The Associate Director of Global Clinical Supply Chain is responsible for the successful execution of supply chain management for clinical trials, providing triage support for rapid start-up of CDMOs and CROs, and ensuring continuous supply of Investigational Medicinal Product (IMP).
Compensation
Salary range for posting: $170,000—$200,000 USD
Responsibilities
Managing and executing overall Project Delivery through coordination of CMC efforts assigned to the entire project team (CMC, Supply Chain, Legal, Procurement, Regulatory, Clinical Development, and Clinical Operations).
Provides recommendations on packaging design, distribution and blinding strategy.
Plans and manages execution of initial supplies and resupplies for assigned studies.
Designs and implements plans to supply study drug to complex global clinical trials using sound supply chain techniques.
Develops and executes inventory management plans for clinical sites and depots to ensure treatment availability for every patient visit.
Requirements
Bachelor's degree in science, engineering, or another relevant field
Lead formulation development and testing for Dove Deodorants, integrating new technologies into the innovation pipeline and collaborating with cross-functional teams.
Compensation
Pay: The pay range for this position is $71,400 to $81,000. Unilever takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. Bonus: This position is bonus eligible. Long-Term Incentive (LTI): This position is LTI eligible.
Responsibilities
Own formulation, stability, safety and performance testing, processing, specifications and regulatory, compliance and patents
Deliver products against technical briefs, ensuring Formulation, Process, Packaging and Quality Assurance specifications are correct and on time
Work with internal R&D teams to translate technology roadmaps into insightful innovations
Build productive relationships with partners including Process Engineering, Packaging, CTI & Claims, Specifications, Safety, Brand Teams, Supply Chain, 3P manufacturers and RM suppliers
Ensure products deliver a delightful, top-quality consumer experience
Requirements
Bachelor's of Science (BS) degree required; Chemical Engineering or Chemistry preferred
Nice to have: Strong, proven technology and/or project deliveries to market
Nice to have: Hands-on laboratory scale-up activities
Nice to have: Fundamental understanding of deodorant category formulation and processing principles
Lead and execute drug product development activities from candidate selection through commercialization, applying biochemical, biophysical, and microbiology principles to formulate, analyze, and optimize biologic drug modalities.
Compensation
Salary Range (annually) $112,100.00 - $182,900.00
Responsibilities
Design and conduct formulation development and stability studies
Perform analytical development and microbial analysis
Develop and transfer new technologies and processes
Prepare and deliver presentations, SOPs, and patents
Maintain accurate laboratory records and comply with data integrity procedures
Requirements
Ph.D. in Pharmaceutical Science, Biochemistry, Chemistry, Microbiology, Biophysics, Engineering, or related field
BS or MS with 8-10 years of experience, or Ph.D. with 0-3 years of experience
The R&D Chemist is responsible for the design and formulation of ink, dispersion, and related chemical technologies through a combination of empirical design and modeling methods, focusing on developing components that expand ink and printing fluid attributes.
Compensation
The pay range for this role is $114,600 to $170,000 USD annually with additional opportunities for pay in the form of bonus and/or equity (applies to United States of America candidates only).
Responsibilities
Design and optimize ink, dispersion, and related formulations to achieve product performance, quality, Regulatory, Manufacturability, cost, and supply objectives.
Lead component development and technical projects from concept through product qualification and introduction
Cross-functional/pan global team participation and leadership
Apply expertise in formulation science, pigment and dye chemistry, polymers, colloidal systems, and surface chemistry to solve complex technical challenges.
Design and execute experiments, analyze data, and translate findings into actionable technical recommendations.
The Associate Director of Formulation Development will provide scientific and strategic leadership for early- and late-stage formulation development activities supporting phase-appropriate formulations of biologic drug products, with a focus on monoclonal antibodies, bispecific formats, and co-formulations.
Locations (2)
Menlo Park, California, United States
Waltham, Massachusetts, United States
Compensation
The anticipated salary range for candidates, who will work in Waltham, MA or Remotely is $182,000 to $208,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.
Responsibilities
Lead phase-appropriate formulation development workflows for biologics, including selection, optimization, and robustness studies, with a focus on high concentration product development.
Experience with co-formulation products.
Experience with PFS and Autoinjector selection and testing.
Partner with drug product and clinical teams to ensure appropriate container closure selections are made that align with QTPP and clinical needs.
Plan, perform and report scientific experiments with SME to support the project portfolio and advance the innovation technical platform of radiopharmaceutical parenteral dosage forms.
Compensation
€30,200.00 - €56,000.00
Responsibilities
Plan and perform formulation development, characterization studies and experiments
Ensure correct, comprehensible, structured, complete and legible documentation according to SOPs, HSE and AdAcAp / Novartis Guidelines
Meet quality, quantity and timelines in all assigned projects
Ensure consumables, excipients, equipment availability as needed
Maintain clean and tidy working place, including waste management activities
Lead formulation and process development activities for early- and late-stage clinical candidates, ensuring alignment with overall development timelines and goals.
Compensation
In the U.S., the hiring pay range for fully qualified candidates is $232,110 - $270,795 per year.
Responsibilities
Lead formulation and process development activities for early- and late-stage clinical candidates
Lead strategic planning for formulation development
Accountable for formulation and process development activities and technical oversight of clinical drug product manufacturing at contract manufacturing organizations
Provide coaching, mentorship, and development support to team members
Support employee performance management activities
Requirements
Advanced degree (Ph.D., M.S., or equivalent) in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or a related discipline
Drive commercial growth by identifying and driving technology opportunities in coated meat applications.
Locations (3)
Beloit, Wisconsin, United States
Springdale, Arkansas, United States
Rome, Georgia, United States
Compensation
The pay range for this position is $102,400 - $168,250 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, internal equity, and Location. In addition, this position is also eligible to earn a performance-based incentive compensation.
Responsibilities
Identify and drive technology opportunities
Become SME on technical creation of new solutions via coatings
Associate Director, Global Clinical Supply ChainNewIMVT Corporation · Remote, US
Associate Director, Formulation Development, Tech Ops (Biologics)Oruka Therapeutics · Menlo Park, US+1 more
Principal Scientist, Product TransferHIKMA · Cherry Hill, US
Technical Business Development Manager - Coated Meat ApplicationsKerry Group · Beloit, US+2 more