Analytical Metrology Chemist

Experience Required

2 years

Minimum Education Required

Master's Degree

Compensation

$91,190.58 / Yearly

Hours Per Week

40

Number Of Positions

1

Job Description

Novel Laboratories, Inc. seeks an Analytical Metrology Chemist in Somerset, New Jersey to conduct metrology analysis for pharmaceutical laboratories. Plan and execute equipment calibration, qualification, and preventative maintenance. Support site procedures and assist with equipment investigations. Review, maintain, and approve master Preventive Maintenance/Calibration schedule. Coordinate and execute preventative maintenance and calibration schedule for equipment and instrumentation used for testing in laboratory operations. Ensure that preventative maintenance and calibration records are produced and maintained in accordance with regulatory requirements. Maintain instrument inventories with preventative maintenance and calibration dates. Participate in analytical method development and method transfer activities. Participate in computer system validation activities associated with new or upgraded equipment or software packages. Review and apply continuous improvement of Standard Operating Procedures, forms, templates, and laboratories tools to ensure compliance with regulatory standards. Troubleshoot laboratory instruments. Collaborate with Quality Assurance, Quality Control, and Engineering teams for audits and CAPAs. Adhere to cGMP and safety procedures. Ensure that all chemical laboratory instruments are in calibration status. Assist in the inventory and procurement of spare parts and equipment in line with established processes, ensuring availability for planned maintenance and unplanned repairs. Annual salary: $91,190.58.

Requirements: Master’s degree in Pharmaceutical Science, Chemistry, or a related field plus 2 years of metrology experience. Must have at least 2 years of experience in each of the following: 1. Conducting metrology analysis for pharmaceutical laboratories; 2. Conducting equipment calibration; 3. Coordinating and executing preventative maintenance and calibration schedule for equipment and instrumentation used for testing in laboratory operations; 4. Ensuring that preventative maintenance and calibration records are produced and maintained in accordance with regulatory requirements; 5. Utilizing computerized standalone systems for GMP validation requirements; 6. Performing analytical method development and method transfer activity; and 7. Preparing, reviewing, and maintaining analytical method development documents, validation protocol, and reports in compliance with regulatory requirements.

To apply, please send resume to USACareers@lupin.com and cite requisition number 00181 or apply at www.lupin.com/US/.

Place of Work

On-site

Requisition ID

00181

Job Type

Full Time

Application Instructions

To apply, please send resume to USACareers@lupin.com and cite requisition number 00181 or apply at www.lupin.com/US/.