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Electro Mechanical Equipment Tech Full-time

at GSK in Pennsylvania (Published at 20-09-2019)

Site Name: USA - Pennsylvania - Marietta
Posted Date: Sep 18 2019
Electro Mechanical Equipment Tech

The Electro Mechanical Equipment Tech is responsible for the set-up, troubleshooting and maintenance of all production areas & equipment within the manufacturing environment for secondary and tertiary packaging operations. Additional responsibilities include supporting equipment related deviation investigations, CAPAs and SOP reviews as the equipment SME. In addition, the EMT is responsible for supporting project work such as equipment modifications, new equipment installations, engineering studies and validations.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Comply with all safety requirements established for the packaging area.
  • Operational Responsibilities
    • Responsible for the set-up and batch change over on all manufacturing lines.
    • Responsible for maintenance (emergency, corrective and preventative), testing, troubleshooting, calibration, and repair of a variety of manufacturing equipment.
    • Ensure timely completion of PMs, calibrations and work orders
    • Provide initial troubleshooting and hands-on support for equipment breakdowns.
    • Ensure the manufacturing lines are operating at peak equipment efficiency with minimal waste and rework.
    • Assists with equipment deviation investigations and CAPA execution.
    • Provide technical input and review to equipment SOPs
    • Work with vendors to get quotes on replacement parts
    • Manufacturing Equipment SME
  • Project Support
    • Help identify and drive OEE and waste reduction activities for the manufacturing lines.
    • Assist with equipment modifications and validation activities.
    • Assist in identifying the user requirements for new or modified manufacturing equipment.
    • Assist with the installation, setup and qualification of new or modified equipment.
  • Maintains full compliance with all assigned learning plans, technical competencies, aseptic technique, documentation practices and procedures as related to the GMP and EHS environments.
  • Perform all job responsibilities in compliance with applicable EHS and GMP regulations, guidelines, policies, standard operating procedures, and industry practice and Industrial Excellence initiatives.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Associates Degree in relevant technical field or High schooltrade school graduate and 5 years? experience in an industrial environment with equipment technician responsibilities
  • 5 years? experience in an industrial environment with equipment technician responsibilities.
  • 2 years? experience in a pharmaceutical, food or research facility working with facility regulatory guidelines standard operating procedures is preferred.
  • Must be able to work independently on off-shifts and call-ins in order to troubleshoot and repair equipment on an emergency basis.
  • Must have prior experience with AC and DC electrical circuits and troubleshooting electrical problems for manufacturing equipment.
  • Must be able to correctly read and understand electrical wiring diagrams, electronic schematics, engineering diagrams isometrics and P&ID drawings.
  • Hands-on experience in the set-up, operation, change-over, troubleshooting, maintenance and calibration of manufacturing equipment.
  • Must be able to address issues and problems related to manufacturing equipment and initiate quick resolution across matrix organization.
  • Must be able to set priorities and successfully adapt to current and changing business needs.
  • Proficient computer skills in Excel and Word in order to create amend and modify documents for individual and team use.
  • Physical requirements include stooping, standing, climbing and frequent lifting of a minimum of 50 lbs. of equipment. Must be able to work while wearing full protective gowning required for GMP areas.
  • The aptitude to correctly troubleshoot and correct problems with a variety of manufacturing equipment.
  • Ability to follow written procedures and document results in a neat and precise manner according to GMP standards and other regulations.
  • Must be a committed team player prepared to work in and embrace a team based culture and work closely with shift team to achieve goals in a 24/7 cGMP production environment. This schedule will include holidays, and weekends; over-time may be required.
  • The capability to maintain attention to detail and quality, while completing multiple or repetitive tasks and meeting timelines and deadlines.
  • The ability to effectively communicate both verbally and in writing with all levels, both inside and outside of the organization.
  • Demonstrate ability to perform all job duties with limited supervision.
  • Maintain a high level of integrity and confidentiality while balancing multiple priorities and responsibilities.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • 2 years? experience in a pharmaceutical, food or research facility working with facility regulatory guidelines standard operating procedures is preferred

Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture.

These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:

Operating at pace and agile decision-making ? using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK HR Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK?s compliance to all federal and state US Transparency requirements. For more information, please visit GSK?s Transparency Reporting For the Record site.



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