SOF) Experience in hosting GCP Inspections Experience in IT Systems validation desirable Experience in implementation of general data protection regulations desirable Operational knowledge of GMP, knowledge of GLP and GCLP desirable Northreach is an equal-opportunity employer and we do not discriminate against any employee or applicant for employment based more »
Royston, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of more »
record in Leading the HSE function across multiple companies in a Pharmaceutical environment. It is key that you have experience within a GXP/GMP environment. Purpose of the Job Health, Safety & Environment Lead and provide oversight and Global strategic leadership covering health, safety, and environment across the Pharmaceutical account. more »
Bishop's Stortford, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
HR GO Recruitment - Bishop's Stortford
to detail and flexibility. Strong communication skills. Ability to handle stressful situations and controversial issues. Willingness to learn and develop new skills. Knowledge of GMP, GDPR, LSAS, and ethical trade issues. Key Tasks: Prepare and submit regulatory documentation for market registration. Support root cause identification and solution resolution. Conduct and more »
in Chemistry/Biochemistry/other related science or equivalent experience in a similar setup. - Competent analytical skills, attention to detail, and understanding of GMP requirements. - Ability to work independently and in a team, with strong computer literacy and communication skills. - 1 year of lab based experience is necessary. Are more »
work environment and that all tools are maintained and accounted for. Liaise with the SHEQ team to resolve H&S issues, environmental, internal audits, GMP, COSHH and ISO quality issues, and ensure all compliance checks are complete and correctly filled. Attend all nominated training modules as necessary. Undertaking any other more »
Chichester, West Sussex, South East, United Kingdom
Natures Way Foods
policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go more »
be paid on a competitive hourly rate. Experience: A minimum of 3 years in sterile drug product development and/or manufacturing Experience in GMP is essential Experienced in liquid product development under aseptic conditions is required Strong technical and practical experience of downstream processing/DSP/DP An more »
Aylesbury, Buckinghamshire, South East, United Kingdom Hybrid / WFH Options
Medik8
to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions more »
in using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion for more »
St. Albans, Hertfordshire, South East, United Kingdom
Evolve Selection Limited
Manager in the Process Engineering department. You will ensure that operations are performed in accordance with the requirements of company standards, industry standards, and GMP/GDP guidelines. Whats on offer? Excellent Salary & Benefits: You will receive compelling salary DOE, along with an exceptional benefits package. Innovative Leadership in Automation more »
and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »
East Kent Hospitals University NHS Foundation Trust
Desirable JAC computer system knowledge Qualifications Essential GCSE grade 4-9 Math and English or equivalent Desirable NVQ2 in Pharmacy Services or evidence meeting GMP standards Other Essential Upholds and models Trust Values Desirable Willing to be flexible to service needs Disclosure and Barring Service Check This post is subject more »
from a Pensions background and ideally Team Leading people working on similar projects as listed below. - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »
and validation of analytical test methods in accordance with regulatory guidelines. Support, release and stability testing performed in-house and at CROs and direct GMP investigations. Develop strategies for evaluating and implementing new technologies within Analytical Development. Support process development, setting of specifications and regulatory filings and responses. Participate in … a relevant biological science. Post-graduate degree in biochemistry or related science is preferred. Experience in a cGMP Quality environment. Experience working in a GMP testing environment with an understanding of regulatory requirements and trends related to analytics and product development. Thorough understanding of current regulatory requirements and practical experience more »
East Kent Hospitals University NHS Foundation Trust
risk assessments Experience of participating in audits/internal monitoring Desirable Knowledge of regulatory requirements relating to clinical trials Awareness of GoodManufacturingPractice (GMP) inc Annex 13 labelling requirements Personal/Professional attributes Essential Excellent attention to detail. High level of initiative Able to problem solve Able to work more »
