Senior Manager Parenteral and Liquids Development

Biopharma Careers; Antwerpen; Hybrid; EUR 120,000 - 160,000; Full time

Job summary

Johnson & Johnson in Beerse, Belgium, seeks a Senior Manager/Associate Director for Parenterals & Liquids Development. You will advance formulation and process development across modalities, run technology transfers, and deliver regulatory submissions to support programs in Beerse.

Lead multiple projects, align with CMC objectives, and uphold GMP, quality, safety, and environment guidelines while driving cross-functional collaboration within Drug Product R&D.

Qualifications

• Leadership experience across multiple programs.
• Strong track record in formulation and process development.
• Experience delivering regulatory submissions.

Responsibilities

• Advance formulation and process development for small molecules, peptides and oligonucleotides.
• Run technology transfers.
• Deliver regulatory submissions.
• Plan resources and set priorities for overlapping programs.
• Ensure GMP, quality, safety and environmental standards are met.

Skills

People leadership

Project management

Regulatory submissions

Technology transfer

GMP knowledge

Job description

# Senior Manager Parenteral and Liquids DevelopmentBeerse, Belgium Full timeOther / Corporate Functions ManagerNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson 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 opportunityAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.**Job Function:**Discovery & Pre-Clinical/Clinical Development**Job Sub Function:**Pharmaceutical Product R&D**Job Category:**People Leader**All Job Posting Locations:**Beerse, Antwerp, Belgium**Job Description:**Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicineWe're hiring a **Senior Manager / Associate Director** into our **Parenterals & Liquids Development (PLD)** department within Drug Product Research & Development in Beerse, Belgium. We'd love to hear from you!In PLD we design every parenteral and liquid formulation and process across the Janssen R&D Synthetics portfolio, from late Discovery through Commercialization. We develop solutions, microsuspensions, nanosuspensions, liposomes, microspheres, biodegradable rods, in situ forming gels and SEDDS. We deliver them through nearly every route: oral, buccal, IV, IM, SC, intra-organ, intra-tumoral, topical, nasal, ophthalmic, transdermal, intra-thecal and lung/inhalation.**The role**Advance formulation and process development for small molecules, peptides and oligonucleotides. Run technology transfers. Deliver regulatory submissions. Guide several programs at once and keep them aligned to CMC objectives and timelines. Apply Best Product at Pivotal and Speed to the Clinic principles. Plan resources, set priorities and decide what comes first when programs overlap. Uphold quality, compliance and safety, and know the rules that apply, GMP included, along with Safety, Health and Environment.