Scientist/Engineer at Serán BioScience

Bend, Oregon, United States

Serán BioScience Logo
Not SpecifiedCompensation
Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
PharmaceuticalsIndustries

Requirements

Candidates must possess a Bachelor's or Master's degree in pharmaceutical science, chemistry, chemical engineering, biological engineering, mechanical engineering, materials science and engineering, or a related field. A minimum of one year of relevant industrial experience is required, along with demonstrated research or product development experience. Strong hands-on laboratory skills, scientific curiosity, excellent analytical and problem-solving skills, strong organization and attention to detail, effective time management, and proficiency with Microsoft Office Suite are essential. Candidates must also be authorized to work in the U.S. without sponsorship.

Responsibilities

The Scientist/Engineer will contribute to the development and scale-up of pharmaceutical manufacturing processes, working independently on experiments using basic laboratory skills and following written protocols. They will execute pharmaceutical unit operations, develop experimental plans, collect, analyze, and summarize data, and develop operating procedures and guidelines for process equipment. The role involves performing routine equipment, laboratory, and instrument maintenance, participating in tech transfers to GMP manufacturing, and executing GMP batches. Responsibilities may increase in scope to align with company initiatives, and the individual will perform other related duties as assigned. They will also develop skills in data analysis and reporting internally and to clients, and communicate effectively with coworkers, clients, and external contacts.

Skills

Data Collection
Data Analysis
Problem-Solving
Laboratory Skills
Pharmaceutical Formulation
Pharmaceutical Manufacturing
Powder Blending
Milling
Granulation
Encapsulation
Tablet Compression
Communication
Continuous Learning

Serán BioScience

Contract development and manufacturing for pharmaceuticals

About Serán BioScience

Serán BioScience specializes in providing drug development and manufacturing services as a Contract Development and Manufacturing Organization (CDMO). They offer a variety of services, including preformulation, formulation development, dosage form development, spray drying, and particle engineering. Their operations adhere to current Good Manufacturing Practice (cGMP) standards, ensuring high quality and safety in their products through rigorous analytical quality control. Serán BioScience serves a wide range of clients, from small biotech startups to large pharmaceutical companies, and is distinguished by its flexibility in tailoring services to meet specific client needs. The company's goal is to enhance the efficiency and effectiveness of drug development processes for their clients.

Bend, OregonHeadquarters
2016Year Founded
$194.5MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
51-200Employees

Benefits

Paid Vacation
401(k) Retirement Plan
Health Insurance
Life Insurance
Disability Insurance
Mental Health Support
Pet Insurance

Risks

Emerging CDMOs in Asia offer lower-cost services, impacting Serán's market share.
Potential delays in new facility construction could affect expansion plans.
Global talent shortage may hinder recruitment for Serán's expansion.

Differentiation

Serán specializes in advanced drug formulation techniques, including spray drying and particle engineering.
The company offers cGMP manufacturing and analytical quality control services.
Serán's flexibility allows tailored services to meet specific client needs.

Upsides

Serán announced a $200 million strategic growth transaction for expansion.
The company plans to build a new commercial-scale manufacturing facility.
Increased demand for personalized medicine aligns with Serán's formulation expertise.

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