1 to 7 of 7 Contract GMP Jobs

changes). This will require close collaboration with Product Development, Production and QA groups on NPIs using product lifecycle approach, preparation and approval of GMP documentations to support such projects, scheduling, raw material acquisition, supervising engineering batch manufacture, etc. Identifying potential process improvements for existing commercial products including proposals for more »

instruments to identify profiles of 'unknown' organic compounds and mixtures, ensuring safe and compliant disposal. Follow approved methods and procedures in accordance with cGLP & GMP requirements. Ensure all Health, Safety, and Environmental standards are met, including workplace organization, work instructions, risk assessments, COSHH assessments, and housekeeping. Participate in method development … Analyst . Skills and Qualifications: Education: Degree in Chemistry. Experience: Minimum 2 years as a QC Analyst in the Fine Chemical or Pharmaceutical industry (GMP/GLP environment). Technical Skills: Proficiency in forensic investigation techniques such as HPLC, GC, GC-HS, LC-MS, GC-MS, FT-IR, XRF, RAMAN more »

and released in compliance with the relevant regulatory standards and our high-quality benchmarks. Key Responsibilities: Certify batches for release, ensuring compliance with EU GMP and relevant regulatory requirements. Conduct audits, both internally and externally, to ensure adherence to quality standards. Collaborate with various departments (eg, Manufacturing, Quality Control, Regulatory … Affairs) to ensure quality assurance throughout the product life cycle. Provide expert guidance on GMP and regulatory compliance issues. Lead and support continuous improvement initiatives in quality systems and processes. Handle deviations, investigations, and CAPAs effectively, ensuring root cause analysis and implementation of corrective actions. Requirements: A valid QP status … as defined by EU Directive 2001/83/EC, with a thorough understanding of UK and EU GMP regulations. Bachelor's degree or higher in Pharmacy, Chemistry, or a related scientific discipline. Significant experience in a GMP environment, preferably within the pharmaceutical industry. Demonstrated ability to work collaboratively and more »

has a broad skillset and excellent oral and written communication skills. An individual who has a number of years of experience working in a GMP and QA environment is therefore essential for this post in order to provide the required support and guidance to our Production and QA departments and … Essential Educated to degree level in relevant scientific discipline or equivalent Postgraduate qualification Experience/Knowledge Essential Regulatory requirements pertaining to ATMPs manufacture Good Manufacturing Practice and Good Clinical Practice Thorough understanding of gene and cell-based therapies Thorough understanding of HTA Proven experience of line managing staff Experience of more »

Technical QA Manager (m/f/d) - Quality Management/Qualification/Validation/CSV of Small Molecules/Data Integrity/GMP/IMP/English & German Project : For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Technical QA Manager (m … Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and GMP-compliance oversight of all Investigational Medicinal Products (IMPs) manufactured and packed for clinical studies in Switzerland. The candidate supports the end to end cGMP activities … products according to Health Authority requirements and Company Standards for IMP products. The main responsibilities are: * QA supervision of qualification- and validation-activities for GMP-relevant equipment (including CSV), Analytics, infrastructure, critical utilities (WFI, PW, Gas) and processes within TR&D in Basel * Support of implementation of DI requirements * Provide more »

Automation Engineer Pharma Engineering (m/f/d) - GMP/Production/Shift Model/Pharma/German Project: For our customer, a large pharmaceutical company based in Kaiseraugst, we are looking for an Automation Engineer Pharma Engineering (m/f/d) Background: The Pharma Engineering department is … units. Technical expertise in network technology and automation software is particularly important: Siemens PCS7, S7, TIA AND WinCC as well as experience in the GMP and GAMP environment. Main tasks and areas of responsibility: * Management of automation projects in all project phases such as initiation, design and implementation (independently and … with the procurement of package units * Technical expertise in network technology and automation software: Siemens PCS7, S7, TIA and WinCC * Solid experience in the GMP and GAMP environment * Ability to work in a team and very good communication and coordination skills within the organization as well as appropriate dealings with more »

to manage/adjust timelines and priorities; escalate issues and concerns as they arise. Ensure all activities are delivered compliant to defined processes and GMP; concerns/risks are identified. Ensure appropriate and complete records arising through operational activities are maintained and TPCs in compliance with GMP and that meet … commitments meet agreed timelines and quality KPIs. Interim Packaging Project Coordinator - The Skills You'll Need to Succeed: Experience working in an R&D GMP environment. Experience working in an operational Packaging Labelling Distribution (PLD) role within Clinical Trial Supplies. Knowledge of Clinical Trial Supply CMOs and their capabilities Knowledge … of the pharmaceutical and clinical development processes and their relationship to the clinical supplies delivery processes; aware of clinical supply GMP requirements and standards. Lean Sigma training/experience Project Management training/experience Experience demonstrating organizational and planning skills coupled with strong written and oral communication skills Demonstrated capability more »