CSL Behring AG (CH) Posted September 4, 2026

Global Regulatory Affairs Manager

Bern, Switzerland Full time
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CSL Behring AG (CH) has closed or removed this posting -- see current similar openings below.

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About this opportunity

Responsibilities: • Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals needed to conduct current and future business activities; and produce, sell, and distribute its goods and services. • Support development of consistent roles and work processes. • Oversee development of plans, cost estimates, and schedules. Acquire the necessary permits and approvals. • Monitor regulatory developments and advise management on the potential impact of regulations on the organization. • Establish and maintain positive relationships with government agencies and other regulatory authorities. • Represent the organization in matters before regulatory, legislative, or industry standards agencies so the organization's interests are advanced. • Prepare materials for legal counsel or external consultants. • Create and compile of registration application documentation. • Regulatory system, data entry and maintenance in/of regulatory systems.

Qualifications: • Bachelor degree in a Life Science or Business Advanced degree in a Life Science (PhD, MD) or Business (MBA) an advantage. • 3+ years regulatory experience in the pharmaceutical industry. Biologics Regulatory experience preferred.

Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor  visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .

 

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL .

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

 

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Bern, Switzerland
Employment type
Full time

How this role compares

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

We currently track 192 comparable Manager Regulatory Affairs roles across 63 biopharma companies.

192Comparable roles tracked
176Currently active
63Companies hiring similar roles
33Countries represented

Salary context

52 of 192 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate, Quality Records · Pfizer $64,600/yr – $107,600/yr
Peer group range $86,100 – $245,000 (median $180,500)

Where these roles are based

Top locations among the 192 comparable roles

United States77
India19
Japan13
United Kingdom12
Poland10
Canada9

+ 27 more countries

Seniority mix

192 of 192 peers have a known seniority level

Manager137
Associate Director45
Associate10

Therapeutic area mix

16 of 192 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology10
Immunology3
Dermatology & Aesthetics2
Neuroscience1

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This posting is closed, but here are live openings closest to it -- ranked by similarity, not by how well you'd qualify for them.

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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.

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.

50%
Associate Director, Regulatory Affairs - Digital Health, Device & Combination Products (all gender)
Merck KGaA · Eysins, Vaud, Switzerland · Associate Director
Function Therapeutic area Adjacent seniority Country
45%
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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Senior Manager, Global Regulatory Affairs – Business Process
McDermott Laboratories Limited · Northern Cross, Ireland · 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.