Net2Source (N2S) is hiring: Other - Manufacturing Associate Manufacturing Assoc

Other - Manufacturing Associate Manufacturing Associate

Other - Manufacturing Associate Manufacturing Associate

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This range is provided by Net2Source (N2S). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$25.00/hr - $28.57/hr

Join a Global Leader in Workforce Solutions - Net2Source Inc.

Who We Are

Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price.

Title: Manufacturing Associate

Location: Andover, MA 01810

Duration: 12+ Months (Extendable)

What You Will Achieve

You will be part of a multi-disciplinary team responsible for cGMP production of phase I/II clinical drug substance supporting the *** Biotherapeutics portfolio. You will be part of the manufacturing team focused on mammalian bio-processing, this includes and not limited to supporting the manufacturing operations team, reviewing Standard Operating Procedures, reviewing batch records, and standard work. As part of technical operations, you will be a team member who is relied to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team's success by sharing of previously acquired knowledge. It is your hard work and focus that will help in making *** ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Manage own time and professional development, be accountable for own results and begin to prioritize own workflow.
• Cross-functional communication with tech transfer team, quality and engineering as necessary.
• Implement {Current} Good Manufacturing Practices {part of GxP} procedures and safe handling techniques for solid dosage processing within the continuous manufacture /PCMM work stream.
• Perform Upstream and Downstream operations in clinical Bio-Manufacturing.
• Ability to follow Standard Operating Procedures and work under minimal supervision.
• Identify and support continuous improvement initiatives and root cause analysis tools.
• Generate, assist and execute documentation associated with solid dosage manufacture, such as, working batch record documentation, in-process run sheets.
• Complete activities identified as Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment.
• Work in electronic systems including QMS, Documentation, Laboratory Information Management System, Enterprise Resource Planning (e.g. SAP) etc.
• Actively participate in shift exchange activities and communication channels.
• Complete training to take part in safety inspections within the facility.
• Understand and comply with the policies, procedures and working practices of Environment, Health & Safety and where necessary contribute to the review and implementation of the practices in the plant.
  
  

Qualifications

Must-Have

• High School Diploma or GED
• Demonstrated experience in a biotechnology manufacturing or laboratory environment
• Operational knowledge of computerized systems, Familiarity with Production Control Systems, Enterprise Resource Planning Systems and other business systems
• Maintains a safe work environment
• Demonstrated capability to work as a team member in a matrix development team
• Excellent oral and written communication skills
• Strong computer skills in Microsoft Office required, especially MS Word, MS Excel
• Understanding of scientific principles, ability to think critically and demonstrate troubleshooting and problem-solving skills
  
  

Nice-to-Have

• Bachelor's Degree
• Knowledge of cell culture and/or downstream processing techniques, manufacturing setting preferred
• Mechanical aptitude and desire to execute hands on manual labor
  
  

Physical/Mental Requirements

• Must be able to climb flights of stairs, and remain standing for extended periods of time
• Must be able to lift up to 50 lbs
• Ability to thrive in dynamic team environment with diverse perspectives
  
  

Non-Standard Work Schedule, Travel Or Environment Requirements

• Ability to work nights and weekends as needed depending upon process needs; non-routine
• Job Location: On premise
• Work Schedule: Monday - Friday 7am - 3:30pm / Weekend OT optional
• Interview: Onsite
  
  

Why Work With Us?

We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.

Our Commitment to Inclusion & Equity

Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.

Awards & Recognition

• America's Most Honored Businesses (Top 10%)
• Fastest-Growing Staffing Firm by Staffing Industry Analysts
• INC 5000 List for Eight Consecutive Years
• Top 100 by Dallas Business Journal
• Spirit of Alliance Award by Agile1
  
  

Ready to Level Up Your Career?

Click Apply Now and let's make it happen.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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