NS Production Tech III - Recovery

Job Title: Night Shift Production Technician III Downstream Recovery and PurificationJob Description

The Night Shift Production Technician III executes and documents downstream recovery and purification manufacturing activities in a highly regulated biomanufacturing environment. This role focuses on downstream processing steps, process monitoring, and process control while maintaining strict adherence to Current Good Manufacturing Practice (cGMP) requirements, quality standards, safety requirements, regulatory expectations, and approved procedures. The position supports a 24/7 manufacturing operation and requires flexibility to work a rotating 2-2-3 day/night shift schedule.

Responsibilities

• Execute and accurately document downstream recovery and purification manufacturing steps in compliance with cGMP requirements and approved standard operating procedures.
• Perform associated support activities for downstream operations, including glass-wash tasks and buffer or solution preparation.
• Conduct process monitoring and process control activities to ensure consistent and reliable operation of downstream processes.
• Perform in-process sampling and testing, including pH measurement, conductivity testing, and visual inspection of materials and equipment.
• Execute validation protocols in accordance with cGMP requirements and established procedures.
• Maintain all required training qualifications to perform assigned downstream manufacturing activities and remain current on procedural updates.
• Operate and execute manufacturing tasks using applicable Distributed Control Systems, including DeltaV, 800xA, Unicorn, and other assigned automated systems.
• Complete takeouts, identity-check returns, and other assigned activities within the Manufacturing Execution System (MES).
• Perform clean-in-place (CIP), steam-in-place (SIP), and other required equipment-cleaning activities to maintain a controlled and compliant manufacturing environment.
• Initiate deviations when necessary, ensuring that issues are documented and escalated according to established procedures.
• Initiate work orders through the Computerized Maintenance Management System (CMMS) to address equipment or facility maintenance needs.
• Apply sound judgment and initiative when completing assignments, recognize the implications of process or equipment issues, and recommend potential solutions.
• Support effective team execution of manufacturing activities and, when assigned, provide informal leadership and guidance to team members.
• Collaborate with cross-functional colleagues to ensure smooth handoffs between shifts and consistent adherence to production schedules.
• Perform other duties as assigned to support overall manufacturing operations and continuous improvement initiatives.

Essential Skills

• High school diploma or GED with at least four years of experience in a cGMP manufacturing environment, or
• Associate degree in life science, engineering, or a relevant technical field with at least two years of experience in a cGMP manufacturing environment, or
• Bachelors degree in life science, engineering, or a relevant technical field with no prior experience required, or
• Equivalent military training or experience in a technical or manufacturing setting.
• Demonstrated experience executing work in a cGMP manufacturing environment.
• Ability to execute and document downstream recovery or purification processing activities in a regulated environment.
• Knowledge of cGMP requirements and applicable safety standards relevant to biomanufacturing operations.
• Ability to perform process monitoring and in-process testing, including pH, conductivity, and visual inspection.
• Ability to use Distributed Control Systems (such as DeltaV, 800xA, Unicorn) for automated process control.
• Ability to use Manufacturing Execution Systems (MES) to document production activities and manage electronic batch records.
• Ability to initiate deviations and create work orders within a Computerized Maintenance Management System (CMMS).
• Effective written and verbal communication skills to document activities clearly and collaborate with team members.
• Ability to work effectively in a team environment and support shared production goals.
• Strong time-management skills and attention to detail to ensure accurate execution and documentation of manufacturing steps.
• Ability and willingness to support a 24/7 manufacturing facility on a rotating 2-2-3 day/night shift schedule.

Additional Skills & Qualifications

• Experience operating a manufacturing unit, with downstream recovery or purification experience strongly preferred.
• BioWork certificate or similar bioprocessing training program certification.
• Demonstrated ability to follow detailed standard operating procedures and execute validation protocols.
• Comfort working with automated systems and electronic documentation tools in a regulated environment.
• Proactive mindset with the ability to recognize process deviations and suggest improvements to enhance quality and efficiency.

Work Environment

This position is part of a night shift team supporting a 24/7 biomanufacturing facility focused on downstream recovery and purification processes. The role follows a rotating 2-2-3 day/night shift schedule, which includes a combination of day and night shifts to ensure continuous operations. Work is performed in a controlled, cGMP-compliant production environment with strict safety and quality standards. The technician regularly works with automated Distributed Control Systems such as DeltaV, 800xA, and Unicorn, as well as Manufacturing Execution Systems and a Computerized Maintenance Management System. The work involves standing for extended periods, working around production equipment, performing clean-in-place and steam-in-place activities, and handling buffers and process solutions while following all safety and gowning requirements appropriate for a regulated manufacturing setting.

Job Type & Location

This is a Contract position based out of Morrisville, NC.

Pay and Benefits

The pay range for this position is $37.00 - $42.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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)

Job Type & Location

This is a Contract position based out of Morrisville, NC.

Application Deadline

This position is anticipated to close on Nov 16, 2026.

Workplace Type

This is a fully onsite position in Morrisville,NC.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

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.