Manufacturing Technician II (AM Swing Shift)

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

Benefits offered by this job

5% shift differential

Job summary

Avecia Pharma is seeking a Manufacturing Technician II for the AM swing shift in Milford, MA. The role operates 8:00 AM to 8:00 PM on a rotating schedule with a 5% shift differential and requires a chemistry-focused education or biotechnology background.

Responsibilities include GMP-compliant documentation, safety oversight, and participating in CAPA tasks while contributing to small process improvements in a cGMP environment.

Qualifications

• High school diploma or equivalent with chemistry background or exposure.
• Biotechnology certificate or college degree preferred.
• Two plus years of experience in a cGMP manufacturing environment.

Responsibilities

• Maintain a clean and organized work environment and follow GMP and safety procedures.
• Identify and submit safety hazards and incidents.
• Complete GMP documentation; review logbooks or other less complex docs.
• May participate in investigations and execute CAPA tasks.
• Identify and implement small continuous improvement projects.
• Ensure training is compliant prior to performing operations.
• Problem solving: recognize abnormal results and report to supervisor.

Skills

cGMP manufacturing

Laboratory instrumentation

Process knowledge

Education

High school diploma or equivalent

Biotechnology certificate or college degree

Tools

pH meter

UV instrumentation

Solution delivery systems

Job description

Manufacturing Technician II (AM Swing Shift)

Jul 5, 2026

Regular Full Time

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 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 role is $61,700.00 - $75,600.00.