1 to 13 of 13 GMP Jobs in the Midlands

facilitate change. The ability to present information coherently, accurately and persuasively. PC literate Experience within food manufacturing, advanced Food Hygiene Certificate & good understanding of GMP/hygiene standards Please click ' Apply Now' to be considered for this fantastic opportunity and to become part of our Proud Bakkavor family. #LI-HF1 more »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and more »

and provide corrective action Use root cause analysis to understand and deliver optimal cost maintenance Delivery of the required standards in relation to Engineering GMP and food safety standards Escalate potential consequences to line manager where work may impact on product quality or safety Key skills & experience: Strong engineering qualifications more »

Safety at work regulations. * Carry out all tasks in a safe and controlled manner, adhering to quality requirements. * Consistently comply with Good Manufacturing Practices (GMP) and act as a role model for others on site. * Understand product safety and customer-specific requirements, and help ensure they are always met. Senior more »

in investigation and corrective action implementation. * Working as a support function to operations to ensure hygiene levels of the facility are maintained by conducting GMP/Glass and Hard Plastic and Fabrication audits in conjunction with departments leads to assess compliance and improve standards. Report findings as identified within the more »

facilitate change. The ability to present information coherently, accurately and persuasively. PC literate Experience within food manufacturing, advanced Food Hygiene Certificate & good understanding of GMP/hygiene standards Please click ‘Apply Now’ to be considered for this fantastic opportunity and to become part of our Proud Bakkavor family. #LI-HF1 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 »

pharmaceutical environment/Medical Device industry required Technical experience within the Manufacturing functions of a pharmaceutical company. Technical knowledge of Pharmaceutical Packaging. Vendor Audits (GMP, Technical and EHS) Knowledge in Supply Chain Risk management, GMP, Quality System requirements, the ‘Orange Guide’, equivalent FDA regulations and systems, procedures, products and organisation. more »

include understanding and applying relevant standards so that Bakkavor, Customer and Legal requirements are achieved and maintained. This role is key to driving improve GMP standards and audit results across the site. You will influence and work collaboratively with the operational teams and agree solutions together. Duties include: To participate … and direct QA team to observe and audit production processes and GMP ensuring products are made to specification and within customer codes of practice and Bakkavor standards, reporting findings to managers as appropriate To ensure products and ingredients are evaluated against specification To assist in delivery of site standards for … Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass and plastic audits. Lead, motivate and inspire QA team to achieve personal development and continuous improvement To promote a quality culture and help 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 »

which will include some weekend working as set by the rota. Day to day duties will be: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and more »

maintained and up to date. Education and experience : *Degree in chemistry, analytical chemistry or equivalent *Previous experience of HPLC, GC analysis with pharmaceutical/GMP regulated environment *Previous experience in analytical method transfer, cleaning validation *your previous experience could be QC analyst, stability analyst, development analyst, principal analyst and raw more »