Supervisor, Manufacturing

Hologic•Marlborough, MA

13d

About The Position

Why join Hologic: You will have the opportunity to get in on the ground floor at a high growth world class manufacturing facility working on life-saving medical devices with potential for future growth. This is a great opportunity to enhance your manufacturing operation skills and knowledge to further your career.

Requirements

Results driven and continuous improvement mindset
Familiarity with mechanical assembly, repairs or testing.
Excellent and proven people skills, professional, self-motivated, high energy, team leader with effective training skills and desire to succeed in a business environment
Excellent organizational and demonstrated problem-solving skills.
Effectively manage and resolve employee conflicts
Strong written and oral communication skills
Strong knowledge of Continuous Improvement and LEAN Manufacturing Practices
Strong record keeping and documentation skills, internal auditing, attention to detail
Proficient in Microsoft Office Suite (Excel, Word, Power Point)
Minimum 3 years of supervisory experience.
Strong electrical/mechanical background with a minimum of 5 years manufacturing related experience
Must follow all applicable FDA regulations and ISO requirements.

Nice To Haves

Minimum of 2-4 years of experience working in a clean room environment preferred. (as per site)
Oracle and Agile experience preferred.
Knowledge of GMP’s, QSR’s, MRP
Experience with ISO and FDA

Responsibilities

Supervise the day-to-day processes of manufacturing operations, ensuring production plans and designed quality specifications are met while complying with regulatory (QSR, ISO, EH & S) and Hologic’s quality standards.
Direct supervision and monitoring of employee's performance to documented procedures and established goals.
Supervises production schedule to max efficiency and timeliness, within assigned budget.
Participates in cost savings events
Provide leadership to direct reports on Continuous Improvement initiatives.
Provides support to Engineering, Manufacturing Engineering, Regulatory Affairs and Quality through participation in process control activities, and special testing, as required.
Ensure 6S compliance as well as drive and lead other Lean initiatives.
Ensure that design, implementation, test and maintenance methods/processes are developed as well as executed in a manner, which supports all Quality Standards.
Responsible for e-time (or similar) reporting and scheduling/approving employee vacation/personal time to ensure that day to day operations needs are met.
Conduct departmental audits of the Production process to ensure compliance with regulatory (QSR, ISO, EH & S) and Hologic policies and identify opportunities for Continuous Improvement.
Provide feedback on the manufacturing process and layout.
Train, motivate and guide employees.
Order necessary equipment and supplies within budget.
Generate and present reports on quality and production.
Interface with Materials, Engineering, EH&S and Quality to facilitate smooth production flow and communication.
Conduct performance reviews for direct reports and ensure coaching and feedback are timely and effective.
Facilitate the engagement of EH&S, Quality and Engineering into the production process.
Interface with document control to maintain current documentation requirements, review DHRs and related regulatory documents.
Prepare, present, and execute plans and procedures that improve processes and efficiency.
Maintain a clean, safe working environment while working to reduce cycle time and scrap.