pharmaceutical scientist

HEOR Scientist - Pneumococcal Vaccines Location: RemoteContract Type: TemporaryRate: £650-800 per day approx. (Umbrella) SRG are supporting a leading global pharmaceutical company with their search for an HEOR Scientist supporting Pneumococcal Vaccines. This will be an initial 9 month contract and the role is predominantly remote based. Reporting to the Global RWE & Health Outcomes Research Lead, you'll play a key role in designing and delivering impactful real-world evidence (RWE) studies that inform strategic decisions and support global market access. Key Responsibilities <ul> <li>Design and execute multiple RWE studies, managing timelines, deliverables, and budgets.</li><li>Ensure quality and compliance across study documentation including protocols, analysis plans, and publications.</li><li>Translate strategic evidence needs into innovative study concepts and protocols.</li><li>Advise internal and external stakeholders on scientific design and data sources.</li><li>Build strong cross-functional relationships across medical, market access, and commercial teams.</li><li>Engage with external thought leaders to ensure robust and credible research approaches.</li></ul> Requirements & Experience <ul> <li>MSc or equivalent in health economics, epidemiology, pharmacy, or life sciences.</li><li>1-3 years' experience in the pharmaceutical industry, ideally within a multinational setting.</li><li>Proven ability to manage projects and budgets in a matrix environment.</li><li>Experience with RWE study designs and HTA/reimbursement evidence generation.</li><li>Experience with Pneumococcal Vaccines would be a major advantage - Vaccines in general or Immunology also useful experience</li><li>Strong communication skills to translate complex data for diverse audiences.</li><li>Knowledge of global healthcare systems and payer decision-making processes.</li></ul> Preferred: PhD/PharmD, launch experience, and direct payer engagement. To Apply If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

HEOR Scientist - Vaccines

Colorado Chromatography

<div>
 
 
 About Colorado Chromatography Labs (CCL)
 
 
 
 Colorado Chromatography Labs (CCL) is a research-driven innovation lab developing next-generation solutions across six R&amp;D verticals: new molecules, dietary supplements, peptide biosynthesis, pharmaceutical formulation, biological testing, and early-stage drug development. Our team is advancing the science of novel molecule design, therapeutic analogs, and bioavailability optimization for underexplored natural products and synthetic compounds. We operate at the interface of chemistry, biology, and formulation science while pushing boundaries through impactful, IP-generating research.
 
 
 
 
 
 
 
 
 
 Position Overview:
 
 
 
 We are seeking a Ph.D.-level Formulation Scientist or PharmD with a strong background in pharmaceutical sciences and a passion for novel delivery systems. This role will join our Formulations R&amp;D team to design and evaluate innovative oral, sublingual, and injectable delivery methods for proprietary compounds. The ideal candidate has experience translating pharmacological targets into bioavailable, scalable dosage forms, and is comfortable operating in a cross-functional, early-stage research environment.
 
 
 This is a technical individual contributor role, not a management position.
 
 
 
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Design and optimize formulations for oral, sublingual, transdermal, and injectable routes of administration.
 </li>
 <li>
 Select and evaluate excipients, carriers, and delivery technologies for solubility and bioavailability enhancement.
 </li>
 <li>
 Conduct pre-formulation studies, including compatibility, stability, and dissolution.
 </li>
 <li>
 Support analytical method development and interface with chemists and biologists for characterization workflows.
 </li>
 <li>
 Collaborate with internal and external teams on PK/PD data to inform iterative formulation changes.
 </li>
 <li>
 Draft technical documentation for internal reports, publications, and patent filings.
 </li>
 <li>
 Stay current on formulation innovations in both the pharmaceutical and dietary supplement spaces.
 </li>
 <li>
 Help transition formulations from benchtop to pilot-scale evaluation when applicable.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Required Qualifications:
 
