1 to 25 of 169 GMP Jobs

CY Partners are currently looking to recruit an Analytical Team Leader on behalf of a growing County Durham based Pharmaceutical CDMO on a permanent basis. As well as routine analysis on raw materials, intermediates and finished products, this quality department 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 »

Proclinical is seeking a dedicated individual for a Director of Quality Assurance position. This role is integral to our mission of developing solutions for some of the most crucial scientific challenges of our age. The successful candidate will be a more »

to help our patients. We value and encourage learning and development. As the Quality Assurance officer you will support the QA Manager in overseeing GMP compliance, contribute to the management of QMS and ensure the maintenance of quality certifications and standards throughout the manufacturing, testing and release of the product. … companies QMS. · Support with assessment of deviation event investigations. · Support closure to plan of Change Controls and CAPA actions. · Issue, review and approval of GMP batch manufacturing records to support certification and release. · Assist in performance of internal self-inspection audits. · Support the Company’s Quality Meetings. · Assist in maintaining … the Company’s quality certifications, e.g. GMP, GDP, HO approvals, etc. · Assist in preparation for inspections from MHRA and other Competent Authorities · Provide quality review and input to manufacturing and business activities. · Ensure compliance with the Company’s Quality Standards. · Engage with the wider team and sector to gain wider more »

selecting and acquiring equipment to ensuring its proper validation. Providing technical support to Manufacturing Operations during troubleshooting and investigations. Conducting data integrity assessments for GMP equipment , safeguarding the accuracy and reliability of collected data. Maintaining the qualification life-cycle of all GMP equipment by performing re-qualification activities as necessary. … a Doctorate (PhD) in a Life Science or Engineering field. Proven experience in validating manufacturing equipment and processes. Solid understanding of Good Manufacturing Practices (GMP) regulations. Experience in collaborating effectively with internal and external stakeholders. Adept at multitasking and thriving in a busy environment. Strong relationship builder with excellent communication 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 »

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 »

data feed. Due diligence on new business transactions. Requirements: Qualified Pensions actuary with experience within a top consultancy or relevant firm. Strong understanding of GMP equalisation, Longevity Swap or risk transfer. Excellent stakeholder skills and ability to lead/drive projects. A tenacity to 'get stuff done' and find ways more »

for scaling up and down of bioprocess operations. - Understanding of how to develop and optimise processes for the purification of biopharmaceutical products. - Understanding of GMP and QbD considerations in a large scale manufacturing environment. - Understanding and experience with statistical and modelling software and tools. - Understanding of in-process assays such 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 »

Develop and implement comprehensive quality management strategies, policies, and procedures to ensure compliance with regulatory requirements (e.g. FDA, EMA, etc.) and industry standards (e.g. GMP, GDP, GCP). Provide leadership and direction to the quality assurance and quality control teams, fostering a culture of quality excellence, accountability, and continuous improvement. more »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »

degree level or above in life sciences, chemistry or a related file with experience of working in a regulated laboratory environment (e.g. GLP or GMP) • Experience in using and troubleshooting ELISA analytical systems as well as the ability to develop and validate analytical methods using ELISA. • The ability to document more »

Lead best practice in the department and become a key contact for the mentoring and training of more junior members of staff. Act as GMP ambassador, take responsibility for ensuring GMP compliance and adoption of GMP principles e.g., right first time. Lead activities to ensure close working with Analytical development … understanding of cell biology and immunology (preferred) Strong verbal and written communication skills. Flexible, self-motivated, and focused on team outcomes. Strong understanding of GMP regulations. Excellent organisational skills with the ability to present results clearly and logically, working co-operatively as part of a team, as well as independently. more »

is a particular need for this role/location An understanding of the principles of Chemistry, Degree/HNC in Chemistry preferred Knowledge of GMP procedures and best practices Valid, clean UK driving license Ability to travel in the UK and willingness to attend training in EU or USA The … responsibilities of the Field Service Technician – Analytical Instruments: Duties include Fault diagnosis, repair, routine servicing, certification, and installation of equipment in accordance with GMP guidelines 80% of your time will be spent on pre-planned maintenance visits and circa 20% breakdown support which will enable you to manage your time more »

profile and past history: 1. Relevant degree in a chemistry related discipline. 2. Proven industry experience in development activities for drug development in a GMP environment. 3. A working knowledge and practical experience with management of an analytical chemistry function/facility in the pharmaceutical industry. Hyper Recruitment Solutions Ltd more »

to release materials. Ensure that the maintenance and qualification of the specified laboratory and equipment within is up to date and at the required GMP standards. To ensure the use only of approved and validated test processes. Co-coordinate department cGMP systems, such as deviation management, closure of corrective and … Chemistry, Biochemistry, etc.) 5 years' quality control experience in the pharmaceutical/biotech/or other regulated industry. Experience with data integrity in a GMP lab. Leadership experience in past roles helps in the success of this position Experience with multi-disciplined team environment Experience in GLIMS Labware system Direct more »

Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »

includes both MSK intra-institutional grant funded projects and projects involving collaboration with the pharmaceutical industry. The RMIP Facility is composed of two radiopharmaceutical GMP manufacturing suites, QC equipment room, and a cyclotron. RMIP produces a wide variety of radionuclides and radiopharmaceuticals, serving both the clinical and research programs of more »

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 »

Work cohesively within the RSM culture to facilitate client introductions and extend other RSM value added services. Experience 12+ years' experience with FDA, GxP, GMP IT validation requirements Bachelor/Master degree in Engineering/Science or in relevant IT field Demonstrated SME level knowledge of process validation and lifecycle more »

or qualitative analysis using classical and instrumental methods. The associate scientist will perform all work in compliance with Standard Operation Procedures, Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Safety Guidelines. As an associate chemist, you will design and perform quantitative and/or qualitative analysis using classical and … ad HPLC, UPLC, GC, dissolution, UV/VIS and wet chemistry techniques. Performed quantitative analysis on routine samples in compliance with Standard Operation procedures, GMP, GLP and safety guidelines. Calculate results from experiments and document all laboratory work in accordance with cGMP requirements. Author and review documents that ensure GMP … skills to achieve our goals: Bachelor's degree in Chemistry, Analytical Chemistry or related sciences. Minimum of 3 years' experience in Good Manufacturing Practices (GMP) operations Experience addressing technical business solutions Strong verbal and written communication skills Proven experience assuring compliance with regulations Preferred Skills Master's degree in Chemistry more »

Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »

Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »

Learn about the Danaher Business System which makes everything possible. The Quality Control Technician Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills more »