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I know many of you want to switch from the bench to office roles, and it's possible! I’m a chemist who -unexpectedly- transitioned to project management in pharma&biotech over the past 3 years. My experience on the bench has greatly influenced my PM journey. What’s helped me most: - Talking to people: especially experienced professionals. Learning about others' career paths helped me understand the roles available to me as a chemistry graduate. I also recommend taking courses in drug development or clinical trials for practical knowledge. - Building transferable skills: skills like managing conflict, organisation, and communication are crucial and can be learned in any role. Successfully handling difficult personalities and conflicts significantly impacts a PM career. These skills are key to keeping people on task and maintaining harmony in projects. For aspiring PMs, talk to current PMs to understand the daily realities of the role. Some discover a different path suits them better, such as procurement or regulatory. Switching from a different background to PM has been rewarding. Good luck to those rebranding themselves! 😊 #ProjectManagement #Pharma #Biotech #CareerSwitch #CareerTips

Biopharma Career Paths: Watch this video if you are considering a career in biopharma. The industry offers diverse opportunities, from research and development to regulatory affairs and quality control. You'll find roles for scientists, data analysts, and project managers, to name a few. Biopharma is a dynamic and rapidly evolving field, making it an exciting career choice. Whether you're interested in lab work or the business side of biopharma, there's a place for you. Here are the top 3 careers in the field include: Research Scientist - Develop new drugs and therapies. Regulatory Affairs Specialist - Ensure compliance with regulations. Quality Control Analyst - Maintain high standards in product development. Explore these roles and find your fit in this impactful industry! Share your options in the comments below. Let’s help the future professional in the comments.

Friends, Colleagues, and Fellow Travelers on the road of life, As some of you may know, Kite Pharma recently made the difficult decision to lay off nearly 7% of their global workforce. Unfortunately, the hybrid in-house Project Management Org/Talent Accelerator that I led was eliminated as part of this change. As such, I now find myself one of many who are in search of new opportunities in a very difficult job market. For those of you who might not be fully acquainted with my background: over the past 10 years, I have grown into a highly skilled Technical Operations leader, with strong management experience in Supply Chain, Quality Operations, and Project/Portfolio Management. Augmenting this is an additional 3 years in Clinical Operations working with both product and sponsor to ensure optimal study execution. Here's just a few of my career highlights to date: -         Spearheaded a Tech Ops focused business rotation dept in the Cell Therapy space (Supply Chain, Quality, Process Dev, MSAT, Biz Ops, and more), mentoring and developing over a dozen junior Project Managers with international impact -         Designed, developed, and deployed an enterprise-wide Order Management System and companion Lot Release Prioritization “SWAT team”, leading to the elimination of a Drug Substance backlog of over 100 lots and the reduction of the Drug Product lot backlog by greater than 50% -         Headed up all Commercial and Clinical planning and operations activities for Dupixent, a Regeneron blockbuster program. This included leading collaboration planning and threat mitigation efforts with ex-US strategic partner Sanofi -         Collaborated with a team of SME’s and PM’s to rapidly bring Regeneron’s life-saving REGN-COV2 anti-COVID monoclonal antibody treatment to market under an Emergency Use Authorization My humble request to all of you is this: if we’ve worked together in the past and you were impressed with the quality or character of my work, would you please consider authoring a recommendation for me via my LinkedIn page? It could go a long way towards helping me earn my next opportunity to make an impact. Additionally, if you should become aware of any open opportunities that you think might be a good fit at companies where you still maintain contacts, would you please consider making a connection? I am currently in search of roles from the Director to Senior Manager level, in the realms of Supply Chain, Quality, and Project/Portfolio Management. I would also be very excited to discuss any Relationship Management/Business Development positions as well. Thank you all in advance for your continued support through these difficult times. I look forward to our future collaborations!

