Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Dynamic Biologics

Electrical Engineer

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
80
out of 100
Average of individual scores

Were these scores useful?

Job Description

Job Overview Position Summary:

The Electrical Engineer is responsible for the uninterrupted, safe, and efficient operation of all electrical systems, power distribution networks, and automated machinery across the pharmaceutical manufacturing plant. This role involves preventive maintenance, rapid troubleshooting of production line electrical faults, managing high-tension (HT) and low-tension (LT) power supply systems, and ensuring strict compliance with NEC and pharmaceutical GMP (Good Manufacturing Practices) guidelines.

Key Responsibilities:

Ø Plant Maintenance & Power Distribution Ø

Uninterrupted Power Supply:

Oversee and maintain High-Tension (HT) and Low-Tension (LT), power distribution, transformers, power Generator sets, and high-capacity UPS systems to ensure zero power fluctuations on sensitive production lines. Ø

Breakdown & Preventive Maintenance:

Schedule and execute preventive and predictive maintenance of manufacturing machinery (e.g., injectable manufacturing and quality control and HVAC systems). Ø

Utility Operations:

Manage electrical systems for plant utilities including boilers, water purification plants (Purified Water/Water for Injection systems) Ø

Compliance, Safety & Documentation:

Ø

GMP/cGMP Adherence:

Ensure all electrical modifications or maintenance work complies with sterile pharmaceutical environment protocols (cleanroom protocols). Ø

Engineering Documentation:

Maintain accurate, audit-ready engineering records, including electrical drawings (SLA/SLD), equipment history cards, preventive maintenance checklists, and change control logs. Ø

Local Safety Standards:

Ensure compliance as per US electrical safety standard. Ø Work in engineering projects related to the design, modification, and optimization of Utilities, systems and equipment. Ø Responsible for preparation and review of Standard Operating Procedures (SOPs) for engineering, maintenance and repair processes. Ø Support the installation and commissioning of new process equipment Ø Perform Validation & Qualification of Utility Systems (e.g. HVAC System, Water System, Nitrogen, Compressed Air) Ø Execute preventive maintenance schedules for machines and equipment. Ø Participate in risk assessments and Failure Mode Effects Analysis (FMEA) on systems and processes to identify potential risks and implement improvements. Ø Collaborate with cross-functional teams to develop and implement innovative engineering solutions Ø Ensure all systems, processes, and equipment comply with FDA, cGMP, and other regulatory standards. Ø Provide technical expertise and support during investigations, audits, and inspections. Ø Ensure effective communication of technical information to both technical and non-technical stakeholder.

Qualifications:

Ø Associate Degree in Electrical Engineering with required Certifications OR Bachelor's or Master's degree in Electrical Engineering, or a related field.

Experience:

Ø minimum of 3-5 years of experience in pharmaceutical engineering or a related field. Ø In-depth knowledge of pharmaceutical manufacturing processes, equipment, and cGMP regulations. Ø Proven experience in project management, process optimization, and cross-functional collaboration. Ø Strong background in equipment qualification, validation, and troubleshooting.

Skills:

Ø Expertise in process control systems, manufacturing equipment, and automation technologies. Ø Experience with mid/large-scale pharmaceutical manufacturing or aseptic processing is a plus. Ø Ability to work in a regulated environment with strict adherence to safety, quality, and compliance standards. Ø Works as a member of a team to achieve all outcomes. Ø Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements. Ø Performs all work in support of our

Values:

Collaboration, Courage, Perseverance, and Passion. Ø All other relevant duties as assigned. Required to stand, walk, sit, talk and hear; required to use hands to operate vehicles and office equipment; must be able to occasionally lift and/or move up to 50 lbs; specific vision requirements for this job include: close, distance and peripheral vision, and the ability to adjust focus, reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position without compromising patient care.

• KriGen Pharmaceuticals LLC dba Dynamic Biologics is an equal opportunity employer. All employment decisions are made without regard to age, color, race, ancestry, national origin, disability, genetic information, military status, religion, creed, sex, pregnancy, childbirth, marital status, citizenship, sexual orientation, gender identity, gender expression, legally protected medical condition, or any other basis prohibited by applicable law. Background checks and drug screens are part of our hiring process. Affirmative Action/Equal Opportunity Employer, Minority/Female/Disabled/Veteran.

Benefits:

Dental insurance Health insurance Paid time off Vision insurance Application Question(s): What is your salary expectation? (Required)

Experience:
Pharmaceutical Manufacturing :

1 year (Preferred)

Work Location:

In person

Benefits

  • Paid Time Off (PTO)
  • Health Insurance
  • Dental Insurance
  • Vision Insurance