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Sharp Sterile Manufacturing Careers

Sharp Sterile Manufacturing
Lee, MA Full Time
POSTED ON 7/8/2026
AVAILABLE BEFORE 8/6/2026
View or apply to [current positions at Sharp Sterile

Manufacturing](https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&type=MP&lang=en_US&selectedMenuKey=CareerCenter){target="_blank"

rel="noopener noreferrer"} **Sharp Sterile Manufacturing is currently

seeking candidates for the below listed positions:** - Senior Project

Engineer - \$97,000-\$122,000/year - Maintenance Technician I&II 1st &

3rd Shift - \$23-\$35/hour - QA Senior Shop Floor Manager -

\$90,000-\$130,000/year - QA Compliance Specialist II -

\$65,000-\$85,000/year - Manufacturing Formulation Supervisor 3rd

Shift - \$80,000-\$110,000/year - Director of Quality Systems -

\$100,000-\$150,000/year - Purchasing Expeditor -

\$58,000-\$85,000/year - Manufacturing Supervisor 3rd Shift (10:30pm -

7:00am) - \$70,000-\$95,000/year - IT Manager -

\$90,000-\$140,000/year - Senior Process Engineer -

\$90,000-\$140,000/year - Staff Accountant - \$60,000-\$85,000/year -

Manufacturing Associate (All Shifts) - \$19.00-\$35.00/hour -

Formulation Associate 2nd & 3rd - \$19.58 - \$36.59/hour **About Sharp

Sterile Manufacturing** Sharp Sterile Manufacturing, is a leader in high

quality clinical and small volume commercial manufacture of sterile

injectable drug/biologic products and medical devices. Sharp Sterile

utilizes state of art isolator technologies to provide the greatest

sterility assurance possible. Sharp Sterile\'s Lee, Massachusetts

facility is FDA inspected and offers a variety of services including:

sterile fill finish, analytical and microbiological testing, stability

services and regulatory support.

Salary : $85,000 - $150,000

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Job openings at Sharp Sterile Manufacturing

  • Sharp Sterile Manufacturing Lee, MA
  • Position Summary The Facilities Maintenance Manager is responsible for the repairs and maintenance of the facility and achieving departmental objectives. T... more
  • 9 Days Ago

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  • Duties Assist in the development, execution and approval of all validation programs and lifecycle documentation, e.g. SOPs, Change Controls, CAPAs, Deviati... more
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  • Position Summary The Quality Systems Director is responsible for developing, implementing, and maintaining a robust Quality Management System (QMS) to ensu... more
  • 6 Days Ago

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  • Position Summary The Formulation Supervisor is a working supervisor role responsible for all aspects of formulation activities to ensure achievement of the... more
  • 7 Days Ago


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