Sr. Associate Mfg Systems

Posted 15 Days Ago
Be an Early Applicant
Juncos
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Provide technical engineering support for automated manufacturing systems, troubleshoot Rockwell PLCs and Cognex/Systech vision systems, ensure cGMP/FDA compliance, assist with inspections and audits, support validation, continuous improvement, maintenance coordination, and engineering optimization in a 24/7 rotating shift environment.
Summary Generated by Built In

The Sr. Associate Mfg Systems provides technical engineering support in a highly automated manufacturing environment. This role supports system and equipment optimization strategies, upgrades, replacements, and modifications while ensuring maintenance and manufacturing systems remain compliant with corporate policies, industry standards, regulatory requirements, and FDA expectations.

This position operates in a 24/7 manufacturing environment and may be assigned to any of four shifts (A, B, C, or D), with availability required for 5:00 AM – 5:30 PM and/or 5:00 PM – 5:30 AM schedules.

Key Responsibilities

  • Provide technical support for automated manufacturing systems and equipment.
  • Support system optimization initiatives and continuous improvement efforts.
  • Troubleshoot PLC systems (Rockwell platforms).
  • Troubleshoot and adjust Vision Systems (Cognex and Systech).
  • Support basic control systems hardware troubleshooting.
  • Ensure automated systems operate reliably and efficiently in compliance with cGMP standards.
  • Evaluate utility systems, instrumentation, calibration, electrical systems, and technical cleaning systems for regulatory compliance.
  • Ensure all maintenance and automation activities comply with cGMP and FDA regulations.
  • Assist during FDA and regulatory agency inspections.
  • Support responses to regulatory observations and audit findings.
  • Assist in maintaining internal audit programs to ensure continued inspection readiness.
  • Coordinate technical support for maintenance teams related to automation, validation, compliance, electrical, and process issues.
  • Ensure training programs, SOPs, and operational standards are consistent and compliant.
  • Support investigations involving high purity water systems and environmental monitoring alerts/actions.
  • Assist in testing and implementing updates to sanitization and maintenance procedures for process, utility, and cleanroom systems.
  • Partner with Plant Engineering to implement engineering improvements and optimization programs.

Core Competencies

  • Strong automation and equipment troubleshooting skills.
  • Comprehensive understanding of validation protocol requirements.
  • Analytical problem-solving capabilities.
  • Ability to identify system gaps and implement effective corrective actions.
  • Leadership and team-building skills.
  • Strong facilitation and cross-functional collaboration abilities.
  • Ability to manage and adapt to change in a dynamic manufacturing environment.
  • Project management and planning skills.
  • Scheduling and prioritization capabilities.
  • Strong organizational skills and attention to detail.
  • Strong verbal communication skills.
  • Strong written communication and technical writing skills.
  • Computer literacy (Microsoft Office and related systems).

Requirements

Education & Experience

  • Master’s Degree OR
  • Bachelor’s Degree + 2 years of Engineering experience OR
  • Associate’s Degree + 6 years of Engineering experience OR
  • High School Diploma/GED + 8 years of Engineering experience

Preferred Qualifications

  • PLC troubleshooting experience (Rockwell).
  • Vision Systems troubleshooting/adjustment experience (Cognex and Systech).
  • Strong knowledge of cGMP requirements.
  • Experience working in FDA-regulated industries.
  • Knowledge of basic control systems hardware.

Benefits

Work Environment

  • Automated manufacturing environment.
  • Rotating 12-hour shifts (A, B, C, or D).
  • Must be flexible to support both day and night operations.

Top Skills

Rockwell Plc,Cognex,Systech,Microsoft Office
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The Company
HQ: Cambridge, MASSACHUSETTS
39 Employees
Year Founded: 2010

What We Do

BioPharma Consulting JAD Group provides a complete portfolio of technical support and solutions for the FDA regulated industry. We deliver solutions with a flexible cost effective approach to meet your company’s needs. BPC JAD group is a company created to help our customers bridge the gap between their business strategy and results.

Our mission is to help our clients succeed by partnering with them and providing value added business solutions on the validation, engineering and compliance fields.

We will carry out our mission by creating a long-term partnership with our customers and provide reliable and cost effective technical solutions.

BPC JAD Group objective is to deliver reliable tailored solutions; from providing consultation to becoming part of your staff. We will develop customized frameworks to help our customers unlock the hidden value in their plants, facilities, equipment and people with an optimal integration of resources regulations and technology.

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