Description
JOB SUMMARY
Support quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to providing general laboratory support for raw material, stability and finished product testing, as well as QA support in AQL inspection and batch release.
ESSENTIAL DUTIES & RESPONSIBILITIES
Comply with all laboratory safety guidelines, both written and implied. Inform management of any safety concerns.
Support the daily operations of laboratory as needed.
Maintain equipment logbooks and other forms to document proper cleaning and use of lab equipment.
Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice.
Stock and maintain laboratory supplies. Monitors inventory levels and order or secure supplies as needed.
Maintain laboratory environment in orderly, operable condition.
Use appropriate respiratory equipment to complete assigned tasks.
Duties will include basic laboratory testing, sample and standard preparation, reagent preparation and maintenance, analysis.
Monitor calibration and expiration dates to ensure compliance with laboratory procedures.
Document generation and filing for QC laboratory
The individual will be required to produce accurate and timely deliverables following appropriate laboratory procedures.
Open to a flexible and fluid work environment. Work on any assignment as directed.
Support Agency, customer and vendor audits as needed.
Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices.
Perform all other tasks, projects, and duties as assigned.
Requirements
DESIRED SKILLS & ABILITIES
Energetic, self-motivated, organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment.
Results oriented and efficient; Acts with a sense of urgency.
Ability to work with a diverse customer base.
Strong attention to detail; Ability to complete tasks with accuracy and efficiency.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Portrays appropriate levels of integrity and professionalism.
Excellent written and verbal skills; Ability to communicate effectively with management, staff, and regulatory agencies by exhibiting excellent interpersonal skills.
Energetic, self-motivated, organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment.
Creative and open-minded individual who fosters an environment in which sharing of ideas is encouraged.
Ability to work well independently and in a cross-functional team environment.
Must have proficient computer skills in Microsoft Word, Excel, and Outlook.
Basic laboratory skills.
Qualified visual inspector or able to become qualified.
Qualified candidates have attained a Bachelor's degree in a related field (e.g. Biochemistry, Biotechnology) and/or applicable professional experience. This is the perfect entry level role for new graduates eager to start their career in a lab setting.
GRAM supports Equal Opportunity Employment