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Associate Manufacturing Specialist Jobs (NOW HIRING)

Manufacturing Associate Location: Vacaville, California Duration: 6 months+ Job Summary: Summary Responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated ...

New

Manufacturing Team Members We Make Doors - Where they lead is up to you... JELD-WEN Holding, Inc ... Our associates are dedicated to bringing beauty and security to the spaces that touch our lives ...

Manufacturing Team Members We Make Doors - Where they lead is up to you... JELD-WEN Holding, Inc ... Our associates are dedicated to bringing beauty and security to the spaces that touch our lives ...

NY · On-site

Process Development & Manufacturing Specialist IResponsibilities / How you will make an impact ... High school diploma with 2+ years of relevant industry experience, or Associate's/Bachelor's degree ...

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Associate Manufacturing Specialist information

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How much do associate manufacturing specialist jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for associate manufacturing specialist in the United States is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

What is an associate manufacturing specialist?

Associate Manufacturing Specialists are entry-level professionals who support the manufacturing process in industries such as pharmaceuticals, biotechnology, or consumer goods. They are responsible for assisting with the production of products by following standard operating procedures, maintaining equipment, documenting processes, and ensuring quality and safety standards are met. These specialists often collaborate with engineers, quality assurance teams, and other production staff to troubleshoot issues and optimize efficiency. The role typically requires strong attention to detail, good communication skills, and adherence to strict regulatory guidelines.

What are the key skills and qualifications needed to thrive as an associate manufacturing specialist?

To thrive as an Associate Manufacturing Specialist, you need a background in life sciences or engineering, along with knowledge of manufacturing processes and quality control principles. Familiarity with Good Manufacturing Practices (GMP), standard operating procedures (SOPs), and relevant software like MES or ERP systems is typically required. Strong attention to detail, effective communication, and problem-solving skills help you excel in this role. These competencies are crucial for maintaining product quality, ensuring regulatory compliance, and contributing to efficient production operations.

How does an associate manufacturing specialist typically collaborate with other departments in a manufacturing facility?

Associate Manufacturing Specialists often work closely with teams such as quality assurance, maintenance, and engineering to ensure production runs smoothly. They may coordinate with quality teams to resolve deviations, communicate with maintenance staff to address equipment issues, and relay feedback to engineering regarding process improvements. This cross-functional collaboration is essential for optimizing workflow, maintaining product quality, and meeting production targets. Being proactive and clear in communication helps build strong relationships and streamlines problem-solving across departments.

What cities are hiring for Associate Manufacturing Specialist jobs?

Cities with the most Associate Manufacturing Specialist job openings:

What are the most commonly searched types of Manufacturing Specialist jobs?

The most popular types of Manufacturing Specialist jobs are:

What states have the most Associate Manufacturing Specialist jobs?

States with the most job openings for Associate Manufacturing Specialist jobs include:

What are popular job titles related to Associate Manufacturing Specialist jobs?

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Infographic showing various Associate Manufacturing Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $43,341 per year, or $20.8 per hour.

Manufacturing Specialist ProQN561

Juncos, PR • On-site

Contractor

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Title: Specialist Manufacturing ProQN561 – Biotechnology Industry

Location: Juncos, Puerto Rico (Only for Puerto Rico residents)

Openings: 6 Positions

Schedule: Administrative Shift (8 hours)

Overtime: Availability to work overtime based on business needs

Contract: 4 months


Position Summary

Our client is seeking Specialist Manufacturing professionals to support manufacturing operations within a regulated biotechnology environment. This role is responsible for supporting manufacturing and quality systems, including deviations, non-conformances, CAPA, process validation, change control, training, and New Product Introductions (NPI). The selected candidate will apply technical expertise, analytical thinking, and troubleshooting skills to ensure GMP compliance, improve manufacturing performance, and support continuous improvement initiatives.


Key Responsibilities

  • Support manufacturing operations by troubleshooting process-related issues and identifying opportunities for continuous improvement.
  • Initiate, revise, review, and maintain manufacturing procedures while serving as a document owner when required.
  • Monitor manufacturing process performance through floor observations and data analysis.
  • Manage the complete lifecycle of deviations, including deviation assessments, investigations, root cause analysis, CAPA implementation, and timely closure using TrackWise.
  • Author investigation reports, support non-conformance management, and monitor incident trends.
  • Assist with process validation activities, including protocol development, execution, data collection, and reporting.
  • Participate in regulatory inspections and maintain compliance with GMP requirements.
  • Support New Product Introductions (NPI), process improvements, equipment modifications, and change control activities.
  • Collaborate with Manufacturing, Process Development, Engineering, and Quality teams to implement process improvements and support special projects.
  • Assist in developing technical training materials and providing process-related training.


Preferred Qualifications

  • Bachelor's degree in Engineering is highly preferred.
  • Biotechnology and pharmaceutical manufacturing experience.
  • Hands-on experience managing deviations and performing deviation assessments.
  • Experience managing the complete lifecycle of deviations from initiation through closure.
  • Experience using TrackWise.
  • Knowledge of GMP manufacturing operations and regulatory requirements.
  • Experience with CAPA, investigations, process validation, change control, and Root Cause Analysis (RCA).
  • Strong analytical, troubleshooting, technical writing, and organizational skills.
  • Ability to collaborate effectively with cross-functional teams.
  • Basic project management and process monitoring knowledge.


Minimum Education & Experience

Candidates must meet one of the following requirements:

  • Doctorate Degree, or
  • Master's Degree with 2+ years of Manufacturing Operations experience, or
  • Bachelor's Degree with 4+ years of Manufacturing Operations experience, or
  • Associate's Degree with 8+ years of Manufacturing Operations experience, or
  • High School Diploma/GED with 10+ years of Manufacturing Operations experience.