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Job Title: Manufacturing Associate

Job Description

Join a dynamic team in a Finished Product Pharmaceutical Facility as a Manufacturing Process Technician to support a brand new product line due to increased market demand. You will be responsible for loading materials, completing electronic batch records, log book entries, documenting work orders, conducting process checks to ensure quality, and managing batch packaging records. The role requires a tech-savvy individual with a mindset for process improvement, capable of identifying and providing solutions to recurring issues.

Responsibilities

+ Load materials into the production line.

+ Complete electronic batch records and log book entries.

+ Document work orders and conduct process checks for quality assurance.

+ Manage batch packaging records for materials loaded and produced.

+ Identify recurring issues on the production line and provide solutions.

+ Communicate effectively and suggest process improvements.

Essential Skills

+ Experience in bioworks and manufacturing operations.

+ Knowledge of biotechnology and GMP (Good Manufacturing Practices).

+ Experience in healthcare or previous manufacturing experience.

Additional Skills & Qualifications

+ Interest in pharmaceutical manufacturing.

+ Exposure to GMP environments (pharma, food, med device, or cosmetic).

+ Bioworks or Associates in Biotechnology degree is advantageous.

Work Environment

This position operates within a manufacturing environment following a 2-2-3 day shift schedule. Initial training occurs during the day shift from Monday to Friday, after which you may transition to the night shift if applicable. Scrubs and closed-toed shoes or work boots are provided, with locker rooms available for changing. The team is currently overworked, and you will be welcomed into an environment where your contributions will be highly valued and appreciated. The company fosters a culture of diversity, inclusion, and work-life balance, with opportunities for career growth.

Pay and Benefits

The pay range for this position is $21.00 - $21.00/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 Clayton,NC.

Application Deadline

This position is anticipated to close on Jun 5, 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.