Director, Bioprocess / Process Development - Pivotal Drug Substance
$184.49k - $249.61kAmgen Inc
Career CategoryProcess DevelopmentJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Director, Bioprocess / Process Development – Pivotal Drug SubstanceWhat you will doIn this leadership role, you will be responsible for the development, characterization, scale‑up, and support of drug substance cell culture and purification processes to enable commercial advancement of programs from Phase II/III through marketing applications. Located in Cambridge, MA and/or Thousand Oaks, CA, you will lead and develop a multi‑site organization of 30+ scientists and engineers while driving program success, safety culture, technical excellence, innovation, automation, and digital strategies.You will support a diverse portfolio of biologics, including monoclonal antibodies (mAbs), BiTEs, bispecifics, biosimilars, and other novel protein‑based modalities, and play a key role in advancing late‑stage and commercial drug substance strategies across Amgen’s manufacturing network.Key ResponsibilitiesLead a high‑impact, multi‑functional drug substance organization integrating cell culture and purification disciplines across multiple sites.Recruit, develop, and retain a strong and diverse team; manage portfolio prioritization and organizational resourcing.Advance integrated drug substance processes through commercial process development, process characterization, lifecycle management, and control strategy development.Partner with engineering, manufacturing, and external network collaborators to enable successful process transfer and commercialization.Author and review global regulatory filings (IND/INDa/MA) and respond to regulatory agency questions.Drive ideation, development, and deployment of innovative and differentiating bioprocess technologies.Contribute to Amgen’s scientific and regulatory eminence through publications, patents, and participation in external conferences and forums.Serve as a member of the Drug Substance Technology extended leadership team and contribute to business, organizational, and change‑management strategies.What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.Basic Qualifications:Doctorate degree and 4 years of scientific process development experience, ORMaster’s degree and 8 years of scientific process development experience, ORBachelor’s degree and 10 years of scientific process development experience AndIn addition to meeting at least one of the above requirements, you must have at least 4 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced abovePreferred Qualifications:PhD in Biochemistry, Biochemical Engineering, Chemical Engineering, or related discipline10+ years of experience in biopharmaceutical process developmentMinimum of 4 years of experience directly managing peopleDeep expertise in either cell culture bioreactor processes OR downstream purification processesStrong understanding of late‑stage biologics development including process design, characterization, validation (PPQ), and regulatory interactionsProven ability to provide scientific and engineering leadership on complex cross‑functional programsDemonstrated experience in statistical data analysis, technical decision‑making, and senior‑level communicationTrack record of developing talent through coaching, mentoring, and feedbackActive engagement in the scientific community (publications, patents, industry forums)What you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accountsA discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plansFlexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.Apply now and make a lasting impact with the Amgen team.careers.amgen.comIn any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.Application deadlineAmgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.SponsorshipSponsorship for this role is not guaranteed.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation..Salary Range184,494.20USD -249,609.80 USDSummaryLocation: US - Massachusetts - CambridgeType: Full time
$154k - $183k
...Venous Diseases (CMVD). Over half of our research and development efforts are focused on targeted therapies to... ...Subject Matter Expert (SME) in the manufacturing processes of commercial small molecule drug substances. The role reports to the Head of Small Molecules Drug...SuggestedFull timeContract workTemporary workRemote workFlexible hours- ...biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization... ...seeking an Associate Director, CMC, Drug Substance to join our CMC Drug... ...for deployment in pre-pivotal and pivotal clinical... ...with the internal process chemistry team, manage...SuggestedContract workTemporary workRemote workFlexible hours
