Serán BioScience

CDMO offering drug formulation & manufacturing

Quality Assurance Associate 2/3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeBend, OR, USANo salary listed

About the Job

Requirements

Knowledge of Good Manufacturing Practice (GMP) and U.S. Food and Drug Administration regulations for clinical trial materials.
Understanding of change control procedures, the corrective and preventive action (CAPA) program, investigations, root cause analysis, and good documentation practices.
Strong organizational skills and attention to detail.
Time management skills and the ability to meet deadlines.
Analytical and problem-solving skills.
Ability to communicate effectively and maintain productive relationships with coworkers, clients, and external contacts.
Ability to collaborate and work in cross-functional teams.
Ability to accept feedback from a variety of sources and constructively manage conflict.
Ability to prioritize tasks and delegate them when appropriate.
Verbal and written communication skills.
Ability to function in a fast-paced and sometimes stressful environment.
Proficiency with Microsoft Office Suite or related software.
Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment across multiple sources of information to make independent decisions.
Bachelor’s degree, preferably in a scientific discipline.
At least 3 years of GMP experience in a quality control (QC) or quality assurance (QA) role for Associate II qualification, or at least 6 years for Associate III qualification.
Pharmaceutical manufacturing experience.
Ability to work in person with consistent and predictable attendance.
Ability to sit or stand for prolonged periods while working at a computer, lift up to 15 pounds at times, and wear required personal protective equipment, including safety glasses, hearing protection, a hard hat, and safety shoes.
Authorization to work for an employer in the United States.

Responsibilities

Author, review, and approve standard operating procedures (SOPs), batch production and quality control records, certificates of analysis, method validations, and equipment qualifications.
Apply working knowledge of best practices in Good Manufacturing Practice (GMP) and understand how Quality integrates with other business areas.
Initiate and oversee investigations.
Manage corrective and preventive actions (CAPA).
Support internal audits, client audits, and regulatory inspections, with potential responsibility for hosting them.
Manage controlled document issuance and archival.
Perform quality reviews with minimal oversight.
Communicate quality-related information to internal teams with minimal guidance.
Perform other related duties as assigned.
Support the Quality Assurance department’s daily activities by ensuring GMP regulations and internal SOPs are followed throughout clinical manufacturing.
Review and approve production records, analytical data, and internal quality assurance documentation.
Conduct risk analyses and investigations and participate in audits and inspections.

Desired Qualifications

Commercial pharmaceutical manufacturing knowledge is desirable but not required.
Oral solid dosage experience is preferred.

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

About the Company

Serán BioScience

CDMO offering drug formulation & manufacturing

Serán Bioscience is a contract development and manufacturing organization that helps pharmaceutical companies develop and manufacture drugs. It offers preformulation, formulation and dosage-form development, spray drying and particle engineering, plus cGMP manufacturing and analytical quality control. It relies on flexible, client-tailored services and a broad technical toolkit to support a range of clients from startups to large pharma. Its goal is to enable efficient, compliant drug development and production with rigorous quality standards.

Company size: 51-200
Company stage: Growth Equity (Venture Capital)
Total funding: $200M
Headquarters: Bend, OR
Founded: 2016

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