Piper Companies
Commissioning Qualification Validation Engineer
Piper Companies, Indianapolis, Indiana, us, 46262
Commissioning Qualification Validation Engineer
Join to apply for the
Commissioning Qualification Validation Engineer
role at
Piper Companies Commissioning Qualification Validation Engineer
4 days ago Be among the first 25 applicants Join to apply for the
Commissioning Qualification Validation Engineer
role at
Piper Companies Get AI-powered advice on this job and more exclusive features. Description
Indianapolis, Indiana (IN).
Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualification protocols (IQ/OQ/PQ) for laboratory equipment, analytical instruments, and systems to ensure compliance with GMP and regulatory standards. Validation: Lead validation efforts for laboratory processes, methods, and equipment, ensuring the reliability, consistency, and reproducibility of results. Support the validation lifecycle of laboratory systems, from planning through execution and reporting. Documentation: Prepare, review, and approve CQV documentation, including protocols, reports, and deviation investigations, ensuring compliance with all internal and external quality requirements.
Description
Piper Companies
is currently looking for an experienced
Commissioning Qualification Validation Engineer (CQV)
in
Indianapolis, Indiana (IN).
Responsibilities for the Commissioning Qualification Validation Engineer (CQV)
include:
Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualification protocols (IQ/OQ/PQ) for laboratory equipment, analytical instruments, and systems to ensure compliance with GMP and regulatory standards. Validation: Lead validation efforts for laboratory processes, methods, and equipment, ensuring the reliability, consistency, and reproducibility of results. Support the validation lifecycle of laboratory systems, from planning through execution and reporting. Documentation: Prepare, review, and approve CQV documentation, including protocols, reports, and deviation investigations, ensuring compliance with all internal and external quality requirements.
Qualifications for the Commissioning Qualification Validation Engineer (CQV)
include:
Bachelor’s degree in engineering, Life Sciences, or a related field (e.g., Biomedical, Chemical, Mechanical Engineering, etc.). Minimum of 3-5 years of experience in Commissioning, Qualification, and Validation (CQV) within a GMP regulated environment, preferably in the biotechnology, pharmaceutical, or cell therapy industry. Strong understanding of GMP, FDA, EMA, and ICH guidelines related to pharmaceutical/biotech operations.
Compensation for the Commissioning Qualification Validation Engineer (CQV)
include:
Salary Range dependent upon experience. Comprehensive benefits package
Keywords
Commissioning, Qualification, Validation, Engineer, Facility build, Laboratory Equipment, IQ/OQ/PQ, Vendor Management, Pharmaceutical Manufacturing
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Quality Assurance Industries Business Consulting and Services Referrals increase your chances of interviewing at Piper Companies by 2x Get notified about new Validation Engineer jobs in
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Join to apply for the
Commissioning Qualification Validation Engineer
role at
Piper Companies Commissioning Qualification Validation Engineer
4 days ago Be among the first 25 applicants Join to apply for the
Commissioning Qualification Validation Engineer
role at
Piper Companies Get AI-powered advice on this job and more exclusive features. Description
Indianapolis, Indiana (IN).
Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualification protocols (IQ/OQ/PQ) for laboratory equipment, analytical instruments, and systems to ensure compliance with GMP and regulatory standards. Validation: Lead validation efforts for laboratory processes, methods, and equipment, ensuring the reliability, consistency, and reproducibility of results. Support the validation lifecycle of laboratory systems, from planning through execution and reporting. Documentation: Prepare, review, and approve CQV documentation, including protocols, reports, and deviation investigations, ensuring compliance with all internal and external quality requirements.
Description
Piper Companies
is currently looking for an experienced
Commissioning Qualification Validation Engineer (CQV)
in
Indianapolis, Indiana (IN).
Responsibilities for the Commissioning Qualification Validation Engineer (CQV)
include:
Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualification protocols (IQ/OQ/PQ) for laboratory equipment, analytical instruments, and systems to ensure compliance with GMP and regulatory standards. Validation: Lead validation efforts for laboratory processes, methods, and equipment, ensuring the reliability, consistency, and reproducibility of results. Support the validation lifecycle of laboratory systems, from planning through execution and reporting. Documentation: Prepare, review, and approve CQV documentation, including protocols, reports, and deviation investigations, ensuring compliance with all internal and external quality requirements.
Qualifications for the Commissioning Qualification Validation Engineer (CQV)
include:
Bachelor’s degree in engineering, Life Sciences, or a related field (e.g., Biomedical, Chemical, Mechanical Engineering, etc.). Minimum of 3-5 years of experience in Commissioning, Qualification, and Validation (CQV) within a GMP regulated environment, preferably in the biotechnology, pharmaceutical, or cell therapy industry. Strong understanding of GMP, FDA, EMA, and ICH guidelines related to pharmaceutical/biotech operations.
Compensation for the Commissioning Qualification Validation Engineer (CQV)
include:
Salary Range dependent upon experience. Comprehensive benefits package
Keywords
Commissioning, Qualification, Validation, Engineer, Facility build, Laboratory Equipment, IQ/OQ/PQ, Vendor Management, Pharmaceutical Manufacturing
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Quality Assurance Industries Business Consulting and Services Referrals increase your chances of interviewing at Piper Companies by 2x Get notified about new Validation Engineer jobs in
Indianapolis, IN . Indianapolis, IN $50,000.00-$240,000.00 1 month ago MV01-080725 Sr Validation Specialist (IN)
Indianapolis, IN $72,800.00-$80,100.00 1 week ago Indianapolis, IN $87,152.00-$94,600.00 1 day ago Indianapolis, IN $56,980.00-$85,000.00 44 minutes ago Greater Indianapolis $80,000.00-$95,000.00 14 hours ago Quality Engineer - Pharma Logistics & Cold Chain
Indianapolis, IN $5,662.27-$7,502.51 4 days ago Computer Systems Quality Assurance (CSQA)
LL02-250725 Validation Specialist for Aseptic Process/Media Fill (IN)
Indianapolis, IN $56,980.00-$85,000.00 5 days ago Indianapolis, IN $40.00-$55.00 17 hours ago Fishers, IN $80,000.00-$100,000.00 1 week ago Westfield, IN $60,000.00-$120,000.00 3 days ago Westfield, IN $60,000.00-$120,000.00 1 week ago Indianapolis, IN $67,500.00-$101,220.00 2 weeks ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr