Director, CMC - Formulations
$190k - $260kCodera
About Codera Codera is a Tang Capital company that provides in-house, end-to-end drug development capabilities for its portfolio companies. Founded in 2002, Tang Capital is a life-sciences focused investment company that creates, acquires and finances companies that develop and commercialize pharmaceutical products. Position Summary The Director, CMC - Formulations will contribute to the oversight, planning and execution of Chemistry, Manufacturing and Controls (CMC) strategy, including drug product formulations, in support of Codera’s development programs. In collaboration with internal departments, such as nonclinical, clinical pharmacology and regulatory teams, the Director, CMC - Formulations will contribute to all aspects of chemistry, manufacturing and controls, including design of drug product formulations, oversight of vendors and production of regulatory documents. Essential Duties and Responsibilities Assist with the design and evaluation of drug product formulations, primarily small molecule formulations, to achieve specific pharmacokinetic (PK) goals Contribute to CMC and development strategy Manage relationships with various contract development and manufacturing organizations (CDMOs), analytical labs and contract research organizations (CROs) Assist with the clinical supply logistics Prepare, analyze and interpret analytical data that integrate into regulatory and intellectual property (IP) documents Draft, edit and review sections of regulatory and IP documents Provide scientific input for analytical protocols and study reports Contribute to a fast‑paced, dynamic, data‑driven scientific culture that embraces innovation and excellence Research CMC and formulation topics to support Tang Capital’s investments Participate in business development activities, as requested Qualifications Bachelor’s degree or higher in life sciences or related discipline required Master’s degree preferred Minimum of 5 years in relevant pharmaceutical industry work experience required Experience with small molecule formulations required Experience with biologics formulations preferred Experience working with CDMOs and analytical labs Experience with one or more of the following drug product formulation strategies: modified/delayed release, fixed‑dose combinations, spray‑dried dispersions Experience with a wide range of excipients and formulation technologies Experience with formulations for oral, subcutaneous and/or inhaled delivery Ability to research, synthesize and summarize complex CMC topics Experience writing and/or reviewing regulatory documents, including Investigational New Drug (IND)/New Drug Application (NDA) sections Ability to effectively organize and manage multiple assignments with challenging timelines from project start‑up through submission Excellent knowledge of Food and Drug Administration (FDA) and International Council for Harmonisation (ICH) regulations and Good Manufacturing Practices (GMP) Outstanding written and verbal communication skills, including the ability to use clear language to explain complex ideas Ability to establish and maintain collaborative working relationships with internal and external stakeholders Additional Information The job description is not designed to cover or contain a comprehensive list of activities, duties or responsibilities that are required. They may change, or new ones may be assigned at any time with or without notice. The estimated annual base salary for this position is $190,000 - $260,000, commensurate with experience and skills. This role may be eligible for discretionary bonuses and other incentive programs. Codera provides a comprehensive benefits package designed to support employees’ physical, mental and financial health and include employer sponsored insurance plans including medical, dental and vision coverage; generous paid time off; retirement plan options and additional wellness and professional development programs. Codera provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression or any other characteristic protected by federal, state, or local laws. Codera participates in E‑Verify. All newly hired employees are required to complete the E‑Verify process as part of their employment eligibility verification. #J-18808-Ljbffr
$170k - $275k
...cancers and immune-mediated inflammatory diseases. We are currently seeking a highly motivated, creative CMC formulation professional at associate director or director level to join our CMC team in San Diego. This candidate will report to the Executive Director and...Suggested$175k - $195k
...Description The Associate Director, Formulation Development, assists in the design and development of drug delivery systems, specifically for oral... ...stability programs. Own drug product development history and CMC documentation (development reports, control strategy,...SuggestedLocal area- ...Associate Director CMC Company Description: Revelation Biosciences, Inc. is a clinical-stage biotech company dedicated to restoring... ...by targeting inflammation through its proprietary Gemini formulation. The company is advancing a diverse pipeline of programs evaluating...SuggestedContract work
$153k - $211k
...CMC / Technical Operations Program Manager - Associate Director Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet...SuggestedTemporary work$204k
...Associate Director, Outsourcing & Vendor Governance & Supplier Management (CMC) page is loaded## Associate Director, Outsourcing & Vendor Governance & Supplier Management (CMC)remote type: Hybrid-San Diegolocations: San Diego, CAtime type: Full timeposted on: Posted 3...SuggestedContract workLocal areaRemote work$175k - $195k
...A biotechnology firm in San Diego seeks an Associate Director of Formulation Development. The role involves leading external collaborations in drug product development, defining formulation strategies, and maintaining compliance with regulations. Candidates should have...$185k - $200k
...Associate Director Of Regulatory Affairs, Cmc The associate director of regulatory affairs, cmc plays a critical role in supporting late-stage development, commercial launch, and lifecycle management activities for artiva biotherapeutics' cell therapy pipeline. This...Remote workFlexible hours$173.6k - $237k
...understanding to guide lead-optimization, process development, and formulation development. Serve as Analytical Development Lead and support... ...accountability for analytical deliverables and progress on CMC and manufacturing plans for all development projectsDirect laboratory...- ...Description Position Summary The Associate Director, Process Chemistry will be responsible... ...This position will report to the Head of CMC. This position can be remote based in the... ...ability to apply regulatory guidance to formulate practical solutions and development...Remote job
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$154k - $192.7k
...Diego, CA. Position Summary The Associate Director in the Early Stage Drug Product... ...responsible for the development of pharmaceutical formulations primarily intended for early-stage... ...documents prepared by CSPs. Liaises with the CMC team, late‑stage formulation team, and...Contract workWork at officeLocal areaRemote work- ...Manufacturing Operations, Quality Assurance, Regulatory Affairs, Process Development and Analytical Development functions to ensure that all CMC deliverables are on track, technically sound, and aligned with IND-enabling requirements under 21 CFR Parts 210/211, 11, 312, and 600...Full timeContract workFlexible hours
$173.9k - $238k
...performing cross‑functional teams Advanced knowledge of drug development process and inter‑dependencies of key functions including research, CMC, non‑clinical development, clinical development and operations, regulatory affairs and commercial Experience as a PM leader on early...Temporary work$126k - $234k
...accommodation or an alternative application process. Associate Director, Analytical Development (Oligonucleotide) Full Time San Diego,... ...Development (Oligonucleotide) Position Type: Full Time / Exempt Department: Analytical Development & Formulation #J-18808-Ljbffr...Full timeContract work$150k - $200k
...Position: Business Development Manager/Director DP&C (Discovery, Preclinical & CMC) Location: Home based - San Diego Salary: $150,000 to $200,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life...Contract workTemporary workImmediate startRemote workWork from homeWorldwideFlexible hours- ...The candidate will be expected to be a medicinal chemistry leader and strong communicator. What You Will Do (Key Responsibilities) Formulate medicinal chemistry strategies and utilize the Genesis platform to execute drug discovery programs from Hit ID through candidate...
