Daniel Campillo Ramos Email & Phone Number

Barcelona, Ct, Es

Madrid, Madrid, Es

Lead the opperations team responsible for Manufacturing activities & TT in Leon Farma site.Responsablities include Solid Bulk of products (Granulation, Direct Blending, Tableting, Coating and Hard capsules workshops), Semisolids Bulk (Gel/Emulsions Manufacturing and Soft Gel Capsules Manufacturing), Dispensing (Excipient, API and Packaging material), Solid & Semisolid Packaging (Bottles Lines, Sachets Lines , Packaging Lines for Solids and Semisolids FDF).The Main functions are the following:Provide lidership for a staff of 310 FTE's (Manufacturing Line Manager, Technicians, Shift Supervisor and Operators) with high complex products Manufacturing. Year output: 4000 M tablets/year, 1200 M Soft gelatin Capsules/year, 360 M hard capsules/year, 20 M Bottles/year, 200 M blister/year & 100 M sachets/YearParticipate in managing Anual Capex for Pharma Production.Assist to establish annual department operating budget.Manage plant assets, personnel and achievement of plant related business goals.Collaborate with Operations, R&D, Engineering, Business Development and Quality to ensure process improvements and innovation are delivered in a collaborative, effective manner.Oversee process transfers, Production and commitments in support of internal business Line stakeholders and external costumers.Expert in Lean Manufacturing (OEE implementation, Continous improvement, 5S, SMED, Lean & Six Sigma).Responsible of the Annual Production Plan in León Farma Site.Identify and lead process optimization opportunities for efficiency and capacity improvements in all areas.Deliver site KPI’s including safety, quality, delivery, cost and people metricsTrends analysis and process monitoring technical investigations and process changes that seek to drive improvements to yield and/or robustness.Participate in internal and external audits. Assure cleanrooms,support areas and staff comply with defined safety and qualityTech Transfer responible of the Site (CMO and internal

Madrid, Madrid, Es

Lead the technical operations team responsible for TT activities in Leon Farma site (Solid & Semisolid FDF) & Farmalán site (Inyectable FDF).-Lead a Technical team of 4 Technicians.-CMO Technical evaluación, Scale-up projects and industrial internal development execution.Coach and mentor a team of technical and engineering experts for new product introductions (NPI), process development, process optimization and tech transfers (TT).Lead the introduction of new Technologies for solids, semisolids, F&F (Injectables/Vaccines) and packaging operations.Lead feasibility review and technology gap analysis for NPI.Be a key member of the Technology Transfer Management team for client-facing projects / Chemo strategic projects.Collaborate with Operations, Engineering, Business Development and Quality to ensure process improvements and innovation are delivered in a collaborative, effective mannerProvide technical oversight and support for all phases of the product lifecycle, including technology transfer, process scale-up, process validation and routine commercial or clinical manufacturing.Identify and lead process optimization opportunities for efficiency and capacity improvements in all areas.Deliver site KPI’s including safety, quality, delivery, cost and people metricsTrends analysis and process monitoring technical investigations and process changes that seek to drive improvements to yield and/or robustness.Technical SME for internal and external audits

Madrid, Madrid, Es

Lead the technical operations team responsible for TT activities in Leon Farma site.Coach and mentor a team of technical and engineering experts for new product introductions (NPI), process development, process optimization and tech transfers (TT).Lead the introduction of new Technologies for solids, semisolids, F&F (Injectables/Vaccines) and packaging operations.Lead feasibility review and technology gap analysis for NPI.Be a key member of the Technology Transfer Management team for client-facing projects / Chemo strategic projects.Collaborate with Operations, Engineering, Business Development and Quality to ensure process improvements and innovation are delivered in a collaborative, effective mannerProvide technical oversight and support for all phases of the product lifecycle, including technology transfer, process scale-up, process validation and routine commercial or clinical manufacturing.Identify and lead process optimization opportunities for efficiency and capacity improvements in all areas.Deliver site KPI’s including safety, quality, delivery, cost and people metricsTrends analysis and process monitoring technical investigations and process changes that seek to drive improvements to yield and/or robustness.Technical SME for internal and external audits

