Medical Device - Director Life Science

Please check your spam/junk email folder in the event any of our follow-on communication ends up there.

Medical Device Industry Experts – Contracting / Contract-to-Hire Opportunities

MetaExperts is proactively seeking candidates to be considered for roles with our growing nationwide customer base for contracting and contract-to-hire opportunities in the medical device/equipment, bioscience and pharma industry. The kinds of roles could vary greatly, and can be full or part-time assignments.

Examples of the talent needed include senior experts in supply chain/sourcing, manufacturing operations management, quality / quality engineering, biomechanical and biomedical engineers, validation engineers, chemists, laboratory engineering, sanitation engineering, pharma sciences, mechanical biomed devices, technical writing/documentation, etc. in the medical device / bioscience manufacturing industry.

>>> This is for Contract and Contract-to-Hire Nationwide

What you’d do
Every client will have different expectations, but in general you’d be responsible for a variety of part time, full time contracting and contract-to-hire assignments involved in a range of key skill areas including: Interim supply chain/operations roles, engineering leadership roles, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), implementing and auditing to ISO 13485/ISO 11607, work as a Bio Medical Engineer, Pharma Sciences Engineering, Mechanical Biomedical Engineering, Biomaterials – chemistry engineering, Cleaning & Sterilization, Medical Device Packaging, Packaging Engineering and Labeling Technologies.

Qualifications
15+ years of work experience in progressively more responsible roles with at least 10 years in medical devices / biosciences and related manufacturing & deployment.
Strong experience and skills / expertise including:
Technical aspects of Quality Management Systems in healthcare related manufacturing.
Quality and Lean Six Sigma certified desirable.
Quality auditing skills in medical industry settings such as ISO 13485 and ISO 11607.
Proven track record with referenced case studies detailing accomplishments.
Engineering, sciences, and / or other related degree or other acumen related to medical device manufacturing and products.

To be considered
Please reply with a resume / CV in Microsoft Word format that includes your contact information and work history along with your minimum hourly rate or annual compensation expectation. Our team will review your information and if you meet our criterion, we will contact you with an invitation to participate in our on-boarding process.

#J-18808-Ljbffr