"As a pharmaceutical professional, I've learned that effective project management is crucial to delivering successful projects. Here are the key things to consider for effective project management in pharma: •⁠ ⁠Clear goals and objectives: Define project scope, timelines, and deliverables to ensure everyone is on the same page. •⁠ ⁠Strong project planning: Develop a detailed project plan, including risk management, resource allocation, and communication strategies. •⁠ ⁠Collaboration and teamwork: Foster a culture of collaboration among cross-functional teams, including R&D, manufacturing, quality, and regulatory affairs. •⁠ ⁠Regulatory compliance: Ensure projects meet all relevant regulatory requirements, such as GMP, GCP, and GLP. •⁠ ⁠Risk management: Identify, assess, and mitigate risks proactively to minimize project delays and ensure patient safety. •⁠ ⁠Effective communication: Keep stakeholders informed through regular updates, progress reports, and transparent communication. •⁠ ⁠Continuous monitoring and improvement: Regularly review project progress, identify areas for improvement, and implement changes as needed. •⁠ ⁠Quality assurance: Ensure projects meet the highest quality standards, from development to delivery. •⁠ ⁠Patient-centric approach: Keep the patient at the forefront of all project decisions, ensuring projects ultimately improve patient outcomes. By considering these factors, pharma project managers can ensure successful project delivery, drive business growth, and ultimately improve patient lives. #pharmaprojectmanagement #projectmanagement #pharmaindustry"

As we approach 2025, the landscape of FDA-regulated industries—whether in pharmaceuticals, medical devices, biotech, or food safety—is evolving faster than ever. Navigating this complex environment requires specialized expertise and a flexible workforce that can keep pace with new regulations, innovations, and challenges. That’s where I come in. I specialize in providing highly skilled, FDA-compliant contractors and consultants tailored to your specific needs. Whether you're looking for short-term project support, long-term strategic guidance, or specialized talent for critical regulatory functions, I can connect you with experts who have a deep understanding of FDA regulations and industry standards. Here’s how I can help: ✔ Experienced Resources: Access a network of professionals with specialized knowledge in FDA regulations, quality assurance, regulatory affairs, clinical trials, validation, and more. ✔ Tailored Solutions: Whether you need a subject matter expert for compliance documentation, a project manager for regulatory submissions, or a team to ensure your product meets FDA guidelines, I’ll match you with the right talent. ✔ Flexibility & Scalability: Contractors and consultants who can seamlessly integrate into your team and scale with your needs, helping you navigate project peaks, expansions, and regulatory shifts. ✔ Time & Cost Efficiency: Avoid the overhead and long hiring cycles. With access to pre-vetted, experienced professionals, you can accelerate timelines and drive faster results without sacrificing quality. Reach out today to learn more about how I can support your projects with top-tier contracted and consulting talent!

Having worked in the pharma industry for over 7yrs, I realised that each role has so much to offer in terms of the learning. However, it is a very common practice that whenever you join a new organization, you are always rushed to learn more about your responsibilities rather than dive deep to learn how actually the industry is functioning. In one of my experiences with an organization where i was working as a Project Coordinator, I was always intrigued to learn about the work that the other team is doing. For e.g., I would see my colleague from the Medical Affairs team, visit the DCGI office with a bundle of documents and I would always wonder what those documents are and what is it’s relevance with the work that I am doing. When I started researching things on my own, I realised that this industry has so much more to offer that I barely know 20% about. Having said that, my major takeaway was that in a rush to meet deadlines and meet your KPIs, do not forget to interact and ask questions to your coworkers on the set of things they are doing, because knowledge is everywhere and the biggest exposure you can get is from the job itself. #pharmaceutical #learning #corporatejourney

