Top 82 Quality improvement specialist Jobs in Juncos, Pr

JT596 - SPECIALIST MANUFACTURING
Quality Consulting Group —Juncos, PR
- Spanish
- English
- Mid-level
13d
JT625 - SPECIALIST MANUFACTURING
Quality Consulting Group —Juncos, PR
- Mid-level
- Analysis skills
- Commercial
1d
Quality Assurance Specialist II
Cytiva —Fajardo, PR
- Full-time
- Clean driving record
- 5 years
- Mid-level
9d
Specialist QA
BioPharma Consulting JAD Group —Juncos, PR
- Contract
- Spanish
- Doctoral degree
- Computer Science
Quick Apply
9d
EHS Specialist (Multi-site visits)
Mentor Technical Group —Caguas, PR
- Full-time
- Engineering
- 8 years
- Ability to lift 50 pounds
Specialist Quality Assurance
InnovaWorkforce Inc. —Juncos, PR
- $40 - $42 an hour
- 8 hour shift
- Doctoral degree
- Word processing
- Master's degree
Quick Apply
5d
QUALITY ASSURANCE SPECIALIST
MENTOR TECHNICAL GROUP CORP —Carolina, PR
- Mid-level
- 3 years
- Continuous improvement
Quick Apply
Quality Assurance Specialist – Utilities & Environmental Monitoring
Mentor Technical Group —Carolina, PR
- Full-time
- Mid-level
- 3 years
- Continuous improvement
Specialist Manufacturing 35561
Inteldot —Municipio de Juncos, PR
- Engineering
- Mid-level
- Master's degree
Quick Apply
12d
Specialist Manufacturing - 35625
Mirus Consulting Group —Municipio de Juncos, PR
- Overtime
- Doctoral degree
- Mid-level
- Master's degree
Quick Apply
1d
Field Application Specialist
Beckman Coulter Life Sciences —Caguas, PR
- Full-time
- Remote
- Spanish
- English
- Mid-level
- Paid time off
JT601 - SPECIALIST MANUFACTURING
Quality Consulting Group —Juncos, PR
- Mid-level
- Analysis skills
- Communication skills
7d
Specialist Manufacturing
BioPharma Consulting JAD Group —Juncos, PR
- Extended hours
- Spanish
- Doctoral degree
- English
Quick Apply
9d
JT615 - SPECIALIST QA
Quality Consulting Group —Juncos, PR
- Bachelor's degree
- Senior level
6d
Specialist Manufacturing
Cencora —Juncos, PR
- Full-time
- Doctoral degree
- Mid-level
- 3 years
- Paid parental leave
- Health insurance
Cleaning Validation Specialist
Cencora —Juncos, PR
- Full-time
- OSHA
- 5 years
- English
- Paid parental leave
- Health insurance
COMPLIANCE SPECIALIST
MENTOR TECHNICAL GROUP CORP —Caguas, PR
- Mid-level
- 3 years
- Analysis skills
Quick Apply
Specialist Manufacturing
Weil Group, Inc —Juncos, PR
- Spanish
- Doctoral degree
- English
Quick Apply
14d
Manufacturing Specialist 35625
ProQualityNetwork —Juncos, PR
- 8 hour shift
- Doctoral degree
- Mid-level
- Master's degree
23h
Manufacturing Specialist- 11
Flexible & Integrated Technical Services, LLC —Juncos, PR
- Spanish
- 5 years
- English
Quick Apply
7d

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JT596 - SPECIALIST MANUFACTURING

Quality Consulting Group -
Juncos, PR

Apply Now

Job Details

13 days ago

Qualifications

Production deviation management
English
Bioprocessing
Presentation creation

Full Job Description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing to a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions.
Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.
May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
Own change controls for manufacturing process changes
Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.
Support Risk Assessments exercises and Microbial assessment evaluations.
Led commercial campaign readiness and effectively communicate and collaborate with cross function areas.
Assist in the generation of training materials and assist in providing training on scientific or technical aspects of the process.
Provide commercial support when needed and assist on the floor troubleshooting.
Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness. Generate technical protocols as needed.
Assist and provide guidance during MBR (Master Batch Record) creation/revisions.
Perform assessment to support process, automation, or equipment modification or implementation of special projects
Initiate, revise, and approve standard manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
Assess process performance and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
Complete assessments for CAPA applicability requests from other plants/sites
Complete assessment for new or changes in BOM's (Bill of Materials)
Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area.

Qualifications:

Bachelor's degree in Life Sciences, Biology, Chemistry, and/or Engineering.
In-depth experience of bio-processing unit operations (Cell Culture, Drug Substance Purification)
Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why’s, Kepner Tregoe)
Previous experience in major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.
Familiar with Lean Manufacturing Practices
Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
Proficiency in GDP (Good Documentation Practices) on a regulated environment
Knowledge in systems: Trackwise, Spotfire, CDOCS, and process monitoring platforms
Strong Technical Writing/presentation abilities, and excellent written/verbal communication skills in English and Spanish

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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Refine Your Search

quality improvement specialist jobs in juncos, pr

JT596 - SPECIALIST MANUFACTURING

JT625 - SPECIALIST MANUFACTURING

Quality Assurance Specialist II

Specialist QA

EHS Specialist (Multi-site visits)

Specialist Quality Assurance

QUALITY ASSURANCE SPECIALIST

Quality Assurance Specialist – Utilities & Environmental Monitoring

Specialist Manufacturing 35561

Specialist Manufacturing - 35625

Field Application Specialist

JT601 - SPECIALIST MANUFACTURING

Specialist Manufacturing

JT615 - SPECIALIST QA

Specialist Manufacturing

Cleaning Validation Specialist

COMPLIANCE SPECIALIST

Specialist Manufacturing

Manufacturing Specialist 35625

Manufacturing Specialist- 11

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