51 to 75 of 176 Permanent GMP Jobs

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 »

track record in this regard. Exhibit adept conflict resolution skills, further enhancing your capacity to lead effectively. Have experience working within environments governed by GMP regulations (at least 4 years). How to Apply: Don't miss out on this amazing opportunity! Submit your application. more »

The site Head of Quality will lead the designated site in terms of GMDP quality and compliance, including in the areas of: QA, QC, GMP, GDP, QP activities and RP activities in line with the business goals and plan. Responsibilities: Establish clear and compliant GMDP standards for all site activities more »

validation requirements for entering ISO classified area. Qualifications Bachelor's Degree in chemistry, engineering, or natural sciences preferred. Need to have experience within a GMP environment & operating an HPLC (6-12 months) Efficient in the use of MS Office Suite required. Ability to lift 50 lbs. required. Why Work Here more »

duties in a safe manner, utilizing all approved safety equipment and successfully completes all safety certification requirements. Maintains awareness and adheres to all FDA, GMP, BATF, EPA, OSHA and employer standards and guidelines. Additional Skills & Qualifications: Science degree OR laboratory experience required Experience with operating standard lab equipment - pH meter more »

cause of quality nonconformance issues. Responsible for receiving trailers of bulk products and testing of raw and heat-treated dairy ingredients. Must follow all GMP's and SOP procedures and complete required documentation/checklists. Maintain area cleanliness, reports leaking or out of spec product and participate in continuous improvement more »

correctly. Ensure that the aseptic process is carried out in compliance with current Standard Operating Procedures following the principles of the Good Manufacturing Practice (GMP). About us Liverpool University Hospitals NHS Foundation Trust was created on 1 October 2019 following the merger of two adult acute Trusts, Aintree University … correctly. Ensure that the aseptic process is carried out in compliance with current Standard Operating Procedures following the principles of the Good Manufacturing Practice (GMP). See Job Description for further information. Person Specification Experience Desirable Experience working in Healthcare Environment Experience of stock rotation Experience of working in stores 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 »

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 »

be paid on a competitive hourly rate. Experience: A minimum of 3 years in sterile drug product development and/or manufacturing Experience in GMP is essential Experienced in liquid product development under aseptic conditions is required Strong technical and practical experience of downstream processing/DSP/DP An more »

or HACCP/Food Safety Experience is a plus Experience Level: Entry Level - 1 plus years of experience in Quality - 1 plus year of GMP and FDA/USDA experience OR Associate/Bachelor's Degree in a science related field About Actalent Actalent is a global leader in engineering more »

for management review Maintain lab equipment in a clean and orderly fashion Communicate non-compliant results immediately to management Monitor plant for compliance to GMP's Accurately weigh ingredients, colors, flavorings and seasonings Test R&D samples for food safety & specification development SKILLS& QUALIFICATIONS AS or BS in science-related more »

verbal and written. Ability to communicate with all levels of the organization including technical teams. Experience working with Food and Food Safety Guidelines (HACCP, GMP, and SQF) experience is a plus. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies more »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions 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 »

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 »

in using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion for more »

installation and commissioning. 2. As the Automation Engineer, you will be responsible for the design and documentation review of Pharmaceutical equipment and adhering to GMP and GAMP 5 guidelines. 3. As the Automation Engineer, you will be responsible for executing and witnessing SAT, IQ/OQ/PQ. You will more »

complete all necessary reporting and documentation within the QC Lab. Must Haves Bachelor's Degree in Chemistry Hands on lab testing experience Skills: chemistry, GMP Top Skills Details: chemistry Additional Skills & Qualifications: Must Haves Bachelor's Degree in Chemistry Hands on lab testing experience - can be academic or professional Experience more »

Fischer - Wet Chemistry testing (Titration, Acid Value, Identification by wet chem, TLC, Iodine value, LOD, ROI etc.) - Assure calibrations, standards, log books and other GMP compliance activities are performed in the laboratory Additional Skills & Qualifications: BS in Chemistry or related Life Science All candidates must have 1+ years of experience more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - 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 »

production Cylinder handling and loading as required Participate in all required safety activities and maintain a safe work environment Skills: Laboratory, Chemistry, Quality Control, GMP, HPLC, Chromatography, Illusion Order, Peak Characteristics, GC Controlling Software, Lab Technician, Chemical Engineer, Analysis Additional Skills & Qualifications: Bachelor's Degree in Chemistry or Chemical Engineering more »

similar role. Paid, owned, website, & commerce data experience. Strong knowledge of key digital platforms, CRM, data and web analytics providers, including Adobe Marketing Cloud, GMP, GCP, Meta and other partners. Strong knowledge of data management, analytics with experience of deploying data & analytics projects across large accounts. Have managed multi- million more »

Assurance Operations to join our growing team The ideal candidate is an experienced within Quality Assurance Operations with a track record of success in GMP environments who understands biologics processes (i.e. cell & gene therapy, aseptic environments, reagent control, contamination control). What You'll Do Here: Review and approve all … GMP documentation including SOPs, batch records, deviations and investigations, QC testing, study reports, validation/qualification protocols and summary reports, etc. Provide document review and feedback for CAL/PM program and Environmental Monitoring for the site. Manage and trend lot/product disposition activities. Provide training and guidance on … in conjunction with logistics/clinical and supply chain functions. Support Tech Transfer activities for new projects. Participate in quality audits in support of GMP operations and regulatory requirements. Partner with Program Management, Manufacturing, Quality Control, Supply Chain and attend meetings in support of relevant manufacturing programs and activities. Present more »