The startups that grew out of the Pfizer redundancies

18 months on, three former Pfizer employees explain how they’ve seized opportunities to fill gaps in the market

In November 2023, Pfizer announced plans to discontinue its pharmaceutical sciences small molecule capabilities at its Discovery Park location in Sandwich, UK, to consolidate the facilities at two sites in the US and India. This decision, which impacted around 500 roles, was met with shock, sadness and an outpouring of support from the scientific community.

However, in the 18 months since, a number of ex-Pfizer employees have led the formation of a variety of startups which, with the support of Pfizer and Discovery Park – where many of them have remained – have been able to hit the ground running.

Chemistry World speaks to three ex-Pfizer employees who have taken the challenge of redundancy and turned it into an opportunity to funnel their expertise into exciting, and much needed, new ventures.

Particology

Ivan Marziano, previously a research fellow at Pfizer, was just about to mark his 25th year at the organisation when the redundancy announcement was made. However, by August 2024 he and his five co-founders, also ex-Pfizer, had launched Particology; a contract research and development organisation providing expert particle technology services to the pharmaceutical, nutraceutical, agrochemical, cosmetics and veterinary medicine industries.

‘When you look at drug development, most of the emphasis is on the synthesis of the active ingredient and then on its formulation, but there’s an often neglected area between the two,’ Marziano explains.

‘Essentially, we aim to fill that space to make sure that when you complete your synthesis and turn your active ingredient into particles, these have the right chemical and physical attributes to ensure successful formulation.’

The company is based at Discovery Park using the same lab space that some of the team were already working in, which, Marziano says, was ideal because many of the facilities were bespoke, with equipment that they themselves had purchased.

When his colleagues came to him with the idea of starting their own company, Marziano says there were three main reasons he agreed to join them, rather than accept an offer of employment from a more established party.

‘The first thing was the fact that we’d applied a certain drug development philosophy in all the projects that we worked on together, so we wanted to try and apply those workflows for the benefit of other companies,’ he says.

‘The second thing was that we share a certain set of values and have a lot of respect for one another, but at the same time, we knew that building that similar environment in another big company was going to be different and difficult, so we wanted to preserve that ethos.’

Finally, he said that they were very keen to remain in the Sandwich area.

‘East Kent is a deprived area and the thought that we could do something to help the scientific community through outreach and creating employment opportunities was particularly appealing,’ he explains.

For Particology, and many other startups that have arisen following the redundancies, the support from Discovery Park has been hugely important in providing advice and contacts to aid them in the legal and practical sides of setting up a new business.

‘They were foundational in helping us form an understanding of the basics of the business, and making contact with other parties that could help us in our journey,’ Marziano says. This support, partnered with their collective expertise, meant that once they’d agreed the lease on the facilities and paid for the equipment they were up and running and able to produce billable hours relatively quickly.

Since then, the company has gone from strength to strength, doubling in size in less than a year and recruiting new talent in a variety of roles. Marziano says he’s also really excited about the fact that they’ve started to establish relationships with local research institutions, including the University of Kent and Canterbury Christchurch University.

The biggest surprise for him venturing out into the startup world was realising just how insular he had become working for a big corporation.

‘I did not feel the incentive to just look outside my immediate environment,’ he says. ‘And now that I find myself in this position, I realise that there is a thriving scientific and business community within Discovery Park – it’s been amazing to talk to people and start thinking about projects that we can work on together.’

Matheus Engineering

Jinu Mathew and her husband Suju both worked at Pfizer for nearly 20 years, so the news that they were being made redundant was met initially with shock and then sadness that they were going to lose the ‘family’ that had formed over that time.

However, several years previously Suju had mentioned that he aspired to venture out alone at some point. ‘[At the time] I brushed the idea aside, saying that nobody in their sound mind would leave a job to start their own business,’ says Mathew. The pair also had to consider that starting a company with just the two of them would mean, to a certain extent, they would have to put ‘all eggs in one basket’.

