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Job Description:

Are you looking for a new opportunity within the healthcare sector?

Do you have experience working in a GP surgery and confidence using EMIS

We are currently working with a friendly and well-established GP Practice in Guildford who are seeking an experienced Medical Receptionist/Administrator to join their team on a temporary contract, permanent placements will also be considered for the right candidate.

Key Responsibilities:

• Handling inbound calls from patients in a professional and friendly manner
• Booking and managing appointments
• Managing incoming and outgoing post
• Scanning and processing documents
• Updating and maintaining accurate patient records on the system

About You:

• Previous experience working within a GP practice is essential
• Strong working knowledge of EMIS
• Excellent telephone manner and customer service skills
• Reliable, organised, and able to work efficiently in a busy environment
• Able to hit the ground running with minimal supervision

This is a great opportunity to join a supportive practice and make a real difference to patient care.

If you are immediately available and feel you have the right skills and experience, we would love to hear from you.

Apply now to be considered.

We are seeking a motivated and detail-oriented Junior QC Analyst to join an established pharmaceutical manufacturing team. This is an entry-level position ideal for recent graduates or individuals starting their career in Quality Control. You will support laboratory testing of raw materials, in-process samples, and finished products to ensure they meet required quality and regulatory standards.

• Perform routine analytical testing on raw materials, in-process samples, and finished products following established methods and SOPs.
• Accurately record and report test results in compliance with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
• Prepare laboratory reagents, standards, and solutions.
• Assist in the maintenance, calibration, and cleaning of laboratory instruments and equipment.
• Support investigations into out-of-specification (OOS) results under supervision.
• Ensure all work is completed within required timelines to support production.
• Maintain a clean, organised, and compliant laboratory environment.
• Follow all health, safety, and environmental procedures.
• Assist with documentation updates and general QC administrative tasks.

• Degree (or equivalent) in Chemistry, Pharmaceutical Science, or a related scientific discipline OR relevant laboratory experience.
• Strong attention to detail and willingness to learn.
• Basic understanding of laboratory techniques.
• Good communication and organisational skills.

• Placement year or internship experience in a laboratory or pharmaceutical environment.
• Basic knowledge of GMP or regulated industries.
• Familiarity with analytical techniques (e.g., HPLC, UV, titration).

If you receive suspicious outreach claiming to be from us, please contact us via the ManpowerGroup website.

Job Title: Quality Control Analyst

Location: Newmarket, England, United Kingdom.

About the Company

We are a leading UK manufacturer of fine chemicals and pharmaceutical intermediates, providing high-quality custom manufacturing and process development services to customers across the pharmaceutical, biotechnology, agrochemical, and specialty chemical industries. As part of our continued growth, we are seeking a motivated and detail-oriented QC Analyst to join our Quality Control team.

About the Role

As a QC Analyst, you will play a critical role in ensuring the quality and compliance of our products. Your key responsibilities will include:

Responsibilities

• Performing routine and non-routine analysis of raw materials, intermediates, and finished products.
• Operating and maintaining analytical instrumentation, including HPLC, GC, UV-Vis, FTIR, Karl Fischer, and wet chemistry techniques.
• Reviewing analytical data to ensure compliance with specifications.
• Preparing analytical reports and laboratory documentation in accordance with GMP and company procedures.
• Investigating Out of Specification (OOS), Out of Trend (OOT), and laboratory deviations as required.
• Supporting analytical method verification, validation, and method transfers.
• Assisting with stability studies and environmental monitoring activities.
• Performing instrument calibration, routine maintenance, and troubleshooting.
• Maintaining laboratory housekeeping and ensuring compliance with Health & Safety procedures.
• Participating in continuous improvement initiatives to enhance laboratory efficiency and quality.
• Collaborating with Production, QA, and Process Development teams.

Qualifications

Essential:

• Degree (or equivalent) in Chemistry, Analytical Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Previous laboratory experience within a pharmaceutical, chemical, CDMO, or GMP-regulated environment.
• Hands-on experience using HPLC and/or GC.
• Good understanding of GMP and laboratory documentation practices.
• Strong attention to detail and excellent organisational skills.
• Ability to work independently and as part of a team.
• Strong written and verbal communication skills.

Desirable:

• Experience working within a pharmaceutical manufacturing environment.
• Knowledge of analytical method validation and transfer.
• Experience investigating OOS/OOT results.
• Familiarity with LIMS, Empower, Chromeleon, or similar chromatography software.
• Understanding of ICH guidelines and data integrity principles (ALCOA+)

Pay range and compensation package

Salary: 28,000 to 36,000 dependent on experience.