 
 <ul>
 <li>
 Ph.D. in Pharmaceutical Sciences, Pharmaceutics, or a closely related discipline (Required) or PharmD (Preferred) with 2+ years R&amp;D formulation experience
 </li>
 <li>
 Demonstrated expertise in solid, liquid, or semisolid dosage forms
 </li>
 <li>
 Experience with excipient screening, solubility optimization, or lipophilic compound formulation
 </li>
 <li>
 Familiarity with analytical tools (HPLC, particle sizing, rheology, etc.)
 </li>
 <li>
 Strong scientific writing skills for technical documentation, manuscripts, or patent support
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Preferred Qualifications:
 
 
 <ul>
 <li>
 Prior experience in startup or early-stage biotech
 </li>
 <li>
 Exposure to cannabinoid, peptide, or alkaloid formulation challenges
 </li>
 <li>
 Knowledge of GRAS and FDA-compliant excipient selection
 </li>
 <li>
 Familiarity with in vitro permeability models or in vivo PK studies
 </li>
 </ul>
</div>

Formulation Scientist - R&D

Intas Pharmaceuticals

<div>
 
 About Intas
 
 
 
 
 Recruitment Fraud Disclaimer:
 
 
 
 
 Intas Pharmaceuticals does not request or accept any fees during recruitment. If someone asks for payment on our behalf, it is a scam. Please report the incident to the local police or cybercrime unit. Your trust and safety are important to us.
 
 
 
 Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world.
 
 
 Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare. The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world.
 
 
 Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA. Substantial in-house R&amp;D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare.
 
 
 At Intas, our success is fundamentally built on the strength of our people. Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence. This approach ensures that every employee plays a meaningful role in driving both the company&rsquo;s growth and advancements in global healthcare.
 
 
 Job Title: Associate Scientist - DPD
 
 
 Job Requisitions No.: 15797
 
 
 
 Job Description
 
 
 
 Competencies
 
 
 Intas - Problem Solving
 
 
 Intas - Action Oriented
 
 
 Intas - Dealing with Ambiguity
 
 
 Intas - Customer Focus
 
 
 Intas - Time Management
 
 
 Purpose of Job
 
 
 Skill Required
 
 
 Roles and Responsibilites
 
 
 <ul>
 <li>
 To support in planning, executing, &amp; performing various drug product development studies and bio-similarity studies.
 </li>
 <li>
 Writing protocols and reports for various drug product development studies
 </li>
 <li>
 To support in process and technology transfer related documentations.
 </li>
 <li>
 To support in executing the stability studies and preparing reports for same.
 </li>
 <li>
 Getting trained on batch manufacturing procedure for drug product and do related documentation.
 </li>
 <li>
 To get trained on HPLC and CE techniques and perform analysis of stability samples.
 </li>
 <li>
 Response to DQA observations and closure of reports.
 </li>
 <li>
 Preparing and updating of SOPs.
 </li>
 <li>
 Ensuring the calibration of the equipment as per the schedules.
 </li>
 <li>
 Attending necessary trainings and following compliance.
 </li>
 <li>
 To follow &lsquo;Good Documentation Practices and Data Integrity&rsquo; requirements during any GxP Operation and recording at site.
 </li>
 <li>
 To take responsibility that application of Data Integrity requirements and potential consequences for not following it are understood and followed.
 </li>
 <li>
 To review in the perspective of compliance to Data Integrity requirements while reviewing any GxP data (Records, Reports) specific to Job description.
 
 
 </li>
 </ul>
 Qualification Required
 
 
 
 Relevant Skills / Industry Experience
 
 
 
 Relevant professional / Educational background
 
 
 
 Any Other Requirements (If Any)
 
 
 
 Compensation / Reward
 
 
 Location:
 
 
 Biotech, Ahmedabad, GJ, IN, 382213
 
 
 Travel: 0%
 
 
 Life at Intas Pharmaceuticals
 
 
 For over three decades, Intas has thrived due to the exceptional talent of its people. Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success. We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape.
 
 
 Date: 26 Dec 2025
</div>

Associate Scientist - DPD

US Pharmacopeia

<div>
 
 Description
 
 
 
 
 Who is USP?
 
 
 
 The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world&rsquo;s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.
 