Darmstadt, De

-Define and improve the Process Control Strategy and the validation status of a process / product. -Identify sources of variation affecting process performance and product quality to reduce or control variation, and implementing the appropriate mitigation activities. -Support to the transfer of new products to the site. edit the validation documents, i.e protocols and reports and close follow-up of the validation execution inside the manufacturing areas. develop industrial projects in accordance with deadlines, costs and quality requirements.-To prepare documents according to transferences and/ or industrial validations together with troubleshooting, risk analysis, process surveillance, industrial process improvement and R&D project processes evaluation-Continous process verification (Use of MiniTab for data analysis)-Industrial technology transfer

Darmstadt, De

As production technician of the unique antibiotics production plant worldwide of Merck group my main duties are the following:-Coordinate a group of 20 people (2 supervisors and 18 operators in two shifts).The production plant is composed by bulk are and packaging area. The solid oral forms manufactured in the plant are: suspensions for reconstitution, tablets and capsules.-Adhere to cGMP or current good manufacturing practices, standard operating methods and legal regulations to maintain a safe and clean work environment.-Maintain equipment operation through responsive troubleshooting, repairs and following operations guidelines.-Review and update manufacturing documentation (SOP´s, BMR, equipment instructions...)-Technical assessment in manufacturing deviations, implment CAPA to improve manufacturing operations, collaborate in cleaning validation.-Lead a project for measuring OEE (Overall equipment effectiveness) and improving this value in packaging area and bulk area.-Equipment qualification (URS,DQ,IQ,OQ,PQ).-Participate in the digitalization program of the company and data integrity compliance.-Provide technical service to other departments in terms of process manufacturing.-Coordinate and control the manufacture of pharmaceutical compounds and related products.-Supervise routine processes related to wet granulation, compression, filling of capsules and suspensions, and packaging.-Check changes in format and control preventative maintenance activities carried out on the different machines.-Carry out adjustments to the production line based on standard operating procedures.-Control processes and coordinate the sampling of intermediary and finished products for being analyzed.-Equipment calibration verification-Comply with the objectives established with regard to production, quality and other deriving ratios (KPI´s)

Sant Joan Despi, Barcelona, Es

- To develop industrial projects in accordance with deadlines, costs and quality requirements- To prepare documents according to transferences and/ or industrial validations together with troubleshooting, risk analysis, process surveillance, industrial process improvement and R&D project processes evaluation- To be responsible for the activities and tasks assigned related to transfers, validations and manufacturing processes- To propose improvements related to scale up- Experience in solid oral dosage forms, injectable forms, BFS technology, oral liquid forms, parenteral bag (terminal sterilization and aseptic filtration) and lyophilized products- Equipment qualification experience (IQ,OQ,PQ)- To contact the CMOs as necessary for the industrialization and commercial life of the product- Support CMOs in process validation, industrial technology transfer, industrial problem solving and support to Regulatory Affairs-GMP, GLP, ICH and FDA regulations and Tech Transfer procedures.

Nijmegen, Nl

- To review manufacturing documentation (Batch records, equipment log-books...)- To prepare documents according to industrial validations and commercial production- Experience in cleaning validation- Knowledge in manufacturing solid oral dosage forms (Tablets, capsules and sachet powder)- Equipment qualification experience (IQ,OQ,PQ)- Equipment calibration and GMP complience- CAPA, change control, manufacturing investigations and risk assessments (FMEA)- To prepare and update SOP´s related to pilot plant

Nijmegen, Nl

Lean Six Sigma Green Belt Certification

Master In Pharmaceutical Industry

Bachelor Of Pharmacy - Bpharm

Bachelor Of Pharmacy - Bpharm