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At PharmaLex, our most valuable asset is our talented team of experts who drive innovation and excellence in the pharmaceutical industry. Today, we’re excited to introduce one of our Nordic team members! Get to know our expert in Quality Management and Compliance, Pia Nelimarkka! 🎤 𝗪𝗵𝗮𝘁 𝗶𝘀 𝘆𝗼𝘂𝗿 𝗿𝗼𝗹𝗲, 𝗮𝗻𝗱 𝘄𝗵𝗮𝘁 𝗮𝗿𝗲 𝘆𝗼𝘂𝗿 𝗱𝘂𝘁𝗶𝗲𝘀 𝗰𝘂𝗿𝗿𝗲𝗻𝘁𝗹𝘆?   As a Senior Manager at PharmaLex, I currently work on-site at a customer, focusing on cleaning validation and quality oversight of environmental monitoring in supply chain manufacturing buildings. Previously, also responsibilities like change management, quality operations, people leadership not only in SC but also in R&D, have been my tasks. So the range of pharma world, not only from quality perspective but also from development, manufacturing, analytics, validations, equipment are familiar to me. All in all, my job involves developing and improving pharmaceuticals for human and veterinary use, ensuring compliance from clinical development to marketed products. 🎤 𝗪𝗵𝗮𝘁 𝗶𝘀 𝘁𝗵𝗲 𝗯𝗲𝘀𝘁 𝗽𝗮𝗿𝘁 𝗼𝗳 𝘆𝗼𝘂𝗿 𝗷𝗼𝗯? 𝗪𝗵𝗮𝘁 𝗱𝗼 𝘆𝗼𝘂 𝗳𝗶𝗻𝗱 𝗳𝗮𝘀𝗰𝗶𝗻𝗮𝘁𝗶𝗻𝗴 𝗮𝗯𝗼𝘂𝘁 𝘆𝗼𝘂𝗿 𝗷𝗼𝗯? The best part of my job is knowing that my work impacts someone's quality of life. I find motivation in knowing that my work saves lives or alleviates symptoms. The variety in my work as a consultant, seeing different companies, processes, and cultures, keeps it exciting. Developing new ideas, solving technical challenges, and collaborating with teams globally gives me a daily boost. It's fascinating to see how a lab concept becomes a product that helps patients. 🎤 𝗪𝗵𝗮𝘁 𝗶𝘀 𝘆𝗼𝘂𝗿 𝘀𝘂𝗽𝗲𝗿𝗽𝗼𝘄𝗲𝗿? My superpower is flexibility in different work tasks, environments, and teams. I connect technical, quality, and management aspects of processes. My natural diplomacy and interpersonal skills, combined with over 20 years of industry experience, enhance my effectiveness. 🎤 𝗪𝗵𝗮𝘁 𝗱𝗼 𝘆𝗼𝘂 𝗱𝗼 𝘄𝗵𝗲𝗻 𝗻𝗼𝘁 𝘄𝗼𝗿𝗸𝗶𝗻𝗴? When not working, I enjoy spending time outdoors with our family dog and practicing yoga for its mental and physical benefits. I stay curious about life and keep up with trends through my three daughters. Time with family and friends is essential to me—it keeps me grounded and balanced. 🔗 Learn more about our team's work: https://lnkd.in/dF4xv7yd #TeamSpotlight #QMC #Nordics

Sometimes, success comes down to being in the right place at the right time—like capturing this photo when the full moon rose perfectly between the lines. In project management, it’s no different. Tangled lines, competing priorities, and shifting timelines are part of the process. But clarity can always be found. As a Project Manager in biotech and pharma, I specialize in finding that clarity. Whether it’s driving complex programs across drug development, manufacturing, and CMC or aligning cross-functional teams for results, I turn tangled lines into a focused path forward. I’m actively seeking my next opportunity to deliver transformative results for biotech teams working on cutting-edge therapies. If you’re looking for someone who thrives at bringing calm, clarity, and focus to complex projects, let’s connect! #projectmanagement #biotech #drugdevelopment #clarityinchaos #jobsearch

The UK Life Sciences sector continues to thrive, offering countless opportunities for innovation and growth. With a projected market value exceeding £94 billion by 2030, the industry is a powerhouse for advancements in biopharma, MedTech, and beyond. For those in QA, this growth means exciting challenges and rewards: 🔴 Increased demand for QA specialists to ensure compliance as innovation accelerates 🔴 The rise of green initiatives, requiring QA teams to adapt processes for sustainability 🔴 New technologies like AI, pushing the boundaries of how we ensure quality Whether you're a candidate seeking your next move or a company looking for top talent, the time to act is now. Are you ready to shape the future of UK life sciences? Let me know if I can help! #LifeSciences #Hiring #QA #Innovation #Sustainability