Scientist Senior Associate
Aequor JD ·www.aequor.com
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Onsite
Based at *** s headquarters in Thousand Oaks, CA, this role in Pivotal Drug Product Technologies will be to provide support of drug product formulation and process development of biologics. The candidate will work closely with a team of engineers and scientists responsible for the technical aspects of *** s drug product commercialization and lifecycle management.
Responsibilities will include:
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 biologics.
Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.).
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.
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.
Preferred Qualifications:
Bachelor s Degree in Engineering, Chemistry, Biochemistry, Pharmaceutics, Materials Science, or related discipline with at least 2 years of relevant laboratory work experience. Or Masters degree without any 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, including Microsoft Office, PowerPoint, Word, and Excel.
Self-motivation, adaptability and a positive attitude.
Critical thinking, problem solving, and independent research skills.
Good organizational skills with strong attention to detail.
Excellent oral and written communication skills.
Based at *** s headquarters in Thousand Oaks, CA, this role in Pivotal Drug Product Technologies will be to provide support of drug product formulation and process development of biologics. The candidate will work closely with a team of engineers and scientists responsible for the technical aspects of *** s drug product commercialization and lifecycle management.
Responsibilities will include:
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 biologics.
Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.).
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.
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.
Preferred Qualifications:
Bachelor s Degree in Engineering, Chemistry, Biochemistry, Pharmaceutics, Materials Science, or related discipline with at least 2 years of relevant laboratory work experience. Or Masters degree without any 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, including Microsoft Office, PowerPoint, Word, and Excel.
Self-motivation, adaptability and a positive attitude.
Critical thinking, problem solving, and independent research skills.
Good organizational skills with strong attention to detail.
Excellent oral and written communication skills.
Frequently asked questions
Who is hiring for the Scientist Senior Associate role?
Aequor JD is hiring for the Scientist Senior Associate position, a Shazamme client. Apply directly on the employer's career site.
Where is the Scientist Senior Associate job located?
The Scientist Senior Associate role with Aequor JD is based in Thousand Oaks, CA, US.
Is the Scientist Senior Associate role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the Scientist Senior Associate role?
The Scientist Senior Associate position is aimed at senior-level candidates.
How do I apply for the Scientist Senior Associate role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.