disposition. The QA officer will ensure assigned tasks are performed in a timely manner to meet batch disposition, supply chain and all associated international GMP/GDP requirements. Key Responsibilities will include: To compile & review batch document sets for completeness & compliance to EU GMP, Pfizer internal requirements and regulatory dossier … s degree in a related scientific discipline with relevant experience (Preferably Biology/Chemistry/Pharmacy/Life Sciences) 2-3 years in a GMP environment Basic experience in pharmaceutical manufacturing, distribution, and control measures Basic experience in Quality administered systems. Previous use of TrackWise® QMS beneficial. Experience in operating more »
trial design, to advise them on goodpractice in accordance with the International Conference on Harmonisation (ICH) guidelines on Good Clinical practice and GoodManufacturingPractice and on the regulatory status of the clinical trial drug. 5. To lead and finalise the set-up of cancer clinical trials, i.e. writing … years post-graduate training above original Masters level qualification) Vocational Masters degree in Pharmacy (4yrs) and 1 years pre-registration training and experience) GMP accredited Desirable Specialist qualification in cancer therapy or equivalent knowledge Qualified Independent Prescriber or willing to undertake training Experience Essential Substantial post registration experience in a more »
also oversee the work of junior QC staff, assist in managing the QC laboratory, and participate in assay transfer activities. This role requires maintaining GMP compliance in the QC laboratory. Key Responsibilities Establish, revise, and maintain procedures for QC testing. Maintain QC systems related to in-process, final drug product … and review of reports. Requirements A BA or BS in Chemistry/Biochemistry/Microbiology or other related science. Experience in a GLP/GMP environment. Computer literacy (including MS Word and Excel). Ability to work well with others. Effective communication skills. Good organizational skills. If you are having more »
naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »
aseptic and non-sterile products for Portsmouth Hospitals University NHS Trust (PHU), and its external customers. You will be working in accordance with GoodManufacturingPractice in order to maintain the standards required by the Medicines and Healthcare products Regulatory Agency (MHRA), and keep the department's manufacturing licence and … local work instructions Proactive attitude to ongoing training and assessment Desirable Previous experience working with aseptics/pharmaceuticals Knowledge of principles of GMP (goodmanufacturingpractice) and Quality Management Systems Good understanding of principles of aseptic manufacturing Customer care skills Additional criteria Essential Punctual and reliable Self-motivated Desirable Willingness more »
and collaboration with Operations and Quality teams. Major Responsibilities Under the QC Manager's direction, the Incoming QC Team Leader will: Ensure GDP/GMP compliance within Incoming Inspection and Quarantine areas through inspection of incoming goods against specifications. Create and maintain incoming inspection procedures and work instructions. Manage QC … external audits (e.g., BSI, FDA). Support and complete other tasks set by the QC Manager. Skills and Experience Working knowledge of GDP/GMP requirements. Ability to create and write Standard Operating Procedures and Work Instructions/Specifications. Understanding of inspection criteria and the use of drawings/specifications. … area for medical devices. Knowledge of SAP (desirable). Knowledge of Master Control (desirable). Strong written and oral communication skills. Good understanding of GMP compliance requirements in Quality Control. Attention to detail. Promotes a collaborative working environment. Understanding of using basic measurement tools (e.g., calipers/jigs and gauges more »
role for you! As a Technical & Quality Coordinator, you will be: Updating and developing technical documentation. Ensuring the organisation remains compliant with food safety, GMP, quality, ACCP , and health and safety procedures . Conducting, and supporting with, internal and external audits and finished product traces . Recording all findings and … in food science or related field. Previous experience in a Quality & Technical role within food manufacturing . A strong understanding of HACCP, BRCGS, and GMP standards and food legislation . Computer literate with MS Office. Able to work well independently and part of a team. If you believe you meet more »
Summary: The Head of Quality Assurance leads strategic QA efforts, ensuring compliance and driving improvement. They oversee operations, manage teams, and maintain high standards. Responsibilities: Define and drive QA strategy. Set and monitor quality standards. Ensure compliance with regulations. Lead more »
GMP Recruitment are proud to be supporting a leading national consultancy seeking a Principal Designer to join their office in the Reading, Berkshire region. This is a full-time permanent position where the Principal Designer will be experienced in their field and have a strong understanding of the Building Safety … If you are a CDM Principal Designer looking to join a consultancy that can offer support, security and progression please click apply or contact GMP recruitment directly. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency. CDM/Principal Designer more »