Astrix Jobs

Analytical Scientist

Laboratory

Johns Creek, GA, US

• Added - 29/03/2024

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Our client is a leading provider committed to women’s healthcare and medical services and is excited to share they are looking for a new Analytical Scientist to join their growing team! This is a great opportunity for a professional analytical chemist with 3-5 years of experience in the medical device, pharmaceutical, or biotech industries.

As an Analytical Scientist, you will be responsible for performing analytical tests to support production and research & development. You will assist in managing the QA Analytical Chemistry Laboratory with their equipment & supplies and participate in projects related to analytical chemistry within product development.

Schedule: 1 st Shift: Monday-Friday, 8am-5pm (with flexibility to work 9am-6pm)

Direct Hire

Responsibilities :

• Organize and maintain laboratory area(s) including equipment parts and consumable supplies in accordance with GMP regulations.

• Initiate, track, and perform routine instrument maintenance, calibrations, and performance troubleshooting, with appropriate documentation in the Quality System.

• Support manufacturing, research and development, and quality assurance in the production, monitoring, and release of medical device products; i.e. set up apparatus for chemical reactions, prepare compounds, monitor commercial production and collect and analyze samples produced and standards by Gas Chromatograph/ HPLC/ titration/ etc.

• Analyze and review data generated prior to submitting the data to the next level of review, including performing routine data calculations.

• Manage OOS/ OOT process in order to identify causes of test failures and detect test result trends.

• Adhere to analytical procedures, quality control protocols, and GMP documentation processes as required by specific methodologies.

• Assist R&D in test method development for QA/ QC related analytical tests.

• Assist with chemical safety program through the management of chemical inventory and Safety Data Sheets.

• Manage test method validation process, leading the efforts to maintain test method validation.

• Assist with process validation activities through protocol and report review/ approval.

• Lead analytical method development activities.

• Support quality assurance activities by performing internal audits, quality inspections, and other quality functions as determined by management.

Education/Experience:

• B.S. in Chemistry or related field.

• Three (5) years’ experience in medical device, pharmaceutical or biotech industry working in Good Manufacturing Practices (GMP) laboratories.

• Must have a strong technical knowledge and experience in the use of GC, HPLC, titrations, pipetting and dilutions, etc.

• Must have a strong technical knowledge and experience in equipment care, maintenance, and troubleshooting performance of GC and HPLC equipment and parts.

Physical Requirements

• Good vision

• Good manual dexterity

• Ability to lift over 25 lbs.

* _This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you_*

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We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.