STADA Arzneimittel Posted October 6, 2026

Regulatory Affairs Placement Student (Huddersfield – The Globe, GB, HD7 5JN)

Huddersfield – The Globe, United Kingdom Type not listed
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STADA Arzneimittel is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s Health as a Trusted Partner. Together we are shaping the future of Thornton & Ross by living our values of Integrity, Entrepreneurship, Agility and One STADA.

STADA UK Thornton & Ross – Regulatory Affairs Placement Student

Huddersfield |U.K.| Full-time | 12-month Fixed Term Contract

Commencing July 2027 | Salary £28,000

Step into the world of Regulatory Affairs and turn theory into real‑world impact. On this year‑long placement, you’ll help keep licensed medicines and everyday healthcare products safe, compliant and on the market – all while being fully trained from day one.

No regulatory experience? Perfect. This role is designed for curious students starting from scratch. You’ll be embedded in our Regulatory Affairs team, getting hands‑on with day‑to‑day submissions, contributing to new and existing product projects, and seeing how products are managed throughout their lifecycle. Along the way, you’ll discover how different healthcare products are regulated and work with teams across the business to help bring compliant, trusted products to patients and consumers.

How You Will Make an Impact

Get hands-on with real regulatory work on medicines and healthcare products, supporting submissions, registrations, packaging, artwork and product updates

Play an active role in New and Existing Product Development projects, maintaining trackers and documentation and joining cross-functional project meetings

Build a strong foundation in how different healthcare products are regulated, from marketing authorisations and product information to post-market activities and regulatory intelligence

Work closely with R&D, Artwork, Vigilance, Quality, Supply Chain, Commercial and Marketing to see how Regulatory Affairs underpins safe, compliant products

Contribute to lifecycle and compliance activities, from tracking safety and regulatory actions to supporting audits and suggesting simple process improvements

Develop your professional work habits: organise your tasks, communicate clearly, follow procedures, protect confidentiality and collaborate respectfully across the business

What We Are Looking For

Open to newcomers – no previous Regulatory Affairs or pharma experience needed

Studying a degree, ideally in science, pharmacy or life sciences, with a strong appetite to learn

Genuine interest in healthcare, medicines, medical devices or how products are regulated

Sharp attention to detail and comfortable working carefully with documents, data and information

Clear written and verbal communicator with basic Microsoft Office skills and readiness to pick up new systems and tools

Organised, curious and collaborative – able to manage your workload, meet deadlines and ask for support when needed

 

How we care for you

At Thornton & Ross our purpose “Caring for people’s health as a trusted partner” motivates us every day. And what would be a better place than starting with our own employees. Which is why we give much in return:

💸 Competitive annual salary of £28,000

🗝 Salary Sacrifice Pension Scheme.

⌚ Hybrid working – we spend three days of your choice in the office, with the remaining days working at home.

🌴 25 days of annual leave plus bank holidays with the potential to buy up to 5 additional days.

💉 Free winter flu jab.

🧠 Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family.

🚲 Cycle to Work Scheme.

🎉 Plus, many more employee benefits & celebration events.

STADA Group values and promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology, or sexual orientation. We use the strength of our uniqueness to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation, and the promotion of an inclusive working environment. We are looking forward to your application and welcome applications without a pharmaceutical background.

#LI – MN1

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Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Huddersfield – The Globe, United Kingdom
Employment type
Not listed

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 554 comparable Regulatory Affairs roles across 108 biopharma companies.

554Comparable roles tracked
532Currently active
108Companies hiring similar roles
49Countries represented

Salary context

152 of 554 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $75,038 – $380,750 (median $198,225)

Where these roles are based

Top locations among the 554 comparable roles

United States231
India44
Japan33
United Kingdom30
Poland25
Ireland21

+ 43 more countries

Seniority mix

432 of 554 peers have a known seniority level

Manager181
Director73
Associate Director53
Senior46
Senior Director22
Intern/Fellow/Postdoc22
Principal15
Associate10
Executive/VP10

Therapeutic area mix

44 of 554 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology14
Immunology10
Rare Disease6
Dermatology & Aesthetics5
Neuroscience3
Vaccines & Infectious Disease3
Cardiovascular / CVRM2
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
AbbVie Maidenhead, ENGLAND Manager
Same function Same country
40%similar
Vertex UK Int'l HQ/R&D Paddington, United Kingdom Director
Same function Same country
40%similar
AbbVie Marlow, England Manager
Same function Same country
40%similar
Ipsen Biopharm Ltd London (UK), United Kingdom Director
Same function Same country
40%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Same country
40%similar
Regeneron UK Limited Uxbridge1, United Kingdom Director
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in the United Kingdom, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Senior Manager, Regulatory Affairs
AbbVie · Maidenhead, ENGLAND · Manager
Function Therapeutic area Seniority Country
40%
Regulatory Affairs Manager Advertising and Promotion
AbbVie · Marlow, England · Manager
Function Therapeutic area Seniority Country
40%
EU Regulatory Affairs Manager (Biosimilars)
Amgen Limited · Uxbridge, United Kingdom · Manager
Function Therapeutic area Seniority Country
40%
Senior Regulatory Submission Project Manager
Ipsen Biopharm Ltd · London (UK), United Kingdom · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.