Clean Room Technician

Cleanroom Technician

Stage 2 Contract Engineering is seeking a skilled and detail-oriented Cleanroom Technician to join our team. As a Cleanroom Technician, you will be responsible for the safe, efficient and routine manufacturing of products.

About us: Stage 2 is an engineering and prototype firm in Farmington Hills, Michigan that creates useful solutions to the world's most pressing problems. Stage 2 works to find, develop, and manufacture products that enable the unlucky half of the world to meet basic needs for electricity, clean water, and effective healthcare. Those products include the HANS™ PowerPack, HANS™ Solar Briefcase, and HANS™ Free Electric bicycle; the HANS™ Premium Water Appliance; and the Renew ECP apparatus. Stage 2 has other clean energy, clean water, and medical technologies that are still under development.

ROLE RESPONSIBILITIES

• Operate Cleanroom equipment, including but not limited to vial washers, de-Pyrogenation ovens, filling machines, autoclaves and packaging equipment.
• Ability to operate in a clean room environment.
• Perform cleaning, and sanitization of equipment.
• Follow batch records, SOPs, and work instructions to accurately execute production processes and ensure compliance with cGMP guidelines and regulatory requirements.
• Record GMP data on controlled documentation accurately and precisely.
• Conduct in-process checks, inspections, and sampling to verify product quality and compliance with specifications.
• Document all production activities, observations, and test results accurately and maintain batch records and production logs.
• Comply with regulatory requirements, quality standards, and company policies related to Cleanroom manufacturing and workplace safety.

QUALIFICATIONS

• High school diploma or equivalent; additional technical or vocational training in pharmaceutical manufacturing or related field is a plus.
• Proven experience as a Cleanroom Operator or in a similar role within the pharmaceutical or healthcare industry is preferred.
• Knowledge of cGMP guidelines, quality control principles, and manufacturing processes in the pharmaceutical sector.
• Familiarity with pharmaceutical manufacturing equipment and processes.
• Attention to detail, ability to follow SOPs and instructions precisely, and maintain accurate documentation.
• Strong organizational skills and ability to multitask in a fast-paced manufacturing environment.
• Basic computer skills for data entry, equipment monitoring, and documentation purposes.
• Good communication skills and the ability to work effectively as part of a team.

Equal opportunity employer

Job Type: Full-time

Pay: $16.45 - $21.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Work Location: In person