‘When there are different founders in an organisation, it’s a bit easier because your family is not at risk, whereas we had to consider that aspect as well,’ she says.

Like Marziano, they were fortunate to benefit from a variety of support offered by Pfizer and Discovery Park, and it was during one of the talks they put on that the Mathews were inspired to ‘take the leap’.

‘You’ve got to do it at the right moment with the right opportunities there. We were getting lots of support, and we felt that was the moment, if we were going to make it, we had to do it.’

Combining the Mathews’ collective expertise in chemistry, physical organic chemistry and chemical engineering, Matheus Engineering covers all aspects of scaling-up chemical processes, with the core mission of bridging the gap between lab and plant.

‘We identify problem statements in a small-scale vessel and design bespoke scale-up solutions,’ she explains. ‘Evaluating and predicting the future performance of a process is vital for scalability and sustainability. Batch failure remains one of the most critical challenges in manufacturing, often leading to production delays, increased cost and compromised quality.’

Their work is not purely lab-based, but a combination of experimental and theoretical approaches. ‘We handle all unit operations,’ Mathew explains. ‘Reaction is only one part of the whole picture when you make a molecule, then you need to get the molecule out of the pot and turn it into an end product.’

‘We knew there was a niche market there, but it takes a lot to turn it around into a business,’ Mathew adds.

Due to the specific skill set required for the work, Mathew says anyone they recruit into the team needs to be carefully trained, so they knew patience and perseverance would be the key to building the company up.

‘There are certain things which require decades of experience and training in highly specialised areas – that’s the heart of the business,’ she explains. In October 2024, they hired another ex-Pfizer colleague and a fourth member of the team will be starting in July.

Also still based at Discovery Park, in a lab that Suju helped to design in 2006, the Mathews were fortunate to have access to advice around setting up the various supporting functions critical for a startup, including accountancy, insurance, waste management and procurement, which Mathew admits she had never had to deal with before.

‘We have an IT group based in Discovery Park who are managing IT infrastructure for all the startups, so that was a massive help,’ Mathew adds. ‘If nothing existed there, it would have been a bit of a challenge.’

Every day they have to wear multiple hats, she says: ‘You are a scientist by heart, but as a business owner that’s not what you do all the time. 10am I am doing lab work, but 11am I’m an accountant, or an EHS [Environmental, Health and Safety] person.’

However, she says there are ‘no regrets’ and that she is looking forward to catering to their niche market and building a vibrant scientific team that in many years’ time they can look back on and be proud of.

Biowaived

A pharmacist by background, Mark McAllister led the global biopharmaceutics group at Pfizer, a group of around 25 scientists spread across the UK, US, Europe and India, focused on predicting formulation performance using laboratory and computational tools.

‘For those of us who were located in the UK, the [redundancy] announcement was hugely impactful but we very quickly came to the conclusion that fundamentally we enjoyed what we were doing,’ says McAllister.

He and his colleagues had had conversations about starting their own business back in 2011, when Pfizer announced it was exiting Sandwich (a decision that was reversed in part). The announcement in 2023 gave them the chance to revisit those conversations, ultimately leading to the establishment of Biowaived, which aims to deliver biopharmaceutics and dissolution strategies to help support companies with drug product development.

‘We felt [Biowaived] would be really valuable to other companies who didn’t have their own biopharmaceutics group, and we thought we could make a difference to them in terms of understanding drug product design and performance in patients,’ says McAllister.

McAllister explains that biopharmaceutics, not to be confused with biopharmaceuticals, is a multidisciplinary area comprising formulation, drug delivery, clinical pharmacology, regulation and analytical science.

‘It’s all around understanding what happens to the drug product when a patient takes it – where physiology meets pharmaceutics. Our science is unravelling the complexity of that process.’

