Pharma Operations Specialist II – GMP Manufacturing

Lever, Inc.; Bend (OR); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Paid time off

Retirement plan

Health plans

Life and long-term disability coverage

Employee Assistance Program

Pet insurance

Job summary

Serán BioScience seeks an Operations Specialist II to support the manufacture of tablets, capsules, and spray dried dispersions in a fast-paced, collaborative setting in Bend, Oregon. You will strictly follow SOPs and GMP, maintain records, and support cross-functional teams to ensure quality and compliance.

Ideal candidates will have GMP experience, strong attention to detail, and the ability to train others while communicating effectively with colleagues and vendors as needed.

Qualifications

• High School Diploma or equivalent.
• Coursework or experience in chemistry or manufacturing field preferred.
• Approximately 2 years of GMP experience.

Responsibilities

• Strictly follows standard operating procedures (SOP).
• Complies with Good Manufacturing Practice (GMP).
• Completes documentation, including logbooks, batch records, and quality records.
• Revises documents for improved compliance and ease of use.
• Maintains an organized, clean, and stocked production area.
• Cleans tools, rooms, and equipment after use.
• Operates specialized machinery to manufacture pharmaceutical products.
• Safety and process improvement participation.
• Works closely and communicates effectively with operations team.
• Involved in safety and process improvement plans.

Skills

Pharma manufacturing

Documentation

Attention to detail

Communication

Time management

Team collaboration

Math

Education

High School Diploma or equivalent

Chemistry/mfg coursework

Tools

Microsoft Office Suite

Job description

Serán BioScience seeks an Operations Specialist II to support the manufacture of tablets, capsules, and spray dried dispersions in a fast-paced, collaborative setting in Bend, Oregon. You will strictly follow SOPs and GMP, maintain records, and support cross-functional teams to ensure quality and compliance.

Ideal candidates will have GMP experience, strong attention to detail, and the ability to train others while communicating effectively with colleagues and vendors as needed.