Job Description

Reference # : 18-06527Title : Compliance Specialist
Location : New Brunswick, NJ
Position Type : Contract
Experience Level : Start Date / End Date : 08/06/2018 / 02/05/2019
Assignment Detail
Industry:Biotech/PharmaJob Category:Scientific / Clinical
Description
Compliance Specialist

Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Compliance Specialist for our client in New Brunswick, NJ.

Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Responsibilities:
  • Managing and coordinating activities related to cGMP Enterprise Electronic Systems. Duties include leading, developing, and maintaining compliance activities across IT Enterprise Services supported regulated GPS applications. Responsible for developing policies and procedures and coordinating all activities relevant between the Quality departments, IT validation and information technology in relation to implementation, maintenance and change control of computerized systems.
  • A key focus of this role will be to provide quality/compliance oversight to all computer system validation related activities across the GPS enterprise. The manager will guide the staff to ensure a comprehensive System Development Lifecycle Methodology in alignment with GAMP 5 requirements..
  • This role will also provide support services and governance to all supporting IT areas (GPS corporate and sites) to ensure global alignment to the computer compliance, global validation and change control standards.
  • Responsibilities also include providing support to assigned Quality programs, such as Data Integrity Governance, Investigations, Global Quality Headquarters Training and other, as assigned
  • Evaluates and administers consultation on computer validation issues related to Quality related computer systems; works closely with Information Technology and Quality Operations on these related issues.
  • Ensures enterprise level metrics and tracking for Corporate Computer related CAPAs are maintained and reported appropriately.
  • Develops and implements policies and procedures related to Quality related system compliance activities related to Risk assessments, validation and the overall maintenance of system state of control.
  • Ensures compliance with all Company policies and procedures, including safety rules and regulations.
  • Partners with IT Validation to ensure risk assessments, incident management and oversight are aligned to corporate and data protection standards.
  • Performs related duties as assigned.

Required Experience:
  • 21CFR11/ EU GMP Annex 11 and GAMP 5 standards
  • Data Integrity Guidance
  • Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements
  • Project management practices and techniques
  • Software development life cycle
  • Computer hardware and software applications including Quality related computer systems, MS Office and MS Project
  • Principles and practices of computer compliance, validation and qualification
  • Knowledge of automated testing practices and tools a plus
  • External and internal inspections

Preferred Skills:
  • Stakeholder management in a cross-functional organization
  • Reviewing user, functional and design specifications.
  • Reviewing and executing protocols and test scripts
  • Sampling, testing and measuring techniques.
  • Analyzing and troubleshooting problems, identifying solutions, recommending, and implementing methods, procedures and/or techniques for resolution.
  • Selecting, training, supervising and evaluating departmental personnel
  • Managing multiple projects, duties and tasks,
  • Communicating clearly and concisely, both orally and in writing.
  • Establishing and maintaining effective working relationships with those contacted in the course of work.

Qualifications:
  • Bachelor’s degree in a related field from an accredited college or university, with a minimum of 5 years of related experience

If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro

If interested, you may contact:
Jane Bautista
Jane@eclaro.com
(201) 285-8622
https://www.linkedin.com/in/froilyn-jane-bautista-88751612a


Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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