Supplier Project Engineer

Katalyst CRO; Acton (MA); On-site; USD 67,000 - 120,000; Full time

Job summary

A leading contract research organization is hiring for a Project Engineer role focused on supplier capital qualification processes within the pharmaceutical and medical device sectors. Candidates should possess a BSc in Engineering and have a minimum of 3 years of relevant experience. This position offers a chance to work collaboratively with diverse teams on global procurement and installation projects, emphasizing analytical skills and a strong ability to communicate effectively.

Qualifications

• Minimum 3 years of relevant experience required.
• Experience in FDA-regulated environments is a plus.
• Six Sigma certification or experience desirable.

Responsibilities

• Lead and manage supplier capital qualification processes.
• Develop and review validation/qualification protocols.
• Collaborate with teams for procurement and installation of manufacturing equipment.

Skills

Analytical skills

Problem-solving

Communication

Team player

Self-motivated

Education

BSc in Engineering (Plastic, Mechanical, Manufacturing/Industrial)

Tools

SAS

JMP

Minitab

MS Office Project

Job description

3 days ago Be among the first 25 applicants

• Katalyst Healthcares & Life Sciences is hiring entry-level candidates for several positions in contract research related to clinical trials of drugs, biologics, and medical devices.
• Immediate job opportunities are available in Drug Safety, Pharmacovigilance, and Clinical Research. We collaborate with university hospitals, pharmaceutical companies, and recruiting partners.

Company Description

Katalyst Healthcares & Life Sciences is hiring entry-level candidates for various roles in clinical trial research involving drugs, biologics, and medical devices. We partner with university hospitals, pharmaceutical firms, and recruitment agencies.

Job Description

• Strong written and verbal communication skills
• Analytical and problem-solving abilities
• Familiarity with SAS, JMP, or Minitab is preferred
• Proficiency in MS Office, including Project software
• Six Sigma certification or experience is desirable
• Experience in regulated industries is a plus
• Knowledge of cGMP practices is beneficial
• Team player who values diverse input and can develop initial proposals
• Highly motivated, self-starter

Responsibilities

• Lead and manage supplier capital qualification processes from initiation to production implementation
• Develop and review validation/qualification protocols; oversee execution and reporting
• Collaborate across functions and lead teams responsible for procurement and installation of manufacturing equipment globally
• Perform other duties as assigned

Requirements

• Minimum 3 years of relevant experience
• BSc in Engineering (Plastic, Mechanical, Manufacturing/Industrial) or related field
• Experience managing supply chain projects from concept to production, including protocol development (IQ/OQ/PQ)
• Experience in FDA-regulated environments
• Proficiency with Minitab or JMP is highly desired

Additional Information

All applicant information will be kept confidential in accordance with EEO guidelines.

Seniority level

• Executive

Employment type

• Contract

Job function

• Engineering and Information Technology

Industries

• Business Consulting and Services

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