Senior Manufacturing Process Technician NS

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Job Title: Sr.Manufacturing Process Technician

Job Description

Join the mission of serving patients living with serious illnesses by becoming a part of a team that pioneers the world of biotech. With a focus on therapeutic areas like Oncology, Inflammation, General Medicine, and Rare Disease, we reach millions of patients each year. As a Sr. Manufacturing Process Technician, you will play a crucial role in operating automated and innovative manufacturing equipment for the packaging operations of our products. This position offers the opportunity to impact patients" lives positively while advancing your career in a collaborative, innovative, and science-based culture.

Responsibilities

• Operate and troubleshoot automated assembly, labeling, printing, and robotic automation equipment.
• Perform equipment setup, operation, and troubleshooting under limited supervision to meet safety, quality, and efficiency standards.
• Maintain machine uptime by clearing faults and stoppages on automated equipment.
• Conduct basic routine manufacturing process operations such as dispensing raw materials, material reconciliation, line clearance, basic analytics, and record transactions.
• Review documentation for assigned areas, including procedures, job plans, logs, area audits, and batch records.
• Assist as a training resource on manufacturing tasks and equipment use.
• Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.
• Ensure components and products are available for continuous operation.
• Carry out equipment inspections and generate emergency corrective or preventative work orders.
• Troubleshoot and identify potential solutions for mechanical errors, safety issues, or general operating inefficiencies within production processes.
• Partner with cross-functional teams to drive improvement opportunities.
• Use computer systems to support material inventory systems, SAP transactions, and electronic batch records.
• Follow standardized operating procedures safely, including material handling, record keeping, assembly, and packaging while adhering to Good Manufacturing Practices (GMPs).
• Report discrepancies to the Team Leader or Production Supervisor to ensure quality standards and safety.
• Train fellow staff on manufacturing processes and equipment.

Essential Skills

• At least a High school diploma or GED.
• 2+ years of regulated manufacturing experience in GMP regulated environments, pharmaceutical manufacturing, pharmaceutical packaging, or food manufacturing.

Additional Skills & Qualifications

• An Associate"s or Bachelor"s degree is preferred but not required.

Work Environment

This role involves working 12-hour shifts from 6pm to 6:30am, alternating between a 3-day work week one week and a 4-day work week the next, with typical work every other weekend. The facility is heavily regulated, offering a clean and climate-controlled environment. This is a valuable opportunity to gain experience in a GMP environment and be part of a rapidly expanding company with potential for growth into level 2 and 3 roles.

Job Type & Location

This is a Contract position based out of New Albany, OH.

Pay and Benefits

The pay range for this position is $27.00 - $29.00/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 New Albany,OH.

Application Deadline

This position is anticipated to close on Jun 4, 2026.

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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.