Evaluate formulation performance through physical, chemical, and biopharmaceutical characterization studies.
Assist in the development and scale-up of drug product manufacturing processes.
Analyze experimental data, summarize results, and communicate findings to project teams and management.
Prepare high-quality technical reports, study protocols, laboratory documentation, and development summaries to effectively communicate experimental results, scientific conclusions, and development recommendations.
Collaborate cross functionally with DMPK, Analytical Development, Chemical Development, and other supporting groups to advance development programs.
Maintain accurate laboratory records and ensure work is performed in compliance with applicable quality and safety standards.
Maintain laboratory equipment, instrumentation, raw material inventory, and samples to ensure effective laboratory operations.
Conduct routine laboratory equipment setup, operation, troubleshooting, cleaning and maintenance of formulation and process equipment. Coordinate calibration and preventive maintenance activities with internal stakeholders and vendors and ensure equipment records are maintained and current.
Serve as a laboratory safety representative and primary liaison with EH&S for assigned laboratory areas. Support implementation of safety initiatives, participate in laboratory inspections and audits, track corrective actions, and promote compliance with laboratory safety procedures and practices.
Proactively Identify opportunities to improve laboratory operations, increase efficiency and expand technical capabilities. Develop subject matter expertise on key processing and characterization equipment and recommend new applications, workflows, or technologies that enhance formulation development and laboratory productivity.
Qualifications
BS in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or related discipline with 6+ years of industry experience; or MS with 4+ years of relevant experience.
Demonstrated experience supporting pharmaceutical formulation and/or drug product development activities in a pharmaceutical or biotechnology environment.
Working knowledge of oral solid dosage form development, pharmaceutical manufacturing, and product development processes.
Experience conducting laboratory experiments, analyzing data, and documenting scientific results.
Demonstrated extensive hands-on experience maintaining, setting up, cleaning and operating equipment used for oral solid dose manufacturing, including but not limited to high shear granulation, milling, blending, tableting, film coating, and spray drying
Advanced knowledge of pharmaceutical characterization techniques.
Experience working with CROs and/or CDMOs is a plus.
Strong scientific curiosity, problem-solving, and analytical skills.
Excellent written, verbal, and technical communication skills.
Highly organized with strong attention to detail and the ability to manage multiple priorities.
Collaborative team player with strong interpersonal skills and the ability to work effectively in a fast-paced, cross-functional environment.
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Pay Range
The expected salary range for this position based on the primary location of South San Francisco, CA is $121,500 - $141,750. The base pay offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. Base salary is just one component of our competitive total compensation package, which includes equity in the form of stock options and/or restricted stock units, comprehensive health, dental, vision, life and disability insurance coverage, 401k retirement benefits with employer match, learning and wellness stipends, and paid time off. Note that benefits are subject to change and may vary based on jurisdiction of employment.
Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.
Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.
Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.
Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers
Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.
Here are some ways to check for authenticity
We do not conduct job interviews through non-standard text messaging applications
We will never request personal information such as banking details until after an official offer has been accepted and verified
We will never request that you purchase equipment or other items when interviewing or hiring
If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com
Please visit our website at: www.cytokinetics.com
Cytokinetics is an Equal Opportunity Employer
