Production Operator
Job in
Cedar Rapids, Linn County, Iowa, 52404, USA
Listed on 2026-09-09
Listing for:
JRS Pharma LP
Full Time
position Listed on 2026-09-09
Job specializations:
-
Manufacturing / Production
Production QC/QA, Pharmaceutical Manufacturing, Production Associate / Production Line
Job Description & How to Apply Below
JRS Pharma LP is seeking a Production Operator to join our Manufacturing & Production team in the pharmaceutical industry. In this role, you will operate and monitor production equipment, follow strict GMP and safety standards, complete batch records, and support routine cleaning and changeovers. You will work closely with cross-functional teams to ensure product quality, line efficiency, and on-time delivery. JRS Pharma LP offers an inclusive, growth-focused culture with opportunities to expand your skills, participate in continuous improvement initiatives, and advance your manufacturing career.
Responsibilities
- Operate, monitor, and troubleshoot pharmaceutical production equipment in accordance with batch records and standard operating procedures (SOPs).
- Set up, calibrate, and change over machinery for different production runs while minimizing downtime and material loss.
- Follow Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and all FDA/EMA regulatory guidelines during production activities.
- Accurately complete batch records, logbooks, and electronic production documentation to ensure full traceability and compliance.
- Perform in-process quality checks, including visual inspections, weight checks, and sampling, and promptly report any deviations or nonconformances.
- Maintain a clean, organized, and safe work area, adhering to site safety policies, personal protective equipment (PPE) requirements, and 5
- S principles.
- Collaborate closely with quality assurance, maintenance, and planning teams to meet daily production schedules and targets.
- Assist in equipment cleaning, line clearance, and basic preventive maintenance to ensure readiness for subsequent batches.
- Participate in continuous improvement initiatives, including root cause analysis and process optimization projects, to improve yield and reduce defects.
- Support training of new team members by demonstrating standard work practices and reinforcing a culture of quality and safety.
Required Skills
- Operation of pharmaceutical or chemical production equipment (granulators, tablet presses, blenders, coating machines, or similar).
- Understanding of c
- GMP, GDP, and basic FDA/EMA regulatory requirements.
- Ability to read and follow technical documents, batch records, and SOPs with strong attention to detail.
- Basic mechanical aptitude for equipment setup, changeover, and minor troubleshooting.
- Use of measuring tools, scales, and basic test instruments for in-process checks.
- Basic computer skills for electronic batch records, data entry, and learning management systems.
- Knowledge of safety practices in a manufacturing environment, including handling chemicals and use of PPE.
- Ability to work in a fast-paced, team-based environment with rotating shifts if required.
- Strong written and verbal communication skills for documenting work and escalating issues.
- Time management and organizational skills to meet production deadlines while maintaining quality.
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