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Director Of Manufacturing Operations Jobs in Puerto Rico

Weil Group, Inc

Specialist Manufacturing

Juncos, PR · On-site

Serve as a document owner. 2. Assess process performance by observation of floor operations and ... Change Control 1. Assist manufacturing change owner on CCRB packages impacting the process.

Inteldot

Specialist Manufacturing 35421

Juncos, PR · On-site

Skilled in performance of GMP production operations * Regulatory knowledge and interactions ... Own change controls for manufacturing process changes * Support major/trend deviation ...

Weil Group, Inc

PR · On-site

Serve as a document owner. 2. Assess process performance by observation of floor operations and ... Change Control 1. Assist manufacturing change owner on CCRB packages impacting the process.

Weil Group, Inc.

Specialist Manufacturing

Juncos, PR · On-site

Serve as a document owner. 2. Assess process performance by observation of floor operations and ... Change Control 1. Assist manufacturing change owner on CCRB packages impacting the process.

Inteldot

Specialist Manufacturing 35326

Juncos, PR · On-site

Experience of bio-processing unit operations * Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why's, Kepner Tregoe) * Familiar with Lean Manufacturing Practices

Weil Group, Inc

PR

Serve as a document owner. 2. Assess process performance by observation of floor operations and ... Change Control 1. Assist manufacturing change owner on CCRB packages impacting the process.

Weil Group, Inc

Specialist Manufacturing

Juncos, PR · On-site

Experience of bio-processing unit operations Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why's, Kepner Tregoe) Familiar with Lean Manufacturing Practices Ability ...

Weil Group, Inc.

Specialist Manufacturing

Juncos, PR · On-site

Serve as a document owner. 2. Assess process performance by observation of floor operations and ... Change Control 1. Assist manufacturing change owner on CCRB packages impacting the process.

Cencora

Specialist Manufacturing

Juncos, PR · On-site

In-depth experience of bio-processing unit operations * Knowledge in Root Cause Analysis ... Familiar with Lean Manufacturing Practices * Ability to communicate and collaborate with technical ...

Cencora

Specialist Manufacturing

Juncos, PR · On-site

In-depth experience of bio-processing unit operations * Knowledge in Root Cause Analysis ... Familiar with Lean Manufacturing Practices * Ability to communicate and collaborate with technical ...

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Director Of Manufacturing Operations information

What is a Director Of Manufacturing Operations job?

A Director of Manufacturing Operations oversees the production process, ensuring efficiency, quality, and cost-effectiveness in manufacturing. They manage plant operations, streamline workflows, implement safety standards, and coordinate with other departments to meet production goals. Additionally, they analyze performance metrics, optimize resources, and drive continuous improvement initiatives to enhance productivity and profitability.

What are the key skills and qualifications needed to thrive in the Director Of Manufacturing Operations position, and why are they important?

To excel as a Director Of Manufacturing Operations, you need strong leadership, process optimization expertise, and a background in engineering or operations management, often supported by a bachelor's or master's degree in a related field. Familiarity with ERP/MRP systems, lean manufacturing methodologies, and industry certifications like Six Sigma or PMP is common in this role. Outstanding soft skills include strategic thinking, decision-making, effective communication, and the ability to motivate and manage large teams. These skills ensure efficient, safe, and high-quality production operations, while driving continuous improvement and organizational success.

What are the typical daily responsibilities of a Director Of Manufacturing Operations?

A Director Of Manufacturing Operations oversees all aspects of a manufacturing facility's production processes, ensuring efficiency, quality, and safety standards are met each day. This typically involves monitoring key performance indicators, addressing operational bottlenecks, collaborating with department heads, and implementing process improvements. Directors also regularly communicate with executive leadership to align production goals with organizational strategy and manage budgets or resource allocation. Additionally, they play a significant role in mentoring managers and supervisors while fostering a culture of continuous improvement on the factory floor.

