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Manufacturing
Quality Control Analyst
Billerica, MA
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Sun Pharmaceutical Industries Ltd

Senior QC Analyst

Job Description

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 Travel Estimate 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

Working knowledge of cGMP/GLP

Benefits

  • Dental Insurance
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