51 to 75 of 192 GMP Jobs

always opportunities to learn and gain exposure. Experience: Previous experience in a QA position within a pharmaceutical, healthcare or food setting Working experience of GMP Operational Quality Assurance experience including batch review/release Exposure to handling complaints processes Lifecycle experience of deviations, CAPAs and change controls Strong stakeholder management … Mark Bux-Ryan for further information quality, assurance, QA, QC, control, analytical, chromatography, HPLC, laboratory, documentation, analyst, officer, specialist, executive, administrator, good, manufacturing, practice, GMP, GLP, audit, SOP, training, complaints, batch, review, release, CAPA, deviation, change, control more »

values, promoting an ethical, positive company culture To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements To work collaboratively with Pharma and Health Tech leadership team to develop a Sustainability Roadmap that supports more »

role will be joining the UK team, as a senior individual contributor and part of a global team. Other essential responsibilities include: Management of GMP and GDP compliance Management of complaints, CAPAs, risk assessments, and validation protocols Review and manage the QMS system Able to manage non-compliance issues and … requirement will be that you are able to travel to West London site and to supplier sites. It is a must that you have GMP and GDP experience. The role will be joining a team which is integral to the business and requires strong communication skills. The team are close more »

opportunity to contribute to the advancement of cutting-edge T cell therapies for the treatment of serious medical conditions. Responsibilities: Batch Manufacturing within a GMP setting Support the scale up of Manufacturing operations in line with GMP standards Draft and maintain SOP’s and batch records Recording all activities and … Support and mentor more junior members of staff Qualifications: BSc or MSc degree in a Biological Science, Biotechnology, Immunology related field Experience in a GMP Manufacturing environment Background in laboratory operations – Immunological cell-based assays Good understanding of and skilled with multi-parameter Flow Cytometry Work co-operatively as part more »

Systems, distributed control system, computer validation, CSV, computer system validation, application software, software, hardware, system software, system hardware, automated production equipment, cGMP, cGMP environment, GMP, Good Manufacturing Practices, Manufacturing, Switzerland, Ireland, UK, Netherlands, Austria, Biopharmaceutical, pharmaceutical, GMP environment, sterile manufacturing, API, aseptic processing, Electrical engineering, pharmaceutical manufacturing, capital investment, project 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 »

duties in a safe manner, utilizing all approved safety equipment and successfully completes all safety certification requirements. Maintains awareness and adheres to all FDA, GMP, BATF, EPA, OSHA and employer standards and guidelines. Additional Skills & Qualifications: Science degree OR laboratory experience required Experience with operating standard lab equipment - pH meter more »

Description: Demonstrate proper laboratory safety and housekeeping practices through weekly 5S Lab audits and monthly laboratory inspections. Assure all activities meet EHS requirements. Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods Reverse Phase SEC Titer concentration CEX Accurately record and report analysis results in … experience. Experience with multitude of HPLC/UPLC assays is a plus SEC CEX Glycans Peptide Map etc. Prior use of EMPOWER Knowledge of GMP regulations in cGMP manufacturing environment. Working knowledge of scientific principles for wide range of analytical techniques strongly preferred. About Actalent Actalent is a global leader more »

suites. Additional facility management responsibilities maintaining equipment logs, following calibration and maintenance schedules, and managing inventory of R&D materials and ingredients. Skills: formulation, GMP, chemist, technician, mechanical, biology Top Skills Details: formulation, GMP, chemist, technician, mechanical, biology Additional Skills & Qualifications: AS or BS Degree in Chemistry or Chemical Engineering … preferred. 6 months of demonstrated industry experience in an GMP or R&D environment preferred but not required. Pilot plant experience a huge plus Mechanical aptitude or experience with small-scale equipment preferred Basic computer knowledge and skillset to work within various systems/interfaces Experience Level: Entry Level About more »

engineering or similar. Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality management" within a technology company including instilling a quality-focused culture and maintainable approach more »

and at conventions. Mentoring and leadership Assist Quality Control in analysis of finished products and received goods when needed Skills: Chemistry, Formulation, Hplc, Laboratory, Gmp, Analytical chemistry, metallurgy Top Skills Details: Chemistry Additional Skills & Qualifications: Bachelor's degree in Chemistry • 10-15 years of formulation experience in a complex product more »

for management review Maintain lab equipment in a clean and orderly fashion Communicate non-compliant results immediately to management Monitor plant for compliance to GMP's Accurately weigh ingredients, colors, flavorings and seasonings Test R&D samples for food safety & specification development SKILLS& QUALIFICATIONS AS or BS in science-related more »

