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Sr Associate

Thousand Oaks, CA
Description:
Note:
  • Onsite 100% Thousand Oaks.

Ideal candidate: 
  • Degree in Engineering, Chemistry, Pharmaceutics, Materials Science, or related discipline. Masters with intern exp, or Bachelors with 2 years analytical industry experience. Eger to learn.
  • This role in Pivotal Drug Product Technologies will be to provide support of drug product formulation and process development of parenteral products, primarily biologics.
  • The candidate will work closely with a team of engineers and scientists responsible for the technical aspects of 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 parenteral products.
  • Support and execute formulation assessments utilizing high-throughput technologies and workflows, working closely with program teams on fast-paced projects.
  • 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.
  • 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.

Preferred 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).

Basic Qualifications
  • Bachelor's Degree with 2+ years relevant experience
  • 0+ Years w/ Relevant MS OR equivalent 2+ Years w/ Relevant BS OR equivalent 4+ Years w/ Relevant AS OR equivalent 6+ Years w/ HS

Top 3 Must Have Skill Sets:    
  • 2+ years of relevant lab experience in industry.
  • Good organizational skills with strong attention to detail.
  • Excellent communication (oral and written).

Day to Day Responsibilities    
  • Lab-based study support and analytical testing
  • Data analysis and documentation
  • Author, review, and data verify technical documents
  • Consistent communication of progress

Pay Rate  between $27 - $29/Hr on W2 based on experience.

"This posting is for Contingent Worker, not an FTE
"

 

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