Associate Director, Formulation Development

Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer.

Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.   Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none.

If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for our patients, for your career, for what’s beyond.  You can view our latest corporate deck and other presentations here. Associate Director, Formulation Development  As the Associate Director, Formulation Development reporting to the Sr. Director, Drug Product, you will lead pre-formulation, formulation development, tech transfer, scale-up, and manufacturing activities at Olema’s CMOs or CDMO partners.

This role provides scientific expertise in solid oral dosage formulation development, early to late-stage process development, oversight of GMP drug product manufacture at contract development sites, authoring global regulatory filings (INDs, IMPDs, NDA, etc.) and technical oversight of packaging validation, shipping validation and transportation studies in preparation for commercial launch.  This position will collaborate with cross functional departments and other CMC functions in a fast-paced high growth environment to ensure progression of Olema’s small molecules from discovery through development/commercialization.  This role is based out of our Dublin, Ireland office and will require 25-30% travel.   Your work will primarily encompass:  Lead preclinical and early clinical phase formulation development effort at CMO and provide oversight of tech transfer to GMP vendor for clinical drug product manufacture and scale up  Design and provide oversight of development and characterization studies in evaluating formulation development and drug product unit process feasibility  Work closely with CMOs to address and refine formulation and process related challenges over the entire course of product development  Develop strategies and execution plans for drug product development from first time in human through development of NDA ready formulations in accordance with timelines and requirements of program strategy  Partner with clinical supply team to ensure uninterrupted drug product supply for ongoing studies and risk-mitigate strategically any supply constraints  Work closely with project management for alignment on study timeline and corresponding drug product supply plan in terms of adequately securing GMP production slots at CDMOs  Work closely with project management to identify critical CMC decision points, gain alignment at Program Team (PT) level and final endorsement from Executive Commitment (EC)   Work closely with regulatory CMC team (or consultants) to align on filing strategies from the perspective of being able to provide drug product for studies by clearing regulatory responsibilities   Engage in identifying high quality drug product manufacture CMOs or CDMOs in expertise, capability and capacity for effective collaboration in developing and/or commercializing Olema molecule  Lead formulation and process development, technology transfer, clinical manufacturing activities & scale-up at CMOs or CDMOs  Review and approve manufacturing documents, protocols and reports  Support manufacturing and quality function in solving technical issues and addressing deviation investigations  Support the design of experiments (DoE) studies to evaluate formulations and process parameter at CDMOs to support NDA filing  Support the late-stage process development and optimization activities to identity CPPs, CQAs etc. leading to process performance qualification and commercialization   Write technical reports and author CMC sections of regulatory submissions related to drug product from IND through NDA stage of development  Lead packaging validation, shipping validation & transportation studies at drug product CDMOs in preparation for Olema drug product commercialization  A love of challenging, important work.

We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role.

Knowledge & Experience  Ph. D. / M.S in Pharmaceutical Science, Chemical Engineering or related field  8+ years' experience in pre-formulation and formulation development for small molecules, preferably solid dosage forms, 5+ years in managing outsourced development activities  Experience in formulation and process development; preferably with direct experience with late-stage oral solid dose manufacturing process  Good working knowledge of GMP requirements for drug product development and manufacturing  Good understanding of ICH, FDA, EMA guidance's in CMC and Quality areas  Effective written, oral communication and interpersonal skills  Experience in leading formulation projects in pre-formulation, formulation development, process selection and scale up, and oversight of GMP manufacture  Experience in leading packaging validation, shipping validation and& transportation studies   Be self-motivated, organized, detail-oriented, team-oriented, & problem-solving oriented  Being proactive, strategic and skillful in multi-tasking  Excel in team settings with ability to think critically, outside of box for problem-solving and work independently  #LI-MK1Important Information >>> We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience.

Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.

Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert:  We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com.

Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.

Olema Pharmaceuticals is a biopharmaceutical company dedicated to developing targeted therapies for women's cancers. With a focus on precision medicine, Olema is committed to advancing innovative treatments that address the unmet medical needs of patients with hormone receptor-positive breast cancer.