Validation Chemist
Chattanooga, Tennessee
- 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 Validation Chemist 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.
Validation Chemist
Chattanooga, TennesseeRESPONSIBILITIES:
- Develops validation protocols for equipment, facilities, processes, and cleaning procedures.
- Plans and schedules validation activities.
- Performs validation studies per schedule and written protocols.
- Accurately accumulates, documents, and communicates data.
- Prepares and submits validation final reports.
- Audit and ensure the site is always audit ready by ensuring compliance to cGMP, SReview and approve batch records as needed to ensure quality compliance.
- Monitor and ensure on-time closures of all QMS records daily.
- Review and approve orders as they ship to ensure quality compliance.
- Available to be the first source of quality information needed by all CCI departments.
- Recognize, recommend, evaluate, and implements steps to improve procedures, SOP’s, and products.
- Complete APQR’s as needed
- Monitor and update QC method training program and method table of contents as needed.
- Assist in all customer, corporate, and regulatory audits as needed.
- Other activities as instructed from time to time.
Qualifications
- B.S. degree in Chemistry, Biology or related field.
- Proficient in the use of Microsoft suite/365.
- Must work effectively both as an individual and as a team member.
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About Us Learn more -
Career Areas Learn more
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