SciPro are working with an exciting, privately owned pharmaceutical company who are looking for an experienced Head of Regulatory & Clinical Affairs to be based in the UK. You will be leading an experienced team of regulatory and clinical professionals, working strategically whilst remaining operational to spearhead regulatory strategy development and drive regulatory submissions for their existing commercial products, and across new product development.The company are a successful, independent business who are developing and marketing leading treatments across primary and secondary care. This is a fantastic opportunity to join a company fostering a culture of collaboration and pride - proud of the work they do and of the leading products they develop and ultimately deliver to patients.The ideal candidate:Previous pharmaceutical marketing experience working at a senior levelExperienced in managing a teamExcellent communication skills with previous experience of liaising with regulatory bodies

SciPro is excited to partner with a leading global biopharmaceutical company in search of a skilled Manager/Associate Director - Contract Manufacturing. This role is crucial in overseeing the manufacturing operations for a liposomal-based ALIS product at the company's Contract Manufacturing Organization (CMO). If you're passionate about transforming patient lives and possess strong expertise in pharmaceutical manufacturing, we encourage you to apply. Key Responsibilities:On-site responsibility for managing manufacturing operations at the CMO, including real-time oversight of commercial batch manufacturing.Provide engineering/technical support, technical review of quality documentation, and manage schedules, raw material consumption, and budgets.Support and evaluate investigations and change controls, and manage process improvement projects.Collaborate with the CMO to ensure process manufacturing, refinement, and enhancements.Ensure compliance with regulatory requirements for pharmaceutical manufacturing.Qualifications:7+ years of experience managing pharmaceutical manufacturing processes, ideally with products marketed in the US and EU.3+ years of experience leading teams tasked with implementing pharmaceutical manufacturing technology improvements in a regulated environment.Experience with commercial CMO operations and design/operation of pharmaceutical aseptic processing equipment, facilities, and supporting utilities.Strong understanding of quality systems, validation principles, engineering design, and statistical process control fundamentals.Proven problem-solving skills using root cause analysis methodology.High energy, innovative "can do" attitude with the ability to work independently, remotely from central leadership.Strong interpersonal skills and effective verbal and written communication.If this role aligns with your experience and you're enthusiastic about contributing to meaningful work in the biopharmaceutical industry, we'd love to hear from you. Apply now through SciPro!

A notable pharmaceutical company is looking to hire a Director of API Process Development to lead drug substance manufacturing operations.   The ideal candidate will have the following background: Academic background in Chemical Engineering ~ 10 years of industry experience in the pharmaceutical industry Strong presentation and leadership skills, with an emphasis on technical and people development Subject matter expert in chemical process development from early phases of development through commercialization Extensive experience with tech transfer to external manufacturing partners Exposure to process modeling and simulation techniques / predictive analytics   The successful candidate will have the following responsibilities: Lead chemical development for a variety of assets from early development to commercial launch, with the potential for life cycle management Lead a team of process, formulation, and analytical chemists Advise on the development of new synthetic routes for API manufacturing Contribute to PAT and continuous manufacturing technical advancements Guide strategy for scale-up of successful chemical assets

This growing pharmaceutical manufacturing team is looking to add a Senior Process Engineer to their TechOps team!   Successful candidates will have the following background: B.S. or M.S. in Chemical Engineering or related subject 3-7 years of pharmaceutical industry experience Expertise in scale-up and manufacturing for APIs Experience in tech transfer activities   This role would be responsible for the successful process scale-up and tech transfer of small molecule API products from early stage development through commercial manufacturing.

SciPro is partnered with an innovative Biotech drug discovery organization in the Greater NYC metropolitan area. The person selected with join a rapidly growing and well-funded organization changing the scientific landscape across a variety of different modalities and indications.   Responsibilities: Help progress drug discovery projects by applying computational tools to invent and advance compounds that have a higher probability of becoming successful drugs. Support small molecule and biologics lead identification and optimization programs using various methods encompassing all computational aspects of drug discovery. design of high throughput screening libraries to support hit finding development of innovative computational methods data analysis and visualization to support multiparameter compound optimization application of machine learning Drive a “predict-first” culture in molecule design that impacts decision making on programs. Create and lead computational methods to study conformationally flexible proteins, identify novel binding sites, and ligand selectivity.   Qualifications: PhD in computational chemistry or related with 4+ years relevant experience Deep understanding of computational biophysical approaches, e.g. molecular dynamics, enhanced sampling methods, free energy calculation and quantum mechanics. Experience with commercial and open-source molecular modeling tools, i.e. Schrodinger, MOE, OpenEye, Amber, NAMD, etc. Experience with computational approaches to compound screening library design including fragment-based ligand design (screening and expansion) and/or DNA encoded libraries (library design, hit-to-lead advancement) Experience with QSAR, machine learning, and/or deep learning   All interested applicants are encouraged to apply below.