Quality Assurance Associate II/III (Swing Shift)

Serán BioScience; Bend (OR); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Over four weeks of paid time off annually

Employer contributions to a retirement account

Various health plans

Employee Assistance Program

Pet insurance

Job summary

A pharmaceutical company in Bend, Oregon, is seeking a Quality Assurance Associate to support regulatory compliance for manufacturing oral solid dosage drug products. Key responsibilities include reviewing production records and ensuring GMP regulations are followed. Candidates should have a bachelor's degree in a scientific discipline, with 3-6 years of GMP experience in QC or QA roles. This role offers various benefits, including paid time off and health plans.

Qualifications

• 3 years of GMP experience within a QC or QA role for Associate II
• 6 years of GMP experience for Associate III
• Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred
• Pharmaceutical manufacturing experience with Oral Solid Dosage preferred.

Responsibilities

• Documents authorships, reviews, and approves of SOPs and production records
• Initiates and oversees investigations and CAPA actions
• Supports internal and client audits
• Support internal and client audits and regulatory inspections.

Skills

Knowledge of GMP and FDA regulations

Analytical and problem-solving skills

Organizational skills

Effective communication

Proficiency in Microsoft Office Suite

Analytical skills

Time management

Problem solving

Education

Bachelor's degree in a scientific discipline

3 years GMP experience in QC/QA

6 years GMP experience in QC/QA

Pharmaceutical manufacturing experience

Tools

MS Office

Job description

Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience.

This role will support the alternative manufacturing schedule from Monday - Thursday, beginning at 2:00 pm and ending at 1:00 am. Experience specific to Serán's manufacturing capabilities and confidence to make independent decisions in alignment with Company policies and risk mitigation philosophies will be critical to this role.

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 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.