Engineering Jobs in Clinton Maine

Company Description

Ranger Construction Corp is a reputable civil construction company headquartered in Fairfield Me.. The organization is dedicated to delivering high-quality construction services across various projects. Known for its professional approach and experienced team, the company takes pride in maintaining strong client relationships. Ranger Construction Corp is committed to excellence, safety, and innovation in every project it undertakes.

Role Description

This is a full-time, on-site role based in Waterville, ME, for a Civil Estimator. The responsibilities include preparing accurate cost estimates for construction projects, analyzing project requirements, reviewing design documents, sourcing materials, and collaborating with project managers and other team members. The role also involves evaluating subcontractor bids, monitoring project budgets, and ensuring that cost estimations align with project goals and company standards.

Qualifications

• Proven experience in cost estimation, project budgeting, and financial analysis for construction projects.
• Strong understanding of construction processes, materials, and methods, as well as blueprint reading and interpretation.
• Proficiency in construction estimation software and tools such as Bluebeam, B2W, Trimble or similar platforms.
• Excellent analytical, organizational, and problem-solving skills to provide precise and efficient estimates.
• Strong communication and collaboration skills to effectively work with project managers, engineers, and subcontractors.
• Bachelor’s degree in Civil Engineering, Construction Management, or a related field is preferred.
• Knowledge of local and national construction codes, standards, and regulations is a plus.
• Ability to manage multiple projects and meet strict deadlines in a dynamic work environment.

Sterility Assurance Associate – 6 Month Contract

We are seeking a Sterility Assurance Associate to support sterility assurance and contamination control initiatives within a sterile/aseptic manufacturing environment. This consultant will partner with Manufacturing, Quality, and Technical Services teams to ensure compliance with GMP and regulatory expectations while strengthening site sterility assurance programs.

Key Responsibilities

• Provide SME support for sterility assurance, aseptic processing, contamination control, and cleaning/process validation activities.
• Support aseptic process simulations (media fills), environmental monitoring programs, and sterile gowning practices.
• Assist with validation and qualification activities for manufacturing processes, equipment, and sterilization cycles.
• Author and maintain SOPs, validation documentation, and contamination control strategies.
• Conduct risk assessments, gap assessments, and remediation activities related to sterile manufacturing operations.
• Support deviations, investigations, root cause analysis, and CAPA implementation.
• Assist with regulatory inspection readiness and GMP compliance initiatives.

Qualifications

• Bachelor’s degree in Engineering, Microbiology, Biology, or related scientific field.
• Experience working in sterile, aseptic, biologics, or parenteral manufacturing environments.
• Familiarity with GMP regulations (FDA, EU GMP) and sterile manufacturing best practices.
• Strong ability to work cross-functionally in a fast-paced, regulated environment.