- ...Xenon Pharmaceuticals Inc. is seeking an Associate Director, CMC, Drug Substance to lead API development and manufacturing programs. You will manage CDMOs, oversee... ...cGMP and regulatory requirements for clinical and pivotal trials. The role reports to the Senior Director,...SuggestedRemote job
$145k - $207k
...potential late-stage pipeline of drug candidates. In this role you will provide leadership in development and execution of robust and cost-effective processes for new small molecule APIs.Your... ...all late-stage small molecule drug substance development and manufacturing...Suggested$170k - $215k
.... Stoke’s first medicine in development, zorevunersen, has demonstrated... ...Purpose The Associate Director of Oligonucleotides Manufacturing... ...Director of Oligonucleotide Drug Substance Development and... ...accurate invoicing and payment processes with CMOs Execute change controls...SuggestedContract workTemporary work$145k - $207k
...Associate Director role leading late-stage small molecule drug substance development and manufacturing at global CMO/CRO sites. Responsible for process development, regulatory compliance, technology transfer, and commercialization support for early and late-stage pipeline...- Xenon Pharmaceuticals is seeking an Associate Director, CMC, Drug Substance to join the CMC Drug Substance team in Boston, MA. The role focuses on overseeing API development and manufacturing programs with CDMOs to support clinical trials and regulatory submissions. The...Remote work
$143k - $203k
...Role: You will be the lead and an integral part of Relay’s drug product development team supporting development programs.You will be responsible... ...and clinical / commercially viable manufacturing process including selection appropriate packaging (container closure...$164.02k - $221.91k
...lives of patients while transforming your career.Associate Director, Commercial Drug Products & Life Cycle ManagementWhat you will doLet’s do... ...world. In this vital role you will be part of Amgen’s Process Development organization, Drug Product Technologies unit that...Full timeTemporary workFlexible hours$175k - $201k
...Entrada is advancing a robust development portfolio of genetic... ...resourceful, and enthusiastic Drug Product Development & Manufacturing... ...The OpportunityThe Associate Director, Drug Product Development & Manufacturing... ..., characterization, process development, technology...Work at officeLocal areaRemote work1 day per week- ...biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life‑... ...About the Role: We are seeking a Director, CMC, Drug Product to join our team.... ...manages and oversees the late phase process development, validation and commercial...Contract workTemporary workWork at office2 days per week
$248.5k
...globally. TM plays a pivotal role in bringing innovative... ..., and bridging drug discovery and clinical... ...profiling, and effective development of medicines. Translational... ...LI- hybridTME Director Cardiovascular MetabolismOversees... ...efficient and timely processing of confidentiality...Full time$212k - $333.19k
...that my employment application process with Takeda will commence and... ...and visionary Senior Director, Small Molecule CMC Advisor to lead the analytical development strategy for our small molecule... ...analytical development strategies for drug substances (API) and drug products....Minimum wageLocal areaRemote work$159k - $195k
...X, LinkedIn and Facebook.Role Summary:The Associate Director, Formulation and Drug Product Development will be accountable for all internal and external activities... ..., tech transfer, and scale-up of drug product processes, and cGMP manufacturing of clinical grade drug...Local areaRemote work$154.4k - $242.55k
Associate Director - MSAT Synthetic Molecule API OBJECTIVES: The... ...manufacturing of commercial Drug Substance. The focus for this position... ...manufacturing of drug substance, process design, optimization, scale‑... ...of phase appropriate CMC development throughout the drug...Minimum wageFull timeContract workFor contractorsWork at officeLocal areaWorldwideNight shift$159k - $219k
About This Role The Associate Director, Antisense Oligonucleotide (ASO) Analytical Development will provide scientific and... ...development activities supporting ASO drug substance and drug product programs.... .... The team partners with process development, Quality Control,...Full timeContract workTemporary workLocal area$159k - $219k
About This Role The Associate Director, Small Molecule Analytical Development will provide scientific and people leadership... .... The team partners with process chemistry, chemical engineering,... ...development activities for small molecule drug substance and drug product programs,...Full timeContract workTemporary workLocal area- ...Job Description SEISMIC THERAPEUTIC Director / Senior Director, Analytical Development and QC About Seismic Seismic Therapeutic... ...critical quality attributes, raw material and in-process testing as appropriate, drug substance and drug product specifications, stability...Contract workWork at officeLocal areaShift work
