VP Head CMC

ProQR Therapeutics is a biotechnology company listed on NASDAQ with offices in Leiden the Netherlands and Cambridge Massachusetts USA. ProQR is focused on the development of life changing RNA therapies to meet the unmet need of individuals and families with common and rare diseases. A team of 150 enthusiastic ProQRians from all walks of life and more than 30 different nationalities is up to this challenge. We have the passion and commitment to make a difference in the lives of the communities we serve. Our proprietary Axiomer RNA editing technology platform enables the editing of specific single nucleotides in RNA using the cells own editing machinery. Axiomer RNA editing technology harnesses ADAR (Adenosine Deaminase Acting on RNA) which is machinery present in all human cells to repair GtoA mutations modulate protein and enable protective mutation functions. Axiomer could potentially yield a new class of innovative medicines and treat currently untreatable diseases.

We are currently looking for an experienced VP Head of Chemistry Manufacturing & Control (fulltime) to join our team.

Location: Leiden NL

The CMC Department:

The Chemistry Manufacturing and Control (CMC) Department has a central role within the ProQR Therapeutics organization. The CMC Department develops manufactures and characterizes oligonucleotides and therapeutic formulations for preclinical and clinical phase development. We have several programs in earlystage development as part of our Axiomer RNA editing platform. Our way of working involves a combined approach of inhouse high throughput manufacture and smallscale early development in newly refurbished laboratories and outsourced development scale up and GxP activities.

The role:

We are looking for an experienced professional in Chemistry Manufacturing & Control to lead the CMC department. The Head of CMC has developed products from Discovery through to late phase clinical studies with a diverse background in CMC drug development and supply chain. In addition the Head of CMC has a strong background in people management and brings a network in the CMC space.

The Head of CMC is ultimately accountable for the ontime delivery of investigational product supplies. In addition the head of CMC is accountable for the CMC content of the regulatory dossier and subsequent authority interactions. The span of control of the Head of CMC ranges from preclinical Phase I Phase II/ Phase III.

The candidate will lead a department of approximately 30 employees covering Drug Substance Drug Product Analytical and Clinical Supplies Management and Logistics and is accountable for inhouse laboratories vendor network and other external relationships. In the current phase of the company the VP CMC also has an enterprise accountability for Quality the training and documentation are coordinated by a small internal team while the other Quality operations are outsourced.

The Head of CMC is part of the companys leadership team.

Tasks and key duties:

• Accountable for developing and executing the Chemistry Manufacturing & Control strategy for pipeline products.
• Accountable for the budget and financial performance of the CMC department
• As a member of the Leadership Team contribute to the development of corporate goals and take accountability for delivery.
• Responsible for overseeing and enabling activities to ensure the efficiency and effectiveness of the CMC department and ProQR as a whole utilizing data trending and risk management tools.
• Identify and analyze highimpact complex and crossfunctional business issues and gaps. Make sure continuous improvement of processes is embedded in the organization. Embed an environment of innovation and cultivate new (scientific) insights.
• Responsible for hiring promotions pay adjustments performance appraisals. Recruiting and developing a highperformance team. Develop individual team members hard and soft skills (challenge motivate reward) using individual development plans. Drive development of intellectual capital and continuous education and capability building. Act as a mentor for teams and individuals.
• Responsible for acting across disciplines with senior leaders and external parties to drive and align strategic and operational activities. Responsible for alignment of functional execution plans with approved corporate plans.
• Continuously monitor progress costs resource allocations timelines and develop corrective actions if deviations occur.
• Communicate effectively across work groups departments and with MT.

We expect our Head of CMC to be/have:

• Independent thinker with demonstrated ability to take the lead
• A deliverableoriented mindset with a strong sense of ownership
• An advanced degree in biochemical engineering pharmaceutical chemistry biochemistry or relevant technical discipline coupled with 15 years of relevant pharma and/or biotech experience
• Experience in development of early and latestage manufacturing process validation and clinical supply chain management
• Proven track record in cGMP manufacturing and IND CTA and NDA/MAA filings; thorough knowledge of relevant FDA and EMEA regulations
• Experience in working with sterile drug products and oligonucleotides is a bonus
• Experience in developing products for rare diseases
• Experience in overseeing outsourced manufacturing models
• Track record in building working processes and organizational structure in a biotech environment
• Strong interpersonal skills with the ability to motivate others influence and negotiate difficult situations.
• Demonstrated ability to mentor and develop strong leaders.
• Able to work adjust and lead in a fastpaced highly dynamic environment.
• Demonstrated ability for innovative and bigpicture thinking.

Skills and competencies that are required for making the difference:

• Lead by example
• Flexible and resistant to change
• Critical thinking decision making and problemsolving skills
• Autonomous
• Analytical and accurate
• Being able to work in a fastpaced environment
• Strong line management skills
• Being able to prioritize
• Excellent communication skills
• Proactive and pragmatic selfstarter with a resultoriented mindset
• A nice person :)

ProQR as an employer

As an employer we are a true believer of the value of a workforce in which people from diverse backgrounds are encouraged to develop themselves personally and professionally. We believe that happy and energized people working well together in an environment in which they thrive will do phenomenal and awesome things.

We are committed to ensure that no employee candidate or job applicant receives less favorable treatment on the grounds of race age disability pregnancy religion gender identity and expression sexual orientation marriage or civil partnership status. At ProQR we want to create an inclusive culture where everyone can be valued for who they are and in which individual differences and contributions in all forms are recognized and valued.

We offer an exciting and innovative working environment in a very committed organization with the following benefits:

• 8% holiday allowance
• 30 vacation days
• An annual performance bonus
• Stock options
• A premiumfree pension plan
• A commuting allowance
• A subsidized staff restaurant
• Unlimited (un)healthy snacks and drinks
• Employee events (boot camp Rebel Caf and other social events)

Do you think you can contribute to achieving our mission If so were looking forward to receiving your application by filling out our application form.

You can contact Silvia Catellani via if you have any questions.