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Validation Engineer - Medical Device or Pharma

DivIHN Integration Inc

Job Description

DivIHN (pronounced Divine) is a nationally-recognized Business Technology Solutions and Staffing services provider headquartered in Chicago. Since our formation in 2002, we have been trusted by Fortune 500 organizations to help them locate and hire best-in-class talent through our Award-winning Professional Workforce Solutions program.  Check out our careers page to see all of our job openings: http://divihn.com/careers/find-a-job/ One of our BEST F500 customers has engaged us to help them hire a Validation Engineer - Medical Device or Pharma to be available to work out of their office in Marion, North Carolina; details can be found below. 10/07/2019 to 10/02/2020 Please apply or call one of us to learn more
This position is with our Direct client based out in Marion NC
Interested candidates can apply to (Phebe) at phebe at divihn dot com and also can reach at 716-598-0700 for further information.
Description: Title: Validation Engineer
Location: Marion, NC
Kronos position
Some travel possible

Job Description:
Summary:
Provide hands on validation support to several facility/utility and equipment qualifications that are planned for the site. This validation engineer will need to have experience with qualification in Mixing Equipment, Clean Room Qualifications, and Water for Injection systems.

Responsibilities:
Must perform process validation, process capability, and process control studies for assigned areas
Must support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process/technology.
Must participate in and contribute to medium to large size projects, own assigned tasks, produce detailed requirements and analysis documents for assigned tasks. Partner with other support groups and manufacturing teams to complete work.
Must ensure computer systems and applications follow regulatory quality standards through validations activities.
Responsible for creating the documents required for the development and validation of computerized systems.
Must be able to understand, test, and debug applicable software while following the software life cycle procedures.
Responsible for ensuring FDA regulations are met for system upgrades/replacements, including the 2011 FDA Guidance for Process Validation.
Responsible for ensuring the quality of facility systems validations:
o Writing and executing protocols and test cases for validations.
o Coordinating testing and documentation of projects.
o Documenting/executing changes to applications.
o Assisting/leading training for systems.
o Develop test requirements and prepare and document test data for complex system testing.
o Provide support to resolve technical issues with systems under validation
Ability to function effectively as a member of a team.
Ability to communicate effectively in written and verbal form.
Must perform all other duties and responsibilities as determined by supervision/management.
This position will be implementing software driven system while working with engineering and IT.
The basic understanding of software systems and how to appropriately test is mandatory.

QUALIFICATIONS:
BS degree in Engineering Discipline (ME, IE, CHE, BME, EE, CE) with at least 1 year of experience.
Knowledge of applications such as MS Office: Word, Excel, PowerPoint, Outlook, Microsoft Project (nice to have).
Wonderware, Allen-Bradley PLC, nice to haves but not required
Experience with installation, administration, and maintenance of servers is helpful
Ability to work with diversified cross functional team across different plant locations.
Self-motivated and work well without direct supervision.
Ability to quickly learn and understand applications.
Quality Assurance or Pharmaceutical industry experience desired.
Candidates must meet visual acuity requirements as documented
IQ / OQ / PQ and Data Integrity (ALCOA)
Soft Skills: Critical thinker, self-starter, team player, sense of urgency, engaged, solution oriented
It will be important for the individual to be able to work days, nights, holidays, and/or weekends as needed by the project timeline to meet manufacturing deadlines.

Physical Requirements (Large manufacturing site)
Requires continuous grasping, pushing/pulling up to 15 pounds and reaching with hands and arms.
Lifting and carrying on average up to 15 pounds frequently throughout the shift.
Normal visual acuity and the ability to distinguish color are necessary.
Have the ability to complete quick and precise repetitive processes using both arms and both hands
Occasionally specialized physicals are required when working with certain drug codes.
Must be able to squat, climb, reach above shoulder level, reach at or below shoulder level, kneel, twist and bend at the neck, twist and bend at the waist and balance

Interview Platform: phone interviews but may do Video WebEx and/or onsite interviews; we are trying to move quickly, and candidates must be able to start quickly.

About us: DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.

DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.

