Manufacturing Technician I
About The Position
About the role: As a Manufacturing Technician I, you will execute all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. You will participate in both departmental projects and any quality working teams which may be applicable. You will initiate new documents for procedures which are simple in nature and may also make minor revisions to existing documents and will troubleshoot simple existing procedures You will demonstrate procedures as a part of a training session and may schedule department or process activities which could involve coworkers. How you will contribute: Prepare media and buffer solutions. Operate Clean-in-Place (CIP) and Steam-in-Place systems. Assemble and operate filtration systems. Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.). Monitor and record critical process parameters. Complete all relevant paperwork following GDP/GMP guidelines. Perform routine maintenance and cleaning of production equipment to maintain in GMP fashion. Perform sampling using aseptic techniques. Participate on Continuous Improvement Teams. Receive and distribute supplies into production areas as necessary. Train and mentor other team members. Revise and review pertinent documentation as appropriate. Assist in troubleshooting process problems and responding to alarms. May perform other duties as assigned.
Requirements
- Typically requires high school diploma or GED plus 1+ years of related experience or associate degree or higher with no prior experience required.
- Knowledge of cGMP manufacturing.
- Knowledge of basic laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, incubators, analytical equipment and CIP/SIP systems.
- Proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurement.
- Must be able to read and follow detailed written instructions and have good verbal/written communication skills.
- Knowledge of basic chemical and biological safety procedures.
- Knowledge of Microsoft Word and Excel
Responsibilities
- Prepare media and buffer solutions.
- Operate Clean-in-Place (CIP) and Steam-in-Place systems.
- Assemble and operate filtration systems.
- Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.).
- Monitor and record critical process parameters.
- Complete all relevant paperwork following GDP/GMP guidelines.
- Perform routine maintenance and cleaning of production equipment to maintain in GMP fashion.
- Perform sampling using aseptic techniques.
- Participate on Continuous Improvement Teams.
- Receive and distribute supplies into production areas as necessary.
- Train and mentor other team members.
- Revise and review pertinent documentation as appropriate.
- Assist in troubleshooting process problems and responding to alarms.
- May perform other duties as assigned.
Benefits
- U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others.
- U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
