Pharmaceutical Operator 1

Par Health, Inc.

North Carolina

On-site

USD 45,000 - 60,000

Full time

14 days+
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Job summary

Par Health, Inc. is seeking a Pharmaceutical Operator I to support APAP production in a regulated GMP environment. You will operate large-scale equipment, follow batch records, and ensure accurate documentation and safety compliance.

Responsibilities include monitoring reaction vessels, performing basic math, maintaining reports, and coordinating with QA/QC and maintenance teams. The role requires attention to detail, teamwork, and adherence to SOPs.

Qualifications

  • High School Diploma, GED or equivalent required.
  • Previous GMP manufacturing experience preferred.
  • Must communicate effectively in verbal and written formats.
  • Must read and follow detailed instructions and procedures.
  • Must perform basic math and have knowledge of safety requirements.

Responsibilities

  • Operates in a regulated environment and complies with cGMP and OSHA regulations.
  • Operates and monitors equipment per batch records and SOPs with proper PPE.
  • Maintains detailed operating reports, batch records, and notes on process parameters.
  • Moves materials using forklifts and other handling devices as needed.
  • Delivers samples to laboratory and retrieves operating supplies from storerooms.
  • Supports Kaizen, safety teams, and cost savings initiatives where applicable.

Skills

Equipment knowledge
Troubleshooting
Decision making

Education

High School Diploma / GED

Job description

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day.

Job Description Summary

This position is responsible for operating large scale manufacturing equipment to produce bulk APIs (Active Pharmaceutical Ingredients) in accordance with Company standards and operating procedures. He/she will be responsible for reports and documentation. Must be able to pay attention to detail due to the nature of chemicals and environment he/she will be working in on a daily basis.

Job Description
  • Operates in a regulated environment and complies with all cGMP and OSHA regulations applicable to manufacturing responsibilities. This includes understanding and following all applicable batch records, standard operating procedures and work instructions, and wearing appropriate personal protective equipment (PPE)
  • Operates and monitors reaction vessels, crystallizers, centrifuges, filters, evaporator, heat exchangers, pumps, valves and other equipment through manual operations, panel boards, indicators, and HMI displays (for PLC and DCS controls) following applicable batch records, procedures, and good documentation practices.
  • Operates and monitors hoists, dryers, mills, sifters, dust collectors, blowers, packaging stations, and other equipment through manual operations, panel boards, indicators, and HMI displays (for PLC controls) following applicable batch records, procedures, and good documentation practices.
  • Packages, weighs, samples, and labels finished goods and intermediate products following applicable batch records, procedures, and good documentation practices.
  • Maintains detailed operating reports and batch records, including notes on problems and records on added weights, volumes, measured temperatures, pH levels, pressures, and flow rates following applicable procedures and as directed by supervisor.
  • Operates forklifts, hoists, and other material handling devices to move bulk raw materials, WIP, and packaged goods to and from pick-up points.
  • Delivers samples to laboratory and retrieves operating supplies from storerooms.
  • Monitors environmental and safety devices (scrubber, rupture discs, relief valves, etc.) to ensure that the equipment is functioning properly.
  • Cleans and maintains work area, process equipment, tools and safety supplies according to regulatory and Company standards and operating procedures.
  • Participates in various employee involvement teams and committees, such as Area/Site Safety Teams, Kaizen events, and Cost Savings Teams, to improve the workplace, increase efficiency, and maximize productivity.
  • Performs Lock Out/Tag Out (LOTO) independently using personal lock.
  • Other duties as assigned by Management.
SKILL LEVEL
  • Has a basic understanding of equipment and processes in their area of responsibility.
  • Can perform basic troubleshooting of equipment or process malfunctions in their area of responsibility.
  • Exercises judgment within defined procedures and practices to determine appropriate actions.
TYPICAL DEMONSTRATED PROFICIENCIES
  • Works toward qualification in either all APAP Wet End operations or all APAP Drying Tower operations.
LEADERSHIP RESPONSIBILITIES
  • No direct responsibility for the work of others
  • Normally receives general instructions on routine work and detailed instructions on new assignments.
MINIMUM REQUIREMENTS
Education

High School Diploma, GED, or equivalent required

Experience

Previous GMP manufacturing experience preferred

Preferred Skills/Qualifications
  • Must be able to communicate effectively in both verbal and written formats.
  • Must be able to read and follow detailed instructions and procedures.
  • Must be able to perform basic math.
  • Must have a working knowledge of chemical and/or powder processing equipment and associated safety requirements.
  • Must possess sound problem solving and decision-making skills.
  • Must work in a team environment to perform job tasks and cover workstations during breaks and lunches
RELATIONSHIP WITH OTHERS/ SCOPE
  • Reports to APAP Shift Supervisor in the APAP production department
  • No positions report directly to the APAP Pharmaceutical Operator I
  • Has frequent contact with: APAP production personnel, Quality (QA/QC), Safety and Maintenance
WORKING CONDITIONS
  • Must be able to wear required Personal Protective Equipment (PPE), including hard hat, safety glasses, ear plugs, steel-toe boots, gloves, chemical resistant aprons and suits, and other personal protec
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