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Entry Level Biocompatibility Jobs in Houston, TX

Assembler 1

Houston, TX · On-site

$16.25 - $20/hr

The Level 1 Assembler is an entry-level role responsible for performing manual and semi-automated ... Conducts passivation and ultrasonic cleaning processes to ensure biocompatibility and cleanliness ...

Entry Level Biocompatibility information

What is an entry level biocompatibility job?

Entry level biocompatibility jobs are positions in the medical device or pharmaceutical industries where professionals help evaluate how materials interact with the human body. These roles typically involve conducting laboratory tests, analyzing data, and preparing reports to ensure that products meet safety standards and regulatory requirements. Individuals in these positions often work under the guidance of more experienced scientists or engineers, and may collaborate with regulatory, quality, and product development teams. Entry level biocompatibility specialists are important for ensuring that new medical products are safe and effective for human use.

What are the key skills and qualifications needed to thrive as an entry level biocompatibility specialist?

To thrive as an Entry Level Biocompatibility Specialist, you need a background in biology, chemistry, or biomedical engineering, often with a relevant bachelor’s degree. Familiarity with ISO 10993 standards, laboratory analysis techniques, and data management systems is typically required. Attention to detail, analytical thinking, and strong written communication skills help you excel in this role. These competencies are crucial to ensure medical devices are safe for patients and to support regulatory compliance.

What are some typical challenges faced by entry level biocompatibility professionals, and how can they be addressed?

Entry-level biocompatibility professionals often face the challenge of interpreting complex regulatory guidelines and translating scientific data into clear risk assessments for medical devices. Navigating evolving standards, such as ISO 10993, can be daunting without prior experience. To overcome these challenges, new professionals should proactively seek mentorship, participate in cross-functional team discussions, and leverage company training resources to build a strong foundation in both regulatory and scientific aspects of biocompatibility. Engaging with professional organizations and staying updated on industry best practices can also provide valuable support and networking opportunities.

What is the difference between Entry Level Biocompatibility vs Entry Level Regulatory Affairs Specialist?

AspectEntry Level BiocompatibilityEntry Level Regulatory Affairs Specialist
Required CredentialsBachelor's in life sciences or related field; some certificationsBachelor's in life sciences, healthcare, or related; certifications like RAC beneficial
Work EnvironmentLaboratories, manufacturing facilities, quality assuranceRegulatory agencies, corporate offices, compliance departments
Industry UsageMedical devices, implants, biomaterialsMedical devices, pharmaceuticals, biotech products

Entry Level Biocompatibility focuses on testing and evaluating materials for safety in medical applications, while Entry Level Regulatory Affairs Specialists handle compliance documentation and regulatory submissions. Both roles require knowledge of industry standards but differ in daily tasks and work settings.

What job categories do people searching Entry Level Biocompatibility jobs in Houston, TX look for?

The top searched job categories for Entry Level Biocompatibility jobs in Houston, TX are:

What cities near Houston, TX are hiring for Entry Level Biocompatibility jobs?

Cities near Houston, TX with the most Entry Level Biocompatibility job openings:

Assembler 1

Halma plc

Houston, TX • On-site

$16.25 - $20/hr

Full-time

Posted 12 days ago


Job description

Help grow a safer, cleaner, healthier future for everyone, every day.
Job Summary:
The Level 1 Assembler is an entry-level role responsible for performing manual and semi-automated assembly tasks in support of surgical device manufacturing. This position requires attention to detail, adherence to quality and safety standards, and the ability to follow work instructions and documentation in a regulated production environment. This position reports into the Assembly Supervisor.
Duties/Essential Job Functions:
  • Performs easy assemblies including blade bending and blade assembly using hand tools and fixtures.
  • Deburrs, tumbles, polishes, and grinds components to meet surface finish and safety requirements.
  • Operates equipment for heat treating, bead blasting, and lasermarking of surgical components.
  • Conducts passivation and ultrasonic cleaning processes to ensure biocompatibility and cleanliness of parts.
  • Cleans and readies product for inventory storage e.g. clean per procedure, bag, inventory
  • Follows detailed work instructions, standard operating procedures (SOPs), and visual aids to ensure accurate and consistent assembly.
  • Performs in-process visual inspections and follows inspection plans to ensure compliance with product specifications.
  • Accurately completes production records, batch documentation, and inspection logs in a timely manner.
  • Uses small hand tools, torque drivers, and measurement devices as required for assembly and verification.
  • Maintains high standards of workmanship and attention to detail in all tasks.
  • Follows all safety guidelines and regulatory requirements, including proper use of PPE and adherence to Good Manufacturing Practices (GMP).
  • Keeps work area clean, organized, and safe in accordance with company policies.
  • Communicates effectively with team members and supports continuous improvement initiatives.
  • Other duties as assigned

Required Education/Licensing/Certification:
  • High school diploma or equivalent.
  • 0-1 year of experience in a manufacturing or assembly environment; medical device experience preferred.
  • Ability to read and follow written instructions, diagrams, and technical documentation.
  • Basic understanding of mechanical assembly and quality control principles.
  • Strong attention to detail and manual dexterity.
  • Willingness to work in a cleanroom or controlled environment as required.

Physical Requirements:
  • Ability to sit or stand for extended periods (up to 8 hours per shift).
  • Frequent use of hands and fingers to handle small parts and tools.
  • Ability to lift and carry up to 25 pounds.
  • Visual acuity to inspect parts and read documentation.
  • Tolerance for repetitive tasks and working in a cleanroom or sterile environment.
  • Use of personal protective equipment (PPE) such as gloves, gowns, and safety glasses as required.

Reasonable Accommodations
Tedan Surgical Innovations is an Equal Opportunity Employer. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions
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