What are popular job titles related to Director Of Manufacturing Operations jobs in Puerto Rico? For Director Of Manufacturing Operations jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Director Of Manufacturing Operations jobs in Puerto Rico look for? The top searched job categories for Director Of Manufacturing Operations jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Director Of Manufacturing Operations jobs? Cities in Puerto Rico with the most Director Of Manufacturing Operations job openings:
Director Of Manufacturing Operations jobs near you
Specialist Manufacturing

Specialist Manufacturing

BioPharma Consulting JAD Group

Juncos, PR • On-site

Full-time

Posted 24 days ago

Job description

With minimal supervision, the Specialist Manufacturing supports the execution of manufacturing and quality systems including non‑conformances, process validation, procedures, training, and new product introductions. The role applies process, operational, and scientific expertise—along with compliance knowledge and troubleshooting skills—to support manufacturing operations. The specialist may serve as a primary process owner for support systems and assist with ownership responsibilities for more complex systems.

FUNCTIONS

  • Initiate, revise, and approve manufacturing procedures; ensure procedures reflect current operations.
  • Serve as document owner for assigned procedures.
  • Assess process performance through floor observation and data review; identify and implement process improvement opportunities.
  • Provide troubleshooting support for manufacturing operations.
  • Assist in generating training materials and delivering technical/scientific training.
  • Support establishment of process monitoring parameters and control limits.
  • Collect process monitoring data and support deviation assessments.
  • Support timely execution of quarterly process monitoring reports.
  • Ensure non‑conformances are triaged within established timelines.
  • Author investigation reports and execute corrective actions.
  • Manage NC/CAPA closure within required goals.
  • Monitor and communicate incident trends.
  • Review equipment/system RCA investigations and support trend evaluations.
  • Assist in generating process validation protocols and reports.
  • Support execution of process validation activities.
  • Collect and analyze validation data.
  • Participate in regulatory inspections, new product introductions, and process/equipment modifications.
  • Assess documentation, materials, training, and equipment needs for NPI.
  • Provide project management support for process or equipment modification projects.
  • Assist manufacturing change owners with CCRB packages impacting the process.
  • Participate in assessments and implementation of special projects or initiatives.
  • Perform additional duties as assigned.

SKILLS

  • Detailed technical understanding of bioprocessing unit operations.
  • Skilled in GMP production operations.
  • Knowledge of regulatory expectations and interactions.
  • Ability to communicate and collaborate with manufacturing, process development, and quality teams.
  • Strong organizational, technical writing, and presentation skills.
  • Basic project management skills.
  • Basic knowledge of control charting and process monitoring.

Requirements

EDUCATION & EXPERIENCE REQUIREMENTS

  • Doctorate OR
  • Master’s + 2 years of Manufacturing Operations experience OR
  • Bachelor’s + 4 years of Manufacturing Operations experience OR
  • Associate’s + 8 years of Manufacturing Operations experience OR
  • High School/GED + 10 years of Manufacturing Operations experience

Preferred Education:

  • Background in Life Sciences, Biology, Chemistry, or Engineering.

PREFERRED QUALIFICATIONS

  • Experience handling deviations, non‑conformances, and investigations.
  • Strong technical writing and report development skills.
  • Proficiency with RCA tools (5 Why’s, Fishbone, Causal Factors, Kepner‑Tregoe).
  • Experience with bioprocessing unit operations and GMP environments.
  • Familiarity with Lean Manufacturing and continuous improvement.
  • Strong project management and action‑tracking skills.
  • Proficiency in GDP and regulated documentation practices.
  • Experience with systems/tools: TrackWise, VEEVA, MES, SmartSheet, Power BI, Spotfire, CDOCS, and process monitoring platforms.
  • Excellent communication skills in English and Spanish.
  • Team‑oriented, strong interpersonal skills, able to work under minimal supervision and high workload.
  • Ability to work extended hours when required.

Benefits

  • 6-month to 1 year contract- with possible extension
  • Administrative Shift