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Actalent Manufacturing Associate I-III in Watertown, Massachusetts

Offering a Career Advancement Program - working with managers and supervisors to develop career goals and plan for growing within the company

Description:

Job Description

The Manufacturing Associate I-III will execute the daily cGMP manufacturing operations of solid oral dose drug product manufacturing in a state-of-the-art commercial biopharmaceutical manufacturing facility in Watertown, MA. This person is accountable for adhering to the production schedule, while ensuring the highest standards of workplace safety and product quality are adhered to. They will support the Manufacturing Suite startup, procedure generation and training to ensure that the technical transfer, scaleup and commercial manufacturing operations are completed on-time and right the first time. The ideal candidate will enjoy working in a team-oriented environment with minimal supervision.

ESSENTIAL JOB FUNCTIONS

-Perform hands-on operations for pharmaceutical manufacturing of solid oral dosage forms, including, but not limited to, dispensing, blending, milling/screening, encapsulation, tableting, banding, coating, weight sorting, packaging, and labeling etc., in a commercial cGMP environment

-Perform equipment set-up, break-down, and cleaning, including appropriate care and storage of all change parts

-Documentation of all activities in Batch Records, Logbooks, Forms, etc. and electronic interfaces

-Maintain the highest standards of workplace Safety and product quality

-Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation.

-Identifies, escalates, and documents events and deviations and subtle variances that deviate from normal operation; participate as needed in investigations.

-Demonstrates ability to troubleshoot basic mechanical operations.

-Work in accordance with site and company EHS programs.

-Work in accordance with regulations, detailed protocols, Batch Records, SOPs, and Work Instructions

-Strong commitment to continuous improvement

Additional Skills & Qualifications:

Experience and Skills

-Technical Degree OR B.S. in Biology, or related field preferred but not required

-Operational Excellence, such as 6S, experience a plus

-Working knowledge of Microsoft Outlook, Word and Excel required.

-Good laboratory skills and excellent record keeping, including GDP, is required.

-Ability to work independently and stay on task in a fast-paced environment without direct supervision.

-Ability to work well with others in a collaborative team environment.

-Regular and reliable performance and attendance required.

-Team player

-Ability to handle multiple tasks while remaining focused

-Reliable, dependable, and organized

COVID19 Vaccine required to come on site; Individuals seeking an exemption from this requirement for medical or religious reasons should reach out to Human Resources for an accommodation

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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