3 Medical Technology jobs in Patna

Job Title: Senior Electrical Engineering Trainer – Pharma & Medical Devices

Location: Remote

Job Type: Part-time

Job Summary:

We are seeking an experienced Electrical Engineering Trainer with over 10 years of hands-on experience in the pharmaceutical and medical devices industries. The trainer will be responsible for designing, developing, and delivering high-quality training programs for engineers, technicians, and operational staff to enhance their technical skills in electrical systems, automation, and compliance with industry standards.

Key Responsibilities:

• Develop and deliver technical training programs related to electrical systems, instrumentation, and control in pharmaceutical and medical device manufacturing.
• Train personnel on maintenance, troubleshooting, and validation of electrical and automation equipment.
• Provide hands-on practical sessions for operational and engineering teams to ensure competence in electrical engineering practices.
• Ensure training content complies with cGMP, ISO 13485, FDA, and other regulatory standards relevant to pharma and medical devices.
• Mentor and guide engineers and technicians on best practices in electrical design, installation, and safety .
• Prepare training manuals, SOPs, presentations, and assessment tools for internal training programs.
• Stay updated on emerging electrical technologies, automation trends, and regulatory requirements in pharma and medical devices.
• Conduct skill gap analysis and propose training plans to address identified gaps.

Required Qualifications & Skills:

• Bachelor’s degree in Electrical Engineering or related field (Master’s preferred).
• Minimum 10 years of experience in electrical engineering roles within pharmaceutical or medical devices industries .
• Strong knowledge of PLC, SCADA, DCS, electrical installations, motors, drives, and control systems .
• Experience with equipment qualification, calibration, and validation (IQ/OQ/PQ).
• Familiarity with cGMP, ISO 13485, FDA regulations, and EHS standards .
• Proven experience in developing and delivering technical training programs .
• Excellent communication, presentation, and interpersonal skills .
• Strong analytical and problem-solving abilities.

Preferred Skills:

• Experience with automation systems, robotics, and MES in pharma/medical devices.
• Certification in training or adult education .
• Hands-on experience with preventive and predictive maintenance techniques.

Key Competencies:

• Technical expertise in electrical engineering for pharma/medical devices .
• Ability to simplify complex technical concepts for trainees.
• Strong leadership, mentoring, and coaching skills.
• Commitment to quality, safety, and regulatory compliance .

Job Title: Senior Labeling Specialist Trainer – Medical Devices Industry

Location: Remote

Job Type: Part-time

Job Summary:

We are seeking an experienced Labeling Specialist Trainer with over 10 years of expertise in medical device labeling, regulatory compliance, and documentation control . The trainer will be responsible for developing and delivering comprehensive training programs that enhance the understanding of global labeling standards, systems, and processes among regulatory, quality, and manufacturing teams.

The ideal candidate will have a deep understanding of medical device labeling regulations (FDA, EU MDR, ISO 15223, ISO 20417, UDI requirements) and experience in label design tools and labeling systems used in the industry.

Key Responsibilities:

• Design and deliver technical and compliance training programs on medical device labeling requirements, standards, and systems.
• Provide hands-on training on labeling software (e.g., Prisym 360, Loftware, Bartender, NiceLabel, etc.).
• Develop and update training materials , SOPs, and competency assessment tools related to labeling processes.
• Ensure trainees understand regulatory and quality requirements (FDA 21 CFR Part 801, EU MDR Annex I, UDI, ISO 15223-1).
• Conduct compliance workshops on global labeling standards, symbols, and risk-based labeling requirements.
• Train cross-functional teams (Regulatory Affairs, QA/RA, Manufacturing, Packaging, IT) on labeling workflows and change management.
• Support audits and internal assessments by providing expert guidance on labeling compliance.
• Evaluate trainee performance and maintain training records as per quality system requirements.
• Collaborate with subject matter experts to continuously improve labeling process training content and delivery.

Required Qualifications:

• Bachelor’s or Master’s degree in Engineering, Life Sciences, Regulatory Affairs, or related field .
• 10+ years of experience in medical device labeling operations , compliance, or artwork management.
• Strong knowledge of global labeling regulations (FDA, EU MDR, CFDA, Health Canada, etc.).
• Proficient in labeling tools and PLM/QMS systems (e.g., SAP, Agile, Windchill).
• Experience in training and mentoring professionals in a regulated environment.
• Familiarity with document control systems and CAPA processes.
• Excellent communication, presentation, and documentation skills .
• Certification or experience in Instructional Design / Training Delivery is a plus.

Preferred Skills:

• Understanding of UDI databases (e.g., GUDID, EUDAMED).
• Knowledge of graphic design principles for labeling (Adobe Illustrator, InDesign basics).
• Experience in label change management workflows .
• Exposure to risk management (ISO 14971) and quality management systems (ISO 13485) .