Serán BioScience

CDMO offering drug formulation & manufacturing

Technician/Specialist 1 - Validation

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

Full-timeBend, OR, USANo salary listed

About the Job

Requirements

A high school diploma is required.
At least 2 years of experience in a manufacturing, quality, engineering, or validation role is required.
Ability to follow detailed procedures and work instructions.
Basic understanding of mechanical and process equipment.
Proficiency with Microsoft Word, Excel, and Outlook, with the ability to learn quality management system (QMS) systems.
Ability to accurately document test results and observations.
Basic troubleshooting and problem-solving skills.
Must be able to lift 25 pounds at times.
Must adhere to consistent and predictable in-person attendance.
Applicants must be authorized to work for an employer in the United States.

Responsibilities

Learn to execute validation protocols under the guidance of Validation Engineers and Quality personnel.
Perform data collection and testing activities during Installation Qualification, Operational Qualification, and Performance Qualification.
Assist with equipment startup, commissioning, and qualification activities.
Record validation results accurately and in accordance with Good Documentation Practices (GDP).
Collect and organize calibration, maintenance, and testing records required for validation packages.
Review completed validation documentation for accuracy and completeness.
Support environmental, utility, and process monitoring activities as required.
Assist in identifying and documenting validation deviations and discrepancies.
Maintain validation logs, binders, and electronic records.
Work closely with Manufacturing, Engineering, Maintenance, Laboratory, and Quality teams to coordinate validation activities.
Ensure all activities comply with safety procedures, current Good Manufacturing Practices (cGMP) requirements, and company policies.
Support regulatory inspections and internal audits by retrieving and organizing validation documentation.
Work for extended periods sitting or standing at a desk, working on a computer, or in a manufacturing environment.

Desired Qualifications

A technical certification or degree is preferred.
Good Manufacturing Practices (cGMP).
Good Documentation Practices (GDP).
Pharmaceutical or biotechnology manufacturing operations.
Equipment calibration and maintenance concepts.
Validation and qualification processes.
Internship, co-op, vocational training, or GMP experience.

Validation is a regulatory requirement and must be conducted in conformance to cGMPs and FDA requirements. The Validation Technician or Specialist I will be part of a cross functional team that will execute validation studies for process, cleaning, computerized systems, and qualification of equipment and critical utilities needed to support clinical and commercial distribution of sterile and non-sterile pharmaceutical products.

The Validation Technician or Specialist I provides hands-on support for validation and qualification activities within a pharmaceutical manufacturing environment. This entry-level role assists with the execution, documentation, and maintenance of validation programs for equipment, utilities, facilities, computerized systems, and manufacturing processes. The position plays a critical role in ensuring compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company quality standards.

This role is ideal for individuals beginning a career in pharmaceutical manufacturing, quality, engineering, or validation.

Duties & Responsibilities

Learn to execute validation protocols under the guidance of Validation Engineers and Quality personnel

Perform data collection and testing activities during, Installation Qualification, Operational Qualification and Performance Qualification

Assist with equipment startup, commissioning, and qualification activities

Record validation results accurately and in accordance with Good Documentation Practices (GDP)

Collect and organize calibration, maintenance, and testing records required for validation packages

Review completed validation documentation for accuracy and completeness

Support environmental, utility, and process monitoring activities as required

Assist in identifying and documenting validation deviations and discrepancies

Maintain validation logs, binders, and electronic records

Work closely with Manufacturing, Engineering, Maintenance, Laboratory, and Quality teams to coordinate validation activities

Ensure all activities comply with safety procedures, cGMP requirements, and company policies

Support regulatory inspections and internal audits by retrieving and organizing validation documentation

Required Skills & Abilities

Technical Skills

Ability to follow detailed procedures and work instructions

Basic understanding of mechanical and process equipment

Proficiency with Microsoft Word, Excel, and Outlook with the ability to learn QMS systems

Ability to accurately document test results and observations

Basic troubleshooting and problem-solving skills

Preferred Knowledge

Good Manufacturing Practices (cGMP)

Good Documentation Practices (GDP)

Pharmaceutical or biotechnology manufacturing operations

Equipment calibration and maintenance concepts

Validation and qualification processes

Education & Experience

High School Diploma required, technical certification or degree prefered

Minimum of 2 years of experience in a manufacturing, quality, engineering, or validation role

Internship, co-op, vocational training, or GMP experience preferred

Physical Requirements

Prolonged periods of sitting or standing at a desk and working on a computer

Prolonged periods of sitting or standing in a manufacturing environment

Must be able to lift 25 pounds at times

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

Recently Posted Jobs

Explore more opportunities at Serán BioScience

See more jobs