 
 At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
 
 
 USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
 
 
 
 Brief Job Overview
 
 
 
 This is a professional, highly technical, non-supervisory position that supports the Excipients program unit team (PUT) within USP&rsquo;s Global Science and Standards Division (GSSD). The incumbent reports to a local management position at the India site as well as functionally reporting to a management position in the Excipients PUT in the US. The incumbent will support the development and technical stewardship of NF standards, other scientific products, outreach and awareness (in India, US, and internationally), and internal strategic initiatives. Key responsibilities include support for the development of missing Excipient monographs and significant revision of the existing Excipient monographs and associated reference standards (RS) in the
 
 USP-NF
 
 that will contribute to USP&rsquo;s success for bridging the gap in introducing missing excipient monographs and keeping existing excipient monographs current. The incumbent will utilize his or her technical expertise, knowledge of excipient compendial monograph standard development process and current regulatory guidelines, and strong organizational and communication skills to ensure timely development of high-quality monographs and associated reference standards. The Science EXC PUT works closely with several other departments including Strategic Customer Development (SCD)/Standard Acquisition (SA), Compendial Operation, Global Laboratory Operations (GLO), Regions Program Operation (RPO) &ndash; Industry Program, and Global External Affairs (GEA).
 
 
 
 How will YOU create impact here at USP?
 
 
 
 As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
 
 
 Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
 
 
 
 The Senior Scientist I/II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Works with USP staff, relevant USP Excipient Expert Committee(s) (EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Excipient monograph and RS development.
 </li>
 <li>
 Supports in the preparation of data packages and briefing materials to present to the Excipients EC/SC/EP; manages projects appropriately and ensures impeccable work-product delivery.
 </li>
 <li>
 Participates in USP EC/SC/EP meetings, scientific conferences/meetings, outreach visits and other events sponsored by USP and/or pharmaceutical industry, trade associations, and regulatory agencies and provides supporting scientific expertise at EC/SC/EP meetings, internal and external meetings, scientific symposia, industry forums.
 </li>
 <li>
 Standard setting responsibilities include:
 </li>
 <li>
 Prepares data summary packages, briefing materials and other technical documents for correspondence with EC/CS/EP.
 </li>
 <li>
 Manages action items from monthly EC /SC/EP telecom meetings.
 </li>
 <li>
 Tracks and reports frequently on the status of assignments to management.
 </li>
 <li>
 Facilitates the accomplishment of key departmental metrics.
 </li>
 <li>
 Assists in writing manuscripts for publication by USP (e.g., PF proposals, stimuli articles) or in peer-reviewed journals.
 </li>
 <li>
 Applies knowledge of current trends in public health to prepare information for Expert Committee to facilitate decision-making.
 </li>
 <li>
 Performs other related duties in support of the Excipients &ndash;Science Program Unit as assigned.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 
 
 <ul>
 <li>
 Scientist I: Ph.D. in Organic Chemistry, Analytical Chemistry, Biochemistry or allied filed and 7-10 years or MS in Organic Chemistry, Analytical Chemistry or Biochemistry or allied field and 11-13 years, respectively, of relevant experience.
 </li>
 <li>
 Scientist II: Ph.D. in Organic Chemistry, Analytical Chemistry, Biochemistry or allied field and 10-13 years or MS in Organic Chemistry, Analytical Chemistry or Biochemistry or allied field and 13-15 years, respectively, of relevant experience.
 </li>
 <li>
 Candidates must have experience related to excipient composition, quality, or analytical chemistry as well as outstanding written and verbal communication skills in English.
 </li>
 <li>
 Ability to review, analyze, and interpret and report on data from various analytical tests such as from HPLC, GC, LC/MS, GC/MS, IR, Raman, UV-Vis, NMR, ICP-MS, AA, etc.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Should possess strong technical knowledge in the areas of complex molecules/compounds such as polymers, fats, oils, waxes and plants.
 </li>
 <li>
 Must be able to share technical information with non-technical or non-scientific staff, and to communicate effectively with representatives from pharmaceutical companies, government, and academic institutions. Ability to rapidly assess technical complications to identify, define, and solve technical issues
 </li>
 <li>
 Well-developed organizational, interpersonal communications, negotiation, writing, and strong listening and presentation skills.
 </li>
 <li>
 Proficient with pharmaceutical testing requirements and test protocols involving USP-NF compendial methods development for Excipient monographs.
 </li>
 <li>
 The ability to influence without direct authority.
 </li>
 <li>
 Results driven demonstrated with successful outcomes.
 </li>
 <li>
 Project Management skills and ability to prioritize tasks and manage multiple projects simultaneously.
 </li>
 <li>
 Able to operate independently where appropriate yet understands when to escalate issues and how to establish effective working relationships.
 </li>
 <li>
 Ability and desire to work well with diverse employees and customers in a cooperative and friendly manner.
 </li>
 <li>
 Ability to handle multiple priorities in a fast-paced environment.
 </li>
 <li>
 Able to work flexible hours when needed.
 </li>
 <li>
 Prior experience in a scientific based industry.
 </li>
 <li>
 Excellent written and verbal communications skills
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 Benefits
 
