We are a staffing company that specializes in providing top talent to the Medical Device, Pharmaceutical, and Engineering industries. We are seeking a highly motivated and experienced IT Bench Sales Recruiter who wants to switch and do bench sales for Medical Device, Pharmaceutical, life sciences and Engineering Professionals in relevant industries. The ideal candidate will have strong bench sales experience in sales recruiting, with excellent communication and negotiation skills, and a desire to succeed in the Medical Device, Pharmaceutical, and Engineering industries. Responsibilities: ?Conduct bench sales for Medical Device, Pharmaceutical, and Engineering professionals, with a focus on Quality Engineer, Manufacturing Engineer, Validation Engineer, and Regulatory Engineer job titles. ?Identify and connect with top talent across the USA. ?Build and maintain relationships with existing clients and vendors, while also identifying and acquiring new business opportunities. ?Approach and acquire new clients and vendors to increase company's business. ?Stay up-to-date on industry trends and regulatory requirements. ?Assist in the preparation of resumes to be presented to potential clients. Requirements: ?Maximum of 2 years experience in bench sales in the IT industry. ?Strong contacts and network within the industry are highly preferred. ?Strong communication and negotiation skills, with the ability to connect with candidates and clients. ?Excellent time management and organizational skills. ?Proven track record of success in identifying, placing top talent and acquiring new clients and vendors. ?Self-motivated, with a strong work ethic and a desire to succeed. ?Experience with writing and speaking to clients and candidates is highly preferred. Benefits: ?Competitive incentives ?Insurance coverage ?Cab dropping facility for females ?Food provided This is an excellent opportunity for someone with a strong background in bench sales who is looking to switch to working with a company that specializes in the Medical Device, Pharmaceutical, and Engineering industries. If you are passionate about connecting top talent with the best companies in these industries and are skilled at acquiring new business, we encourage you to apply.
We are seeking an experienced Supplier Quality Professional Trainer with 10+ years of expertise in managing supplier quality assurance , supplier development, and compliance in regulated industries (pharmaceutical, biotech, or medical devices). The role involves ensuring suppliers meet company , industry, and regulatory standards by leading audits, driving quality improvement initiatives , and building strong supplier partnerships. Job Responsibilities: Develop and manage supplier quality strategies, policies, and risk management processes. Lead supplier qualification, selection, and approval in alignment with regulatory standards (FDA, EMA, ISO 13485, ICH Q10, GMP). Conduct supplier audits, assessments, and performance reviews to ensure compliance with quality and regulatory requirements. Oversee supplier corrective and preventive actions (CAPA) , root cause analysis, and continuous improvement programs. Collaborate with cross-functional teams (procurement, R&D, operations, quality) to resolve supplier-related issues. Monitor supplier KPIs (on-time delivery, defect rates, deviations, complaints) and drive improvement initiatives. Support new product development (NPD) by ensuring supplier capability for components, raw materials, and services. Manage supplier change control processes and evaluate impact on product quality and regulatory compliance. Train, mentor, and guide internal teams and suppliers on quality systems and compliance expectations. Ensure alignment with global regulatory requirements (FDA 21 CFR Part 11/210/211, ISO standards, EU MDR, ICH guidelines). Core Competencies & Skills Strong expertise in supplier quality management, auditing, and regulatory compliance . In-depth knowledge of GMP, GDP, ISO 9001, ISO 13485, IATF 16949 (if automotive/industrial) . Proficiency in risk management, root cause analysis, CAPA, Six Sigma, Lean methodologies . Excellent communication, negotiation, and stakeholder management skills. Ability to lead supplier development programs and strategic quality initiatives. Experience in global supplier management and multicultural environments. Qualifications: Bachelor's/Master's degree in Engineering, Life Sciences, or related field. 10+ years of experience in supplier quality assurance, preferably in pharma/medical devices/regulated manufacturing industries. Certified Lead Auditor (ISO 9001/13485, GMP, or equivalent) preferred. Six Sigma Green/Black Belt certification is a plus. Proven track record in managing global suppliers and delivering measurable quality improvements.