$185k - $225k
....Position Overview:The Associate Director of Product Quality Assurance (PQA... ...procedures, equipment, personnel and processes to ensure that they consistently... ...industry in combination with drug substance/drug product manufacture, development and quality. Must have Biologics...Full timeContract workWorldwide$185k - $200k
...Editor! Decoding The Role: The Process Development team is seeking an experienced Associate Director of Lipid Process Chemistry to... ...of lipid raw materials into drug product manufacturing. Define... ...expectations for clinical-stage drug substances. Ideally, you would also have...Contract workFlexible hours- ...research operations in Tübingen, Germany. JOB DESCRIPTION We are seeking an experienced and innovative Associate Director to lead drug product development and manufacturing efforts for oligonucleotide-based therapeutics, with an emphasis on novel delivery technologies...3 days per week
$160k - $235k
OverviewGilbane Development Company is seeking a Director, Asset Managment to lead asset management strategy across... ...and multi-year capital planning process in coordination with Finance, Operations... ...must pass a pre-employment substance abuse test.Gilbane is an Affirmative...Summer work$237.9k - $356.9k
...DescriptionGeneral Summary:The Senior Director, Immunology will oversee... ...support the research and development of the Vertex portfolio, and... ...closely with manufacturing, process and analytical development colleagues... ...to advance novel, next gen drug discovery in T1DProvide...Full timeSummer workFlexible hours$210k - $260k
...for products in the Beam portfolio. The Director of Pharmacovigilance will contribute to... ...activities, PV organization and process development, inspection readiness, PV vendor management... ...reports.Thorough understanding of the drug development process and context applicable...Full time3 days per week1 day per week$192.7k - $289.1k
...is in-house, and our Writers are strategic partners in our drug development process, collaborating with cross functional teams, authoring and driving... ...Seaport office. Relocation assistance is available.The Director, Medical Writing Science has responsibility for the...Full timeSummer workWork at officeRemote workRelocation packageFlexible hours2 days per week3 days per week$132.5k - $201.6k
OverviewGilbane Development Company is seeking a Director of Leasing & Revenue to lead leasing strategy, revenue... ...must pass a pre-employment substance abuse test.Gilbane is an Affirmative... ...considered property of Gilbane and will be processed accordingly. Job...Work at officeRemote workShift work- ...develop, and market innovative drugs across our main therapeutic... ...020 and focused on research, development and commercialization of treatments... ...is what you will doThe Director, RWE is responsible for leading... ...influencing adoption of new processes and approaches. This includes...Hourly payWork at officeLocal areaRemote workRelocation packageFlexible hours
$204k - $306k
...DescriptionGeneral Summary:The Director, Biostatistics will... ...the company’s Global Medicines Development and Affairs (GMDA) area on new... ...Biostatistics activities with a drug developer mindset. As a people... ...drug discovery and development processes.Represents Biostatistics as a...Full timeSummer workRemote workFlexible hours2 days per week$166k - $249k
...Automation of Machinery and Processes (AMP) Team is seeking a high... ...Genetic Therapies programs. This pivotal role is at the forefront of... ...novel equipment & systems development, vendor selection, equipment... ...systems and robotics, in bioprocessing, medical device, pharmaceutical...Full timeSummer workFlexible hours- Meet Life Sciences Ltd. is seeking an Associate Director of Drug Product Technical Services to lead validation activities for injectable... ...requires collaboration with regulatory, manufacturing, quality and development teams to ensure robust validation and a smooth transition...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Director, Bioprocess / Process Development - Pivotal Drug Substance. Be the first to apply!
- organizational development manager Cambridge, MA
- research and development chef Cambridge, MA
- development manager Cambridge, MA
- senior development executive Cambridge, MA
- development chef Cambridge, MA
- medical director clinical development Cambridge, MA
- director corporate development Cambridge, MA
- manager corporate development Cambridge, MA
- senior director corporate development Cambridge, MA
- franchise development manager (remote) Cambridge, MA


