Sr Associate
Aequor Technologies
- Thousand Oaks, CA
- Permanent
- Full-time
- Participate in the planning, design, execution, and documentation of studies related to drug product formulation and process development in support of commercialization and life cycle management of parenteral products.
o Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc.
o Support and conduct related studies (e.g., stability, UF/DF, filtration, freeze/thaw, fill/finish, etc for products in various formulations and presentations (e.g., liquid, lyophilized, etc.).
- Data analysis and documentation/review in electronic notebooks.
- Author, review, and data verify technical documents such as protocols, reports, regulatory documents, etc.
- Clearly and consistently communicate data in progress reports and presentations.
- Participate in cross-functional teams in a fast-paced environment to progress product development.
- Adhere to all training, compliance, and safety guidance.
- Support lab operations and inspections as required of all lab-based staff.
- Work primarily onsite with remote work as appropriate to role and tasks.
Bachelor's Degree with 2+ years relevant experiencePreferred Qualifications:
- Degree in Engineering, Chemistry, Pharmaceutics, Materials Science, or related discipline.
- 2+ years of relevant lab experience.
- Understanding of physical/chemical stability of proteins.
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with procedures and policies.
- Proficient computer skills.
- Self-motivation, adaptability and a positive attitude.
- Critical thinking, problem solving, and independent research skills.
- Good organizational skills with strong attention to detail.
- Excellent communication (oral and written).