Documentation Consultant for Pharmaceutical Industry

We're looking for a highly skilled Pharmaceutical Industry Consultant to join our team at Devote Consulting. As a Senior Consultant, you'll be responsible for delivering changes in the life sciences industry focused on processes, data, and systems.About the RoleBusiness process optimization: Redesign and improve business workflows for greater...

We are seeking a highly skilled Validation Engineer to join our team at Hamlyn Williams. As a Validation Expert for the pharmaceutical industry, you will play a critical role in ensuring the quality and safety of our clients' products.Your key responsibilities will include validating equipment and processes to ensure compliance with regulatory requirements,...

Quality Assurance Documentation Engineer 3 days ago Be among the first 25 applicants Direct message the job poster from Think IT Resources Recruitment Consultant at Think IT Resources I am currently looking for a Quality Assurance Documentation Consultant, someone in the pharmaceutical industry who is experienced with GMP, GAMP, and GDP. You will have good...

About the JobWe are seeking a highly skilled Pharmaceutical Industry Security Advisor to join our client in the pharma industry. The ideal candidate will possess expertise in both management and strategy, as well as experience in industrial manufacturing (OT).The consultant will evaluate our current security solution and provide recommendations to ensure an...

At AM Group, we approach consulting differently. We believe in leveraging well-established management and engineering tools to deliver tangible improvements to our clients' businesses.We are seeking an experienced Process Engineer in the life sciences industry to join our team. As a Process Engineer, you will play a key role in designing, optimizing, and...

Job Description: Global Quality Assurance Specialist within Pharmaceutical IndustryIn this role, you will be responsible for ensuring the quality of pharmaceutical products manufactured by contract manufacturers. This includes conducting audits, reviewing documentation, and providing training to partners. You will also be responsible for implementing quality...

AM Group - partner of Consultys - is a consulting company based on experience and a desire to challenge the norm. We believe in approaching consulting differently. Instead of relying on complex theories that only work in ideal scenarios, we utilize well-established management and engineering tools to deliver tangible improvements to our clients' businesses....

Company OverviewRamboll is a global architecture, engineering, and consultancy company founded in Denmark. We believe that the purpose of sustainable change is to create a thriving world for both nature and people. Our history is rooted in a clear vision of how a responsible company should act and being open and curious is a cornerstone of our culture.We...

We are seeking a highly experienced Pharma Documentation Specialist to join our team at Think IT Resources. As a Quality Assurance Expert, you will be responsible for establishing and maintaining traceability from documented requirements through design documentation to test execution.Key responsibilities include:Establishing and maintaining...

As a HSEQ Senior Consultant, you will play a critical role in supporting our global teams to achieve HSEQ excellence. You will work closely with stakeholders and partners to identify and mitigate potential risks, ensuring that our business operates safely, sustainably, and responsibly.About the RoleThis is an exciting opportunity to contribute to the growth...

Job DescriptionOur client, a global Contract Development and Manufacturing Organization (CDMO), is recruiting for an Automation CSV Engineer to join their new CAPEX investment programme in Denmark.The successful candidate will contribute to providing process development and cGMP production in cell culture, microbial fermentation, and gene therapies.Essential...

Job DescriptionWe are seeking a Senior Pharmaceutical Engineer to support the commissioning and qualification of critical process and utility systems. The ideal candidate will have strong field commissioning experience, troubleshooting skills, and the ability to work collaboratively with a team.Key Responsibilities:Lead and perform CIP commissioning for...

Project Planner Job SummaryWe are seeking an experienced Project Coordinator to join our team at TRS Staffing Solutions. This role involves creating, maintaining, and monitoring project schedules, ensuring timely delivery and efficient resource management.Key Responsibilities:Schedule Development: Develop and maintain project schedules, identifying key...

Senior/Principal Medical Writing ConsultantsPharma IT is hiring experienced Senior/Principal Medical Writer Consultants to join our Regulatory Affairs & Medical Writing TeamIn this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries.In this position, you will work on-site at the client's location or...

**Job Summary:**We are looking for a skilled Mechanical Design Engineer - Pharmaceutical Sector to join our team at IPS. In this role, you will be responsible for designing and developing equipment, utilities, and process pipework systems for our pharmaceutical clients.Key Responsibilities:Develop and implement mechanical design solutions for pharmaceutical...

Are you an experienced professional from the pharmaceutical industry, passionate about improving business processes and driving impactful change? Devote Consulting is expanding its team and is looking for a Senior Consultant with expertise in organizational change management (OCM) in the life science industry.Join Our Team at Devote ConsultingAre you an...

We are seeking a talented and motivated individual with a Ph.D. or Master's degree in analytical chemistry and pharmaceutical science, or equivalent education with relevant practical experience.A proven track record in method development, stability studies, and trending on stability data is essential.Experience in preparing regulatory documentation and...

We are seeking a highly skilled and experienced management consultant specializing in Identity & Access Management (IAM) for one of our clients in the pharmaceutical industry.Main ResponsibilitiesSupport the execution of strategic IAM initiatives while collaborating with architects and product owners.Develop tactical plans to transition existing strategies...

A career as a Validation Engineer with Hamlyn Williams offers many benefits and opportunities for growth and development. As a Validation Expert for the pharmaceutical industry, you will play a critical role in ensuring the quality and safety of our clients' products.Your key responsibilities will include validating equipment and processes to ensure...

About Lundbeck A/SLundbeck A/S is a global leader in the discovery, development, and commercialization of innovative treatments for brain disorders. Our mission is to improve the lives of people affected by brain disorders, and we are committed to making a difference through our cutting-edge science and strong partnerships.We are proud to be part of the...