Engineer Manufacturing Systems

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Cencora PharmaLex is a highly successful and growing consulting company for the Healthcare industry around the world. Cencora PharmaLex offers professional development, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in an atmosphere that values trust, respect, teamwork, creative talent, enthusiasm, and diligence.
What we offer:
Competitive salaries
Ability to earn additional income based on hours worked (Biweekly basis)
Free High-Quality webinars provided by experts from around the world
Committed to keeping our consultants in project continuity
Referral Program
Wellness Program
Recognition Program (for employees only)
Service Award Program (for employees only)
Discount Program (for employees only)
An administrative team that is oriented to providing excellent service that pursues satisfying the needs of our consultants.
For our projects in the US, we cover travel/lodging/transportation expenses (employees only)
General Description:
In a full automation role, the Sr. Associate Mfg Systems will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are maintained in compliance concerning current corporate policies, industry standards, regulatory standards, and FDA standards.

Responsibilities:
Evaluate and determine if utility systems, process maintenance, instrumentation/calibration/electrical systems, and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards, and FDA standards.
Ensure the maintenance team training program, standard operating procedures, and equipment/system operational standards are consistent throughout the team.
Participate in the coordination of technical support to the maintenance team on engineering issues, regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues, and process maintenance issues.
Assist the maintenance team during FDA and other regulatory agency inspections. Provide technical support to the maintenance team in response to the FDA and other regulatory agencies.
Assist the maintenance team when responding to high-purity water systems and environmental monitoring alert/action notifications.
Assist with the investigation of all alert/action notifications.
Assist with the development and maintenance of an audit program for the maintenance team and facilitate routine audits of activities, documentation, operations, and related areas to ensure a continued state of compliance
Assist plant engineering in the evaluation and implementation of engineering improvements, policy changes, compliance improvements, and optimization programs.
Assist with the testing of proposed sanitization and maintenance procedure changes and modifications for process, utility, and clean room systems.
Knowledge, Skills, and Abilities
Background in programming, installation of manufacturing process controls, automation, and field instrumentation technologies.
Working knowledge of pharmaceutical/biotechnology processes.
Familiarity with validation processes and documentation in a highly regulated environment.
Strong verbal communication skills in English and Spanish.
Skills in the following areas: Problem-solving and root cause analysis, basic technical report writing, basic technical presentations, dealing with and managing change, technical (Equipment Specific)Analytical Problem Solving, and ComputerLiteracy.
Knowledge of Rockwell Automation Platform and Allen-Bradley PLCs.
Knowledgeable on Rockwell Automation Factory Talk & ControlLogix PLC Platform.
Knowledgeable on Rockwell SLC500 PLC family Controllers.
Knowledgeable on Rockwell Automation FTView SE and FTBatch systems.
Knowledgeable on DeviceNet technologies.
Work schedule flexibility to support 24/7 operations.
Knowledge of a programming language (e.g. VBA, SQL)
Knowledge of vision system technology
Knowledge of the serialization process.
Basic Knowledge of robot or cobot programming.
Minimum Education and Experience
Master's degree or Bachelor's degree and 2 years of Engineering experience
Associate's degree and6 years of Engineering experience
High school diploma and 8 years of Engineering experience

PharmaLex is an Equal Opportunity Employer.
Job Types: Full-time, Contract - Temporary Hourly - Overtimedepending on 12-hour Shift -

Pay Rate starts at $25

Shift: 5:00 am to 5:30 pm or 5:00 pm to 5:00 am including alternate weekend
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, creed, national origin, ancestry, sex, age, handicap or disability, marital status, sexual orientation, gender identity or expression, pregnancy or pregnancy-related condition, genetic information, veteran status, immigration or citizenship status, military obligations, status as a domestic violence victim or a victim of sexual assault or stalking, participation in discrimination complaint-related activities, or any other status protected under applicable federal, state or local law.
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