Serán BioScience is looking for a scientist with laboratory experience to support manufacturing of pharmaceutical drug products within our In-Process Control group. As a scientist within the Quality Control department you will work alongside a team of scientists and operators to ensure the highest quality product by testing raw materials and production equipment within GMP manufacturing and laboratory environments. Qualified candidates will demonstrate expertise in utilizing specialized laboratory equipment, techniques, and methodologies for technical assessments and data analysis purposes. Preference will be given to those with experience in GMP environments and technical data review specific to the pharmaceutical industry.

Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.

Duties and Responsibilities

Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies
Performs routine testing using analytical equipment including but not limited to HPLC, GC, KFC, Disso, etc.
Conducts appearance testing, solution preparation, raw material sampling, and pH measurement
Drafts stability tables, sets-up stability studies, logs-in samples and standards
Cleans lab and glassware and disposes of analytical waste appropriately
Participates in process improvement and other non-routine projects
Enters clean spaces with appropriate PPE to collect various samples
Is familiar with introductory analytical equipment (e.g., HPLC, GC-HS, TOC, FT-IR)
Is familiar with raw materials testing requirements (compendial and client testing)
Conducts peer review of routine testing at the discretion of the relevant supervisor
Performs technical writing and reporting including but not limited to: incident reporting, laboratory investigations, CAPAs, SOPs, trend reports, risk assessments, etc.
Performs hypothesis testing or investigative work for OOS results under management and SME guidance
Demonstrates cross-functional support capabilities with other QC teams
Responsibilities may increase in scope to align with company initiatives
All other related duties as assigned

Required Skills and Abilities

Hands-on lab experience in HPLC, CG-HS, TOC, FT-IR
Hands-on lab experience with raw materials testing
Strong verbal and written communication skills
Demonstrated ability to collaborate and work in cross-functional teams
Strong organizational skills and attention to detail
Follows detailed written and oral instructions
Strong time management skills with a proven ability to meet variable and competing deadlines
Strong analytical and problem-solving skills
Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs
Accepts feedback from a variety of sources and constructively manages conflict
Ability to prioritize tasks and to keep leadership apprised of performance to timelines
Ability to function well in a high-paced and at times stressful environment
Proficient with Microsoft Office Suite or related software

Education and Experience

Bachelor's degree in related scientific discipline
3 years of hands-on laboratory experience required, cGMP preferred
Minimum of 2 years of GMP experience required to be considered for Scientist II

Physical Requirements

Prolonged periods of sitting or standing at a desk and working on a computer
Prolonged periods of sitting or standing in laboratory environment
Must be able to lift up to 25 pounds at times
Adheres to predicable in-person attendance
Motor skills required for basic laboratory operations

Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Benefits Summary:

Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.

The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701

Serán BioScience

Quality Control Scientist 1/2 - In-Process Control-Day Shift

About the Job

Requirements

Responsibilities

Desired Qualifications

Duties and Responsibilities

Required Skills and Abilities

Education and Experience

Physical Requirements

About the Company

Serán BioScience

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