QC Analyst II
Billerica, Massachusetts
- Full Time
- Level: Entry
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Overview
You’re the one who will help us meet and exceed the quality standards that medical professionals and patients expect from us. Collaborating with like-minded, inventive colleagues, you’ll take a balanced approach, tackling challenges, learning from mistakes, and creating solutions that empower our fast-growing company. Join a workplace that’s big on open communication and fueling your career growth. When can you start?
Success Profile
What makes a great QC Analyst II at Sun Pharma? Take a look and see how you match up.
- Collaborative
- Communicator
- Detail-oriented
- Independent
- Problem-solver
- Team player
Our Culture
Discover an environment that’s open and transparent. Every day is a new opportunity to learn and grow, surrounded by powerful reminders of the impact your role has on patients’ lives. This is the Sun Pharma way of life. And we can’t wait for you to be a part of it.
Benefits
We’re in your corner – in so many different ways. Sun Pharma wants you to have the benefits, support, and rewards of a job well done.
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Career Growth
Get support for your career growth and development.
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Benefits Programs
Discover comprehensive benefits to support the health and wellness of you and your family.
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Time Off
Enjoy paid time off and leave-of-absence options.
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Compensation
Earn competitive compensation with incentive programs that reward our shared success.
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Working Conditions
Work confidently in the safe, clean, and regulated work environment that we foster.
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Team Environment
Collaborate in a workplace that’s rooted in our values and encourages cross-team engagement.
QC Analyst II
Billerica, MassachusettsJob Summary:
Performs various quality control tests on raw materials, in-process and final product using Standard Operating Procedures (SOPs) and works in accordance with current Good Manufacturing Practices (cGMPs). Monitors and evaluates systems, equipment, records and trends data. Review/revise documentation (i.e. SOPs). Works under limited supervision following established procedures.
Areas of Responsibility:
Perform release, stability, validation and complaint (follow-up) 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
Monitor, calibrate, maintain and evaluate systems or equipment (i.e. water systems, environmental chambers, analytical instrument/equipment)
Analyze data and interpret results
Maintain data records in manual or computer based logs following GDPs
Revise SOP documentation
Send samples to contract laboratories and collect test data
Wash glassware, prepare reagents, solutions, equipment for chemical tests and assays
Provide training to junior analysts on laboratory tests and skills
Able to operate complex laboratory instrumentation to analyze product
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
Job Qualifications and Experience:
B.S. in a related scientific major required
Good oral and written communication skills
Ability to follow specific instruction and report assay results (i.e. written SOPs)
Proficient with wet chemical methods and tests (USP, ACS, Titration, Limit tests, etc.)
Fundamental knowledge of chemical principles
Proficient with basic laboratory instrumentation
Understanding of cGMPs and GLPs
Strong analytical skills with attention to detail
Able to perform basic troubleshooting and repair of complex instrumentation
Proficient computer skills including word processing and spread sheet programs
Minimum 2-4 years related experience
Use of Trackwise, Novatech, and Empower software
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About Us Learn more -
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