Technician - Manufacturing​/Production

Associate Manufacturing Technician

Location:

Wilson, NC

Duration: 12+ months W2 Contract with possible extension

Notes from Manager:

- Role is 100% onsite in Wilson, NC, Mon-Fri 8am-5pm for the rest of 2026

- The role might shift into a possible 2nd shift or night shift in 2027

- This position is an Associate Manufacturing Technician

- Will be working with Manufacturing Technicians

- Will work on SOPs, and work instructions

- Will help or assist with equipment

- Will learn how alarms work

- Could have "minimal travel" - domestic, if any travel at all

- Will be working in construction area in 2027

- Must have previous GMP experience/knowledge

- Must have at least 1 previous year of experience

- Candidates that have knowledge of "chromatography" is very helpful

- Candidates that have continuous improvement experience is also very helpful

- SAP is very helpful

- Prior experience with Batch Records, preferred

Essential

Job Duties and Responsibilities:

The Manufacturing Technician is responsible for performing manufacturing procedures and the execution of scheduled tasks within a GMP environment.

Key Responsibilities include:

Responsible for quality and maintaining the highest standards in compliance and safety within company policies, procedures and all applicable regulations in alignment with the Site Vision. Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum. Accurately complete documentation in SOP's, logbooks and other GMP documents and/or systems. This position requires the ability to work collaboratively and independently, time management, orientation towards action & solutions, ability to learn, and the ability to communicate & understand others.

• Execute technical processes in assigned areas.

o Maintain equipment and instruments.

o Accountable for maintaining a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations.

o Support schedule adjustments to meet production, material receipt and shipping requirements.

o Retrieve and analyze trend charts and process data on trained procedures.

o Verify and enter production parameters per SOP and Batch Records.

o Demonstrate training progression through assigned curriculum.

o Support the ongoing production schedule by reporting to work on-time and according to the shift schedule.

o Ensure materials are available for production.

o Attend departmental and other scheduled meetings.

• Accountability for quality, safety and compliance in GMP environment.

o Wear the appropriate PPE when working in manufacturing and other hazardous working environments.

o Proactively maintain a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors

o Adhere to the safety code of Conduct & Pharmaceutical EHS policies and attend all required EHS training.

o Carry out duties in compliance with all state and federal regulations and guidelines including FDA, EPA and OSHA.

o Offer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity.

o Responsible for audit preparation and participation

• Provide ideas for continuous improvement & foster a sense of curiosity.

o Champions programs and initiatives that support our business, environment and communities

o Review and understand non-conformances

o Learn new skills, procedures and processes as assigned by management and continue to develop professionally.

• Exercise independent leadership skills as outlined by Pharmaceutical's Leadership Imperatives.

o Practice good interpersonal and communication skills.

o Demonstrate positive team-oriented approach in the daily execution of procedures.

o Promote and work within a team environment.

Minimum Qualification:

• 0-3 years or more with trade school equivalent

• Interpret a variety of instructions furnished in written, oral, diagram or schedule form.

• Follow instructions.

• Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.

• Working knowledge of cGMP's in a biopharmaceutical or pharmaceutical…