methods. • Follows and complies with all safety and work rules and regulations. Maintains departmental housekeeping standards. • Other duties as assigned. Skills: Quality control, Laboratory, Gmp, Quality assurance, Qc Additional Skills & Qualifications: QUALIFICATIONS: Education and Experience • 3-5 years related experience and or/training; or equivalent combination of education and more »

the laboratory function in executing daily operations and testing necessary to support commercial products. • Anticipates and resolves problems independently while conforming to SOPs and GMP regulations • Monitors the scientific and financial progress of projects that they are assigned • May have responsibility for a laboratory group or function and may have … timely manner and are completed within established target completion dates o Ensure that the Quality Control staff have been appropriately trained before performing a GMP task 3. Productivity o Serve as primary resource for planning and scheduling of tests o Assist analysts as needed and troubleshoot if required o Witness … and organizational skills o Ability to work with a sense of urgency in a fast-paced environment o Strong technical writing and investigational skills GMP DECISION-MAKING AUTHORITY The Team Leader Quality Control is responsible for decisions related to: o When an investigation is warranted o When analyst training is more »

activities related to finished product and NPI testing. Maintain accurate documentation and a laboratory environment consistent with laboratory key safe behaviors, Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP). Responsibilities: Prepare sample solutions, standards, and reagents. Perform wet chemical and instrumental analysis, including Near IR, FTIR, HPLC, UV more »

samples. Demonstrate proper laboratory safety and housekeeping practices through weekly 5S Lab audits and monthly laboratory inspections. Assure all activities meet EHS requirements. Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods Reverse Phase SEC Titer concentration CEX Accurately record and report analysis results in … experience. Experience with multitude of HPLC/UPLC assays is a plus SEC CEX Glycans Peptide Map etc. Prior use of EMPOWER Knowledge of GMP regulations in cGMP manufacturing environment. Working knowledge of scientific principles for wide range of analytical techniques strongly preferred. Skills: HPLC, GMP, chemistry, EMPOWER, Quality control … analytical chemistry, wet chemistry Top Skills Details: HPLC,GMP,chemistry,EMPOWER Additional Skills & Qualifications: Strong knowledge and understanding of chemistry and chromatographic analytical instrumental technologies. Good knowledge of quality and regulatory requirements in the pharmaceutical industry. Good problem-solving skills and ability to multi-task Strong interpersonal and communications skills more »

Description: The QA Technician will be responsible for testing product samples from Production and Incoming Materials as well as ensuring HACCP/quality/GMP regulations are being followed accurately. Running lab tests including GC and LC testing. Will also complete floor tests include metal checks, screen checks, weight checks … the Manufacturing team on the floor and in a lab environment. Will be required to ensure employees uphold Food Safety and Quality standards including GMP's, SQF, FDA, PCQI and customer requirements. 60% lab (running physical and sensory tests)/40% floor (pulling samples, swabbing, etc.) All products are powder more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

any trends •Support Technical department and site with document creation and review which may include records, procedures, and communication boards •Complete audits on bakery GMP standards & Technical compliance such as G&HP, CCP, Process controls, Mobile phone audits, paperwork completion etc •Lead for Site Traceability exercise •Promote and maintain high … standards of food safety culture, promote and challenge site GMP standards including Technical, Food Safety, Quality, Compliance and Business values.. •To verify accuracy of handheld temperature probes, temperature-controlled storage equipment Qualifications&Requirements - Quality Systems & Compliance Assistant •Good IT skills with knowledge of Microsoft Office •Level 3 Food Safety •Internal more »

and maintenance of the company's Quality Management System (QMS) in accordance with regulatory requirements. Assist in conducting internal audits to assess compliance with GMP/GDP standards and company policies. Participate in the review and approval of GMP documentation, including batch records, SOPs, and change controls. Assist in deviation … Bachelor's degree in Pharmacy, Chemistry, or related field. Some experience or internship in a pharmaceutical quality assurance role is preferred. Basic knowledge of GMP/GDP regulations and quality management systems. Strong analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal skills. Ability to work more »

you will be responsible for testing and reporting laboratory activities to enable compliant, on time delivery of products to the customer whilst adhering to GMP standards. Your contribution will be the regular completion of on the bench testing of Asthma Inhalers (MDIs). You will be part of a quality more »

and supply chain as well as external partners like CDMOs to achieve objectives and ensure adequate product availability for launch. Ensure compliance with regulatory & GMP/GDP requirements for generic & specialty drug launches in relevant markets. Establish key performance indicators (KPIs) to track launch performance and evaluate post launch success more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

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 »

and vision systems integrated within packaging equipment including interfaces with enterprise systems. Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11. Key Experience Essential - Practical experience working within manufacturing and packaging environments Experience of the automation project lifecycle including design, configuration, implementation, testing, commissioning more »