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Description

This position is a part of a team that provides around the clock technical support and expertise to sterile pharmaceutical production. And will provide shift assistance to the Customer Facing Process Engineers on their respective lines with customer technical transfers, modifications to existing processes and auxiliary support systems. Initiates process improvements to increase safety, reduce costs, improve quality, and improve Overall Equipment Effectiveness (OEE). Emphasis on minimizing production equipment downtime to increase equipment availability and efficiency along with regulatory compliance for process and support systems. Works closely with Engineering, Operations, Maintenance, Validation and Quality to maintain cGMP compliance, injury-free workplace, and on-time product delivery. • Provide technical expertise and support with meeting business unit objectives and increasing production’s Overall Equipment Effectiveness (OEE). Maintains system design and associated documentation. • Diagnoses and resolves difficult process and equipment interactions to maintain system readiness. Frequently, this effort requires collaboration with other teams. Communicates resolution summary to Area Leadership. • Subject Matter Expert (SME) on Equipment and Process functionality for Production and Utilities. • Develops process flow diagrams, problem solving guides and advanced troubleshooting aides to increase process efficiencies and repeatability. Trains internal resources to increase overall Technical Knowledge in Steriles East. • Will provide SME input in the development of CAPEX Equipment Upgrades on Sterile Fill / Finish processing equipment for compliance to regulatory requirements, quality initiatives / requirements, and to increase line efficiency. • Coordinate planned interruptions of processing areas and/or entire building during shutdown activities, as required pending magnitude of scope. • Creates, modifies, and approves process equipment recipes following all relevant SOPs. • Provides supporting data on process systems and equipment to production and quality investigations along with proposing solutions and improvement opportunities. • Performs daily floor interactions with Engineering, Operations, Maintenance, Quality, and Safety. With the expectation of spending 70-90% of time on shift on the production floor. • Works in partnership with key stakeholders to prioritize line activities and resolve conflicts. • Documents conditions, actions, and results of work performed following company policies and procedures in logbooks and shift reports. • Owns results by taking actions to correct deficiencies and reports variances and exceptions in processes. • Drives Continuous Improvements using metrics, TPM, 5S, and the PPI process.

Additional Skills & Qualifications

• BS Degree, preferably in Mechanical, Electrical or Industrial Engineering, with three (3) years of process experience. • 3+ years of Process Improvement experience using Six Sigma, Lean, 5S, Trend Analysis methodologies preferred. • Successful history in a regulated manufacturing environment in the Biotechnology, Pharmaceutical, and Medical Device industry a plus. • Experience with Data Integrity principles for automation systems and audit trail data a plus. • Outstanding attention to detail and organizational skills to manage time and prioritize tasks. • Strong verbal and written communication skills, and people skills to establish and maintain effective working relationships. • This is a 12-hour rotating shift position following a 2-2-3 schedule straight days or nights. • Adhere to OHS policies and procedures and ensure a safe and healthy workplace environment. • Other duties as assigned.

Pay and Benefits

The pay range for this position is $38.00 - $50.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Greenville,NC.

Application Deadline

This position is anticipated to close on Jun 20, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.