Eclaro
Plant Document Specialist
Eclaro, Sanford, Maine, us, 04073
Plant Document SpecialistJob Number: 24-02785
Use your skills where innovative technology solutions begin. ECLARO is looking for a
Plant Document Specialist
for our client in
Sanford, ME.
ECLARO's client is a leading consumer products company with a global presence. If you're up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
The Plant Document Specialist is responsible for managing Document Control programs that ensure all documents related to the product quality meet the requirements this includes, maintaining, controlling, and auditing documentation for compliance, and reviewing assigned production documentation.
Responsibilities:
Maintain, control and audit site documentation in electronic and paper systems to ensure compliance with cGMP.Standard Operating Procedures & Associated Documents.Manufacturing Batch Production Records & Associated Documents.GMP Training Records.Create records as per site procedures and provide to Operations for manufacturing activitiesCreate and maintain Standard Operating Procedures (including but not limited to procedures, forms, maintenance work, logbooks, etc.) for the cGMP compliance programsManage site's electronic and paper document control systems designed to achieve cGMP compliance and provide training on its useManage filing system for current and archived documents required for cGMP compliance, including management of documents on site and those sent to an off-site 3rd party storage locationManage libraries of SOPs (Standard Operating Procedures), Formulas, Manufacturing SOPs, Lab SPIs, and general SOPs to ensure accuracy and reliabilityManage SOP (Standard Operating Procedures) periodic review program and track/report KPI (Key Performance Indicators)Audit/review all assigned documentation required to support the business, including logbooks, preventive maintenance forms, etc.
Qualifications:
1-3 years of industrial experience in FDA regulated consumer products, pharmaceutical or Food industries.This experience should include working in a quality system environment with exposure to governmental audits and assessments.Self-driven, detail-oriented, and able to work independently on regularly scheduled (daily, weekly, etc.) tasks.Possess excellent ability to understand, read, speak, and write in English.Excellent interpersonal and communication skills.Able to communicate information clearly, simply and in a timely manner.Strong multitasking skills and excellent time management skills.Working knowledge of Google Docs, Sheets, Slides, as well as Microsoft Word, Excel, and PowerPoint. SAP experience is a plus
If hired, you will enjoy the following ECLARO Benefits:
401k Retirement Savings Plan administered by Merrill LynchCommuter Check Pretax Commuter BenefitsEligibility to purchase Medical, Dental & Vision Insurance through ECLARO
If interested, you may contact:Lester Candiladojan.candilado@eclaro.com6466800168Lester Candilado | LinkedIn
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.
Use your skills where innovative technology solutions begin. ECLARO is looking for a
Plant Document Specialist
for our client in
Sanford, ME.
ECLARO's client is a leading consumer products company with a global presence. If you're up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
The Plant Document Specialist is responsible for managing Document Control programs that ensure all documents related to the product quality meet the requirements this includes, maintaining, controlling, and auditing documentation for compliance, and reviewing assigned production documentation.
Responsibilities:
Maintain, control and audit site documentation in electronic and paper systems to ensure compliance with cGMP.Standard Operating Procedures & Associated Documents.Manufacturing Batch Production Records & Associated Documents.GMP Training Records.Create records as per site procedures and provide to Operations for manufacturing activitiesCreate and maintain Standard Operating Procedures (including but not limited to procedures, forms, maintenance work, logbooks, etc.) for the cGMP compliance programsManage site's electronic and paper document control systems designed to achieve cGMP compliance and provide training on its useManage filing system for current and archived documents required for cGMP compliance, including management of documents on site and those sent to an off-site 3rd party storage locationManage libraries of SOPs (Standard Operating Procedures), Formulas, Manufacturing SOPs, Lab SPIs, and general SOPs to ensure accuracy and reliabilityManage SOP (Standard Operating Procedures) periodic review program and track/report KPI (Key Performance Indicators)Audit/review all assigned documentation required to support the business, including logbooks, preventive maintenance forms, etc.
Qualifications:
1-3 years of industrial experience in FDA regulated consumer products, pharmaceutical or Food industries.This experience should include working in a quality system environment with exposure to governmental audits and assessments.Self-driven, detail-oriented, and able to work independently on regularly scheduled (daily, weekly, etc.) tasks.Possess excellent ability to understand, read, speak, and write in English.Excellent interpersonal and communication skills.Able to communicate information clearly, simply and in a timely manner.Strong multitasking skills and excellent time management skills.Working knowledge of Google Docs, Sheets, Slides, as well as Microsoft Word, Excel, and PowerPoint. SAP experience is a plus
If hired, you will enjoy the following ECLARO Benefits:
401k Retirement Savings Plan administered by Merrill LynchCommuter Check Pretax Commuter BenefitsEligibility to purchase Medical, Dental & Vision Insurance through ECLARO
If interested, you may contact:Lester Candiladojan.candilado@eclaro.com6466800168Lester Candilado | LinkedIn
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.