Senior QC Analyst

Sun Pharmaceutical Industries, Inc.; Billerica (MA); On-site; USD 85,000 - 110,000; Full time

Job summary

Sun Pharmaceutical Industries, Inc. (USA) is seeking a QC Analyst to perform GMP testing of raw materials, in-process and finished products, following established procedures. The role includes monitoring data, reviewing documentation, and working under limited supervision.

You will calibrate and maintain systems, develop IQ/OQ/PQ protocols, and mentor junior analysts while ensuring cGMP compliance and contributing to continuous improvement in QC operations.

Qualifications

• B.S. or equivalent degree in chemistry or related field.
• Excellent oral and written and interpersonal communication skills.
• Fundamental knowledge of chemical principles and analytical instrumentation.
• Ability to follow SOPs and instructions precisely.
• Proficient with wet chemical methods and instrumentation (USP/EP).
• Proficient computer skills (word processing, spreadsheets, instrumentation software).
• Able to troubleshoot analytical instruments and maintain calibration programs.

Responsibilities

• Perform release, stability, validation, and QC tests on raw materials, in-process, and final products per GLPs.
• Perform QC tests and assays using USP and EP methods.
• Document and follow up on assay issues and investigations (Trackwise).
• Calibrate, monitor, maintain, and evaluate laboratory systems and equipment.
• Maintain data logs in compliance with GDPs and cGMP."
• Develop, author, and execute IQ/OQ and PQ protocols for instruments.
• Provide mentoring and training to junior analysts.
• Lead monthly equipment maintenance and participate in lab inspections.

Skills

Oral and written communication

Interpersonal communication

Analytical instrumentation knowledge

Wet chemistry methods

HPLC/GC

Education

Bachelor's degree in Chemistry or related

Tools

Trackwise

Novatech

Empower

Job description

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Company: Sun Pharmaceutical Industries, Inc (USA)

Job Summary

Performs GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. Monitors and evaluates systems, equipment, records and trends data. Reviews and revises documentation (i.e. SOPs). Works under limited supervision following established procedures.

Area Of Responsibility

• Perform release, stability, validation, analytical quality control tests and assays on raw materials, in-processing and final products following GLPs
• Perform quality control tests and assays including USP test methods and EP test methods
• Conduct, document and follow up on assay issues, failures and complaint investigations (Trackwise)
• Calibrate, monitor, maintain and evaluate systems and equipment (i.e. water systems, environmental chambers, analytical instrument/equipment)
• Maintain data in manual or computer based logs following GDPs
• Develop, author, and execute instrument IQ/OQ and PQ protocols
• Maintain major laboratory programs (i.e. calibration program, reference standard program)
• Serve as liaison to service, calibration and technical representatives
• Send samples to contract laboratories and collect test data
• Wash glassware, prepare reagents, solutions, equipment for chemical tests and assays
• Maintain laboratory in cGMP compliance and conduct internal lab inspections
• Record and review GMP data, monitor and evaluate QC systems and equipment, recommend improvements to procedures, and revise GMP documentation as required
• Serve as a leader within the QC group and a knowledge resource within the company
• Provide mentoring and training to junior analysts on laboratory tests, skills, and lab processes
• Perform monthly equipment/instrument maintenance and cleaning
• Follow work-flow procedures from receiving test samples, monitoring inventories, to waste disposal
• Train towards Visual Inspection qualifications
• Other duties as assigned

Work Conditions:

• Office
• Lab
• Noise, heat, open flame and radiation in specific areas requiring appropriate safety equipment (i.e. gloves, lab coat, safety glasses and respirator)
• Work with non-hazardous and hazardous chemicals, toxic metals, cryogenic gases and radioactive materials.
• Exposure to or use of syringes and needles
• Requires access/work in chemical fume hoods
• Requires access/work in class 100K, 10K or 100 clean room (mask and boots in conformance with environmental dress codes)

Physical Requirements:

• Stand, walk, sit, use hands and fingers to handle or feel, reach with hands and arms, climb or balance, stoop, kneel, crouch or crawl, hear and talk
• Close vision
• Lift up to 25 lbs.
• Operates computer/office machines
• Ability to wear Personal Protection Equipment

Up to 5%

Education and Job Qualification

• B.S. or equivalent experience
• Excellent oral and written and interpersonal communication skills
• Fundamental knowledge of chemical principles and analytical instrumentation
• Ability to follow specific instruction (i.e. written SOPs)
• Proficient with wet chemical methods and tests (USP, ACS, Titration, Limit tests, etc.)
• Proficient knowledge of basic and complex laboratory instrumentation (theory, function, basic and complex troubleshooting)
• Strong analytical skills with attention to detail
• Able to troubleshoot and repair complex instrumentation
• Proficient computer skills including word processing, spreadsheet, and instrumentation control software programs
• Able to perform standard and non-standard analytical techniques to analyze product
• Proficient in use of Balances, Ultraviolet/Visible (UV/VIS) Spectrometer, Conductivity Meter, TOC Meter, pH Meter, Autotitrator, Karl Fischer Titrator, High temperature furnaces and oven, Fume hoods, Stirrer/hot plates, Propane burners, Compressed Gas Regulators and Cylinders, Melting Point, Infrared (IR), Gamma Ray Spectrometer and RCP assays, Flame Atomic Absorption (AA), Polarograph, Osmometer, High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC)

Experience

• Minimum 5-7 years of related experience
• Use of Trackwise, Novatech, and Empower software
• Experience with qualitative and quantitative analysis using good analytical laboratory practices