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Compliance Specialist

Job Description

ACS group has an immediate need for a 'Compliance Specialist' with experience in the Pharmaceutical Industry. This is a 06- month contract opportunity in New Brunswick NJ. Our client is a leading Pharmaceutical company.

Please review the job description below:

Top Skills:

  • Pharmaceutical
  • IT Quality Assurance
  • Gxp
  • compliance
  • CSV

Key Requirements and Technology Experience:

Manage and coordinate activities associated with the GxP IT Quality Assurance (QA) program for GPS and R&D computerized systems regulatory compliance across the end-to-end product lifecycle (GPS and R&D) for software development and validation lifecycle activities associated with regulated computerized systems to ensure conformance to cGxPs, guidance documents, applicable industry accepted standards and requirements.

Carries out functions of the GxP-ITQA as directed including but not limited to:

Review and approval of key computer system Validation Life Cycle (VLC) deliverables; Review and approval of test scripts and defects associated with computer system validation; Oversight of key Software Development Life Cycle (SDLC) process such as incident, problem, change, release, etc.; Ensure adequate and timely regulatory compliance support.

Partner with IT Validation to ensure risk assessments, incident management and oversight are aligned to corporate and data protection standards.

Provide backup support for the department as needed and perform other assignments as required.

Support internal and external (regulatory) inspection activities related to validated systems.

Provide support to assigned Quality programs, such as Data Integrity Governance, Investigations, Global Quality Headquarters Training and other, as assigned.

Ability to manage multiple projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross-functional team.

Operate effectively and with minimal supervision, within a team or independently, performing special projects and related duties, as assigned.

Qualifications:

Experience in the BioTech/Pharmaceutical industry or similar regulated industry required.

Good understanding of the drug and device development process from discovery through to regulatory filing and approval of drug applications as well as commercial manufacturing processes.

Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), Good Pharmacovigilance Practices (GVP), Food & Drug Administration (FDA), and other regulatory

requirements.

FDA 21 CFR 11, EU GMP Annex 11 and GAMP 5 standards.

Data Integrity Guidance.

In-depth understanding of industry-accepted software development and validation life cycle programs and related IT controls.

Experience with relevant GxP systems such as quality management systems, document management systems, ERP, training/learning management systems, clinical and laboratory systems preferred.

Understanding of quality risk-management concepts (ICH Q9) preferred;

Understanding of ITIL Framework concepts (e.g., Incident, Problem, Change management processes)

Understanding of Good Documentation Practices

Project management practices and techniques;

Experience with automated testing practices and tools preferred;

Computer hardware, software including MS Office and MS Project;

External and internal inspections support a plus;

Excellent analytical, interpersonal, and communication skills, including written and verbal communication.

Education:

Bachelor's degree in a related field from an accredited college or university, with a minimum of 5 years of related experience.

Thanks & Regards
Parag PATEL

Team Recruitment

P: (+1) 678 487 8366


ABOUT ACS GROUP.
- ACS Group is a premier provider of IT Consulting, Engineering Consulting, Healthcare, Talent, and Workforce Management Solutions tFortune 1000 companies globally. Our operating brands have provided targeted services and solutions for more than 50 years. We serve our clients through four operating companies:
* AIC
*Analysts
*ComforceHealth
*HireGenics
Recent Recognitions:
#No. 6 Largest IT staffing Firm in the U.S. (2019 SIA)
#Largest Minority-Owned IT Staffing Firm in the U.S. (2018 SIA)
# No. 8 Largest IT Staffing Firm in the U.S. (2018 SIA)
#Inavero's Best of Staffing® Client Diamond Award (2018).
#National Class lV Supplier of the Year Finalist and a Regional Class IV Supplier of the Year by NMSDC
#Inavero's Best of Staffing®Client Diamond Award Winner(2017)

Website: www.acsicorp.com

Job Requirements

 

Job Snapshot

Location US-NJ-New Brunswick
Employment Type Contractor
Pay Type Year
Pay Rate N/A
Store Type Energy, Oil & Gas, IT & Technical, Clinical & Scientific
Apply

Company Overview

Analysts

Analysts International Corporation (AIC) is an IT services firm fully dedicated to the success and satisfaction of its customers. From IT staffing to project-based solutions, AIC provides a broad range of services designed to help businesses and government agencies drive value, control costs and deliver on the promise of a more efficient and productive enterprise. Learn More