We are seeking an experienced Industrial Automation Trainer (freelancer role) with hands-on expertise in PLC, HMI, SCADA, and DCS systems . The ideal candidate will be responsible for providing training in the fields of designing, delivering, and evaluating training programs that build technical capabilities in automation, instrumentation, integration, and troubleshooting across multiple industries, including pharmaceutical/biotechnology, FMCG, and technology sectors. Key Responsibilities: Design and deliver training modules on PLC, HMI, SCADA, and DCS programming for engineers and technical professionals. Provide hands-on workshops on instrumentation, system integration, and process optimization in industrial automation. Train participants in diagnostics, troubleshooting, and preventive maintenance of automation systems. Develop training content, manuals, case studies, and simulation-based learning exercises. Stay updated on emerging automation technologies and integrate them into training programs. Conduct assessments and provide feedback to ensure participants achieve desired competency levels. Collaborate with industry experts to align training with current regulatory and operational standards (e.g., pharma and biotech compliance). Mentor and guide professionals to apply automation solutions effectively in manufacturing and process environments . Required Skills & Expertise: Strong proficiency in PLC programming (Siemens, Allen Bradley, Schneider, etc.). Hands-on experience in HMI and SCADA development and configuration . Knowledge of DCS systems and their applications in process industries. Expertise in instrumentation, sensors, and control systems integration . Ability to train on system optimization and troubleshooting techniques . Familiarity with pharma, biotech, FMCG, and technology sector automation needs . Excellent communication, presentation, and mentoring skills. Qualifications & Experience: Bachelor's degree in Electrical, Pharma, Instrumentation, Automation, or related engineering field . 10+ years of industry experience in automation, with at least 35 years in training, mentoring, or coaching roles . Certifications in PLC/SCADA/DCS systems will be an added advantage.
Position Summary: We are looking for an experienced R&D Engineer Trainer with 1015+ years of expertise in the medical device industry . This role will focus on leading training programs in the design , development , and optimization of innovative medical technologies . The trainer will provide guidance on the full new product development (NPD) lifecycle from concept through commercialization while ensuring alignment with global regulatory requirements. The position also involves close cross-functional collaboration to support the delivery of safe, effective, and high-quality medical devices that enhance patient outcomes. Key Responsibilities: Lead the design and development of new medical devices, from feasibility studies through product launch. Oversee product development lifecycle including concept generation , prototyping , design verification & validation , risk analysis , and design transfer to manufacturing . Ensure compliance with FDA, ISO 13485, MDR, IEC 60601, ISO 14971 and other applicable regulations and standards. Drive innovation by identifying new technologies, materials, and processes that enhance product performance and cost-effectiveness. Lead technical design reviews, root cause analysis, and continuous improvement initiatives. Collaborate with cross-functional teams including Quality, Manufacturing, Regulatory Affairs, and Marketing to ensure successful product development and launch. Manage design documentation including Design History File (DHF), Design Inputs/Outputs , and Risk Management Files . Provide technical leadership and mentorship to junior engineers and project teams. Interface with clinicians, key opinion leaders (KOLs), and end-users to incorporate clinical feedback into design. Lead problem-solving initiatives for product performance, reliability, and usability. Stay updated with medical device industry trends, regulatory changes, and emerging technologies. Qualifications & Requirements: Bachelor's or Master's degree in Biomedical Engineering, Mechanical Engineering, Materials Science, or related field . 10-15+ years of progressive experience in R&D within the medical device industry. Strong knowledge of medical device product development processes, including Design Control per 21 CFR Part 820. Proven track record of successfully launching medical devices into global markets. Expertise in CAD tools (SolidWorks/Creo/AutoCAD) , prototyping, and testing methods. Experience with risk management (ISO 14971), usability engineering (IEC 62366), and biocompatibility standards (ISO 10993) . Strong project management and leadership skills with experience in leading cross-functional teams. Excellent problem-solving, analytical, and communication skills. Experience with Class II and Class III medical devices preferred. Core Competencies: Innovation & Creativity in Medical Device Development Regulatory & Quality compliance mindset Leadership & Mentorship abilities Cross-functional Collaboration Strong Analytical and Technical problem-solving Strategic thinking with hands-on execution
Job Title: CNC Swiss Machinist Location: Remote Position Overview We are seeking a CNC Swiss Machinist to join our production team. This role is responsible for operating and maintaining CNC Swiss machines in a collaborative environment, ensuring high-quality output that meets medical device standards. While prior experience is preferred, training will be provided in blueprint reading, geometric dimensioning and tolerancing (GD&T), inspection methods, and tooling adjustments. Key Responsibilities Operated and maintained multiple CNC Swiss machines in a production environment. Performed daily preventive maintenance on machines to support consistent operations. Conducted in-process inspections to verify quality using calipers, micrometers, visual checks, and programmed CMM equipment (training provided). Read and interpreted blueprints and applied basic GD&T principles (training provided). Made tooling changes and offsets per production layouts (training provided). Ensured compliance with all safety protocols and company guidelines. Documented production status, inspection results, and communicated progress or quality issues with team members and supervisors.