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The successful candidate will play a key role in managing regulatory activities across multiple products, primarily small molecules, with the opportunity to expand into development projects over time. Prepare and manage regulatory submissions including IMPDs and CTAs. Contribute to strategic plannin

Operations Analytics Lead – Pharma - £650 pd Outside IR35 Our global pharmaceutical client now requires an Operations Analytics Lead to join them on a 12-month contract assignment. This is a great opportunity for a talented professional to join a widely recognised brand during a time of significant transformation as they embed SAP S4HANA. The Operations Analytics Lead will be responsible for leading a team of senior business analysts, task managing, providing them with oversight and creating best practices. They will be designing new operating models for areas such as network, supply chain, manufacturing and distribution etc. Key Skills: • Senior Business Analysis skills, • Knowledge of ERP analytics in pharma, • Supply Chain Operations experience, • Proven experience of team leadership/management, • Experience of SAP Analytics Cloud and Datasphere, • Experience managing senior stakeholders, • S4HANA implementation experience (desirable) Rate: £650 per day Outside IR35 Duration: 12 months Location: Hybrid/Luton

Working Instructions Writer 6 months + possible extension Remote- ad hoc Luton site attendance if required by HM £175 day PAYE / UMB – Inside IR35 We are now looking for Working Instructions Writer to join our team! What you'll do: The Working Instruction Writer is responsible for developing clear and comprehensive Working Instructions intended for end users. This role involves creating step-by-step guidance that enables users to understand and execute procedures accurately. Activities / Accountabilities • Develop Step-by-Step Instructions: Create clear, detailed working instructions using SAP Enable Now that guide end users through tasks and processes in a logical sequence, ensuring ease of understanding and accuracy, • Engage with Subject Matter Experts: Collaborate with process owners and technical specialists to gather the necessary information and validate content, ensuring instructions reflect current practices and standards., • Review and Revise Documentation: Regularly update and improve working instructions based on feedback, process changes, or lessons learned, maintaining the relevance and accuracy of each document., • Ensure Regulatory and Quality Compliance: Align documentation with internal policies, quality standards, and regulatory requirements, supporting audit readiness and operational integrity., • Standardize Document Formats: Adhere to approved templates and formatting guidelines to ensure working instructions are consistent, professional, and easy to follow across different departments or functions. Essentials: • Previous experience in working instructions writing, • Finance (Planning and budgeting, O2DC, PM&M) or Operations (Manufacturing and Warehouse, Supply Chain, Quality), • S/4HANA Knowledge, • Ability to understand/work with various online IT systems / applications including Microsoft Office suite, • Strictly follow a template to allow development of content to be produced in a consistent and uniformed manner., • Ability / experience to follow a project plan and be able to adhere to tight deadlines Desired: • Experience in large scale S4 Hana implementations, • Pharma experience, • SAP Enable Now Knowledge

Knowledge of Analytics tools and Data Warehouses like PowerBI, Qlik, Azure Data Lake, Snowflake, SAP B4H, SAP Analytics Cloud etc. SAP FICO Consultant – Pharma - £580 pd Outside IR35. Our global pharmaceutical client now has an opportunity for an SAP FICO Consultant to join them on a 12-month con

PhD or MSc in Biostatistics, Statistics or a closely related field. Associate Director, Statistics, hemel hempstead. Associate Director, Statistics | Global Pharma | UK | Home Based |.

Packaging Operator – Pharmaceutical Industry. Pharmaceuticals / GMP Manufacturing. Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London.

Senior Research Executive - Pharma. Are you currently an RE or SRE with experience in the pharmaceutical sector, looking to join a friendly, independently-owned research agency where your research career will be nurtured through peer support and robust continuous professional development?.

We're Hiring: Market Access Specialist (UK).Field-based | 💼 Medical Devices | 🕐 Min.Are you a hands-on Market Access professional who thrives on face-to-face engagement with payers and healthcare stakeholders? We're looking for someone who doesn’t just write reports — but gets out on the r

Head of Operations - Warehousing (Pharma). We’re pleased retained exclusively with a growing pharmaceutical distribution business on their search for a high-impact Head of Operations. Strong experience in operations leadership within a pharmaceutical/medical-grade or strictly regulated environment

Deliver high-quality CMC regulatory services to support global pharmaceutical development and commercialization. Bachelor’s degree in Chemistry, Biological Sciences, Pharmacy, or a related discipline. Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Man

You will be responsible for growing and maintaining a portfolio of clients – predominately in the pharmaceutical sector. To create an account strategy to drive sales and relationships across the business for owned pharmaceutical SMM accounts.

A global biopharma company is seeking a skilled scientist to support non-clinical pharmacokinetics/pharmacodynamics (PKPD) and toxicokinetics strategy within early drug development. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts,

Alternatively, please send your CV to grant@pharma-search.

Proven track record in CMC-regulatory affairs within the pharmaceutical industry.

Drafting, reviewing, and negotiating commercial and clinical contracts, third party vendor agreements, service agreements, consulting agreements and various pharmaceutical related agreements for the Group e. Partnering with other functions to ensure compliance with industry codes of practice and app

Planet Pharma is partnered with a global leading pharmaceutical company who are currently hiring for a Data Sourcing & Contract Management Support - Project Manager to join their team on a critical project for 5 months initially, on a fully remote basis in the UK. Interested? Apply now for immediate

Referrals increase your chances of interviewing at Envision Pharma Group by 2x. How will you make an impact at Envision Pharma Group?. Pharmaceutical Manufacturing and Biotechnology Research.