A Quality Control Manager has become available, offering a salary of 40,000 - 45,000 (DOE) plus a competitive benefits package of up to 12% employer pension contribution, life assurance, enhanced sick pay, 33 days annual leave, long service awards and many more!

This global chemical manufacturer specialises in high-quality speciality chemicals, supplying major brands across the fragrance, cosmetics, and personal care industries. They are seeking a Quality Control Manager to join their manufacturing team in Leek.

Salary and benefits available for Quality Control Manager:

• Annual Salary: 40,000 - 45,000
• Up to 12% Employer Pension Contribution
• Days based role
• 33 days Annual Leave
• Life Assurance Policy
• Enhanced Company Sick Pay
• Long Service Awards

Quality Control Manager Role Overview:

You will lead the sites QC function, ensuring laboratory operations, testing activities, and quality systems support safe, compliant, and efficient manufacturing. The role is responsible for developing the QC team, maintaining compliance with customer and regulatory requirements, managing laboratory resources, resolving quality issues, and driving continuous improvement across the site.

Skills and Experience Required from Quality Control Manager:

• Lead and manage the sites QC system and laboratory operations, ensuring effective testing, inspection, and release of raw materials, intermediates, finished products, returns, waste, and environmental samples.
• Oversee QC laboratory resources, equipment maintenance, consumables, and budget planning, including monthly and annual forecasting to meet operational requirements.
• Develop and maintain QC team capability through coaching, training, competency management, and ownership of the QC Competency Matrix.
• Manage product and raw material specifications, inspection data, and concession processes to ensure compliance with quality and regulatory requirements.
• Support supplier approval activities for raw materials and collaborate with suppliers to maintain quality standards.
• Coordinate and support the investigation and timely resolution of customer complaints, driving effective corrective actions and continuous improvement.
• Support the sites ISO 14001 Environmental Management System, including environmental compliance activities and delivery of the internal audit programme

To apply for this Quality Control Manager opportunity, please submit your CV for review. Alternatively, contact Kate Wadsworth at E3 Recruitment for further information.

Job Description:

Are you looking for a new opportunity within the healthcare sector?

Do you have experience working in a GP surgery and confidence using EMIS?

We are currently working with a friendly and well-established GP Practice in The South Woodford area who are seeking an experienced Medical Receptionist/Administrator to join their team on a temporary contract.

Key Responsibilities:

• Handling inbound calls from patients in a professional and friendly manner
• Booking and managing appointments
• Managing incoming and outgoing post
• Scanning and processing documents
• Updating and maintaining accurate patient records on the system

About You:

• Previous experience working within a GP practice is essential
• Strong working knowledge of EMIS
• Excellent telephone manner and customer service skills
• Reliable, organised, and able to work efficiently in a busy environment
• Able to hit the ground running with minimal supervision

This is a great opportunity to join a supportive practice and make a real difference to patient care.

If you are immediately available and feel you have the right skills and experience, we would love to hear from you.

QC Scientist
Location: Near Peterborough, Cambridgeshire
Job Type: Full-Time, Permanent

Talentmark is recruiting for a QC Scientist to join a growing bioscience organisation operating within a GMP-regulated environment.

This is an excellent opportunity for an analytical scientist with experience in chromatographic techniques to play a key role in quality control testing, supporting the manufacture and processing of high-quality, plant-derived active pharmaceutical ingredients (APIs).

Key Responsibilities:

• Perform analytical testing of plant-derived molecules in accordance with approved SOPs.
• Prepare working solutions, mobile phases, standards, and laboratory reagents.
• Maintain accurate GMP-compliant documentation and ensure data integrity requirements are met.
• Carry out routine maintenance, calibration, and verification of laboratory instrumentation, including GC-MS and HPLC-UV systems.
• Manage laboratory stock levels and consumables to support uninterrupted testing activities.
• Support internal audits and regulatory inspections where required.
• Participate in data review activities and continuous improvement initiatives.
• Collaborate closely with QA, Production, and other cross-functional teams.

• Degree-qualified in Chemistry or a related scientific discipline, or possess equivalent laboratory experience.
• Experience working within a regulated laboratory environment, ideally GMP.
• Familiarity with analytical techniques such as HPLC and/or GC-MS.
• Strong understanding of laboratory safety practices, including COSHH, risk assessments, and PPE requirements.

• Opportunity to join an innovative bioscience organisation with ambitious growth plans.
• Collaborative and fast-paced working environment.
• Work within a modern GMP-regulated laboratory environment.
• Exposure to cutting-edge products and technologies.

