Top 31 Quality document control specialist Jobs in Barceloneta, Pr

Quality - Document Control Specialist
Viant Medical —Vega Baja, PR
- Full-time
- Customer service
- Writing skills
- Mid-level
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8d
QA / Documentation Specialist
Qualitech Management Solutions —Barceloneta, PR
- $20 - $40 an hour
- Part-time
- Background check
- Mid-level
- Bachelor's degree
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14d
Documentation Specialist
Artech LLC —Barceloneta, PR
- Overtime
- Microsoft Word
- Spanish
- 5 years
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1d
Regulatory QA Specialist
HR Works —Barceloneta, PR
- $30 - $45 an hour
- Contract
- Senior level
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Documentation Specialist
Mentor Technical Group —Barceloneta, PR
- Full-time
- Mid-level
- Business development
- Analysis skills
10d
Quality Assurance (QA) Specialist II
Artech LLC —Barceloneta, PR
- $20.00 - $21.16 an hour
- Contract
- Bilingual
- Mid-level
- Manufacturing
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QA Specialist
PSC Biotech —Manatí Municipio, PR
- Full-time
- 5 years
- English
- Mid-level
9d
C&Q Specialist | Pharmaceutical
LPMP | Legal Project Management Partners —Manatí, PR
- Contract
- Spanish
- Microsoft Excel
- Microsoft Outlook
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Computer System Validation (CSV) Specialist (EBR System)
Validation & Engineering Group, Inc —Barceloneta, PR
- Full-time
- 5 years
- Senior level
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Cleaning Validation Specialist
Moriah Engineering —Jayuya, PR
- Engineering
- Mid-level
- Ability to climb stairs
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Cleaning Validation Specialist
Validation & Engineering Group —Barceloneta, PR
- Spanish
- OSHA
- 5 years
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Validation Specialist (Cleaning-In-Place)
Validation & Engineering Group, Inc —Barceloneta, PR
- Extended hours
- 7 years
- Senior level
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Validation Specialist – Water System & Equipment Qualification
Mentor Technical Group —Vega Baja, PR
- Full-time
- Spanish
- Engineering
- English
Validation Specialist
Flexible & Integrated Technical Services, LLC —Dorado, PR
- Spanish
- Customer service
- Engineering
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Senior Parenteral Inspection Technology Specialist
Weil Group, Inc —Manatí, PR
- Temporary
- Background check
- Master's degree
- 8 years
Quick Apply
JT678 - QUALITY APPLICATIONS SPECIALISTS
Quality Consulting Group —Villalba, PR
- Product management
- Senior level
- Leadership
Sr. Quality Applications Specialist
Flexible & Integrated Technical Services, LLC —Villalba, PR
- Spanish
- Customer service
- Engineering
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Senior Parenteral Inspection Technology Specialist
Flexible & Integrated Technical Services, LLC —Manatí, PR
- Spanish
- 5 years
- Engineering
Quick Apply
Real Estate Agent - High Quality Leads, Expert Training, Coaching and Support!
ADT Realty —United States
- $80,000 - $250,000 a year
- Full-time
- Remote
- Mid-level
- Real Estate License
- Professional development assistance
- Flexible schedule
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Quality Assurance Specialist
Accel Inc —New Albany, OH
Assist with non-conformance assessments, findings, reports, CAPAs, and root cause analysis. Accel is hiring a *Quality Assurance Specialist* to perform routine…
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Assist in training floor associates on procedures & quality gauges / tools. 401k Retirement Plan- Company matching. Assist in tracking trends or quality issues.
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Quality - Document Control Specialist

Viant Medical -
Vega Baja, PR

Quick Apply

Job Details

Full-time
8 days ago

Qualifications

Customer communication

Full Job Description

Title: Quality - Document Control Specialist

Position Description/Responsibilities:
The employee will be responsible for reporting training and KPI metrics, leading compliance and CRB meetings, managing changes to Bill of Materials (BOM), reviewing and updating documents, supporting various projects related to injection molding and combination products, and maintaining the integrity of the quality systems procedures. Additionally, the employee will assist in audits, ensure customer requests are addressed, verify manual mixing processes, inspect incoming raw materials, and manage the record retention area.

Position Authority:
The employee has the authority to make decisions regarding the review and update of quality systems procedures, BOM changes, document change orders (DCOs), and incoming inspection processes. They also have the authority to lead com compliance meetings and ensure adherence to audit requirements.

Essential Functions:
Report training metrics as required.
Report KPI metrics as required.
Lead Compliance and CRB meetings.
Make necessary changes to BOM.
Review DCOs and ECOs.
Support Injection Molding and Combination Product projects by reviewing DCOs, ECOs, phase reviews, and requests made by Project Managers Project Engineers and Customers. Review and update quality systems procedures and related forms as required.
Assist with regulatory, external, internal and customer audits.
Assist with the completion of Certificates of Compliance (COCs).
Handle customer requests related to procedures and COCs.
Verify the manual mixing (resin and colorant) process and review related documentation.
Assist with incoming inspection of raw materials.
Responsible of record retention area.
Identify and destroy documents after the required retention period is complete.
Provide new and/or revised manufacturing documents to manufacturing areas and ensure that obsolete documents are removed upon updates.
Make IT tickets for Master Control accounts, BMRAM accounts, password resets, among others as required.
Assist with New Employee Orientation onboarding activities such as creating and presenting overview presentations.
Perform other functions as required.

Skills:
Strong organizational written and project management skills. Attention to detail, particularly with documentation and compliance, effective communication, both verbal and written, for internal and external interactions. Analytical thinking for reviewing DCOs, ECOs, and phase reviews. Knowledge of quality management systems and regulatory standards. Proficiency in handling customer requests and audit preparations. Strong interpersonal skills.

Physical Requirements:
Ability to sit or stand for extended periods while reviewing documentation. Capacity to lift and move boxes or records in the retention area. Regular manual handling of materials during the inspection and mixing processes.

Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.

Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.

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Refine Your Search

quality document control specialist jobs in barceloneta, pr

Quality - Document Control Specialist

QA / Documentation Specialist

Documentation Specialist

Regulatory QA Specialist

Documentation Specialist

Quality Assurance (QA) Specialist II

QA Specialist

C&Q Specialist | Pharmaceutical

Computer System Validation (CSV) Specialist (EBR System)

Cleaning Validation Specialist

Cleaning Validation Specialist

Validation Specialist (Cleaning-In-Place)

Validation Specialist – Water System & Equipment Qualification

Validation Specialist

Senior Parenteral Inspection Technology Specialist

JT678 - QUALITY APPLICATIONS SPECIALISTS

Sr. Quality Applications Specialist

Senior Parenteral Inspection Technology Specialist

Real Estate Agent - High Quality Leads, Expert Training, Coaching and Support!

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