From their own experiences of trying to access new technologies, new capabilities and additional support at Pfizer, McAllister and his four co-founders knew there were ‘only a handful’ of companies that do what Biowaived does with the same level of expertise.

‘We’re not a big [contract research organisation] like some of the other players who specialise in this area, and I think that’s where our strength is,’ he says.

Biowaived was established in April 2024 and became operational in September. As well as receiving considerable support from Pfizer and Discovery Park – where they too are based – they also worked with Kent County Council on their small business boost loan to provide them with the funding to expand in those early months.

They were able to work quickly to secure lab space, reconfigure the laboratory operation and agree a deal to buy equipment from Pfizer. However, moving from a science-based role to a business that delivers the science required them to adopt a new way of thinking.

‘The challenge … is thinking about the balance between consolidation and growth and being able to have everything that you need to go out and talk to other companies confidently; to be able to say “we can do this work for you”.’

As a team they have had to dedicate time to thinking about what Biowaived looks like to the outside world.

‘None of us are really good at social media – it’s that external aspect that is difficult and it’s only in the last few months that we’ve begun to be a bit more confident about that and think about how we tell our story to others,’ McAllister says.

Moving from a big company to a small startup also comes with the realisation that ‘there’s stuff you’ve just got to do’, McAllister says, which can mean the boundaries between life and work can become blurred. But there are benefits to this too.

‘We were able to set up a three-way collaboration with just a half hour meeting,’ says McAllister. ‘That would have taken a couple of months in big pharma.’

Biowaived is now starting to grow, with the recruitment of three employees and plans to bring on more in the next year. McAllister admits they are further along than they initially expected.

‘If somebody had said to me this time last year, we will be running a business that can pay its bills, that is engaging with a number of different clients, is growing in terms of we’ve got first employees coming on board, we’ve got access to all the laboratory equipment we need, we, importantly, also have the critical software we need through a strategic partnership with Certara … I wouldn’t have believed them.’

Article originally published on ChemistryWorld, written by Julia Robinson, Science Correspondent. 

Copyright: ChemistryWorld /Julia Robinson. 

https://www.chemistryworld.com/careers/the-startups-that-grew-out-of-the-pfizer-redundancies/4021629.article

Macmillan Coffee Morning

📅 Wednesday 24th September 2025 📍 Innovation House, 2nd Floor, opposite the Social Zone

From 11am until the last slice is gone, we’ll be serving delicious cakes and treats in support of Macmillan Cancer Support.

If you’d like to get involved, you can either whip up something tasty at home or pick up a sweet treat from the shop — just let Janice know at J.Noble@newappointmentsgroup.co.uk.

Or, simply drop by, join the fun, and help us in the most enjoyable way possible… by eating cake! 🍰

 

Unbe-leaf-able Free Salad

📅 Thursday 21st August 2025 📍 Innovation House Foyer

GrowUp will be showing up at Innovation House with free salad bags worth leaf-ing your desk for. No pesticides, no cutlery, no fuss – just bags full of bold, fresh flavour.

Senior Manager, Global Labelling Lead

Position: Senior Manager, Global Labelling Lead at Pfizer
Location: Discovery Park, Sandwich, Kent 
Role: Permanent

About the job

The Senior Manager, Global Labelling Lead (GLL) has overall accountability for the development and execution of global labelling strategy for their assigned products.

This includes managing the end-to-end process of Target Labeling in early development, creation and maintenance of Core Data Sheets (CDS), and submission and label negotiations for US Prescribing Information (USPI), and EU Summary of Product Characteristics (EU SmPC).

This role offers high visibility and the opportunity to work cross-functionally with SMEs, contribute to organizational strategic initiatives, and support Pfizer’s Internal Medicine, Inflammation & Immunology, and Non-malignant Hematology pipeline. The successful candidate should possess an eagerness to grow, an aptitude for strategic thinking, and a focus on delivering for patients.

