8 Biomedical Engineering jobs in Hyderabad

We are seeking skilled medical devices recruiters to join our team. In this role, you will support US-based clients in sourcing top talent for engineering, medical devices, and pharmaceutical roles.

• Source and engage candidates for engineering, pharma, and medical devices positions.
• Collaborate with account managers and hiring teams to understand role requirements.
• Conduct interviews and assess candidate fit.
• Coordinate interview scheduling, feedback, and follow-ups.
• Maintain accurate records in the applicant tracking system.

• 6 months to 2 years of experience in US staffing, preferably in engineering/medical devices/pharmaceuticals.
• Excellent communication and interpersonal skills.
• Ability to work independently in a remote setup.

• Permanent remote position.
• Opportunity to work with leading clients in the US market.

Job Title: Senior Microbiology Trainer – Medical Devices

Location: Remote

Job Type: Part-time

Job Summary:

We are seeking an experienced Microbiologist with over 10 years of hands-on expertise in microbiology, sterilization, and quality assurance in the medical devices industry. The ideal candidate will design, develop, and deliver training programs to enhance the knowledge and technical capabilities of staff across R&D, quality control, manufacturing, and regulatory teams. The trainer will ensure compliance with global standards, including ISO 13485, FDA, and GMP requirements.

Key Responsibilities:

• Design and deliver training programs on microbiology concepts, testing methods, and aseptic processing techniques relevant to medical devices.
• Develop curriculum covering sterility testing, bioburden testing, microbial limit testing, endotoxin testing, and cleanroom practices.
• Conduct hands-on workshops, practical demonstrations, and assessments for lab personnel and manufacturing teams.
• Stay updated on latest industry trends, regulatory requirements, and technological advancements in microbiology.
• Collaborate with cross-functional teams (QA/QC, Production, R&D) to identify training needs.
• Ensure all training programs meet compliance standards and are documented properly.
• Mentor junior microbiologists and support their professional development.
• Review and update training materials, SOPs, and protocols as per regulatory changes.

Qualifications & Experience:

• Master’s or Ph.D. in Microbiology, Biotechnology, or related field.
• Minimum 10 years of experience in microbiology within the medical devices or pharmaceutical industry.
• Hands-on experience with sterility testing, microbial limit tests, endotoxin testing, environmental monitoring, and aseptic techniques.
• Strong knowledge of regulatory standards: ISO 13485, ISO 14698, USP <71>, FDA, and GMP.
• Proven experience in delivering technical training and preparing training materials.
• Excellent communication, presentation, and mentoring skills.
• Experience with cleanroom operations and GMP documentation preferred.

Key Competencies:

• Deep understanding of microbiological principles and testing methods.
• Ability to translate complex technical concepts into effective training modules.
• Strong analytical and problem-solving skills.
• Attention to detail and commitment to quality and compliance.

Job Title: Senior Microbiology Trainer – Medical Devices

Location: Remote

Job Type: Part-time

Job Summary:

We are seeking an experienced Microbiologist with over 10 years of hands-on expertise in microbiology, sterilization, and quality assurance in the medical devices industry. The ideal candidate will design, develop, and deliver training programs to enhance the knowledge and technical capabilities of staff across R&D, quality control, manufacturing, and regulatory teams. The trainer will ensure compliance with global standards, including ISO 13485, FDA, and GMP requirements.

Key Responsibilities:

• Design and deliver training programs on microbiology concepts, testing methods, and aseptic processing techniques relevant to medical devices.
• Develop curriculum covering sterility testing, bioburden testing, microbial limit testing, endotoxin testing, and cleanroom practices.
• Conduct hands-on workshops, practical demonstrations, and assessments for lab personnel and manufacturing teams.
• Stay updated on latest industry trends, regulatory requirements, and technological advancements in microbiology.
• Collaborate with cross-functional teams (QA/QC, Production, R&D) to identify training needs.
• Ensure all training programs meet compliance standards and are documented properly.
• Mentor junior microbiologists and support their professional development.
• Review and update training materials, SOPs, and protocols as per regulatory changes.

Qualifications & Experience:

• Master’s or Ph.D. in Microbiology, Biotechnology, or related field.
• Minimum 10 years of experience in microbiology within the medical devices or pharmaceutical industry.
• Hands-on experience with sterility testing, microbial limit tests, endotoxin testing, environmental monitoring, and aseptic techniques.
• Strong knowledge of regulatory standards: ISO 13485, ISO 14698, USP <71>, FDA, and GMP.
• Proven experience in delivering technical training and preparing training materials.
• Excellent communication, presentation, and mentoring skills.
• Experience with cleanroom operations and GMP documentation preferred.

Key Competencies:

• Deep understanding of microbiological principles and testing methods.
• Ability to translate complex technical concepts into effective training modules.
• Strong analytical and problem-solving skills.
• Attention to detail and commitment to quality and compliance.

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 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) .

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) .