Specialist Manufacturing 35380

Inteldot; Juncos (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Inteldot, a leader in the life science industry, is seeking an Administrative Shift professional in Puerto Rico. This role involves supporting manufacturing/quality systems and driving process optimization with minimal supervision.

Candidates should possess engineering experience, familiarity with compliance standards, and a collaborative mindset to troubleshoot issues effectively. A range of educational backgrounds will be considered, including degrees in Engineering, Life Sciences, or related disciplines.

Qualifications

• Engineering experience in manufacturing operations is essential.
• Hands-on experience in biotech or pharmaceutical production is required.
• Familiarity with Lean Six Sigma and process optimization methodologies is expected.

Responsibilities

• Support manufacturing operations with minimal supervision.
• Assist with process ownership and complex manufacturing systems.
• Troubleshoot and drive process optimization initiatives.

Skills

Engineering Experience in Manufacturing Operations

Hands-on experience in process engineering

Technical Knowledge of automation systems

Problem-Solving Skills

Cross-Functional Collaboration

Regulatory/GMP Knowledge

Strong communication

Education

Doctorate or Master's with 2 years of experience

Bachelor's degree with 4 years of experience

Associate's degree with 8 years of experience

High school/GED with 10 years of experience

Preferred background in Engineering or Life Sciences

Job description

Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Administrative Shift

Description

With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.

Requirements & Qualifications

• Engineering Experience in Manufacturing Operations
• Hands‑on experience in process engineering, manufacturing support, or production systems within a regulated environment (biotech, pharmaceutical, or similar).
• Technical Knowledge – Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean Six Sigma, Kaizen, root cause analysis).
• Problem‑Solving Skills – Demonstrated ability to troubleshoot manufacturing issues, implement corrective/preventive actions (CAPA), and drive process optimization.
• Cross‑Functional Collaboration – Proven experience working with operations, quality, and maintenance teams to deliver results in a fast‑paced environment.
• Regulatory / GMP Knowledge – Understanding of cGMP, compliance, and documentation practices for regulated industries.
• Additional Strengths – Strong communication, adaptability to change

Education

• Doctorate, or a Master's degree with 2 years of Manufacturing Operations experience, a Bachelor's degree with 4 years of Manufacturing Operations experience, an Associate's degree with 8 years of Manufacturing Operations experience, or a High school/GED with 10 years of Manufacturing Operations experience.
• Preferred academic background in Engineering disciplines, particularly Life Sciences, Engineering, Biotechnology, Chemistry, or a related technical discipline.