Role Responsibilities

  • Lead the development, maintenance, and implementation of high quality labeling including CDS, USPIs, EU SmPCs, and patient labeling
  • Author labeling content de novo based on scientific source data, understanding of regulations and guidance, and label precedent
  • Manage cross-functional Labeling Team and collaborate with stakeholders including Clinical, Medical, Safety, Regulatory, and Commercial
  • Drive global labeling strategy through development of target labeling, scenario planning, and risk mitigation
  • Manage label negotiations with US FDA and EMA
  • Provide guidance on labeling regulations, industry best practices, and competitor label assessments
  • Act as the primary labeling representative on Global Regulatory Strategy Teams, Submission Working Groups, and other relevant product teams
  • Contribute to strategic initiatives and process improvements across the organization

Qualifications:

  • Degree in a scientific or technical discipline plus years of relevant labeling experience in the pharmaceutical or biotech industry:
    • PhD/PharmD with 1+ years work experience
    • Master’s degree with 5+ years work experience
    • Bachelor’s degree with 6+ years work experience
  • Advanced knowledge of external labeling guidelines and regulations
  • Ability to successfully understand regulatory implications of product strategy with regards to the product label, assessment and practical management of associated impacts.
  • Ability to develop strong and positive working relationships with cross-functional stakeholders and SMEs
  • Excellent written and verbal communication skills; complete fluency in English language
  • Proven strength in logical, analytical, and writing ability
  • Strong project management skills and attention to detail
  • Proven ability to negotiate, influence, and problem solve

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Additional Information:

  • Work Location Assignment: Hybrid and will require 2 to 3 days a week to work from site
  • Last Day to Apply: August 8, 2025

The annual base salary for this position ranges from $120,800.00 to $201,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

For more information and to apply

Respiratory Technical Leads (Analytical, Formulation and Project Lead Roles)

Position: Respiratory Technical Leads (Analytical, Formulation and Project Lead Roles) at Viatris
Location: Discovery Park, Sandwich, Kent 
Role: Permanent

The Role & What You Will Be Doing

We have exciting new opportunities in our global respiratory R&D group at Senior Manager and Director level across multiple technical disciplines (analytical, formulation, and project lead).  These roles will play a central part within Viatris in creating new respiratory products by applying technical expertise and leadership to the development of our portfolio of NCE and generic products.  Technical leadership opportunities exist for candidates with specialised expertise of inhaled and nasal products, including pressurised metered dose inhalers and solutions / suspensions for nebulization.  Candidates with substantial experience in the development of inhalation products will be ideal to join our science-focused department where technical excellence delivers innovation for Viatris.

Every day, we rise to the challenge to make a difference and here’s how the Respiratory Technical Leads (Analytical, Formulation and Project Lead Roles) role will make an impact:

  • Lead the delivery of project activities to take new respiratory products to clinical studies and commercialization.
  • As a member of multidisciplinary project teams, support the planning and execution of experiments to generate scientific understanding in development of analytical methods, formulations and/or manufacturing processes.
  • Ensure the smooth transfer of analytical methodologies or manufacturing processes to commercial facilities.
  • Lead the review and/or approval of data, interpretation of results and reporting of experimental outcomes to project development teams.
  • Lead scientific input to troubleshooting and investigations.
  • Shape formulation design and scale up strategies and overall project plans through input and leadership at matrix team technical discussions.
  • Prepare, review and approve documentation (e.g.  protocols, reports, procedures, specifications) as required.
  • Deliver and/or lead the input to investigational and commercial drug product regulatory filings.
  • For people manager roles, take responsibility for performance management and professional development of staff within the team.
  • Lead the improvement of departmental capabilities, e.g. by implementation of new technologies.

