Yoh
Yoh | Quality Assurance Engineer IN
Yoh, Noblesville, Indiana, United States,
Yoh is seeking a
Quality Assurance Engineer
for our pharmaceutical client here in Noblesville, IN. This is a 6 month contract opportunity on day shift and
must be able to work on W2 Location:
Noblesville, IN (onsite) Pay:
$30-$40/hr. Hours:
M-F, 8 am - 5 pm Type:
6 month Contract Summary of Position The Senior Quality Assurance Engineer is responsible for the Quality oversight for Validation, Engineering and Maintenance at the site. This position requires strong technical and quality skills. The position reports directly to the Senior Manager or Senior Director of Quality Assurance. Knowledge in pharmaceutical quality systems with proficiency in quality oversight of: Validation, Engineering, Maintenance, Manufacturing, QC, Regulatory, CAPA, Deviations, Out of Specification Investigations, and Annual Product Reviews. Essential Skill/Functions Take a lead role for site/corporate development and maintenance of facility's quality systems and procedures. Review and approve Change Control/Process Management Documents involving product or process changes. Key personnel for FDA or other regulatory agencies for on-site audits. Reviews and approves IOQs, requirement documents, SOPs, validation documents and data integrity assessments. Assemble, analyze and report QA system data to ensure regulatory compliance, identify trends and to identify areas of improvement. Conduct quality audits and develop and assess subsequent corrective action recommendation(s). Developing procedures, statistical evaluations, and remediation of systems. Ability to adapt quickly in a fast-paced dynamic environment. Ability to communicate with and positively influence broad and diverse populations within and outside the organization. Ensure a safe and quality working environment through training, awareness and compliance to safety guidelines and SOP's. Ensure the maintenance of the department, premises and equipment. Additional areas of responsibility may include developing specifications, standard operating procedures; providing quality system training and actively participating in Quality Review Board meetings. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)
Requirements Bachelor of Science in Biology, Chemistry, Life Sciences or related field required Five or more years of relevant Quality or Validation experience in a finished pharmaceutical manufacturing environment with strong understanding of and exposure to applicable quality systems. Experience in supporting on-site inspections for regulatory agencies. Significant experience investigating Deviations and other variances. Must be thoroughly familiar with applicable regulatory guidelines concerning the establishment, validation, and documentation of test procedures, equipment, processes and facility systems. Working knowledge of cGMP guidelines and their application in a controlled aseptic environment Must be able to work with other groups to seek understanding and resolve issues, close gaps, and seek compliant outcome. Must have experience with statistical tools Proficient in use of Microsoft suite of products.
#IND-SPG Note: Any pay ranges displayed are estimations.
Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description.
All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit
https://www.yoh.com/applicants-with-disabilities
to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Quality Assurance Engineer
for our pharmaceutical client here in Noblesville, IN. This is a 6 month contract opportunity on day shift and
must be able to work on W2 Location:
Noblesville, IN (onsite) Pay:
$30-$40/hr. Hours:
M-F, 8 am - 5 pm Type:
6 month Contract Summary of Position The Senior Quality Assurance Engineer is responsible for the Quality oversight for Validation, Engineering and Maintenance at the site. This position requires strong technical and quality skills. The position reports directly to the Senior Manager or Senior Director of Quality Assurance. Knowledge in pharmaceutical quality systems with proficiency in quality oversight of: Validation, Engineering, Maintenance, Manufacturing, QC, Regulatory, CAPA, Deviations, Out of Specification Investigations, and Annual Product Reviews. Essential Skill/Functions Take a lead role for site/corporate development and maintenance of facility's quality systems and procedures. Review and approve Change Control/Process Management Documents involving product or process changes. Key personnel for FDA or other regulatory agencies for on-site audits. Reviews and approves IOQs, requirement documents, SOPs, validation documents and data integrity assessments. Assemble, analyze and report QA system data to ensure regulatory compliance, identify trends and to identify areas of improvement. Conduct quality audits and develop and assess subsequent corrective action recommendation(s). Developing procedures, statistical evaluations, and remediation of systems. Ability to adapt quickly in a fast-paced dynamic environment. Ability to communicate with and positively influence broad and diverse populations within and outside the organization. Ensure a safe and quality working environment through training, awareness and compliance to safety guidelines and SOP's. Ensure the maintenance of the department, premises and equipment. Additional areas of responsibility may include developing specifications, standard operating procedures; providing quality system training and actively participating in Quality Review Board meetings. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)
Requirements Bachelor of Science in Biology, Chemistry, Life Sciences or related field required Five or more years of relevant Quality or Validation experience in a finished pharmaceutical manufacturing environment with strong understanding of and exposure to applicable quality systems. Experience in supporting on-site inspections for regulatory agencies. Significant experience investigating Deviations and other variances. Must be thoroughly familiar with applicable regulatory guidelines concerning the establishment, validation, and documentation of test procedures, equipment, processes and facility systems. Working knowledge of cGMP guidelines and their application in a controlled aseptic environment Must be able to work with other groups to seek understanding and resolve issues, close gaps, and seek compliant outcome. Must have experience with statistical tools Proficient in use of Microsoft suite of products.
#IND-SPG Note: Any pay ranges displayed are estimations.
Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description.
All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit
https://www.yoh.com/applicants-with-disabilities
to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.