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Manufacturing Specialist - 33614

🌟 Exciting Opportunity: Specialist Manufacturing (33614) 🌟

Location: Puerto Rico (East of the island) – Hybrid Opportunity

Shift: 8:00 am to 5:00 pm (8-hour shift)


Are you ready to take the next step in your career? Our client is seeking a Specialist in Manufacturing to join their team and support critical manufacturing and quality systems. This hybrid role offers the opportunity to apply your operational and scientific expertise while making a real impact! 🌱


✨ What You'll Do

With minimal supervision, you will support key areas such as:

β€’ Non-conformances

β€’ Process validation

β€’ Procedures

β€’ Training

β€’ New product introductions


You’ll apply your troubleshooting skills and process expertise to support manufacturing operations while also playing a key role as a primary production process owner on support systems.


✨ Qualifications

You must meet one of the following:

πŸŽ“ Doctorate degree

πŸŽ“ Master's degree + 3 years of Manufacturing Operations experience

πŸŽ“ Bachelor's degree + 5 years of Manufacturing Operations experience

πŸŽ“ Associate's degree + 10 years of Manufacturing Operations experience

πŸŽ“ High school diploma / GED + 12 years of Manufacturing Operations experience


πŸ” Preferred Skills:

β€’ Experience handling deviations and non-conformances investigations

β€’ Strong technical writing skills

β€’ Proficiency in root cause analysis tools (e.g., causal factors analysis, 5 Why’s)

β€’ Excellent project management skills


🌟 Key Responsibilities


πŸ›  Applied Process Expertise

β€’ Create, revise, and approve manufacturing procedures.

β€’ Assess and improve process performance through data review.

β€’ Provide troubleshooting support and generate training materials.


πŸ“Š Process Monitoring

β€’ Support process monitoring parameters and ensure timely reporting.

β€’ Collect and analyze process-monitoring data for deviations.


⚠️ Non-Conformance and CAPA

β€’ Author and manage investigation reports.

β€’ Execute corrective actions and track NC/CAPA closures.

β€’ Monitor trends and review equipment/system Root Cause Analysis investigations.


πŸ“ Process Validation

β€’ Assist with validation protocols and support data analysis.


πŸ” Regulatory

β€’ Participate in regulatory inspections as needed.


πŸš€ New Product Introductions & Process Modifications

β€’ Collaborate on documentation, training, and equipment modifications for new products.


πŸ”„ Change Control

β€’ Assist in managing manufacturing change requests impacting the process.


πŸ”§ Projects and Initiatives

β€’ Support special projects or initiatives as assigned.


πŸ”‘ Competencies & Skills

β€’ Technical understanding of bioprocessing unit operations

β€’ Skilled in GMP production operations

β€’ Regulatory knowledge and interactions

β€’ Strong communication and collaboration skills across technical and management teams

β€’ Organizational, technical writing, and presentation skills

β€’ Basic project management and control charting knowledge


🌟 Ready to Apply? 🌟

This is a fantastic opportunity to work in a hybrid role in Puerto Rico while advancing your career in manufacturing operations. πŸ’Ό



πŸ‘‰ Share with your network and take part in our referral program! You could earn a referral bonus if your referral is hired.

Click here to view the full job description and apply with your updated resume inside the job: Specialist Manufacturing Job Description


ο»ΏDon't miss out – apply today and be part of something impactful! 🌟



Thank you. We will be in contact soon.

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