About Your Skills & Experience

For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

  • Minimum of a Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Forensics, Chemical Engineering, Pharmacy, Pharmaceutical Sciences) or equivalent.
  • Substantial experience of pharmaceutical product development, including the development of inhalation products.
  • Substantial experience in the management of activities to achieve project deliverables.
  • Highly effective verbal and written communication skills.
  • For people manager roles, substantial experience in performance management and personal development of others.
  • Substantial   experience   in   authoring   GMP   documentation   and   preparing   regulatory submissions.
  • Substantial experience of the challenges involved in the validation and transfer of complex analytical methods or transfer of manufacturing processes to commercial facilities.
  • Substantial experience of the specific challenges involved in the development, approval and commercialization of inhaled products.
  • Able to lead the interpretation of complex data to solve product development issues.
  • Able to proactively identify and address barriers to collaborative working with internal and external partners.
  • Able to work autonomously to deliver multiple tasks of high complexity across a portfolio of products, working with internal or external teams to plan work to consistently achieve output of high-quality results in a timely manner.
  • Has a good understanding of cGMP requirements for analytical work in support of clinical studies and product registration.
  • Familiar with the use of project management tools, e.g. Microsoft Project.
  • Occasional business travel as required.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Benefits At Viatris

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary:

  • Top Employer Accreditation, demonstrating that we provide excellent people policies and practices
  • Focus on career progression with growth and development opportunities
  • Emphasis on Health & Wellness programmes
  • 100% paid medical insurance and Employee Assistance Programme
  • Life cover
  • Excellent employer-matched pension scheme with Viatris contributing up to 11%
  • 2 paid volunteer days per year

For more information and to apply

Principal Scientist/Engineer, Device and Product Performance

Position: Principal Scientist/Engineer, Device and Product Performance at Viatris
Location: Discovery Park, Sandwich, Kent 
Role: Permanent

Key responsibilities for this role include:

  • Provision of subject matter expertise to support the development of Combination Products
  • Leading a team to plan and execute design verification and reliability strategies.
  • Responsible for technical interface between drug product and device teams during combination product development ensuring formulation and manufacturing development activities are compatible and align with device development.
  • Responsible for the development of design requirements and specifications based on characterization of comparator products, regulatory requirements, design intent and user requirements.
  • Responsible for developing test methods and specifications to assess device functionality and product performance including evaluation, procurement & implement new, state-of-the-art lab testing equipment as applicable.
  • Responsible for material assessment of device components including biological evaluation, extractables profiling and material certification.
  • Provide technical support to manufacturing sites during filling and assembly process development by providing device controls and sampling plans.
  • Use of statistical techniques or data analysis such as hypothesis testing, confidence and tolerance intervals, regression, capability analysis, DOEs, etc., to inform design decision making and conclusions for deliverables like test method validations, design characterizations and verification, and reliability.
  • Ensures all activities within team are conducted and executed to the appropriate quality standards within the GDD Quality Management system.
  • Lead support activities for external and internal audits and inspections as applicable.

The minimum qualifications for this role are:

  • Degree in Science/Engineering (Master’s preferred)
  • Proven experience in pharmaceutical and/or medical device development
  • Working knowledge of design control requirements in line with FDA 21 CFR part 820 and ISO 13485 would be an advantage
  • Experience in the development and validation of analytical methods
  • Experienced in application of statistical techniques for data analysis
  • Experience of writing and supporting regulatory submissions
  • Highly driven and motivated person who can work as part of a flexible, dynamic team whilst taking responsibility for individual tasks in a Subject Matter Expert role.
  • Well-developed communication skills to lead or facilitate effective discussions. Able to communicate technical and/or project information to key stakeholders.
  • Some travel will be required as part of this role.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Benefits At Viatris

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary:

  • Top Employer Accreditation, demonstrating that we provide excellent people policies and practices
  • Focus on career progression with growth and development opportunities
  • Emphasis on Health & Wellness programmes
  • 100% paid medical insurance and Employee Assistance Programme
  • Life cover
  • Excellent employer-matched pension scheme with Viatris contributing up to 11%
  • 2 paid volunteer days per year

 

For more information and to apply