Duties and Responsibilities

• Documents authorships, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications
• Applies working knowledge of best practices in GMP and understands how Quality integrates with other business areas
• Initiates and oversees investigations
• Manages corrective and preventive actions (CAPA)
• Supports internal audits, client audits and regulatory inspections, with the potential to host 
• Manages controlled document issuance and archival
• Performs quality reviews with minimal oversight 
• Communicates quality-related information to internal teams with minimal guidance
• Responsibilities may increase in scope to align with company initiatives
• Performs all other related duties as assigned

Required Skills and Abilities

• Knowledge of GMP and FDA regulations for clinical trial materials; commercial knowledge is desirable but not required
• Confident understanding of change control procedures, CAPA program, investigation and root cause analysis, and good documentation practices
• Excellent organizational skills and attention to detail
• Excellent time management skills with a proven ability to meet deadlines
• Strong analytical and problem-solving skills
• Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
• Demonstrates the ability to collaborate and work in cross-functional teams
• Accepts feedback from a variety of sources and constructively manages conflict
• Ability to prioritize tasks and to delegate them when appropriate
• Excellent verbal and written communication skills
• Ability to function well in a high-paced and at times stressful environment
• Proficient with Microsoft Office Suite or related software
• Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions

Education and Experience

• Bachelor’s degree, preferably in a scientific discipline
• 3 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate II
• 6 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate III
• Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred

Physical Requirements

• Prolonged periods of sitting or standing at a desk and working on a computer
• Must be able to lift up to 15 pounds at times
• Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
• Adheres to consistent and predictable in-person attendance

Visit  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