Manager Global Technology Transfer (Sant Just Desvern (Barcelona), ES, 8960)
About this opportunity
Manager Global Technology Transfer
Barcelona | Spain | Full-time | Permanent
ABOUT US
At STADA we pursue the purpose of "Taking care of people's health as a trusted partner." All our decisions and actions are driven by our purpose, vision and values. With our wide range of products: Generics, Consumer Healthcare and Specialties, we offer patients, doctors and pharmacists a wide range of therapeutic options.
Around 13,000 employees live our values of Integrity, Entrepreneurship, Agility and One STADA, in order to achieve our ambitious goals and shape a successful future
for our company. We continually expand our goals in line with our ambition, and we achieve them with passion, commitment and a growth mindset.
Do you want to be part of a successful international pharmaceutical company and grow with us?
Manager Global Technology Transfer is responsible for leading end-to-end Technology Transfer execution providing Project Management, scientific and technical expertise, e.g., in quality, technology transfer, regulatory.
KEY RESPONSIBILITIES
Lead and manage Tech Transfer projects effectively and independently, ensuring deliverables are completed in time, at agreed costs and carefully balancing benefits & risks
Define Project strategy, Project Team and create end-to-end Project Plan capturing project risks including mitigation strategy
Coordinate cross-functional Project Team across internal stakeholders (Global and local TechOps functions: QA, QC, AS&T, MS&T, ESO, RA, Commercial Transfer Team), as well as the third parties when involved in the project scope (CMOs) e.g. transfer Projects to the Contract Manufacturer
Run project meetings to monitor project milestones, track project execution and report on progress
Ensure cross-functional alignment and joint decision-making, define actions in project meetings and follow up on execution with project team members
Provide scientific and technical expertise, e.g., in quality, regulatory, tech transfer and resolve issues which occur as part of daily business to ensure cross-functional information flow on the way to adhere to the project schedule
Consolidate Master Documentation (Technical Package) for BC calculation and provide technical expertise on transfer feasibility to the target site
Check that content of GMP documents is correct and complete and in compliance with the dossiers
Support manufacturing sites to produce trial and validation batches (provide onsite support)
Write Product Performance Review – Report after feasibility trials that summarizes conclusions and recommendation for validation batches
Prepare the updates to Module 3 according to technology transfer results
Prepare the variation documentation in accordance with local regulatory requirements of impacted countries
Support product launches from the new site following transfer in cooperation with Commercial Transfer Team, Supply Chain, QA, RA.
EXPERIENCE
University degree in Pharmacy, Chemistry/Chemical Engineering, Biology (Life Sciences) or comparable field
Fluent in English (written and spoken)
More than 5 years of work experience in Pharma Industry (in depth knowledge preferably in technology transfers, product development, manufacturing, or regulatory affairs). It can independently manage all areas of Tech Transfer Projects: quality, regulatory and technical
Project management experience and capability to lead multi-functional teams
Learning agility – as ongoing, proactive, and self-motivated pursuit of knowledge
Business/market/technology savvy - understanding business and impact on business
Growth mindset- sees obstacles as surmountable challenges
Strong problem solver with the ability to multitask and make sound decisions in a fast-moving environment
Integrity as concept of consistency of actions, values, methods, measures, principles, expectations, and outcomes
Open to travel globally flexibly
STADA Group promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of this diversity 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.
STADA offers a competitive environment for personal and professional development in a growing company full of opportunities.
Our future project requires dynamic and proactive professionals, capable of adding value in a changing environment.
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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 661 comparable Manager Manufacturing & CMC roles across 88 biopharma companies.
Salary context
205 of 661 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.
Where these roles are based
Top locations among the 661 comparable roles
+ 35 more countries
Seniority mix
661 of 661 peers have a known seniority level
Therapeutic area mix
9 of 661 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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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.
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.