Contact Information

US-NJ-New Brunswick
AIC
(770) 493-5588
Snapshot
Analysts
Company:
US-NJ-New Brunswick
Location:
Contractor
Employment Type:
Year
Pay Type:
N/A
Pay Rate:
Energy, Oil & Gas, IT & Technical, Clinical & Scientific
Store Type:

Job Description

ACS group has an immediate need for a 'Compliance Specialist' with experience in the Pharmaceutical Industry. This is a 06- month contract opportunity in New Brunswick NJ. Our client is a leading Pharmaceutical company.

Please review the job description below:

Top Skills:

  • Pharmaceutical
  • IT Quality Assurance
  • Gxp
  • compliance
  • CSV

Key Requirements and Technology Experience:

Manage and coordinate activities associated with the GxP IT Quality Assurance (QA) program for GPS and R&D computerized systems regulatory compliance across the end-to-end product lifecycle (GPS and R&D) for software development and validation lifecycle activities associated with regulated computerized systems to ensure conformance to cGxPs, guidance documents, applicable industry accepted standards and requirements.

Carries out functions of the GxP-ITQA as directed including but not limited to:

Review and approval of key computer system Validation Life Cycle (VLC) deliverables; Review and approval of test scripts and defects associated with computer system validation; Oversight of key Software Development Life Cycle (SDLC) process such as incident, problem, change, release, etc.; Ensure adequate and timely regulatory compliance support.

Partner with IT Validation to ensure risk assessments, incident management and oversight are aligned to corporate and data protection standards.

Provide backup support for the department as needed and perform other assignments as required.

Support internal and external (regulatory) inspection activities related to validated systems.

Provide support to assigned Quality programs, such as Data Integrity Governance, Investigations, Global Quality Headquarters Training and other, as assigned.

Ability to manage multiple projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross-functional team.

Operate effectively and with minimal supervision, within a team or independently, performing special projects and related duties, as assigned.

Qualifications:

Experience in the BioTech/Pharmaceutical industry or similar regulated industry required.

Good understanding of the drug and device development process from discovery through to regulatory filing and approval of drug applications as well as commercial manufacturing processes.

Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), Good Pharmacovigilance Practices (GVP), Food & Drug Administration (FDA), and other regulatory

requirements.

FDA 21 CFR 11, EU GMP Annex 11 and GAMP 5 standards.

Data Integrity Guidance.

In-depth understanding of industry-accepted software development and validation life cycle programs and related IT controls.

Experience with relevant GxP systems such as quality management systems, document management systems, ERP, training/learning management systems, clinical and laboratory systems preferred.

Understanding of quality risk-management concepts (ICH Q9) preferred;

Understanding of ITIL Framework concepts (e.g., Incident, Problem, Change management processes)

Understanding of Good Documentation Practices

Project management practices and techniques;

Experience with automated testing practices and tools preferred;

Computer hardware, software including MS Office and MS Project;

External and internal inspections support a plus;

Excellent analytical, interpersonal, and communication skills, including written and verbal communication.

Education:

Bachelor's degree in a related field from an accredited college or university, with a minimum of 5 years of related experience.

Thanks & Regards
Parag PATEL

Team Recruitment

P: (+1) 678 487 8366


ABOUT ACS GROUP.
- ACS Group is a premier provider of IT Consulting, Engineering Consulting, Healthcare, Talent, and Workforce Management Solutions tFortune 1000 companies globally. Our operating brands have provided targeted services and solutions for more than 50 years. We serve our clients through four operating companies:
* AIC
*Analysts
*ComforceHealth
*HireGenics
Recent Recognitions:
#No. 6 Largest IT staffing Firm in the U.S. (2019 SIA)
#Largest Minority-Owned IT Staffing Firm in the U.S. (2018 SIA)
# No. 8 Largest IT Staffing Firm in the U.S. (2018 SIA)
#Inavero's Best of Staffing® Client Diamond Award (2018).
#National Class lV Supplier of the Year Finalist and a Regional Class IV Supplier of the Year by NMSDC
#Inavero's Best of Staffing®Client Diamond Award Winner(2017)

Website: www.acsicorp.com

Job Requirements

 
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