appropriate to their role Have experience in cGMP application Have an awareness of the requirements for equipment and method validation Have awareness of root cause analysis Be computer literate and be able to demonstrate an understanding of electronic systems </td> </tr> </tbody> </table> </td> </tr> </tbody> </table> Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser <a href="#">https://www.adecco.co.uk/candidate-privacy </a></div>

<div>Pharmaceutical QC Analyst Location– Oxfordshire Sector – Pharmaceutical Salary– Competitive Full-time, permanent opportunity (day shift pattern) Our client is a leading contract manufacturing organisation based in Oxfordshire, looking for an enthusiastic and hard-working individual to join their Quality Control team as a QC Analyst. This role is well suited to candidates with experience in undertaking analytical testing in a pharmaceutical environment, ideally carrying out method development and validation using techniques such as HPLC, GC, NMR, etc in a GMP environment. This role is available as a ‘traditional’ working pattern (09:00 – 17:00, weekdays), and on a 12-hour day shift pattern (07:00 – 19:00, 4 on, 4 off). The Role This position is suitable for individuals with experience in using analytical techniques to conduct pharmaceutical testing in an industry setting following Good Manufacturing Practice (GMP), ideally including method development/method validation. As a Quality Control Analyst, you will be responsible for the following: <ul> <li>Utilising analytical chemistry techniques to undertake method development and validation at all stages of the pharmaceutical development process, from raw materials to finished products,</li> <li>Producing high quality assessments and reports related to QC,</li> <li>Ensuring all work is conducted following Good Manufacturing Practice (GMP).</li> </ul> Skills and Experience Needed An ideal candidate will have: <ul> <li>A degree in Pharmaceutical Science, Analytical Chemistry, or a related field,</li> <li>Experience in working in an industry setting following GMP,</li> <li>Hands-on proficiency using HPLC and GC (essential), as well as NMR, FTIR, Karl Fischer, UV-vis (desirable),</li> <li>Strong communication skills (written and verbal),</li> <li>Knowledge of method development using HPLC/GC is desirable.</li> </ul> The Package Our client is offering this opportunity on a full-time, permanent basis. The starting base salary is competitive, dependant on experience and interview performance, with a generous benefits package. The 12-hour day shift pattern has an extra shift allowance added to the base salary.</div>

Pharmaceutical QC Analyst

<div>Working closely with production team and reporting to QC Manager, the Senior Analyst will be responsible for microtesting of products before they are released alongside additional responsibilities; supporting investigations, and duties detailed below. You will be working in a busy environment ensuring products are released in a timely manner complying with Baxter standards and GMP guidelines.Essential Duties and Responsibilities<ul><li>Technical Leadership - specifically within the testing of samples to support validation studies and implementing process improvements through the development of a team</li><li>Make detailed observations, documents results and perform data analysis</li><li>Provide assistance to management in investigating out of specs and trend results for microbiological data</li><li>Create / Revise SOPs, Laboratory records, logs and other related documents</li><li>Contribute ideas and suggestions to improve standard laboratory techniques, improve protocols, processes and equipment</li><li>Identify and develop corrective actions for out of compliance issues</li><li>Perform microbiological validations as needed for products and processes</li><li>Assist in reviewing the data and support timely product release</li><li>Well versed with knowledge and understanding of current standards and methods pertaining to microbiology, sterility assurance, bioburdens, environmental monitoring, water testing, validations and other testing related to microbiology in drug and device industry</li></ul>Qualifications<ul><li>Science degree/ Qualification in Chemistry / or relevant Science</li><li>Knowledgeable with regards to GMP and have a GMP background within the pharmaceutical industry</li><li>Experienced with Quality Control analytical testing techniques and industry best practice</li><li>Have proven leadership skills in supervision of teams as well as good time management and communication skills</li><li>Knowledgeable with regards to continuous improvement techniques and root cause analysis techniques</li><li>Have experience in test and equipment validation</li></ul></div>

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