12 Manufacturing jobs in Kakinada
Manufacturing Specialist
Posted 4 days ago
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Job Description
Job Description: Manufacturing Specialist
Work time: EST and PST time zone work hours
Location: India (Anywhere)
Job Summary
This role focuses on driving continuous improvement in factory operations. The Manufacturing Process Improvement Engineer will work with internal and external teams to optimize production processes and enhance operational efficiency.
Key Responsibilities
- Analyze factory flow and identify areas for improvement.
- Implement lean manufacturing and Six Sigma methodologies.
- Collaborate with manufacturing engineering teams to improve performance.
- Support ramp-up and sustaining operations.
- Track and report on key performance indicators (KPIs).
Qualifications
- Bachelor’s degree in Industrial, Mechanical, or Manufacturing Engineering.
- 5–7 years of experience in process improvement or lean manufacturing.
- Six Sigma Green Belt or Black Belt certification preferred.
- Strong problem-solving and data analysis skills.
Senior Core Engineering – Calibration, Quality & Manufacturing Trainer
Posted 2 days ago
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Job Description
Job Title: Core Engineering – Calibration, Quality & Manufacturing Trainer
Location: Remote
Job type: Part-time
Job Summary:
We are looking for an experienced Core Engineering Trainer with 8 to 10+ years of expertise in Calibration, Quality Assurance, and Manufacturing . This role is ideal for professionals passionate about training, mentoring, and enabling career growth for engineers. The trainer will deliver hands-on sessions , conduct interview preparation , and guide candidates through industry best practices and certification pathways to make them industry-ready.
Key Responsibilities:
- Deliver training on Calibration Techniques (instruments, equipment, standards)
- Guide on QA & Manufacturing Best Practices (ISO 9001, Lean, Six Sigma, GMP )
- Provide real-world manufacturing project case studies & problem-solving scenarios
- Train on documentation : SOPs, Deviations, CAPA, Audit Reports
- Mentor candidates on Equipment Qualification & Preventive Maintenance
- Conduct Mock Technical & HR Interviews
- Assist candidates in building career-ready resumes & structured project stories
- Guide on Certification Pathways (Lean Six Sigma, CQE, CMQ/OE )
Requirements:
- 8–10+ Years in Core Engineering (Calibration, QA, Manufacturing )
- Strong Calibration Expertise (instruments, sensors, process equipment)
- Experience in Quality Management Systems & Manufacturing Operations
- Prior Mentoring/Training Experience preferred
- Excellent Communication, Documentation & Presentation Skills
Senior Quality Control (Microbiology + Chemistry) Trainer
Posted 3 days ago
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Job Description
Job Title: Quality Control (Microbiology + Chemistry) Trainer
Location: Remote
Job Type: Part-time
Job Summary:
We are seeking an experienced QC (Microbiology and Chemistry) Trainer to design and deliver technical training programs , mentor professionals , and support their career success in the pharmaceutical and healthcare industries. This role involves hands-on guidance , GMP/GLP compliance training , documentation mentoring , and interview preparation .
Key Responsibilities:
- Deliver training on QC techniques:
- Microbiology: Environmental Monitoring (EM), Sterility Testing, Bioburden
- Chemistry: HPLC, GC, UV-Vis Spectroscopy, FTIR
- Mentor and coach on GMP, GLP, Data Integrity & Regulatory Compliance
- Guide candidates on laboratory practices, documentation & audit readiness
- Prepare real-world case studies on OOS, OOT investigations & CAPA handling
- Train on SOP creation, deviation management & lab report preparation
- Conduct mock interviews (Technical + HR) with actionable feedback
- Support career enablement: Resume building, project story development, certification guidance (ASQ, Microbiology, Analytical Chemistry)
Requirements:
- 10+ years of experience in QC (Microbiology + Chemistry) in a regulated Pharma / Healthcare environment
- Hands-on expertise with laboratory equipment & analytical techniques (HPLC, GC, UV, FTIR)
- Strong knowledge of regulatory standards: FDA, WHO, ICH, MHRA
- Experience with GMP, GLP, Data Integrity, CAPA investigations, OOS/OOT analysis
- Training/mentoring experience with excellent presentation skills
- Strong documentation skills and ability to prepare audit-ready records
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