 
 
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Sr Scientist I/ Sr. Scientist II, Documentary Standards (Excipients)

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a dynamic and experienced Formulation Scientist in Injectable division for designing and development of formulation process, ensuring quality by design (QbD) implementation, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 
 <ul>
 <li>
 You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval.
 </li>
 <li>
 You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections.
 </li>
 <li>
 You will be responsible to support in scale-up to pilot/plant scales for Injectable Products.
 </li>
 <li>
 You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions.
 </li>
 <li>
 You will be responsible for technology transfer and execution of the batches.
 </li>
 <li>
 You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up).
 </li>
 <li>
 You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development.
 </li>
 <li>
 You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 Masters in Pharmaceutical/M.Tech in Chemical Engineering
 
 
 
 
 
 Minimum work experience:
 
 5 to 8 years of experience in pharmaceutical company in Injectable products.
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Have work experience on Formulation Development and expertise in inhalation/injectable dosage form.
 </li>
 <li>
 Experience in areas of product development for Generic Injectable
 </li>
 <li>
 Experience in Quality by Design (QbD).
 </li>
 <li>
 Experience in Process Optimization and scale up.
 </li>
 <li>
 Experience in Operational Excellence.
 </li>
 <li>
 Knowledge on Good Manufacturing Practice and Good Laboratory Practice.
 </li>
 <li>
 Experience in Technology Transfer.
 </li>
 </ul>
 
 
 Behavioral
 
 
 Skills
 
 
 
 
 <ul>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Strong analytical and problem-solving abilities.
 </li>
 <li>
 Ability to work collaboratively with own team and cross-functional teams.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

Formulation Scientist

Veranova

<div>
 
 Discover Veranova:
 
 
 
 At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
 
 
 Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
 
 
 Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.
 
 
 
 Role Overview:
 
 
 
 The Process R&amp;D Scientist plays a key role in developing and optimizing synthetic routes for complex active pharmaceutical ingredients (APIs). This position conducts small- to large-scale chemical reactions and generates high-quality data that supports project decision-making and innovation. Working under the guidance of technical leads, the role contributes to delivering projects on time, on spec, and within budget. It&rsquo;s an excellent opportunity to deepen expertise while supporting impactful pharmaceutical development.
 
 
 
 Core Responsibilities:
 
 
 
