Quality Control Chemist
At Elvis Eckardt Recruitment & Sales Solutions Limited, we're not just your average recruiters or HR professionals.
We're a team driven by passion, committed to revolutionizing the way you experience recruitment and HR.
With over a decade of hands-on experience, we've honed our craft and specialize in delivering exceptional Recruitment and HR Solutions to SMEs, Start-Ups, and even the industry giants like the Big Four.
Our journey started from the ground up, and that's what makes us stand out – we're a bootstrapped endeavour that's all about connecting with businesses and candidates alike on a personal level.
We understand that one size doesn't fit all. That's why our approach to recruitment goes beyond the mundane.
Our aim is simple, yet profound – to exceed your expectations and create tailor-made, practical, and memorable experiences for you, whether you're a client looking for the perfect addition to your team, a candidate seeking the next big opportunity, or a partner sharing our vision.
At the heart of our mission is the drive to add real value to your operations. We're not here to simply provide solutions; we're here to optimize your entire Recruitment and sales processes, helping you achieve your goals more effectively.
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Let's make this personal. Reach out to us today at [email protected], and let's embark on this exciting journey together – where Recruitment and Sales Solutions meet a personal touch.
The Role
Role: Quality Control Chemist
Location: Central Islip, NY, USA
Industry: Pharmaceuticals/Biotechnology/Clinical Research
Type: Full-Time | Onsite | General Shift: 8:30 AM – 5:00 PM
Experience Required: 2 – 15 years
Visa Status: Only US Citizens and Green Card Holders. No employment sponsorship or visa transfers.
Relocation Support: Up to USD 6,000 provided for eligible candidates.
About The Job:
We are seeking a QC Chemist I with a solid background in pharmaceutical Quality Control testing.
The role is suited for professionals who are detail-oriented, analytically skilled, and experienced in handling a variety of testing techniques within a cGMP-regulated environment.
Key Responsibilities:
- Conduct in-process testing (e.g. weight, thickness, hardness, disintegration, friability) in accordance with manufacturing batch record instructions.
- Perform routine and advanced testing of raw materials and finished products.
- Operate instruments including Karl Fisher, HPLC, GC, Particle size, and ICP.
- Ensure adherence to data integrity and cGMP documentation practices.
- Lead or assist in investigations and lab documentation processes.
- Collaborate with team members to support timely and compliant laboratory operations.
Work Conditions:
- Must be comfortable working in a regulated lab with PPE (e.g., lab coats, goggles, masks).
- Ability to stand/walk unaided for long periods and lift up to 10 kg.
- Must be open to shift flexibility and occasional weekend work as required.
Application Process:
To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling basis, so early submissions are encouraged.
Equal Opportunity Employer:
We value diversity and are committed to creating an inclusive work environment. We encourage applicants from all backgrounds to apply.
Contact: Elvis Eckardt
Ideal Profile
MUST HAVE Qualifications:
- Bachelor’s degree (BS or BA) in Chemistry or a Physical Science discipline.
- Experience in the pharmaceutical industry (strictly no bio-pharma).
- Educational background in Chemistry (BS/BA preferred).
- Working knowledge of Inhalation products (MDI) is a plus (also open to experience with tablets, capsules, liquids, and solids).
- Familiarity with key instruments: Karl Fisher, HPLC, GC, Particle Size Analysis, ICP.
- Strong English proficiency (spoken, written, and reading) for scientific documentation.
What's on Offer?
- Work in a company with a solid track record of performance
- Flexible working options
- Opportunity to make a positive impact
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