QC Chemist required on a permanent basis, based in the Greater Manchester. Requiring proven industrial experience within quality control (QC) testing with wet chemistry techniques, ideally within paints & coatings. A range of other industrial chemical QC experience can be considered.

Title: QC Chemist
Location: Greater Manchester
Salary: 28,000 - 34,000 (dependent on experience)
Term: Permanent

SRG are working with a respected and well-established manufacturer of premium coating products. Renowned for high-quality formulations, expertise and product performance, they are now seeking to hire a QC Chemist to join their technical team in Greater Manchester. This role will be laboratory-based and hands-on, focusing on quality control (QC) testing, batch approval support and technical problem-solving across raw materials, intermediates and finished products. This represents an excellent opportunity for candidates with proven QC or technical laboratory experience within paints, coatings, chemicals or other related manufacturing environments within industrial chemicals.

Benefits: You will join a well-established and highly successful coatings manufacturer. 39 hours per week. 8:30am-5:00pm Mon-Thurs and 8:30am-4:00pm on Friday. 25 days holiday plus bank holidays.

Role / Description

• Perform quality control (QC) assessments on incoming raw materials, products in manufacture and finished goods to ensure compliance with established quality standards.
• Undertake a variety of laboratory evaluations including colour, viscosity, density, pH, gloss, opacity, drying characteristics, adhesion, stability and application performance testing.
• Contribute to batch release activities by interpreting test data, identifying deviations and highlighting any quality concerns requiring further investigation.
• Support the investigation of manufacturing, product quality and customer-related issues, helping to identify root causes and implement effective solutions.
• Assist with colour verification, tint accuracy checks and shade correction activities to maintain consistency across product ranges.
• Produce test panels, drawdowns and application samples to assess both the visual appearance and functional performance of coating products.
• Ensure all laboratory results, quality records, specifications and supporting documentation are completed accurately and maintained in accordance with company procedures.
• Carry out routine calibration, verification and upkeep of laboratory instruments to guarantee reliable and reproducible test results.
• Liaise with colleagues across production, technical and commercial functions to support product quality objectives and continuous improvement projects.
• Provide support with raw material assessments, competitor product reviews and formulation-related activities where required.

Requirements

• Proven industrial experience within a QC, or analytical testing laboratory within the chemicals sector.
  • Experience gained within decorative paints, surface coatings, chemicals or a manufacturing environment would be advantageous.
• A degree, HNC, HND or similar qualification in Chemistry or a related scientific discipline would be beneficial.
• Practical understanding of paint and coatings testing methods including colour, viscosity, pH, density and applied coating performance.
• Excellent attention to detail with strong documentation and record-keeping skills.
• Ability to investigate technical and quality issues and provide practical solutions.
• Good communication skills with the ability to work collaboratively across technical and production teams.
• Knowledge of laboratory safety procedures and quality systems.
• Full UK driving licence would be advantageous.

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're 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 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 Chris on (phone number removed).

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Role Overview:

We are looking for a proactive and organised Business Administrator to support the day-to-day operations of our care home. This varied role combines administration, customer service, HR, finance and compliance, ensuring the home operates efficiently while delivering an excellent experience for residents, families, visitors and colleagues.

Key Responsibilities:

• Act as the first point of contact for residents, families, visitors and professionals.
• Manage reception, enquiries and visitor records while maintaining confidentiality and GDPR compliance.
• Provide administrative support, including preparing reports, letters, meeting minutes and maintaining compliance trackers.
• Support recruitment, onboarding, HR administration, payroll preparation and employee record management using Planday.
• Monitor HR compliance, including DBS checks, Right to Work, probation reviews, supervisions, appraisals and absence management.
• Maintain resident funding records, petty cash, procurement and liaise with the central finance team.
• Monitor mandatory training compliance and update Skills for Care workforce data.
• Support CQC compliance, safeguarding, health and safety, infection prevention and emergency procedures.

We are looking for:

Essential :

• Previous administration experience.
• Excellent communication, organisation and customer service skills.
• Strong IT skills, including Microsoft Office.
• Knowledge of HR administration or payroll systems.
• GCSE (or equivalent) in English and Maths.
• Ability to prioritise workload and maintain accuracy.

Desirable

• Experience working in a care home or healthcare setting.
• Knowledge of CQC standards and care sector regulations.
• NVQ Level 2 or 3 in Business Administration or Health & Social Care.

Please Note:

• This job description is not an exhaustive statement of the job. Other duties may need to be undertaken commensurate with this position.
• This is not a sponsorship role.