Job Requirements

Medical Device, Pharma, Data Integrity, OQ, PQ, ALCOA
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Job Snapshot

Location US-NC-Marion
Employment Type Full-Time
Pay Type Hour
Pay Rate $0.00 - $75.00 /Hour
Store Type Other

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Snapshot
DivIHN Integration Inc
Company:
US-NC-Marion
Location:
Full-Time
Employment Type:
Hour
Pay Type:
$0.00 - $75.00 /Hour
Pay Rate:
Other
Store Type:

Job Description

DivIHN (pronounced Divine) is a nationally-recognized Business Technology Solutions and Staffing services provider headquartered in Chicago. Since our formation in 2002, we have been trusted by Fortune 500 organizations to help them locate and hire best-in-class talent through our Award-winning Professional Workforce Solutions program.  Check out our careers page to see all of our job openings: http://divihn.com/careers/find-a-job/ One of our BEST F500 customers has engaged us to help them hire a Validation Engineer - Medical Device or Pharma to be available to work out of their office in Marion, North Carolina; details can be found below. 10/07/2019 to 10/02/2020 Please apply or call one of us to learn more
This position is with our Direct client based out in Marion NC
Interested candidates can apply to (Phebe) at phebe at divihn dot com and also can reach at 716-598-0700 for further information.
Description: Title: Validation Engineer
Location: Marion, NC
Kronos position
Some travel possible

Job Description:
Summary:
Provide hands on validation support to several facility/utility and equipment qualifications that are planned for the site. This validation engineer will need to have experience with qualification in Mixing Equipment, Clean Room Qualifications, and Water for Injection systems.

Responsibilities:
Must perform process validation, process capability, and process control studies for assigned areas
Must support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process/technology.
Must participate in and contribute to medium to large size projects, own assigned tasks, produce detailed requirements and analysis documents for assigned tasks. Partner with other support groups and manufacturing teams to complete work.
Must ensure computer systems and applications follow regulatory quality standards through validations activities.
Responsible for creating the documents required for the development and validation of computerized systems.
Must be able to understand, test, and debug applicable software while following the software life cycle procedures.
Responsible for ensuring FDA regulations are met for system upgrades/replacements, including the 2011 FDA Guidance for Process Validation.
Responsible for ensuring the quality of facility systems validations:
o Writing and executing protocols and test cases for validations.
o Coordinating testing and documentation of projects.
o Documenting/executing changes to applications.
o Assisting/leading training for systems.
o Develop test requirements and prepare and document test data for complex system testing.
o Provide support to resolve technical issues with systems under validation
Ability to function effectively as a member of a team.
Ability to communicate effectively in written and verbal form.
Must perform all other duties and responsibilities as determined by supervision/management.
This position will be implementing software driven system while working with engineering and IT.
The basic understanding of software systems and how to appropriately test is mandatory.

QUALIFICATIONS:
BS degree in Engineering Discipline (ME, IE, CHE, BME, EE, CE) with at least 1 year of experience.
Knowledge of applications such as MS Office: Word, Excel, PowerPoint, Outlook, Microsoft Project (nice to have).
Wonderware, Allen-Bradley PLC, nice to haves but not required
Experience with installation, administration, and maintenance of servers is helpful
Ability to work with diversified cross functional team across different plant locations.
Self-motivated and work well without direct supervision.
Ability to quickly learn and understand applications.
Quality Assurance or Pharmaceutical industry experience desired.
Candidates must meet visual acuity requirements as documented
IQ / OQ / PQ and Data Integrity (ALCOA)
Soft Skills: Critical thinker, self-starter, team player, sense of urgency, engaged, solution oriented
It will be important for the individual to be able to work days, nights, holidays, and/or weekends as needed by the project timeline to meet manufacturing deadlines.

Physical Requirements (Large manufacturing site)
Requires continuous grasping, pushing/pulling up to 15 pounds and reaching with hands and arms.
Lifting and carrying on average up to 15 pounds frequently throughout the shift.
Normal visual acuity and the ability to distinguish color are necessary.
Have the ability to complete quick and precise repetitive processes using both arms and both hands
Occasionally specialized physicals are required when working with certain drug codes.
Must be able to squat, climb, reach above shoulder level, reach at or below shoulder level, kneel, twist and bend at the neck, twist and bend at the waist and balance

Interview Platform: phone interviews but may do Video WebEx and/or onsite interviews; we are trying to move quickly, and candidates must be able to start quickly.

About us: DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.

DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.

Job Requirements

Medical Device, Pharma, Data Integrity, OQ, PQ, ALCOA
Validation Engineer - Medical Device or Pharma Apply now