What are the responsibilities and job description for the Facilities Engineer position at Aurobindo Pharma USA, Inc.?
Division Overview
Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has give Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in.
Job Overview
The Facilities Engineer performs day-to-day tasks under the guidance of F&E Director. The Facilities Engineer ensures that the completion of the new manufacturing area is being performed as per the guidelines. The Facilities Engineer has to communicate with vendors to assign work and also to keep a record of all the activity which is being performend in the site location.
Responsibilities
Preparation of master equipment list. Preparation and finalization of preventive maintenance checklist and schedules. Preparation of master calibration list and calibration schedules. Ensure the execution of preventive maintenance and calibration schedules with internal or external sources. Review and verification of all calibration certification details and their archival. Issuance, execution and archival of all approved documents on timely basis as per respective SOPs. Must be detail oriented and ensure that all action items in QAMS related to Change Control, CAPAs, Deviation are attended and thoroughly closed according to the action plans. Preparation, Review and Effectiveness of SOP in DMS. Must train people on the SOP belonging to respective departments by preparing question banks, initiating a self-study course or offline course or external training in Nichelon. Review the logbooks related to utilities, Facility and executed documents. Adhering to safety, good documentation and Good Manufacturing Practices. Practicing/ implementation of good Engineering practices. Follow the laid down Quality Culture Principles and Behaviors.
Qualifications - Skills & Requirements
Must have a Mechanical/Industrial Background or Electrical Background
Education & Experience
Bachelor's degree required, Master's degree preferred. Minimum of 2-3 years of relevant experience required.
Physical Requirements
FIELD - While performing the duties of this job the employee is required to:
Job requires you to worker to reach or work above the shoulderLifting 1-4 Hours - 0-10 Pounds Blood/Fluid Exposure Risk Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.
We Are An Equal Opportunity Employer
Aurobindo Pharma USA, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training., Must have a Mechanical/Industrial Background or Electrical Background, Preparation of master equipment list. Preparation and finalization of preventive maintenance checklist and schedules. Preparation of master calibration list and calibration schedules. Ensure the execution of preventive maintenance and calibration schedules with internal or external sources. Review and verification of all calibration certification details and their archival. Issuance, execution and archival of all approved documents on timely basis as per respective SOPs. Must be detail oriented and ensure that all action items in QAMS related to Change Control, CAPAs, Deviation are attended and thoroughly closed according to the action plans. Preparation, Review and Effectiveness of SOP in DMS. Must train people on the SOP belonging to respective departments by preparing question banks, initiating a self-study course or offline course or external training in Nichelon. Review the logbooks related to utilities, Facility and executed documents. Adhering to safety, good documentation and Good Manufacturing Practices. Practicing/ implementation of good Engineering practices. Follow the laid down Quality Culture Principles and Behaviors.
Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has give Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in.
Job Overview
The Facilities Engineer performs day-to-day tasks under the guidance of F&E Director. The Facilities Engineer ensures that the completion of the new manufacturing area is being performed as per the guidelines. The Facilities Engineer has to communicate with vendors to assign work and also to keep a record of all the activity which is being performend in the site location.
Responsibilities
Preparation of master equipment list. Preparation and finalization of preventive maintenance checklist and schedules. Preparation of master calibration list and calibration schedules. Ensure the execution of preventive maintenance and calibration schedules with internal or external sources. Review and verification of all calibration certification details and their archival. Issuance, execution and archival of all approved documents on timely basis as per respective SOPs. Must be detail oriented and ensure that all action items in QAMS related to Change Control, CAPAs, Deviation are attended and thoroughly closed according to the action plans. Preparation, Review and Effectiveness of SOP in DMS. Must train people on the SOP belonging to respective departments by preparing question banks, initiating a self-study course or offline course or external training in Nichelon. Review the logbooks related to utilities, Facility and executed documents. Adhering to safety, good documentation and Good Manufacturing Practices. Practicing/ implementation of good Engineering practices. Follow the laid down Quality Culture Principles and Behaviors.
Qualifications - Skills & Requirements
Must have a Mechanical/Industrial Background or Electrical Background
Education & Experience
Bachelor's degree required, Master's degree preferred. Minimum of 2-3 years of relevant experience required.
Physical Requirements
FIELD - While performing the duties of this job the employee is required to:
- Work in a temperature controlled office environment or travel via vehicle or commercial transportation
- While performing the duties of this job, the employee is occasionally required to handle or feel objects, talk, hear, and walk during the course of employment
- Position requires some degree of travel for business purposes
- Employee may use computer, phone, copier and other office equipment in the course of a day
- Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and an ability to adjust focus Sedentary work Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met. Additional
Job requires you to worker to reach or work above the shoulderLifting 1-4 Hours - 0-10 Pounds Blood/Fluid Exposure Risk Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.
We Are An Equal Opportunity Employer
Aurobindo Pharma USA, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training., Must have a Mechanical/Industrial Background or Electrical Background, Preparation of master equipment list. Preparation and finalization of preventive maintenance checklist and schedules. Preparation of master calibration list and calibration schedules. Ensure the execution of preventive maintenance and calibration schedules with internal or external sources. Review and verification of all calibration certification details and their archival. Issuance, execution and archival of all approved documents on timely basis as per respective SOPs. Must be detail oriented and ensure that all action items in QAMS related to Change Control, CAPAs, Deviation are attended and thoroughly closed according to the action plans. Preparation, Review and Effectiveness of SOP in DMS. Must train people on the SOP belonging to respective departments by preparing question banks, initiating a self-study course or offline course or external training in Nichelon. Review the logbooks related to utilities, Facility and executed documents. Adhering to safety, good documentation and Good Manufacturing Practices. Practicing/ implementation of good Engineering practices. Follow the laid down Quality Culture Principles and Behaviors.