Job Purpose

To provide a professional, friendly and efficient reception and administrative service, ensuring that all visitors, residents, relatives, healthcare professionals and staff receive a positive first impression of the home. The Receptionist is responsible for managing the reception area, handling telephone enquiries, providing administrative support, maintaining accurate records and ensuring the smooth day-to-day operation of the reception function. The post holder will promote an excellent service experience, uphold confidentiality, and contribute to the efficient and professional running of the home in accordance with company policies, procedures and regulatory requirements.

Reception Duties

• Welcome residents, relatives, visitors, contractors and healthcare professionals in a courteous and professional manner.
• Operate the main reception desk during working hours.
• Answer and direct telephone calls promptly and accurately.
• Take clear messages and ensure they are passed to the appropriate person.
• Monitor visitor sign-in and sign-out procedures.
• Issue visitor badges where required.
• Ensure safeguarding and security procedures are followed for all visitors.
• Maintain a clean, tidy and welcoming reception area at all times.

Administration

• Provide general administrative support to the management and administration team.
• Prepare, scan, photocopy and file documents accurately.
• Maintain both paper and electronic filing systems.
• Process incoming and outgoing post.
• Order and maintain office stationery and supplies.
• Assist with data entry onto the home's electronic care and administration systems.
• Produce letters, reports and other documents as requested.
• Support the smooth day-to-day running of the office and reception.

Digital Marketing

Whilst not essential, we would particularly welcome applications from candidates who have experience of, or an interest in, creative digital marketing. This may include creating social media content, taking photographs, promoting the home online, designing simple promotional materials, or helping to maintain the home's digital presence.

About You

Previous experience in a reception, administration or office management role (care or healthcare experience is desirable but not essential. Excellent communication and customer service skills. Strong organisational and record-keeping skills. Confident handling confidential and sensitive information. Comfortable working independently and prioritising workload. An interest in digital marketing or social media would be an advantage.

What We Offer

• ompetent in Microsoft Office, including Word, Excel and Outlook.
• A positive, calm, professional and reliable approach.
• Friendly, approachable and well presented.

• School-hours working pattern available, but prefer full time hours (9-5)
• Flexible and supportive working environment.
• Permanent role with long-term stability.
• Competitive salary dependent on experience.
• Opportunity to work within a respected, long-established care service.
• Supportive management team with a structured handover and ongoing support.

How to Apply

Please submit your CV together with a short covering letter outlining your relevant experience, why you are interested in joining our team, and your current availability.

Talent STEM are partnering with an established chemical manufacturer to recruit a Temporary QC Analyst to support their Quality Control laboratory during a busy production period.

This is an excellent opportunity for an experienced QC Analyst to join a busy manufacturing laboratory, carrying out routine analytical testing to support production and ensure products consistently meet quality standards.

The Opportunity

Working as part of the Quality Control team, you will perform routine analysis of raw materials, in-process samples and finished products using a range of analytical techniques. This is a hands-on laboratory role within a fast-paced manufacturing environment.

Key Responsibilities

- Perform analytical testing of raw materials, intermediates and finished products.

- Operate GC, HPLC, FTIR and Karl Fischer instrumentation.

- Carry out wet chemistry techniques including titrations.

- Prepare samples, standards and reagents.

- Record, review and report analytical results accurately.

- Support investigations into out-of-specification results.

- Maintain laboratory equipment and documentation.

- Ensure compliance with laboratory quality, HSE and COSHH procedures.

- Work closely with production and technical teams to support manufacturing.

About You

To be considered, you should have:

- A BSc (or equivalent) in Chemistry or a related scientific discipline.

- Previous experience within a QC or analytical laboratory.

- Essential: Hands-on industrial experience operating both GC and HPLC.

- Experience using FTIR and Karl Fischer would be advantageous.

- Wet chemistry experience, including titrations.

- Strong attention to detail and good laboratory documentation skills.

- A good understanding of laboratory safety and quality procedures.

- The ability to work effectively within a busy laboratory environment.

Why Apply?

- Immediate start available.

- Join an established chemical manufacturing business.

- Work with a wide range of analytical techniques.

For a confidential discussion, please contact Talent STEM directly.

Important: Applicants must have the unrestricted right to work in the UK. Unfortunately, this role is not eligible for visa sponsorship, and we are unable to consider applications from candidates who require sponsorship now or at any point in the future.

Talent STEM is a specialist recruitment consultancy supporting the scientific, engineering, chemical, pharmaceutical, environmental, waste, biotechnology, medical device and manufacturing sectors.