Job summary
Job post source
This job is directly from Alcami Corporation
Job overview
The Sr. Scientist I at Alcami Corporation performs analytical testing and method development to support pharmaceutical product development and manufacturing, impacting product quality and regulatory compliance.
Responsibilities and impact
The role involves developing, validating, and transferring analytical methods using HPLC, CE, icIEF, and UV, performing GMP reviews, analyzing data for accuracy, writing protocols and reports, maintaining lab safety and equipment, and handling hazardous materials.
Experience and skills
Requires a Bachelor's degree with 8+ years, Master's with 4+ years, or Ph.D. with 2+ years of experience, including 2+ years in pharmaceutical drug product development under cGMP; CDMO experience is preferred. Strong communication, problem-solving, organizational skills, and proficiency with lab software and Microsoft Office are essential.
Work environment and culture
The company emphasizes a safe, clean, and organized work environment with adherence to cGMP and safety protocols, including handling potent compounds and hazardous waste.
Company information
Alcami Corporation specializes in delivering solutions for pharmaceutical development and commercialization with industry expertise and regulatory experience.
Job location and travel
This is a 100% on-site position working first shift Monday to Friday, 8:00am to 5:00pm, with up to 5% domestic travel.
Unique job features
The position requires expertise in multiple analytical techniques and compliance with stringent safety and regulatory standards, including handling hazardous waste and potent compounds.
Company overview
Alcami Corporation is a leading contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical development and manufacturing services. They make money by offering a range of services including drug product development, analytical testing, and commercial manufacturing to pharmaceutical and biotechnology companies. Founded in 1979, Alcami has a rich history of innovation and expansion, including strategic acquisitions to enhance their service offerings and global reach. Their expertise spans across various therapeutic areas, making them a vital partner in bringing new drugs to market efficiently and safely.
How to land this job
Tailor your resume to highlight your expertise in analytical techniques such as HPLC (SEC, AEX, CEX), CE, icIEF, and UV methodologies, emphasizing your experience with method development, validation, and GMP compliance to align with Alcami Corporation's Sr. Scientist I role.
Showcase your proficiency in pharmaceutical product development under cGMP conditions, including your ability to interpret analytical data, write detailed protocols and reports, and maintain laboratory safety and documentation standards, as these are key responsibilities.
Apply through multiple platforms including Alcami Corporation’s official career page and LinkedIn to maximize your application visibility and increase chances of consideration for the position.
Network by connecting with current employees in the analytical sciences or pharmaceutical development divisions at Alcami Corporation on LinkedIn; start conversations with ice breakers such as commenting on recent Alcami projects, asking about their experience working with specific methodologies like icIEF or HPLC, or expressing enthusiasm about their commitment to cGMP and quality standards.
Optimize your resume for ATS by incorporating keywords from the job description such as 'HPLC,' 'method validation,' 'cGMP,' 'pharmaceutical product development,' 'analytical methodology,' and specific instruments like 'Empower3' and 'ProCal' to ensure your resume passes initial automated screenings.
Use Jennie Johnson’s Power Apply feature to automate tailoring your resume, applying across multiple job boards, and identifying relevant LinkedIn contacts to message, giving you more time to prepare for interviews and refine your professional skills.
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