Job Details

Job Summary:

The company is seeking an entry-level scientific professional to support manufacturing and laboratory operations within a regulated pharmaceutical development environment. This role focuses on operating automated fill and finish equipment, supporting prefilled syringe production activities, documenting technical processes, and assisting with laboratory procedures while maintaining strict compliance with quality standards. The ideal candidate will bring strong scientific fundamentals, technical writing ability, and a collaborative mindset.

Key Responsibilities:

• Set up, operate, and monitor moderately complex automated fill and finish equipment used in prefilled syringe production

• Support routine laboratory and manufacturing activities with minimal supervision in a controlled environment

• Work with process equipment including mixing vessels, filters, tanks, utilities, and related system connections

• Accurately document manufacturing activities, observations, and results in electronic systems in compliance with GLP and GMP standards

• Draft technical documents, reports, and process records using clear and professional scientific writing

• Assist with troubleshooting equipment or laboratory process issues through scientific problem solving

• Utilize Microsoft Office tools for documentation, reporting, and data tracking

• Collaborate effectively with cross-functional team members while maintaining adherence to quality procedures

Required Qualifications:

• Bachelor's degree in Engineering, Pharmaceutical Sciences, Chemistry, Pharmaceutics, or related scientific discipline

• Hands-on laboratory experience and familiarity working with automated process equipment

• Basic knowledge of laboratory or manufacturing documentation practices in regulated settings

• Strong technical writing and documentation skills

• Scientific problem-solving, experimental design, and troubleshooting ability

• Proficiency with Microsoft Office applications

• Strong verbal and written communication skills with the ability to work in a team environment

Preferred Qualifications:

• Experience in a regulated pharmaceutical manufacturing or laboratory environment

• Familiarity with sterile processing operations

• Exposure to fill and finish manufacturing processes

• Understanding of GLP and GMP compliance requirements

Benefits:

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

Pay Range: $30/hr to $38/hr