$119.7k - $222.3k
...accommodation or an alternative application process. Associate Director, Process Development and Manufacturing Full Time US 6 days ago... ...timely release of AOC DS. Work with QC, QA and Analytics & Formulations to refine AOC DS specifications for late‑stage clinical trials...Full time- ...Neomorph, located in San Diego, California, is seeking a knowledgeable Director of Analytical Development, CMC to lead their analytical strategy for small-molecule drug development. The role demands expertise in method development and strong regulatory knowledge to guide...
- ...Description The Associate Director Clinical Pharmacology and Pharmacokinetics will play a crucial role in our drug discovery and development... ...(non-GLP and GLP), from in vitro ADME, in vivo PK, PK/PD, formulations and IND enabling toxicology and TK analysis, along with...Local area
$166k - $208k
...Associate Director, Clinical Pharmacology page is loaded## Associate Director, Clinical Pharmacologyremote type: Remotelocations: Remotetime... ..., drug-drug interactions, enzymology of drug metabolism, formulation bridging, bioequivalence, food-effect, exposure-QTc...Local area- ...-solving skills • Expanding program offering and enhancing the quality of existing programs Coordinate cross-project activities • Formulate, organize and monitor inter-connected projects • Decide on suitable strategies and objectives .• • Lead and evaluate project managers...Work experience placementWork at officeLocal areaImmediate start
- ...responsibility for all spectrum HR affairs, develop HR framework according to global HR strategy and provide local insights 3. Formulate local pay philosophy, structures to ensure the achievement of equitable and competitive compensation for attracting and retaining...Local area
$179.2k - $268.8k
...manufacturing, quality, test, marketing, and distribution as the product(s) and/or product line(s) move through their lifecycle. Formulates and executes long-term roadmaps for cost/profit control. Promotes use of new technologies and industry-leading trends. Directs those...Temporary workWork experience placementImmediate startWork from home- ...innovation and collaborative teams, then Debut is for you. Summary Debut is seeking a commercially driven, highly connected Director of Formulation Sales to own and grow our West Coast formulation business. This is a hunter and closer role focused exclusively on selling...Contract workImmediate start
- ...Associate Director Regulatory Affairs - Hybrid - San Diego We are partnering with a clinical stage biopharma who are focused on developing... ...functionally with Clinical Development, Clinical Operations, CMC, Nonclinical, Biometrics, Medical Writing, and Quality teams to...Odd job
$100k - $140k
...Director of Advancement WHO WE ARE - OPPORTUNITY & MISSION If you are interested in diving into a mission-driven culture... ...President, Board of Trustees, and Leadership Team, engage in formulating and executing a comprehensive strategic resource vision ● Serve...Full timeInternshipWork at officeLocal areaFlexible hours- ...Role Reporting to the Chief Medical Officer, the (Associate/Sr) Director of Translational Medicine is responsible for leading translational... ..., Clinical Development, Drug Discovery, Regulatory, and CMC teams to ensure translational excellence and mechanism‑driven insights...
$143.76k - $174.2k
...Working Months: 12 Description To apply for The Director of the Personnel Commission position, please view the information... ...regarding assigned functions; assist as needed in the formulation and development of policies, procedures and programs. Direct...Full timeContract workPart timeFor contractorsWork experience placementWork at officeImmediate startFlexible hours$162.4k - $243.6k
...manufacturing, quality, test, marketing, and distribution as the product(s) and/or product line(s) move through their lifecycle. Formulates and executes long-term roadmaps for cost/profit control. Promotes use of new technologies and industry-leading trends. Directs those...Work experience placementWork from home$172.9k - $263.3k
...IP Sourcing Team is seeking a highly skilled and experienced Director to source and manage Electronic Design Automation (EDA) tools... ...functional areas and/or entire organization. Has influence over the formulation and achievement of long-term business plans and objectives....Full timeContract workTemporary workWork experience placementWork from home
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