Senior Compliance Specialist (Pharma, Bio technology, Life Science any experince)

GXP, Pharmaceutical, Bio technology
Contract W2, Contract Independent, Contract Corp-To-Corp, 12 Months
Depends on Experience

JOB DESCRIPTION:

Additional Job Information: TitleSenior Compliance Specialist
Start Date: 02/08/2021
End Date: 08/07/2021
# of Openings: 1
Priority: null
Position Type:
Location: Morris Plains, NJ, United States

Description:

GENERAL SUMMARY (FUNDAMENTAL PURPOSE OF THE POSITION)
Reporting to the Manager, Technical Investigations and Writing, the Sr. Investigations Compliance Specialist will work with Validation, Supply Chain, Warehouse, and Quality Assurance to support clinical/commercial Biotechnology Products. The Sr. Investigations Compliance Specialist will also be responsible for collaborating with different areas to agree on appropriate CAPAs as needed. In addition, the Sr. Investigations Compliance Specialist may revise or create Standard Operating Procedures, Protocols, and/or Risk Assessments.

ESSENTIAL JOB FUNCTIONS* (PRIMARY RESPONSIBILITIES)
• Perform root cause analysis and product impact investigations for major and critical deviations, related to Validation/ Supply Chain/ Warehouse, to support clinical and commercial biotechnology products.
• Collaborate with GxP Subject Matter Experts to write, review, or edit technical GxP documents in a clear, concise format.
• Meet key timing commitments, with well-investigated and well-documented reports.
• Coordinate and follow-up with personnel/department managers where the event occurred to gather additional information, facts, documents and applicable data.
• Utilize root cause analysis techniques during the deviation investigation process and perform prompt and thorough investigation in compliance with associated regulatory requirements.
• Determine scope, root cause, and product impact of the event
• Assist in determining appropriate CAPA plans to address identified deficiencies, or prevent reoccurrences and potential nonconformances.
• Assist the Data Integrity Governance Committee with DI investigations.
• Assist Quality Assurance in the review of investigation reports.
• Ensure Good Documentation Practices (GDP) are followed.
• Assist in the retrieval and compilation of quality metric data for the investigative process.
• Understand and apply global regulations to processes to ensure compliance.
• Create, review and/or approve appropriate policies, directives and procedures in alignment with relevant governmental regulations and guidelines.
• Provide active participation during regulatory agency inspections, as needed.
• Assist Quality Compliance management maintain a state of inspection readiness and compliance.
• Perform other related tasks and assignments as needed and specified by management related to document generation and control.

EDUCATION/ EXPERIENCE (MUST INCLUDE MINIMUM REQUIREMENTS NECESSARY TO PERFORM ESSENTIAL JOB FUNCTIONS; ADDITIONAL PREFERENCES OPTIONAL)
• Minimum of a Bachelor’s degree in a Technical/Science related field (e.g. Biochemistry, Engineering, Chemistry, Biology, etc.) or equivalent is required; with 5-7+ years of experience in the biotechnology, pharmaceutical, (GxP) industry; or equivalent combination of education and experience.
• Training in investigations technique and root cause analysis tools (5 WHY, Fishbone analysis, Is/Is-Not, etc). is preferred.
• Must have a thorough understanding of pharmaceutical validation, supply chain, and warehousing as it related to the Biologics space.
• Strong experience with investigations/technical writing.

CORE COMPETENCIES (KNOWLEDGE, SKILLS, AND ABILITIES)
• Excellent written and verbal communication skills required, including responsible business communication.
• Comfortable with ambiguity and can adapt style and tactics based on situation.
• Focus on achieving objectives within specified timeframe and to meet quality expectations.
• Knowledge of relevant GxP regulations and guidance to include but not limited to 21 CFR, ICH Q10, EU GDP/GMP, PIC/S.
• Superior attention to detail, organizational skills, and the ability to handle multiple tasks in a timeline-driven environment necessary.
• Must be proficient with all MS Office applications. The Sr. Investigations Compliance Specialist
• Ability to work independently and to make decisions based on experience.

Candidate Details:

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