other DSP, Facebook, Twitter Experience of managing vendor relationships Regularly contributes to platform best practices and campaign processes Experience with Google stack and have GMP & Adwords certifications (desirable) Experience with running campaigns across multiple countries/languages Experience with managing a mid- to large-sized team across a range of more »
Pontefract, West Yorkshire, Yorkshire, United Kingdom
Refresco UK
focus: Actively participate in the implementation of site quality improvement projects, where necessary providing support to train operation teams and monitor project effectiveness. Complete GMP and Hygiene audits to required schedules. Assist in the investigation of consumer complaints and non-confirming items determining root cause and corrective action necessary to more »
in place to meet legal and statutory requirements. Keep records and provide reports in accordance with good engineering practices to external audit standards. Upholding GMP engineering standards across site, statutory inspections are compliant, and any non-conformances are closed out with root cause analysis to avoid repeat failure. Lead the more »
the manufacturing teams in these areas. The role will mostly be factory facing and will have responsibilities for auditing compliance against Quality Management Systems, GMP standards, Due Diligence and Customer Standards. Accountabilities : Supporting the Technical Manager in implementing our Food Safety. Quality and Hygiene systems in line with business growth more »
as part of the remuneration. Experience: Experienced project engineer or project manager in a pharmaceutical setting A strong understanding and hands on experience of GMP Engineering or validation experience is essential Exposure to the full validation lifecycle and the ability to walk through the full CQV phase Hands on experience more »
skills in previous positions. Worked as an engineer or come from an analytical background carrying out on site support. Experience working in GLP/GMP environment. Be prepared to travel and stay away as required. Package: Salary up to £43,000 D.O.E Bonus Scheme (£6.5k) Company Car + Expenses Covered more »
safety guidelines and protocols. Continuous Improvement: Driving factory process improvements through techniques like root cause analysis and downtime analysis. Contributing to plant housekeeping and GMP audits and managing logistics team standard tasks. Measures of Success: Clear logistics strategy and plans. Adherence to logistics budget. Decrease in logistic complaints. On-time more »
Durham area. Salary and Benefits of QC Analyst Salary up to £28,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP Standards Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience HPLC and GC Experience Responsibilities of the QC Analyst The more »
renowned for their commitment to excellence. Role Overview: As a Senior Project Manager, you will oversee the entire project lifecycle, focusing on Grade C GMP cleanrooms for this Micro Bio Pharma facility. From initial feasibility to full construction, commissioning, and qualification, you will ensure projects meet the highest standards of more »
Huddersfield, West Yorkshire, Yorkshire, United Kingdom Hybrid / WFH Options
Thornton Ross
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 »
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 »
Wetherby, West Yorkshire, Yorkshire, United Kingdom
Unity Personnel
all levels - work under own initiative 2+ Years QA experience within Food Manufacturing, ideally with both private label and branded product experience. Proficient in GMP and Quality Standards. Level 3 HACCP Level 3 Food Safety Auditor qualification Recognised allergen qualification Recognised microbiology qualification Working hours: 18:00/ more »
in a multi-talented and compliance orientated team. You have · A background in a scientific discipline (MSc is a plus) · Experience working within a GMP environment, preferably in a CDMO · Strong experience of QC environment and organisation · Experience of reagent preparations and material handling Touchlight Benefits Touchlight is a successful more »
developing products used in hazardous environments (i.e. ATEX, nuclear or chemical industries) is preferred but not essential, as would experience of GoodManufacturing Practices (GMP) for the pharmaceutical industry, although neither are essential. Hybrid and flexible working can be discussed. More information available upon application. When applying for this role more »
and operational support OR 3+ years in a similar role with Manufacturing OT equipment, in Healthcare/Pharma. 3+ years working with GxP and GMP environments. If you're interested and would like to find out more, reach out on LinkedIn or send your CV to lauren.mckinley@skillsalliance.com. more »
who is adaptable, can show initiative and pick up lots of new skills quickly Good general laboratory experience, ideally with GLP and/or GMP certification For the chance to join an exciting company on their journey to change the world for the better, please apply today! Bond Williams Professional more »
on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated more »
a relevant engineering discipline Pharmaceutical/BioPharma Projects experience Full lifecycle Project Management Cost Control Scheduling and achieving schedules Delivery of projects within a GMP environment Thorough understanding of engineering principles, concepts, industry practices and standards 16 hours (2/3 days onsite) Outside IR35 Till October more »
archiving and ensure document control. Assist the team with technical issue resolution and continuous development of food safety & quality Complete site internal audits (CCP, GMP, Glass and plastic, hygiene etc) Collect and coordinate samples for routine micro/analytical analysis Actively reinforce the company's goodmanufacturing practices and hygiene more »
Skipton, North Yorkshire, Yorkshire, United Kingdom
Dechra
good stead: Experience with HPLC testing (desirable) Experience within a manufacturing environment (ideally within pharmaceutical, food, chemical etc) Understanding of data integrity (ALCOA principles GMP) Strong attention to detail Ambition and drive, not afraid to challenge the status quo 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 »
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 »
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 »
development, licensure, and marketing of chemical drugs, biologics, or gene therapies. Liaise with U.S. and UK/Shanbally teams to prepare change controls and GMP documentation to support global submissions for product registrations and/or renewals. Participate in cross-functional project teams as a regulatory CMC representative for project more »
