Calibration Technician II

Be the First to Apply

Division
Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.
Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Calibration Technician II Job Description
The Calibration Technician II is responsible for performing calibration, preventive maintenance, troubleshooting, and documentation activities for manufacturing, laboratory, process, and utility equipment. This role ensures instrumentation and equipment remain compliant with GMP, regulatory, and company requirements while supporting safe and efficient operations. Essential Duties & Responsibilities

- Perform calibration activities on process, utility, laboratory, and manufacturing instrumentation, including temperature, pressure, flow, conductivity, pH, humidity, level, and weight measurement devices.

- Execute preventive maintenance and calibration work orders in accordance with approved procedures and schedules.

- Troubleshoot instrumentation and control system issues and implement corrective actions as needed.

- Support equipment installation, commissioning, qualification, and validation activities.

- Maintain calibration documentation and records in accordance with GMP requirements and data integrity standards.

- Complete and review work orders within the site's computerized maintenance management system (CMMS).

- Support investigations and corrective actions related to calibration or instrumentation deviations.

- Partner with Manufacturing, Quality, Engineering, and Facilities teams to resolve equipment issues and maintain operational readiness.

- Ensure compliance with all applicable site safety, environmental, quality, and regulatory requirements.

- Participate in continuous improvement initiatives to enhance equipment reliability and operational efficiency.

- Perform other duties and responsibilities as assigned to support departmental objectives and business needs.

Education & Experience

- Associate degree in Instrumentation, Electronics, Engineering Technology, Industrial Maintenance, or a related technical discipline preferred.

- 2-3 years of calibration and instrumentation experience in a pharmaceutical, biotechnology, medical device, chemical, or other regulated manufacturing environment.

- Equivalent combinations of education and relevant experience may be considered.

Knowledge, Skills & Abilities

- Knowledge of calibration principles, instrumentation, and related equipment.

- Ability to read and interpret P&IDs, electrical schematics, wiring diagrams, and technical manuals.

- Familiarity with GMP regulations and documentation requirements.

- Experience troubleshooting electrical, mechanical, and instrumentation systems.

- Proficiency with CMMS systems and Microsoft Office applications.

- Strong organizational skills and attention to detail.

- Ability to prioritize workload and work independently with minimal supervision.

- Effective verbal and written communication skills.

- Strong teamwork and collaboration skills.

Physical Requirements

- Ability to stand, walk, bend, kneel, and climb ladders for extended periods.

- Ability to work in manufacturing, laboratory, and utility environments.

- Ability to lift up to 50 pounds.

- Ability to wear required personal protective equipment (PPE).

Work Environment
This position operates in a GMP-regulated pharmaceutical manufacturing environment and may require occasional off-shift, weekend, or on-call support based on business needs.