Manufacturing Engineer (Instrumentation) 12 Month Contract (56942)

binx health; Trowbridge; On-site; GBP 45,000 - 60,000; Full time

Job summary

binx health is seeking a skilled Manufacturing Engineer for a 12-month contract in Trowbridge. The ideal candidate will design, implement, and maintain manufacturing processes in the medical device industry, ensuring quality and compliance with regulatory standards.

Responsibilities include evaluating workflows, documentation maintenance, and project management. Candidates should have experience in medical device manufacturing and a strong background in process development. This role offers an opportunity to contribute to critical projects in a growing company.

Qualifications

• Proven experience in medical device or diagnostics manufacturing, owning and improving manufacturing processes.
• 5+ years of experience in a regulated industry where Quality Systems are essential.
• Hands-on experience with process development, troubleshooting, and continuous improvement initiatives.

Responsibilities

• Evaluate manufacturing processes and workflows to identify improvements.
• Support verification and validation activities at CMO.
• Maintain manufacturing process documentation including technical reports.

Skills

Familiarity with Design for Manufacturability (DFM) and Design for Assembly (DFA) principles

Knowledge of manufacturing methods relevant to instrumentation or electromechanical assembly

Strong analytical and problem-solving skills

Excellent verbal and written communication skills

Ability to manage projects with minimal supervision

Job description

JOB DESCRIPTION – Manufacturing Engineer (Instrumentation) 12 MONTH CONTRACT

binx Health is looking for a skilled manufacturing engineer to design, implement, monitor, and maintain manufacturing processes and work instructions within the medical device industry.

Key Responsibilities

• Evaluate manufacturing processes and workflows to identify areas that could benefit from changes and improvements, through interfacing with line operators, component vendors and key suppliers.
• Support verification and validation activities of manufacturing line at CMO, ensuring appropriate testing suites, including in‑line process controls, are identified and implemented for our product.
• Apply working knowledge of product design and assembly to the manufacturing process.
• Maintain manufacturing process documentation, including technical reports (e.g., process capability studies), BOM, process specifications in line with regulatory and quality assurance requirements.
• Create processes and procedures to help the company meet performance quotas.
• Design systems and equipment that reduce time, cost and improve quality and safety.
• Work with design engineers to improve product design for ease of manufacturing and assembly.
• Ensure products and sub‑assemblies can be manufactured reliably and perform consistently.
• Manage projects using engineering principles and techniques.

Required Experience

• Proven experience in medical device or diagnostics manufacturing, owning and improving manufacturing processes in a regulated industry (e.g., medical devices, diagnostics, or similar).
• Experience supporting manufacturing transfer, scale‑up, and production in collaboration with CMOs or external partners.
• Experience working with suppliers and cross‑functional teams, including design engineering and quality.
• Demonstrated experience maintaining manufacturing documentation within a Quality Management System (e.g., ISO 13485).
• Hands‑on experience with process development, troubleshooting, and continuous improvement initiatives.
• 5+ years’ experience in a regulated industry where Quality Systems are essential, e.g., ISO 13485.

Required Skills

• Familiarity with Design for Manufacturability (DFM) and Design for Assembly (DFA) principles.
• Knowledge of manufacturing methods relevant to instrumentation or electromechanical assembly.
• Ability to design and implement efficient, scalable manufacturing processes.
• Strong understanding of verification and validation (V&V), including process validation and in‑line testing strategies.
• Strong and demonstrated analytical and problem‑solving skills, with a hands‑on approach to troubleshooting and experimentation.
• Excellent verbal and written communication, and teamwork skills.
• Capable of managing projects with minimal supervision.

binx health is proud to be an Equal Opportunity Employer, committed to equal employment opportunity and fair, equitable compensation regardless of race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.