 <ul>
 <li>
 Delivers experimental output with high scientific integrity, meeting targets, timelines, and quality expectations with guidance.
 </li>
 <li>
 Exhibits strong safety awareness, conducts laboratory and operational activities safely, and maintains accountability for safe behavior in the work environment.
 </li>
 <li>
 Maintains technical equipment and related services to ensure proper functionality.
 </li>
 <li>
 Acts on feedback and demonstrates a continuous commitment to learning and professional development.
 </li>
 <li>
 Leads technical and operational areas and supports troubleshooting for complex scientific issues with minimal guidance.
 </li>
 <li>
 Shares knowledge, skills, and experience effectively with internal and external stakeholders; may lead focused projects as a key contact.
 </li>
 <li>
 Keeps accurate, legible, and complete records of all experiments, observations, and equipment use.
 </li>
 <li>
 Writes high-quality reports and delivers presentations to customers and management with some guidance, aligned with project milestones.
 </li>
 <li>
 Contributes to maintaining strong customer relationships and identifies new commercial opportunities.
 </li>
 <li>
 Actively supports the technical development of the department and the broader organization.
 </li>
 <li>
 Ensures all documentation meets Veranova standards; supports audit readiness and participates in regulatory and customer audits as needed; reports near misses and safety incidents per company procedures; and ensures all work complies with applicable state and federal regulations, including GMP, DEA, and FDA requirements.
 </li>
 <li>
 Adheres to all EHS policies and procedures; demonstrates strong technical and procedural proficiency in applying EHS standards; supports EHS audit readiness and participates in audits; reports and cooperates fully in investigations of near misses and incidents; and upholds Veranova&rsquo;s EHS commitments by integrating ISO 14001, OHSAS 18001, and Sustainability 2025 principles into daily work.
 </li>
 <li>
 Performs additional duties within the employee&rsquo;s skills and abilities as reasonably assigned.
 
 
 
 </li>
 </ul>
 
 Qualifications:
 
 
 
 
 Required
 
 
 
 <ul>
 <li>
 PhD degree (or equivalent experience) in a chemistry related discipline.
 </li>
 <li>
 Proficiency with relevant lab and analytical techniques.
 </li>
 <li>
 Previous industry experience in relevant areas.
 </li>
 <li>
 Proficiency with relevant analytical techniques within an industry environment.
 </li>
 <li>
 Ability to write clear and concise technical reports.
 </li>
 <li>
 Good understanding of Microsoft Office and other relevant technical software platforms.
 </li>
 <li>
 Skilled in written and spoken communication and proven ability to effectively interact with management.
 </li>
 <li>
 Demonstrates good judgment, quick decision-making skills, and the ability to work independently and in a team environment.
 
 
 
 </li>
 </ul>
 
 Special Factors
 
 
 
 <ul>
 <li>
 Must be able to stand, walk, and manually operate objects, tools, or controls; reach with hands or arms; and climb, balance, stoop, kneel, or crouch when necessary for the job activity.
 </li>
 <li>
 Must be able to lift and/or move up to 50 pounds.
 </li>
 <li>
 Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus.
 </li>
 <li>
 May regularly work with moving mechanical parts and may work with toxic or caustic chemicals.
 </li>
 <li>
 May work in humid areas with low or high temperatures.
 </li>
 <li>
 May be required to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.
 
 
 
 </li>
 </ul>
 
 Salary Range
 
 : $105,000 - $120,000 annual base salary
 
 
 
 Our Commitment:
 
 
 
 <ul>
 <li>
 Health &amp; Wellness: Comprehensive health &amp; wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
 </li>
 <li>
 Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
 </li>
 <li>
 Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
 </li>
 <li>
 Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don&rsquo;t meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.
 
 
 
 </li>
 </ul>
 
 Additional Information:
 
 
 
 Applicants for this role must be authorized to work in the United States without further employer sponsorship.
 
 
 Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.
 
 
 All your information will be kept confidential according to EEO guidelines.
 
 
 Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
 
 
 All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .
 
 
</div>

Scientist - Process Research & Development

ONE NUCLEUS

3 Month Contract Near Cambridge UK Scientist / Bioanalytics, PK assays, MSD Candidates will need to be available to start quickly, be able to be based in Cambridge, have right to work in the UK and have experience with the above techniques. Some training could be given to certain areas lacking. Please send CV's direct via LinkedIn to Louisa Hodgson in the first instance and for suitable candidates she will organise a call to discuss more insight. This role will support a leader in a time of need, so if you can confidently help us with the above then we would welcome hearing from you with your CV. Candidates without the immediate right to work in the UK unfortunately cannot be considered.

Scientist / Bioanalytics, PK assays, MSD

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