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Critical to your success will be your ability to develop and expand new business opportunities within established and new clients within USA, particularly big Pharma, mid Pharma, BioPharma, Biotech and CROs. Our client is a knowledge-based, science-led business providing a wide range of innovative a

At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.

Direct message the job poster from Envision Pharma Group. How will you make an impact at Envision Pharma Group?. Proven track record of leading high-impact, strategic value communication projects for pharma clients, driving organic growth.

At Planet Pharma, we connect top talent with impactful roles that drive innovation in life sciences — and this is one of them.

Proven recent background managing big Pharma/Biotech accounts. Proven experience hunting for and winning new business for alternate revenue streams within existing big-pharma accounts. Degree qualified in Life Science/Pharma related discipline.

Previous experience in pharmaceutical, biotech, or FMCG packaging operations preferred (training will be provided). Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Centra

We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies.

Associate Director / Director – Clinical Pharmacology & Pharmacometrics. Role Summary: Are you a Clinical Pharmacology leader with strong Neuroscience experience looking for a high-impact role in a global biopharma environment? This is a unique opportunity to join an organisation at the forefront

Industries: Pharmaceutical Manufacturing and Biotechnology Research. In/Out Licensing Specialist - Pharma. BSc (or equivalent) in Pharmacy or a related discipline.

Direct message the job poster from Planet Pharma. This opportunity allows you to step into a pivotal role within a global biopharmaceutical leader at the forefront of oncology innovation. Pharmaceutical Manufacturing and Biotechnology Research.

Critical to your success will be your ability to develop and expand new business opportunities within established accounts and prospective new clients within USA, particularly big Pharma, mid Pharma, BioPharma, Biotech and CRO client companies.

Pharmaceutical Manufacturing and Biotechnology Research. Planet Pharma is seeking a talented and motivated Biostatistician to support the design, analysis, and reporting of clinical trials and observational studies. PhD with some experience, or Master’s degree in Biostatistics with substantial exp

Experience in clinical trials from CRO or pharma/biotech company or as an investigator.

Planet Pharma are working with a global biopharmaceutical company focused on developing innovative treatments for severe diseases. Market Research & Insights Specialist - Fully remote in UK - Leading Bio-Pharmaceutical!*. Market Research & Insights Specialist - Fully remote in UK - Leading Bio-Pharm

Biotechnology Research and Pharmaceutical Manufacturing. Legal Contracts Specialist – Pharma | FTC to Year-End. Are you a contracts whizz with pharmaceutical industry experience, available to jump into a high-impact role straight away?.

Proven track record in CMC-regulatory affairs within the pharmaceutical industry. Industries: Pharmaceutical Manufacturing.

Opportunity to work with leading pharma clients on strategic digital/data programs. Pharma Commercial Data / Technical / AI Ecosystems. Partner with offshore and onshore teams to design scalable data and analytics solutions tailored to pharma commercial use cases.

Critical to your success will be your ability to develop and expand new business opportunities within prospective new clients within DACH, particularly with mid Pharma, BioPharma, Biotech and MedTech client companies.

Ready to lead the future of pharma marketing on a global scale? Apply now to take the next bold step in your career. Chemical Manufacturing and Pharmaceutical Manufacturing. Are you a strategic marketing leader with a passion for innovation in the pharmaceutical industry? An established global playe

Head of Operations - Warehousing (Pharma). We’re pleased retained exclusively with a growing pharmaceutical distribution business on their search for a high-impact Head of Operations. Strong experience in operations leadership within a pharmaceutical/medical-grade or strictly regulated environment

Critical to your success will be your ability to develop and expand new business opportunities within established accounts and prospective new clients within Europe and North & South America, particularly within big Pharma, mid Pharma, BioPharma, Biotech and CRO client companies. Ideally you will ha

Global Pharma, UK remote based. Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have extensive functional expertise including: Regulatory Affairs, Phar

A unique opportunity to play a key leadership role within an exceptionally successful, extremely dynamic, and remarkably ambitious business.Having achieved unbridled success over recent years you can help lead the next phase of their growth, development and success.Do you have the passion, enthusias

A global biopharma company is seeking a skilled scientist to support non-clinical pharmacokinetics/pharmacodynamics (PKPD) and toxicokinetics strategy within early drug development. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical

Clinical Pharmacology & Pharmacometrics Director – Oncology & Neuroscience Focus. Phase 1–4), and analyze pharmacokinetic and pharmacodynamic data. Are you ready to make a meaningful impact in the lives of patients with serious medical conditions? A leading global biopharma company is seeking an

Business Development Director, Clinical Pharmacology - Pharma Sales. Business Development Director, Clinical Pharmacology - Pharma Sales. Business Development Director, Clinical Pharmacology - Pharma Sales.

Dermatology Territory Manager - Toronto North York Ajax page is loaded.Dermatology Territory Manager - Toronto North York Ajax.Apply locations Thornhill posted on Posted 10 Days Ago job requisition id JR014627.Galderma is the emerging pure-play dermatology category leader, present in approximately 9

Quality Assurance Manager - GMP Pharma. Our client is a pharmaceutical business based in Hertfordshire. This is a GMP accredited Pharma Manufacturing site.

Direct message the job poster from Verbatim Pharma. This is a high-impact role overseeing complex partnerships with key biopharma clients across the clinical development lifecycle. Work with leading biopharma sponsors in a high-visibility role.

Our client is a pharmaceutical business based in Hertfordshire. This is a GMP accredited Pharma Manufacturing site. Understanding of best practise within a GMP Pharma environment.