9 days old

Bulk Adjuvant Electro-Mechanical Equipment Technician

GSK
Marietta, PA 17547
Site Name: USA - Pennsylvania - Marietta
Posted Date: May 18 2020

As a Bulk Adjuvant Electro-Mechanical Equipment Technician, you will be responsible for the maintenance of the equipment and processes used in the Bulk Adjuvant manufacturing process at the GSK Marietta facility. The position serves as technical lead for the assigned production shift operation, troubleshoots related problems and drives continuous improvement.

Key Responsibilities:

Operational Responsibilities:

  • Ensure timely completion of PMs, calibrations and work orders
  • Provide initial troubleshooting and hands-on support for equipment breakdowns.
  • Responsible for the set-up and batch change on production equipment.
  • Responsible for maintenance (emergency, corrective and preventative), testing, Troubleshooting, calibration, and repair of a variety manufacturing equipment, calibration, and repair of a variety manufacturing equipment.
  • Ensure equipment the is operating efficiently within specified
  • 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 and secure onsite support

Project Support:

  • Help identify and implement continuous improvement initiatives.
  • Assist with equipment modifications and validation activities.
  • Assist in identifying the user requirements for new or modified equipment.
  • Assist with the installation, setup and qualification of new or modified equipment.
  • Comply with all established safety requirements
  • Maintains full compliance with all assigned learning plans, technical competencies, 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:

  • Associates Degree in relevant technical field with 0-1 years experience or high school\\trade school graduate and completion of a recognized apprenticeship program totaling 2 years or a combination of formal training in a relevant technical field and experience equal to 2 years in an industrial environment.
  • Must be able to work independently on off-shifts and call-ins in order to troubleshoot and repair equipment on an emergency basis.
  • Prior hand-on experience working with controls, instrumentation, automation, and PLCs systems with at least one of the following systems: Allen Bradley, Siemens, ControlLogix, RSLogix, and Step 7or Delta V.
  • 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.
  • Must be able to address issues and problems related to manufacturing equipment and initiates quick resolution across matrix organization.
  • Must be able to set priorities and successfully adapt to current and changing business needs.
  • 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.

Preferred Qualifications:

  • Experience in an industrial environment with equipment technician responsibilities.
  • Experience in a pharmaceutical, food or research facility working with facility regulatory guidelines standard operating procedures is preferred.
  • Specific training in microprocessors, automatic machine controls, and programmable logic controllers is required.
  • Hands-on experience in the set-up, operation, change-over, troubleshooting, maintenance and calibration of production equipment to include packaging, labeling and inspection machines are required.
  • 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.
  • 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.

Why GSK?

Our values and expectationsare 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, rigor 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

US work authorization is required for this role. Sponsorship is not available for this position

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

GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that 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 GSKs compliance to all federal and state US Transparency requirements. For more information, please visit GSKs Transparency Reporting For the Record site.

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Posted: 2020-05-20 Expires: 2020-06-19

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Bulk Adjuvant Electro-Mechanical Equipment Technician

GSK
Marietta, PA 17547

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