Manufacturing Technician II (AM Swing Shift)

Nitto Avecia; Milford (MA); On-site; USD 61,700 - 75,600; Full time

Job summary

A biotechnology manufacturing company is seeking a Manufacturing Technician II in Milford, Massachusetts. This role involves responsibilities such as maintaining compliance with GMP standards, executing production activities, and completing necessary documentation. With a salary range of $61,700 to $75,600, it requires a high school diploma or equivalent, and a preferred background in biotechnology or related fields. Experience in a cGMP environment is essential, making this an excellent opportunity for those looking to advance their career in the biotech industry.

Qualifications

• Minimum education requirement is a high school diploma or equivalent.
• Preferred qualification includes a biotechnology certificate or college degree.
• Must have two plus years of experience in a cGMP manufacturing environment.

Responsibilities

• Maintain a clean and organized work environment.
• Complete GMP documentation in a compliant manner.
• Identify and implement small continuous improvement projects.

Skills

Knowledge of basic laboratory instrumentation

Problem solving

Compliance with GMP and safety regulations

Education

High school diploma or equivalent

Biotechnology certificate or college degree

Job description

About This Opportunity

As a Manufacturing Technician II, you'll be responsible for the implementation of assigned production operations working within defined production schedules in a cGMP environment. This is a swing shift position which runs from 8:00 AM - 8:00 PM (1st week M,T and F - Sn / 2nd week W-Th). This role comes with a 5% shift differential.

Key Responsibilities

• Maintain a clean and organized work environment. Responsible for following GMP and safety cultures, procedures, and regulations.
• Identify and submit safety hazards and incidents.
• Complete GMP documentation in a compliant manner. May review less complex documentation like logbooks.
• May revise procedures under direct supervision.
• May participate in investigations. May execute CAPA tasks.
• Identify and implement small continuous improvement projects.
• Responsible for assigned production activity and ensuring training is compliant prior to performing operations.
• Problem solving: basic understanding of process and documentation. Ability to identify abnormal results and report to higher position.
• Proficient in the assigned area of the process.

Required Skills/Abilities

• Minimum education requirements: high school diploma or equivalent with college level Chemistry degree or equivalent work experience.
• A biotechnology certificate or college degree is preferred.
• Must have knowledge of basic laboratory instrumentation such as use of pH meter, UV instrumentation, and solution delivery systems (process skids).
• Two plus years of experience in cGMP manufacturing environment. Performance/other experience can be considered pending manager discretion.

The annualized salary range for this roles is $61,700.00 - $75,600.00.