Senior Process Development Specialist

Ferring Pharmaceuticals·
Kastrup, Denmark
5d ago
Full-timeSeniorManufacturingGastroenterology
Market Rate — Industrial Engineers
25th
$78K
Median
$99K
75th
$123K

BLS 2024 data (national)

Description

<h2><b>Job Description:</b></h2><h1><b>Senior process specialist for late-stage drug product development </b></h1><p></p><p><b>Are you passionate about l</b><b>ate-stage drug product development</b><b>? Do you thrive by leading activities in a fast-paced environment that demands clear decisions and strong execution with high scientific standards?</b></p><p><br />This role offers broad organizational exposure and collaboration and is a chance to truly stand out in a lean organization where great work is quickly recognized. You will collaborate closely across device development, formulation, and other key functions, and have a real opportunity to make an impact on critical late-stage projects within a small, dedicated team.</p><p><br /><b>Our International Pharma Science Center (IPC) in Denmark – Part of Ferring Pharmaceuticals</b><br />Ferring Pharmaceuticals is a global leader in reproductive medicine, maternal health, and key areas within gastroenterology and urology.<br />By joining our International Pharma Science Center (IPC) in Kastrup, you become part of Ferring’s global network—collaborating across functions in a state-of-the-art waterfront building with stunning views of Sweden and easy access to Copenhagen Airport.<br />You’ll work mostly on-site with 600 highly skilled colleagues in an international, dynamic, and collaborative environment.<br /> </p><p><b>Ferring &#43;You – Our collaboration</b><br />You will join a small, highly dedicated team supporting projects at late stages of development. The team is working with the development of drug products in a variety of dosage forms and modalities including peptides and small molecules, proteins, gene therapies, and more recently, microbiome-based therapies.  For us, the key to success is collaboration and support, and we expect a future team member to actively take part in preserving this culture. The team is based in Kastrup and reports to the Senior Director, Process Development, Manufacturing and Device.</p><p></p><p><b>Your day at Ferring - Tasks where you are accountable </b><br />You will work with process development and IMP manufacturing, focusing on developing a robust manufacturing process which comply with regulatory requirements whilst meeting the expectations of commercial manufacturing.</p><p></p><p>Your primary tasks will be to:  </p><ul><li><p>Represent Process Development and GMP manufacturing in CMC project teams and drive development strategies.</p></li><li><p>Establish, oversee, and support process development at CMOs, ensuring timelines and quality standards are met.</p></li><li><p>Author and review technical reports and regulatory documentation (e.g., IND/BLA/CTD) and handle authority questions.</p></li><li><p>Facilitate technology transfer to Ferring’s commercial manufacturing organization.</p></li><li><p>Take key responsibility for lates-stage development work</p></li></ul><p>Your work location will be on-site at our state-of-the-art International PharmaScience Center in Kastrup</p><p></p><p><b>Behind our entrepreneurship … there´s your skills</b><br />Most importantly, you bring process development and GMP manufacturing expertise. However, the role also requires an interest in project management, as you will be responsible for coordinating activities with external and internal partners. You will also need to apply structured problem-solving tools for troubleshooting</p><p></p><p>Therefore, you should have:</p><ul><li><p>Experience as a Subject matter expert ( &gt; 10 years) in process development and IMP manufacturing</p></li><li><p>Strong expertise in GMP and aseptic/sterile drug product manufacturing (fill–finish).</p></li><li><p>Proven experience in late-stage drug product development, including phase II all the way up to submission activities.</p></li><li><p>Solid track record in CTD authoring, responding to authority questions, and late-stage lifecycle management.</p></li><li><p>Demonstrated scientific project management skills and the ability to drive cross-functional work.</p></li><li><p>Collaborative mindset and the ability to work effectively across cultures and functions.</p></li><li><p>Excellent written and verbal English communication skills.</p></li><li><p>M.Sc. in pharmaceutical process science or a related scientific discipline.</p></li></ul><p><br /><b>Become a part of Ferring – apply now</b><br />If our mission and your vision are aligned, apply via the link in the job ad and include a short motivation in your CV.<br />Please note that applications are reviewed continuously, and we close the process when we find the right match.<br /><br /><b>Candidates must be located in the Øresund region as the position is onsite.</b></p><p><b>Note to agencies:</b><br />This search is being managed by Ferring’s Talent Acquisition team. Kindly do not send us unsolicited profiles.<br /><br /><i><span><b>About Ferring Pharmaceuticals.</b><br />At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused in the areas of reproductive and women’s health, gastroenterology, and urology. Ferring &#43; You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. Read more at ferring.com.</span></i></p><p></p><h3></h3><h2><b>Location:</b></h2>Ferring Denmark
Ferring Pharmaceuticals

Ferring Pharmaceuticals

PHARMACEUTICAL

Small Molecule Manufacturing

LocationArgentina - Buenos Aires
Employees5000+
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Neurology
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AMPLEXN/A
MesalazineN/A
EUFLEXXA™N/A
hMG-HP/r-FSHN/A
Sodium Picosulfate, Magnesium Oxide and Citric AcidN/A