Supervisor, Equipment Mechanic
Curia
Summary
The Equipment Mechanic Supervisor is responsible for supervising and coordinating the activities of employees engaged in the installation, repair, and maintenance of industrial machinery and equipment. This role provides technical guidance in diagnosing and resolving mechanical, electrical, hydraulic, pneumatic, and electronic issues, while ensuring safe and efficient work practices. The supervisor plans and assigns work based on production schedules, interprets specifications and blueprints, and oversees adherence to company policies and safety regulations. In addition to managing spare parts inventory and production records, the Equipment Mechanic Supervisor mentors and develops team members, collaborates with cross-functional departments, and partners with Process Engineers to improve equipment performance, manufacturing processes, and overall operational efficiency.
Job description
Essential Duties and Responsibilities
- Directs workers in electrical, electronic, mechanical, hydraulic, and pneumatic maintenance and repair of machinery and equipment. Assists workers in diagnosing malfunctions in machinery and equipment. Directs workers engaged in dismantling, assembling, and installing industrial machinery.
- Requisitions and keeps a supply of spare parts. Studies production schedules and estimates worker hour requirements for completion of job assignments. Interprets company policies to workers and enforces safety regulations.
- Interprets specifications, blueprints, and job orders to workers, and assigns duties. Establishes or adjusts work procedures to meet production schedules. Recommends measures to improve production methods, equipment performance, and quality of the product.
- Suggests changes in working conditions and use of equipment to increase the efficiency of the shop, department, or work crew. Analyzes and resolves work problems, or assists workers in solving work problems. Initiates or suggests plans to motivate workers to achieve work goals.
- Maintains time and production records. Confers with other supervisors to coordinate activities of individual departments. Interfaces and communicates with the operations team.
- Supports manufacturing personnel and schedule adherence. Leads the team by example. Mentors and develops Equipment Mechanics.
- Works closely with Process Engineer to provide multi-disciplinary support for Processes, equipment, and manufacturing. Performs activities of workers supervised. Instruct team on technical issues SME for Equipment Mechanics.
- Read/interpret SOPs to ensure compliance.
- Maintain up to date trainings.
- Other duties as assigned.
Education and Experience
- High school diploma or general education degree (GED).
- Minimum of five (5) years' relevant experience in a pharmaceutical manufacturing or relevant industry.
- Minimum of one (1) year experience in a leadership role.
- Bachelor's or Associate's degree in Engineering or related field of study with a minimum of three (3) years' experience in a pharmaceutical manufacturing or relevant industry, preferred.
- Industrial GMP experience in an FDA-regulated environment, preferred.
Supervisory Responsibilities
Responsible for leading and supporting a team to achieve organizational objectives. This role also involves fostering a positive work environment, providing guidance and support to your team members, and evaluating performance to drive continuous improvement and achieve both departmental and organizational objectives.
Other Skills and Abilities
- Leads with integrity and respect.
- Provides guidance, coaching, and mentorship to team members.
- Demonstrates business acumen.
- Fosters a collaborative and positive work environment.
- Champions change.
- Coaches and Develops.
- Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
- Demonstrates strong attention to detail.
- Experience with industrial safety programs (i.e., LOTO, Confined Space, etc.).
- Ability to work at elevated heights.
Other Qualifications
- Must pass a background check.
- Must pass a drug screen.
- May be required to pass Occupational Health Screening.
- Must be able to obtain and maintain gowning certification.
- May be required to wear a respirator.
Requirements
- High school diploma or general education degree (GED)
- Minimum of five (5) years' relevant experience in a pharmaceutical manufacturing or relevant industry
- Minimum of one (1) year experience in a leadership role
- Bachelor's or Associate's degree in Engineering or related field of study with a minimum of three (3) years' experience in a pharmaceutical manufacturing or relevant industry, preferred
- Industrial GMP experience in an FDA-regulated environment, preferred
- Experience with industrial safety programs (i.e., LOTO, Confined Space, etc.)
- Ability to work at elevated heights
- Must pass a background check
- Must pass a drug screen
- May be required to pass Occupational Health Screening
- Must be able to obtain and maintain gowning certification
- May be required to wear a respirator
Benefits
- Generous benefit options
- Paid training
- Paid vacation
- Paid holidays
- Career advancement opportunities
- Education reimbursement
- 401(k) matching
- Learning platform
Company overview
Curia is a leading global Contract Development and Manufacturing Organization (CDMO) with over 30 years of experience in the pharmaceutical industry. Headquartered in Albany, New York, the company operates an integrated network of 25 global sites across North America, Europe, and Asia, employing approximately 3,500 professionals. Curia provides comprehensive end-to-end solutions spanning drug discovery, development, and manufacturing services for both small molecules and biologics. Their expertise covers active pharmaceutical ingredient (API) manufacturing, sterile drug product development, analytical testing, and regulatory support. The company specializes in complex areas including high-potency compounds, controlled substances, sterile APIs, and mRNA manufacturing. With state-of-the-art GMP facilities and a strong focus on innovation, Curia partners with pharmaceutical and biotechnology companies to accelerate the development and commercialization of life-changing therapeutics, from early-stage discovery through commercial-scale production.