Manufacturing Associate Job at Net2Source (N2S) in Andover

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Why This Role Matters

Our pharmaceutical manufacturing team plays a crucial role in delivering life-changing medicines to patients worldwide. We rely on dedicated and agile professionals who understand the impact of their work and strive to continuously improve outcomes. Your contributions will help ensure that patients and healthcare providers receive the medicines they need, when they need them.

What You Will Do

You will be part of a multi-disciplinary team responsible for cGMP production of phase I/II clinical drug substances, focusing on mammalian bioprocessing. This includes supporting manufacturing operations, reviewing Standard Operating Procedures (SOPs), batch records, and standard work. Your understanding of procedures, techniques, tools, materials, and equipment will help prioritize workflows and complete tasks of varying complexity. Sharing your knowledge and dedication will contribute to the team’s success.

How You Will Achieve It

• Manage your time and professional development, prioritizing your workflow independently.
• Communicate cross-functionally with tech transfer, quality, and engineering teams as needed.
• Implement current Good Manufacturing Practices (GxP) and safe handling techniques within the manufacturing process.
• Perform upstream and downstream operations in clinical bio-manufacturing.
• Follow SOPs and work with minimal supervision.
• Support continuous improvement initiatives and root cause analysis.
• Generate and execute documentation such as batch records and in-process run sheets.
• Perform operator care tasks related to pharmaceutical manufacturing equipment maintenance and operation.
• Work with electronic systems including QMS, LIMS, ERP (e.g., SAP).
• Participate actively in shift exchanges and communications.
• Complete safety training and contribute to facility inspections.
• Adhere to Environment, Health & Safety policies and contribute to ongoing improvements.

Qualifications

Must-Have:

• High School Diploma or GED
• Experience in biotechnology manufacturing or laboratory environment
• Knowledge of computerized systems, production control, and ERP systems
• Ability to maintain a safe work environment
• Team player with strong communication skills
• Proficient in Microsoft Office (Word, Excel)
• Critical thinking with troubleshooting and problem-solving abilities

Nice-to-Have:

• Bachelor’s Degree
• Experience with cell culture or downstream processing in manufacturing
• Mechanical aptitude and willingness to perform hands-on manual tasks

Physical Requirements:

• Ability to climb stairs and stand for extended periods
• Ability to lift up to 50 lbs
• Willingness to work nights, weekends, or non-standard schedules as needed

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Manufacturing

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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